Gene editing in primary immune cells using a cell membrane-permeable CRISPR-CAS system

Abstract

The present disclosure provides compositions and methods for in vitro and in vivo gene editing using a cell-membrane-permeable CRISPR-Cas system comprising a cell-membrane-permeable Cas and an endosomal escape peptide. TIFF2024520644000034.tif94128

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 63 / 196,144, filed June 2, 2021, which is incorporated by reference in its entirety.

[0002] STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT This invention was made with Government support under Grants AI117950, AI108565, and CA077831 awarded by the National Institutes of Health. The Government has certain rights in this invention. [Background technology]

[0003] 2. Background of the Invention CRISPR-Cas system provides a useful tool for gene editing.However, many methods for editing primary T cells require electroporation, which may cause off-target effects on genome and can be expensive.There is a need in the art for a CRISPR-Cas system that can achieve high gene editing efficiency both in vitro and in vivo, and is less expensive and can be more easily introduced into experimental workflow.The present invention addresses this need. Summary of the Invention

[0004] SUMMARY OF THE PRESENT APPLICATION As described herein, the present disclosure provides compositions and methods for peptide-assisted genome editing (PAGE). In one aspect, the present disclosure provides a peptide-assisted genome editing (PAGE) system, comprising (a) a CRISPR-associated (Cas) protein linked to a cell membrane-permeable peptide (CPP), and (b) an endosomal escape peptide linked to the CPP.

[0005] In some embodiments, Cas is Cas9 or Cas12a or a Cas derivative. In some embodiments, Cas derivative is a Cas protein linked to another protein or catalytic domain. In some embodiments, the protein or catalytic domain is selected from the group consisting of AID deaminase, APOBEC deaminase, TadA deaminase, TET enzyme, DNA methyltransferase, transactivation domain, reverse transcriptase, histone acetyltransferase, histone deacetylase, sirtuin, histone methyltransferase, histone demethylase, kinase, and phosphatase.

[0006] In some embodiments, the endosomal escape peptide comprises any of the amino acid sequences set forth in SEQ ID NOs: 1434-1523. In some embodiments, the endosomal escape peptide comprises dTAT-HA2.

[0007] In some embodiments, the Cas comprises a nuclear localization signal (NLS) sequence. In some embodiments, the NLS sequence comprises the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). In some embodiments, the NLS sequence further comprises a GGS linker.

[0008] In some embodiments, the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10-1422. In some embodiments, the CPP comprises a sequence derived from the transactivating transcription activator (Tat) from HIV-1. In some embodiments, the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO:2).

[0009] Another aspect of the present disclosure provides an in vitro method of gene editing, comprising: introducing a PAGE system and at least one sgRNA or crRNA into a cell, wherein the PAGE system comprises a Cas protein linked to a CPP and an endosomal escape peptide linked to the CPP.

[0010] Another aspect of the present disclosure provides an in vivo method of gene editing, comprising: introducing a PAGE system and at least one sgRNA or crRNA into a cell, wherein the PAGE system comprises a Cas protein linked to a CPP and an endosomal escape peptide linked to the CPP, and administering the cell to a subject.

[0011] In some embodiments, Cas is Cas9 or Cas12a or a Cas derivative. In some embodiments, Cas derivative is a Cas protein linked to another protein or catalytic domain. In some embodiments, the protein or catalytic domain is selected from the group consisting of AID deaminase, APOBEC deaminase, TadA deaminase, TET enzyme, DNA methyltransferase, transactivation domain, reverse transcriptase, histone acetyltransferase, histone deacetylase, sirtuin, histone methyltransferase, histone demethylase, kinase, and phosphatase.

[0012] In some embodiments, the endosomal escape peptide comprises any of the amino acid sequences set forth in SEQ ID NOs: 1434-1523. In some embodiments, the endosomal escape peptide comprises dTAT-HA2.

[0013] In some embodiments, the Cas comprises an NLS sequence. In some embodiments, the NLS sequence comprises the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). In some embodiments, the NLS sequence further comprises a GGS linker.

[0014] In some embodiments, the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10-1422. In some embodiments, the CPP comprises a sequence derived from the transactivating transcription activator (Tat) from HIV-1. In some embodiments, the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO:2).

[0015] In some embodiments, the method does not require electroporation. In some embodiments, the PAGE system is introduced into the cells in serum-free medium. In some embodiments, the endosomal escape peptide is introduced into the cells at a concentration of about 25-75 μM. In some embodiments, the Cas is introduced into the cells at a concentration of about 0.5-5 μM.

[0016] In some embodiments, the cell is an immune cell.

[0017] In some embodiments, the cells are selected from the group consisting of primary human CD8 T cells, human iPSCs, and CAR T cells.

[0018] In some embodiments, the sgRNA targets Ano9, Pdcd1, Thy1, Ptprc, PTPRC, or B2M.

[0019] In some embodiments, the subject is in need of treatment for a disease or disorder, and when the edited cells are administered to the subject, the disease or disorder is treated in the subject.In some embodiments, the disease or disorder is an infection.In some embodiments, the disease or disorder is associated with T cell exhaustion. [Brief description of the drawings]

[0020] The above and other features and advantages of the present invention will be more fully understood from the following detailed description of illustrative embodiments, taken in conjunction with the accompanying drawings.

[0021] [Figure 1A] FIG. 1A: Schematic for the generation of the TAT-4xMyc NLS-Cas9 expression construct. [Figure 1B] Figure 1B: Purification of TAT-4xMyc NLS-Cas9. The TAT-4xMyc NLS-Cas9 expression construct was transformed into Rosetta 2 (DE3) pLysS and induced with IPTG. Lane 1: bacterial lysate after IPTG induction; lane 2: flow-through of Strep-Tactin affinity purification; lane 3: flow-through after in-column digestion with SUMO protease ULP1; lane 4: TAT-4xMyc NLS-Cas9 after IEC (HiTrap SP HP); lane 5: TAT-4xMyc NLS-Cas9 after SEC (Superdex 200 increase 10 / 300 GL). [Figure 1C]Figure 1C: In vitro cleavage assay by TAT-4xMyc NLS-Cas9. Cas9 RNP was assembled by incubating purified spCas9 or TAT-4xMyc NLS-Cas9 with sgRNA targeting a 8.7 kb DNA fragment, and Cas9 RNP was incubated with the DNA fragment for 1 minute, 5 minutes, 10 minutes, and 15 minutes at 37 degrees. The reaction was stopped, and the DNA products were separated in a 0.8% agarose gel. An uncut band (approximately 8.7 kb) and two kinds of cut bands (approximately 2.7 kb and approximately 6 kb) are shown on the gel. [Figure 2A] Figure 2A: Schematic of the EL4 mCherry reporter cell line used for Cas9 editing efficiency and experimental workflow. EL4 cells were infected with a lentiviral reporter construct stably expressing mCherry and an sgRNA targeting mCherry. When incubated with TAT-4xMyc NLS-Cas9 and dTAT-HA2, the cells lost mCherry fluorescence as measured by flow cytometry, leading to an increased frequency of mCherry-cells after 4 days. [Figure 2B] Figure 2B: Higher concentrations of endosomal escape peptide (dTAT-HA2) and TAT-4xMyc NLS-Cas9 increased the editing efficiency. EL4 reporter cells were incubated for 1 h in the absence or presence of 10 μM or 40 μM dTAT-HA2 and in the absence or presence of 0.5 μM or 4.0 μM TAT-4xMyc NLS-Cas9. Complete medium was replaced after incubation, and flow analysis was performed after 4 days of incubation. [Figure 2C]Figure 2C: Low FBS increased editing efficiency. EL4 reporter cells were incubated for 1 hour in the presence of 10% FBS or in the absence of FBS, in the absence or presence of 10 μM or 40 μM dTAT-HA2, and in the absence or presence of 0.5 μM or 4.0 μM TAT-4xMyc NLS-Cas9. Flow analysis was performed after 4 days of incubation. [Figure 2D] (D) EL4 reporter cells were incubated for 30 min in the presence or absence of 75 μM dTAT-HA2 and / or 5.0 μM TAT-4xMyc NLS-Cas9 in the presence or absence of 10% FBS or FBS. Flow analysis was performed after 4 days of incubation. [Figure 3A] Figure 3A: Testing the efficiency of CD45.2 sgRNA in RN2-Cas9 cells. RN2-Cas9 cells stably expressing Cas9 were infected with a retrovirus expressing mCherry and an sgRNA targeting the cell surface marker CD45.2, or with a retrovirus expressing mCherry and a control sgRNA targeting Rosa26. CD45.2 expression levels were measured by flow cytometry 3 days after infection. [Figure 3B] FIG. 3B: Schematic of the experiment showing in vitro editing with TAT-4xMyc NLS-Cas9 in mouse primary T cells. [Figure 3C] FIG. 3C: An example of a flow plot showing the percentage of sgRNA+Cas9+ for Rosa and CD45.2. [Figure 3D] Figure 3D: Target gene is knocked down between days 1 and 5 of in vitro culture as measured by flow cytometry. [Figure 3E](Figure 3E) Normalized MFI of GFP(TAT-4xMyc NLS-Cas9) of sorted sgRNA+ cells during in vitro culture. The MFI of sgRNA+ cells is normalized to the MFI of sgRNA+ cells that did not receive TAT-4xMyc NLS-Cas9 treatment. [Figure 4A] Figure 4A: Schematic of the workflow showing in vivo editing by TAT-4xMyc NLS-Cas9 in mouse primary T cells. CD8 P14 cells from donor mice were isolated and activated, while recipient mice were infected with LCMV clone 13 on day -2. 24 hours later (day -1), cells were infected with retroviral vectors (VEX+) expressing sgRNAs targeting Ano9 or expressing sgRNAs targeting Pdcd1 (encoding PD-1) for 24 hours. Cells were then treated with TAT-4xMyc NLS-Cas9, dTAT-HA2, 0.25% trypsin, and DNase I, and sgRNA+Cas9+(VEX+GFP+) P14 cells were sorted. 5 x 104 sorted cells were adoptively transferred into recipient mice infected with LCMV clone 13. Six days later, spleens and livers were harvested and analyzed by flow cytometry for PD-1 expression levels and expansion of P14 cells. [Figure 4B] Figure 4B: Flow plot of Cas9GFP+ transduction into sgRNA+ P14 cells. [Figure 4C] (C) Histograms and statistical analysis of PD-1 knockdown efficiency of P14 cells in the liver and spleen on day 6 after cell transplantation. Ano9_e3.2 sgRNA is used here as a control. [Figure 4D] FIG. 4D: Knockdown of PD-1 induces T cell expansion in the liver and spleen 6 days after cell transfer. [Figure 5A]Figure 5A: Schematic of the workflow showing in vitro editing with TAT-4xMyc NLS-Cas9 in human primary T cells. Human total T cells were isolated from PBMCs of normal donors and activated with CD3 / CD28 Dynabeads, IL-2, and IL15 on day 0. After 24 hours (day 1), cells were infected with lentiviral reporter constructs for 2 days as in Figure 2A. mCherry+ cells were selected by blasticidin on days 3-9 and subsequently treated with TAT-4xMyc NLS-Cas9 and dTAT-HA2. The frequency of mCherry- cells was measured on days 12-14 by flow cytometry. [Figure 5B] Figure 5B: The percentage of mCherry-human T cells was measured by flow cytometry on days 3 and 5 after treatment of cells with dTAT-HA2 and TAT-4xMyc NLS-Cas9. T cells were isolated from three normal donors. [Figure 5C] FIG. 5C: An example histogram of mCherry-human T cells on day 5 after treatment of cells with 0.5 μM TAT-4xMyc NLS-Cas9 and 50 μM dTAT-HA2. [Figure 6A] Figure 6A: iPSCs were infected with the same lentiviral reporter constructs as in Figure 2A. When incubated with TAT-4xMyc NLS-Cas9 and dTAT-HA2, the cells lost mCherry fluorescence as measured by flow cytometry, resulting in an increased frequency of mCherry-cells after 4 days. [Figure 6B] FIG. 6B: An example histogram of mCherry- iPSCs on day 4 after treatment of cells with dTAT-HA2 and TAT-4xMyc NLS-Cas9. [Figure 7]Figure 7: Schematic diagram of peptide-assisted genome editing (PAGE) system constructs used in this study. TH is dTAT-HA2; T is TAT; H is HA2; Cas9-T6NCPP is TAT-4xNLSMYC-Cas9-2xNLSSV40-sfGFP; Cas9-T8NCPP is TAT-6xNLSMYC-Cas9-2xNLSSV40-sfGFP; Cas9-TH6NCPP is TAT-HA2-4xNLSMYC-Cas9-2xNLSSV40-sfGFP; Cas9-R6NCPP is R9-4xNLSMYC-Cas9-2xNLSSV40-sfGFP; Cas9-6NCPP is 4xNL opCas12a-T8NCPP is TAT-6xNLSMYC-opCas12a-2xNLSSV40-sfGFP; Cas9-BE-T6NCPP is TAT-4xNLSMYC-evoA1-nCas9-2xNLSSV40-sfGFP; RNP is ribonucleoprotein; sgRNA is single-stranded guide RNA (associated with Cas9); crRNA is crispr RNA (associated with opCas12a); P14 is LCMV-P14 T cell receptor; Cas9-BE is Cas9 base editor; d2GFP is destabilized GFP fluorescent protein. [Figure 8A]Figures 8A-8E: Optimization of peptide-assisted cell membrane permeable Cas9 system in EL4 reporter cells. Figure 8A: Schematic diagram of EL4 mCherry reporter cell line used for editing efficiency of Cas9-CPP. EL4, mouse T lymphoblasts, were lentivirally transduced with a dual expression vector stably expressing mCherry (mChe) fluorescent reporter and sgRNA targeting mCherry gene or with a dual expression vector stably expressing mCherry (mChe) fluorescent reporter and sgRNA targeting Ano9 gene as a negative control. EL4-mChe cells were incubated with various Cas9-CPP proteins as well as various endosomal escape or cell membrane permeable chemicals and peptides. Proteins, chemicals, and peptides were washed off after 30 min of incubation. On the fourth day after treatment, gene editing efficiency was assessed based on loss of mChe fluorescence using flow cytometry. [Figure 8B] Figures 8A-8E: Optimization of peptide-assisted cell membrane permeable Cas9 system in EL4 reporter cells. Figure 8B: Quantification of editing efficiency of Cas9-T6NCPP in combination with various endosomal escape or cell membrane permeable chemicals and peptides in EL4-mChe reporter. EL4 mChe reporter cells were treated with 0.5 μM Cas9-T6NCPP in the presence of chemicals 200 mM chloroquine or 1 mg / ml polybrene, or in the presence of 75 μM supporting peptides KALA, transportan, penetratin, penetratin-Arg, dTAT-HA2E5, or TH. To measure editing efficiency, the percentage of cells that lost mCherry was measured by flow cytometry on the fourth day after treatment. Among these chemicals and CPP peptides tested, the highest percentage of mCherryOFF (>90%) was shown by incubation with TH(dTAT-HA2), suggesting that incubation with TH strongly induced gene editing. [Figure 8C]Figures 8A-8E: Optimization of peptide-assisted cell membrane permeable Cas9 system in EL4 reporter cells. Figure 8C: Western blotting for levels of Cas9-T6NCPP, lamin-B1, and α-tubulin in nuclear, cytoplasmic, and whole cell lysates prepared from EL4 cells treated with Cas9-T6NCPP and TH. EL4 cells were treated with 5 μM Cas9-T6NCPP and 75 μM TH at 37°C for 30 min. Cells were washed with PBS and trypsinized to remove Cas9-T6NCPP bound to the cell surface. Nuclear and cytoplasmic fractions were separated and subjected to immunoblotting analysis using antibodies against Cas9, nuclear marker lamin B1, and cytoplasmic marker α-tubulin. The data showed that addition of TH increased the translocation of Cas9-T6NCPP into cells, into the cytoplasmic fraction, and especially into the nuclear fraction, compared to cells without TH treatment. [Figure 8D] Figures 8A-8E: Optimization of peptide-assisted cell membrane permeable Cas9 system in EL4 reporter cells. Figure 8D: Quantification of editing efficiency of Cas9CPP variants in combination with various concentrations of TH peptide in EL4-mChe reporter. EL4 mChe reporter cells were treated with 0.5 μM Cas9CPP variants in the presence of 25-75 μM TH. To measure editing efficiency, the percentage of cells that lost mCherry was measured by flow cytometry on the fourth day after treatment. [Figure 8E] Figures 8A-8E: Optimization of peptide-assisted cell membrane-permeable Cas9 system in EL4 reporter cells. Figure 8E: Final workflow of Cas9-PAGE system for gene editing in EL4 mCherry reporter cell line. The combination of cell membrane-permeable Cas protein and endosomal escape peptide is called peptide-assisted genome editing (PAGE). [Figure 9A]Figure 9A-9E: Optimization of the Cas9-PAGE system in EL4 reporter cells. Figure 9A-9B: Quantification of gene editing efficiency using titration of either TH or Cas9-T6NCPP. The percentage of cells that lost mCherry was measured by flow cytometry on the second day after treatment. Figure 9A: EL4 mCherry reporter cells were incubated with 0.5 μM Cas9-T6NCPP and various concentrations of TH from 5 to 100 μM. The concentration of TH positively correlated with increased gene editing efficiency. [Figure 9B] Figure 9A-9E: Optimization of the Cas9-PAGE system in EL4 reporter cells. Figure 9A-9B: Quantification of gene editing efficiency using titration of either TH or Cas9-T6NCPP. The percentage of cells that lost mCherry was measured by flow cytometry on the second day after treatment. Figure 9B: EL4 mCherry reporter cells were treated with various concentrations of Cas9-T6NCPP from 0.05 to 5 μM, and TH at 75 μM. Increasing the concentration of Cas9-T6NCPP resulted in increased gene editing efficiency. [Figure 9C] Figures 9A-9E: Optimization of the Cas9-PAGE system in EL4 reporter cells. Figure 9C: Quantification of viable cell recovery of EL4 cells treated with increasing concentrations of TH. [Figure 9D] Figures 9A-9E: Optimization of the Cas9-PAGE system in EL4 reporter cells. Figure 9D: Quantification of the GFP-positive cell population as a function of increasing amounts of Cas9-T6NCPP. The percentage of GFP-positive cells is a surrogate for cell membrane permeabilization efficiency. [Figure 10]Figure 10A-10B: TH aids PAGE system in trans. Figure 10A: Quantification of gene editing efficiency when TH is truncated. TH (dTAT-HA2) peptide enhanced the editing efficiency of Cas9-T6NCPP in EL4 mCherry reporter cells, whereas neither T (dTAT) nor H (dHA2) peptides alone enhanced the editing efficiency. EL4 mCherry reporter cells were incubated with 0.5 μM Cas9-T6NCPP in the presence of 75 μM T, H, or TH peptides. The percentage of cells that lost mCherry was measured by flow cytometry on the fourth day after treatment. Figure 10B: Quantification of gene editing efficiency of Cas9-T6NCPP and gene editing efficiency of Cas9-TH6NCPP when dTAT-HA2 (TH) was added in cis. The percentage of cells that lost mCherry was measured by flow cytometry on the fourth day after treatment. TH promoted Cas9CPP in trans, regardless of whether the TH peptide was present in cis. [Figure 11] Figure 11: PAGE system for gene editing in various cell types. Quantification of the efficiency of gene editing mediated by the Cas9-PAGE system in various cell types. mCherry positive reporters were established in the indicated cell types: MOLM-13, a human myeloid cell line model, NK-92, a human natural killer cell line, and human primary T cells isolated from PBMCs of three healthy donors. mCherry reporter cells were incubated with Cas9-T6NCPP and TH as indicated for 30 min. The percentage of cells that had lost mCherry was measured by flow cytometry on the fourth day after treatment. [Figure 12A]Figures 12A-12G: Cas9-PAGE-mediated genome editing with retroviral sgRNA in primary mouse CD8 T cells ex vivo. Figure 12A: Schematic of the experimental workflow to evaluate the PAGE system ex vivo in primary mouse CD8 T cells. Primary mouse T cells were activated with anti-CD3, anti-CD28, and IL-2, followed by retroviral transduction with sgRNA expression vectors linked to mCherry fluorescent marker. mCherry-positive cells enriched by FACS sorting were incubated with Cas9-T6NCPP and TH peptide, which were then washed out after 30 min of incubation. Gene editing was assessed at various time points by flow cytometry for the indicated gene products or by direct Sanger sequencing of the targeted genomic regions. Figures 12B-12E: TH promoted gene editing by Cas9-T6NCPP in primary mouse CD8 T cells. Cells were transduced with either sgThy1_IG1 or sgNeg, followed by incubation with various concentrations of TH and 5 μM Cas9-T6NCPP for 30 min. Flow cytometry analysis was performed on the indicated days after treatment. Figure 12B: Time course analysis of CD90 protein expression in CD8 T cells treated with increasing concentrations of TH. Figure 12C: Quantification by mean fluorescence intensity (MFI) of flow cytometry analysis after 4 days of treatment as described in Figure 12B (left panel). Figure 12D: Representative flow cytometry plot of CD90 after 4 days of treatment in cells transduced with either sgThy1_IG1 or sgNeg. Figure 12E: Quantification of viable cell recovery of CD8 T cells treated with increasing concentrations of TH. FIG. 12F: Schematic bar graph of gene editing efficiency in mouse primary CD8 T cells at day 4 post-treatment for PAGE with additional sgRNA targeting Thy1 gene and PAGE with additional sgRNA targeting Ptprc gene.Figure 12G: Tracking of Indels by DEcomposition (TIDE) mutagenesis assay for PAGE sgRNAs used in Figure 12F. Dot plots show TIDE assay scores (% of indels) for the indicated sgRNAs. Genomic DNA was isolated on day 6 after PAGE and Sanger sequenced, followed by quantification with the online TIDE analysis tool. sgThy1_IG1, sgThy1_IG2, sgThy1_IG3 are sgRNAs targeting the immunoglobulin domain of the Thy1 gene; sgPtprc_CAT1 and sgPtprc_TM1 are sgRNAs targeting either the catalytic or transmembrane domain of the Ptprc gene; sgNeg, an sgRNA targeting the Ano9 gene, was used here as a negative control. [Figure 12B] See legend to Figure 12A. [Figure 12C] See legend to Figure 12A. [Figure 12D] See legend to Figure 12A. [Figure 12E] See legend to Figure 12A. [Figure 12F] See legend to Figure 12A. [Figure 12G] See legend to Figure 12A. [Figure 13]Figures 13A-13D: Cell membrane permeable ribonucleoprotein (RNP) complexes for ex vivo PAGE genome editing in mouse primary T cells. Figure 13A: Schematic of a series of CasCPP variants for RNP-PAGE experiments in mouse primary T cells. Cas9-T6NCPP (TAT-4xNLSMYC NLS-Cas9-2xNLSSV40-sfGFP); Cas9-T8NCPP (TAT-6xNLSMYC NLS-Cas9-2xNLSSV40-sfGFP); opCas12a-T8NCPP (TAT-6xNLSMYC NLS-opCas12a-2xNLSSV40-sfGFP). Figure 13B: Schematic of an experiment showing ex vivo editing by Cas9 / opCas12a-RNP-PAGE in mouse primary T cells. Mouse primary CD8 T cells, either naive or activated for 2 days, were incubated with 5 μM RNP complex and various concentrations of TH at 37°C for 30 minutes. Cells were washed once and cultured for 5 days with or without sorting GFP+ cells, and editing efficiency was measured by flow cytometry for expression of target genes. Figure 13C: Analysis of CD90 expression levels in either naive or activated CD8 T cells treated with various Cas9 / opCas12a-RNP-PAGE systems. Mouse primary CD8 T cells, either naive or activated, were treated with 5 μM Cas9-T6NCPP RNP complex, Cas9-T8NCPP RNP complex, or opCas12a-T8NCPP RNP complex with guide RNA targeting the IG domain of CD90 in combination with 25 μM TH as described in Figure 13B. CD90 expression was measured by flow cytometer on the 5th day after treatment. opCas12a-RNP-PAGE showed superior gene editing efficiency over Cas9-RNP-PAGE in primary mouse T cells. Figure 13D: Optimization of TH concentration for delivery of opCas12a-RNP-PAGE in primary mouse CD8 T cells.Primary mouse CD8 T cells were activated for 2 days and then treated with 5 μM opCas12a-T8NCPP RNP targeting the IG domain of CD90 in the presence of various concentrations of TH ranging from 25 to 50 μM. CD90 expression was measured by flow cytometry on day 5 after treatment. [Figure 14] Figures 14A-14C: Genome editing by opCas12a-RNP-PAGE ex vivo in human chimeric antigen receptor (CAR) T cells. Figure 14A: Schematic of the experiment showing ex vivo editing by opCas12a-RNPCPP in CAR T cells. Human primary T cells from healthy donors were isolated and activated with anti-CD3, anti-CD28, and IL-2. Activated T cells were transduced with CAR19 lentivirus on day 1. On day 6, CAR19+ cells were FACS sorted, followed by incubation with 5 μM opCas12a-T8NCPP RNP and 25 μM TH for 30 min. Cells were cultured for an additional 10 days after treatment, and expression of the target gene was measured by flow cytometry. Figures 14B-14C: Human CAR T cells were treated with 5 μM opCas12a-T8NCPP RNPs targeting the catalytic domain of CD45 (encoded by PTPRC) or the immunoglobulin domain of beta-2-microglobulin (encoded by B2M) in the presence of 25 μM TH. Expression of CD45 (Figure 14B) or B2M (Figure 14C) was measured by flow cytometry on day 6 after treatment. [Figure 15A]Figures 15A-15G: Highly efficient in vivo editing of clinically relevant genes by the Cas9-PAGE system in primary mouse T cells. Figure 15A: Schematic of the experimental workflow for evaluating the PAGE system in vivo in primary mouse CD8 T cells. Donor CD8 T cells from P14 transgenic (CD45.1+ or CD45.1 / 2+ congenic) mice were isolated and activated with anti-CD3, anti-CD28, and IL-2, followed by retroviral transduction with either test or negative control sgRNA expression vectors linked to fluorescent markers. sgRNA-transduced T cells were incubated with 5 μM Cas9-T6NCPP and 25 μM TH peptide for 30 min, followed by FACS sorting to enrich for Cas9-positive and sgRNA-positive (double-positive) populations. P14 T cells transduced with test sgRNA and negative control sgRNA were mixed at a 1:1 ratio and then adoptively transferred into CD45.2+ congenic recipient mice infected with LCMV clone 13 virus. Gene editing and P14 T cell populations were assessed over time by flow cytometry over a 30-day period. Figure 15B: Example of flow cytometry plot of CD90 surface expression after sgThy1_IG1-mediated editing at day 8 post-infection, and (Figure 15C) quantification of CD90 surface expression. Figures 15D-15E: As in Figures 15B-15C, except for PD-1 after sgPdcd1_IG44-mediated editing. Figure 15F: Percentage of P14 T cells transduced with the indicated sgRNA and co-transferred in blood over time. (FIG. 15G) P14 T cells transduced with the indicated sgRNAs as a percentage of total CD8 T cells in blood over a 30 day period. n=5-10 per time point, data are representative of two experiments. [Figure 15B] See legend to Figure 15A. [Figure 15C]See legend to Figure 15A. [Figure 15D] See legend to Figure 15A. [Figure 15E] See legend to Figure 15A. [Figure 15F] See legend to Figure 15A. [Figure 15G] See legend to Figure 15A. [Figure 16] Figure 16A-16C: Cas9-BE PAGE shows base editing in K562 d2GFP reporter cell line. Figure 16A: Schematic of Cas9-BE expression construct. Figure 16B: Schematic of experimental workflow to evaluate base editing efficiency of Cas9-BE PAGE system in K562 d2GFP reporter cell line. K562 cells were lentivirally transduced with a dual expression vector stably expressing d2GFP fluorescent reporter and sgRNA targeting d2GFP fluorescent reporter gene, or a dual expression vector stably expressing d2GFP fluorescent reporter and sgRNA targeting Ano9 gene as negative control. K562 d2GFP cells were incubated with Cas9-BE-T6NCPP and TH peptide for 30 minutes, followed by washing removal of the protein and peptide. Base editing was assessed 5 days after treatment based on the loss of d2GFP reporter fluorescence upon complete degradation of the Cas9-BE protein linked to GFP (Figure 16C: Quantification of loss of d2GFP expression in the K562 d2GFP reporter cell line described in Figure 16B). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0022] Detailed Description Herein, an optimized, highly efficient, inexpensive and novel gene editing method is established in cells, using a cell membrane permeable Cas protein linked to an endosomal escape peptide. This study creates a novel composition for this cell membrane permeable Cas tool. Compared with previously reported gene editing methods using cell membrane permeable CRISPR-Cas system (Ramakrishna et al., (2014) Genome Res 24, 1020-1027; Staahl et al., (2017) Nat Biotechnol 35, 431-434), this method achieves high gene editing efficiency both in vitro and in vivo. Compared with previously reported gene editing methods for mouse primary T cells that use the CRISPR-Cas system, which requires electroporation of ribonucleoprotein (RNP) complexes (Kornete et al., (2018) J Immunol 200, 2489-2501; Nussing et al., (2020) J. Immunol), our method is less expensive and easier to implement into experimental workflows. Our method does not require electroporation, but instead requires either (1) incubation of cell membrane-permeable Cas proteins and endosomal escape peptides with cells infected with sgRNA expression constructs, or (2) incubation of cell membrane-permeable Cas·sgRNA ribonucleoprotein (RNP) complexes and endosomal escape peptides with cells. Furthermore, our method does not require transgenic mice expressing Cas proteins to achieve gene editing, thus eliminating the time and expense of generating specific Cas transgenic mouse lines. Importantly, after 2 days of incubation, cells lose most of the plasma membrane-permeable Cas protein, which reduces the immunogenicity of the Cas protein and / or reduces the genomic off-target effects observed in other studies.

[0023] Researchers can use this method to achieve gene editing in mouse and human primary T cells, or other primary immune cells, including human immune cells, and to enable CRISPR-CAS screening. The settings used in this method can also be applied to other Cas proteins, i.e., Cas12a, and Cas9 base editors, in addition to Cas9.

[0024] It should be understood that the methods described in this disclosure are not limited to the particular methods and experimental conditions disclosed herein, as such methods and conditions may vary. It should also be understood that the terminology used herein is for the purpose of describing certain embodiments only, and is not intended to be limiting.

[0025] Furthermore, the experiments described herein use conventional molecular and cell biological techniques and conventional immunological techniques that are within the skill of the person skilled in the art, unless otherwise specified. Such techniques are well known to those skilled in the art and are fully described in the literature. For example, see Ausubel et al., eds., "Current Protocols in Molecular Biology", John Wiley & Sons, Inc., NY, NY (1987-2008), including all supplements, MR Green and J. Sambrook, "Molecular Cloning: A Laboratory Manual" (4th edition), and Harlow et al., "Antibodies: A Laboratory Manual", Chapter 14, Cold Spring Harbor Laboratory, Cold Spring Harbor (2013, 2nd edition).

[0026] A. definition Unless otherwise defined, scientific and technical terms used herein have the meanings that are commonly understood by those skilled in the art. In the event of any potential ambiguity, the definitions provided herein take precedence over dictionary or external definitions. Unless the context requires otherwise, the singular includes the plural and the plural includes the singular. The use of "or" means "and / or" unless otherwise specified. The use of the term "including" as well as other forms such as "includes" and "included" is not limiting.

[0027] Generally, the terminology used in cell and tissue culture, molecular biology, immunology, microbiology, genetics, and protein and nucleic acid chemistry, and hybridization described herein is well known and widely used in the art.Unless otherwise specified, the methods and techniques provided herein are generally carried out according to conventional methods well known in the art and as described in various general references and various more detailed references cited and discussed throughout this specification.Enzymatic reactions and purification techniques are carried out according to manufacturer's specifications as commonly performed in the art or as described herein.The terminology used in analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein, and the experimental techniques and techniques in these fields are well known and widely used in the art.Standard techniques are also used for chemical synthesis, chemical analysis, pharmaceutical preparation, pharmaceutical formulation, and pharmaceutical delivery, and patient treatment.

[0028] In order that the present disclosure may be more readily understood, selected terms are defined.

[0029] The articles "a" and "an" are used herein to refer to one or to more than one (i.e., to at least one) of the grammatical object of the article. By way of example, "an element" means one element or more than one element.

[0030] "About," as used herein, when referring to a measurable value, e.g., amount, duration, etc., is meant to encompass a ±20% or ±10% variation from the specified value, more preferably a ±5% variation, even more preferably a ±1% variation, and even more preferably a ±0.1% variation, as appropriate for performing the disclosed methods.

[0031] "Activation" as used herein refers to the state of T cells that are stimulated sufficiently to induce detectable cell proliferation. Activation can also be associated with induced cytokine production and detectable effector function. The term "activated T cells" refers, inter alia, to T cells undergoing cell division.

[0032] As used herein, "alleviating" a disease means reducing the severity of one or more of the symptoms of the disease.

[0033] The term "antigen" as used herein is defined as a molecule that induces an immune response. This immune response can involve either antibody production or activation of certain immunocompetent cells, or both. Those skilled in the art will understand that virtually any macromolecule, including any protein or peptide, can act as an antigen.

[0034] Furthermore, the antigen may be derived from recombinant DNA or from genomic DNA. Thus, one skilled in the art will understand that any DNA containing a nucleotide sequence encoding a protein that induces an immune response or such a partial nucleotide sequence will code for an "antigen" as the term is used herein. Furthermore, one skilled in the art will understand that it is not necessarily only the full-length nucleotide sequence of a gene that codes for an antigen. It is clear that the present invention includes, but is not limited to, the partial use of nucleotide sequences of multiple genes, and that these nucleotide sequences are arranged in various combinations to induce a desired immune response. Furthermore, one skilled in the art will understand that an antigen does not have to be encoded by a "gene" at all. It is clear that an antigen may be synthetically produced or may be derived from a biological sample. Such biological samples may include, but are not limited to, tissue samples, tumor samples, cells, or biological fluids.

[0035] As used herein, the term "autologous" is intended to refer to any material that is derived from the same individual into which it is subsequently reintroduced.

[0036] "Costimulatory molecule" refers to a cognate binding partner on a T cell that specifically binds to a costimulatory ligand, thereby mediating a costimulatory response by the T cell, such as, but not limited to, proliferation. Costimulatory molecules include, but are not limited to, MHC class I molecules, BTLA, and Toll ligand receptors.

[0037] A "costimulatory signal," as used herein, refers to a signal that, in combination with a primary signal, such as TCR / CD3 engagement, leads to T cell proliferation and / or upregulation or downregulation of key molecules.

[0038] A "disease" is a state of health in an animal in which the animal is unable to maintain homeostasis and in which the animal's well-being continues to deteriorate if the disease is not reversed. In contrast, a "disorder" in an animal is a state of health in which the animal is able to maintain homeostasis, but in which the animal's health is not as favorable as would be the case in the absence of the disorder. If left untreated, the disorder does not necessarily cause a further deterioration of the animal's health.

[0039] The term "downregulation," as used herein, refers to a decrease or elimination of gene expression of one or more genes.

[0040] "Effective amount" or "therapeutically effective amount" are used interchangeably herein and refer to an amount of a compound, formulation, substance, or composition described herein that is effective to achieve a certain biological result or to provide a therapeutic or prophylactic benefit. Such results may include, but are not limited to, an amount that, when administered to a mammal, induces a detectable level of immune suppression or immune tolerance compared to the immune response detected in the absence of the composition of the present invention. Immune response can be readily assessed by many art-recognized methods. Those skilled in the art will understand that the amount of the composition administered herein will vary and can be readily determined based on several factors, such as: the disease or disorder being treated, the age and health and physical condition of the mammal being treated, the severity of the disease, the particular compound being administered, etc.

[0041] "Encoding" refers to the inherent property of a particular nucleotide sequence in a polynucleotide, such as a gene, cDNA, or mRNA, to act in biological processes as a template for the synthesis of other polymers and macromolecules that have either a defined sequence of nucleotides (i.e., rRNA, tRNA, and mRNA) or a defined sequence of amino acid sequences and also have biological properties due to them. Thus, a gene codes for a protein when transcription and translation of mRNA corresponding to the gene produces a protein in a cell or other biological system. The coding strand is the one whose nucleotide sequence is identical to the mRNA sequence and is usually provided in a sequence listing, and the non-coding strand is the one used as a template to transcribe the gene or cDNA, both of which may be referred to as encoding the protein or other product corresponding to the gene or cDNA.

[0042] As used herein, "endogenous" refers to any material that is derived from or produced within an organism, cell, tissue, or system.

[0043] The term "epitope" as used herein is defined as a small chemical molecule on an antigen that is capable of eliciting an immune response, which induces a B-cell response and / or a T-cell response. An antigen may have one or more epitopes. Most antigens have multiple epitopes; that is, they are multivalent. In general, the size of an epitope is roughly about 10 amino acids and / or sugars. Preferably, an epitope is about 4-18 amino acids, more preferably about 5-16 amino acids, and even more preferably about 6-14 amino acids, more preferably about 7-12, and most preferably about 8-10 amino acids. Those skilled in the art will appreciate that in general, the overall three-dimensional structure of a molecule, rather than the specific linear sequence, is the primary criterion for antigen specificity, and thus distinguishes one epitope from another. Based on the present disclosure, a peptide used in the present invention may be an epitope.

[0044] As used herein, the term "exogenous" refers to any material introduced from outside an organism, cell, tissue, or system, or produced outside an organism, cell, tissue, or system.

[0045] The term "expanded" as used herein refers to an increase in number, such as an increase in the number of T cells. In one embodiment, the T cells expanded ex vivo are increased in number compared to the number originally present in the culture. In another embodiment, the T cells expanded ex vivo are increased in number compared to other cell types in the culture. The term "ex vivo" as used herein refers to cells that are transferred from a living organism (e.g., a human) and cells that are grown outside of the organism (e.g., in a culture dish, in a test tube, or in a bioreactor).

[0046] The term "expression", as used herein, is defined as the transcription and / or translation of a particular nucleotide sequence driven by its promoter.

[0047] "Expression vector" refers to a vector that contains a recombinant polynucleotide that includes an expression control sequence that is operably linked to a nucleotide sequence to be expressed. An expression vector contains sufficient cis-acting elements for expression; other elements for expression can be supplied by the host cell or in an in vitro expression system. Expression vectors include all those known in the art, such as cosmids, plasmids (e.g., naked or contained in liposomes), and viruses (e.g., Sendai virus, lentivirus, retrovirus, adenovirus, and adeno-associated virus) that contain recombinant polynucleotides.

[0048] "Identity" as used herein refers to the identity of subunit sequences between two polymer molecules, particularly between two amino acid molecules, such as between two polypeptide molecules. If two amino acid sequences have the same residue at the same position; for example, if a position is occupied by arginine in each of the two polypeptide molecules, then both sequences are identical at that position. Identity, or the degree to which two amino acid sequences have the same residue at the same position in an alignment, is often expressed as a percentage. The identity between two amino acid sequences is a direct function of the number of positions that are matched or identical; for example, if half of the positions in two sequences (e.g., 5 positions in a polymer 10 amino acids long) are identical, the two sequences are 50% identical; if 90% of the positions (e.g., 9 out of 10) are matched or identical, the two amino acid sequences are 90% identical.

[0049] The term "immune response," as used herein, is defined as a cellular response to an antigen that occurs when lymphocytes recognize the antigenic molecule as foreign and induce antibody production and / or activate lymphocytes to eliminate the antigen.

[0050] The term "immunosuppression" is used herein to refer to the overall decrease in immune response.

[0051] "Insertion / deletion", commonly abbreviated as "indel", is a type of genetic polymorphism in which a particular nucleotide sequence is present (insertion) or absent (deletion) in the genome.

[0052] "Isolated" means altered or separated from the natural state. For example, a nucleic acid or peptide that is naturally present in a living animal is not "isolated," but the same nucleic acid or peptide that is partially or completely separated from the coexisting materials in its natural state is "isolated." An isolated nucleic acid or protein may exist in a substantially purified form, or may exist in a non-native environment, such as, for example, within a host cell.

[0053] The term "knockdown," as used herein, refers to a decrease in gene expression of one or more genes.

[0054] The term "knock-in," as used herein, refers to an exogenous nucleic acid sequence that is inserted into a target sequence (e.g., an endogenous locus. In some embodiments, when the target sequence is a gene, the knock-in results in an exogenous nucleic acid sequence that is operably linked to any upstream and / or downstream regulatory elements that control expression of the target gene. In some embodiments, the knock-in results in an exogenous nucleic acid sequence that is not operably linked to any upstream and / or downstream regulatory elements that control expression of the target gene.

[0055] The term "knockout," as used herein, refers to the elimination of gene expression of one or more genes.

[0056] "Lentivirus" as used herein refers to one of the genera of the Retroviridae family.Lentivirus is unique among retroviruses in that it can infect non-dividing cells; it can deliver a significant amount of genetic information to the DNA of host cells, making it one of the most efficient approaches for gene delivery vectors.HIV, SIV, and FIV are all examples of lentivirus.Vector derived from lentivirus provides a means to achieve significant levels of gene transfer in vivo.

[0057] The term "modified" as used herein refers to an altered state or structure of a molecule or cell of the invention. Molecules can be modified in many ways, including chemical, structural, and functional modifications. Cells can be modified by the introduction of nucleic acids.

[0058] The term "modulate" as used herein means to cause a detectable increase or decrease in the level of response in a subject, compared to the level of response in the subject in the absence of treatment or compound, and / or compared to the level of response in an otherwise identical subject that is untreated.The term encompasses disrupting and / or affecting natural signals or responses, thereby causing a beneficial therapeutic response in a subject, preferably a human.

[0059] In the context of the present invention, the following abbreviations are used for commonly occurring nucleobases: "A" refers to adenosine, "C" refers to cytosine, "G" refers to guanosine, "T" refers to thymidine, and "U" refers to uridine.

[0060] The term "oligonucleotide" typically refers to a short polynucleotide. When a nucleotide sequence is represented by a DNA sequence (i.e., A, T, C, G), it is understood that this also includes an RNA sequence in which "T" is replaced by "U" (i.e., A, U, C, G).

[0061] Unless otherwise specified, a "nucleotide sequence encoding an amino acid sequence" includes all nucleotide sequences that are degenerate versions of each other and that encode the same amino acid sequence. A nucleotide sequence encoding a protein or RNA can also include introns, to the extent that some versions of a nucleotide sequence that encodes a protein may contain introns.

[0062] "Parenteral" administration of the immunogenic compositions includes, for example, subcutaneous (sc), intravenous (iv), intramuscular (im) or intrasternal injection or infusion techniques.

[0063] The term "polynucleotide" as used herein is defined as a chain of nucleotides. Furthermore, nucleic acid is a polymer of nucleotides. Thus, nucleic acid and polynucleotide are interchangeable as used herein. Those skilled in the art have general knowledge that nucleic acid is a polynucleotide, which can be hydrolyzed into monomeric "nucleotides". Monomeric nucleotides can be hydrolyzed into nucleosides. As used herein, polynucleotide includes, but is not limited to, all nucleic acid sequences obtained by any means available in the art, including recombinant means, i.e., cloning nucleic acid sequences from recombinant libraries or cell genomes using conventional cloning techniques and PCR, and also includes, but is not limited to, synthetic means.

[0064] As used herein, the terms "peptide", "polypeptide" and "protein" are used interchangeably and refer to compounds composed of amino acid residues covalently linked by peptide bonds. A protein or peptide must contain at least two amino acids, but there is no limit on the maximum number of amino acids that can make up a protein or peptide sequence. A polypeptide includes any peptide or protein that contains two or more amino acids linked together by peptide bonds. As used herein, the term refers to both short and long chains, where short chains are commonly referred to in the art as, for example, peptides, oligopeptides, and oligomers, and long chains are commonly referred to in the art as proteins, of which there are many types. "Polypeptides" include, for example, biologically active fragments, substantially homologous polypeptides, oligopeptides, homodimers, heterodimers, variants of polypeptides, modified polypeptides, derivatives, analogs, fusion proteins, and the like, among others. A polypeptide includes natural peptides, recombinant peptides, synthetic peptides, or combinations thereof.

[0065] The term "specifically binds" as used herein with respect to an antibody refers to an antibody that recognizes a specific antigen in a sample, but does not substantially recognize or bind to other molecules. For example, an antibody that specifically binds to an antigen from one species may also bind to antigens from one or more species. However, such species cross-reactivity does not in itself change the point at which the antibody is classified as specific. In another example, an antibody that specifically binds to an antigen may also bind to different allelic forms of the antigen. However, such cross-reactivity does not in itself change the point at which the antibody is classified as specific. In some examples, the term "specifically binds" or "specifically binds" can be used with respect to the interaction of an antibody, protein, or peptide with a second chemical species to mean that the interaction is dependent on the presence of a specific structure (e.g., an antigenic determinant or epitope) in the chemical species; for example, an antibody recognizes and binds to a specific protein structure, rather than to proteins in general. If an antibody is specific for epitope "A," then in a reaction involving labeled "A" and the antibody, if a molecule containing epitope A (or free, unlabeled A) is present, the amount of labeled A that is bound to the antibody will be reduced.

[0066] The term "stimulation" refers to a primary response induced by the binding of a stimulatory molecule (e.g., the TCR / CD3 complex) to its cognate ligand, which mediates a signal transduction event, such as, but not limited to, signal transduction via the TCR / CD3 complex. Stimulation may mediate changes in the expression of certain molecules, such as, for example, downregulation of TGF-β, and / or rearrangement of cytoskeletal structure.

[0067] As the term "stimulatory molecule" is used herein, it refers to a molecule on a T cell that specifically binds to a cognate stimulatory ligand present on an antigen-presenting cell.

[0068] "Stimulatory ligand," as used herein, refers to a ligand that, when present on an antigen-presenting cell (e.g., aAPC, dendritic cell, B cell, etc.), is capable of specifically binding to a cognate binding partner (herein referred to as a "stimulatory molecule") on a T cell, thereby mediating a primary response by the T cell, including, but not limited to, activation, initiation of an immune response, proliferation, etc. Stimulatory ligands are well known in the art and include, inter alia, peptide-loaded MHC class I molecules, anti-CD3 antibodies, superagonist anti-CD28 antibodies, and superagonist anti-CD2 antibodies.

[0069] The term "subject" is intended to include a living organism (e.g., a mammal) capable of generating an immune response. A "subject" or "patient" as used herein may be a human or a non-human mammal. Non-human mammals include, for example, livestock and pets, such as, for example, ovine, bovine, porcine, canine, feline, and murine mammals. Preferably, the subject is a human.

[0070] "Target site" or "target sequence" refers to a nucleic acid sequence that defines a portion of a nucleic acid to which a binding molecule can specifically bind under conditions sufficient for binding to occur. In some embodiments, a target sequence refers to a nucleic acid sequence of a genome that defines a portion of a nucleic acid to which a binding molecule can specifically bind under conditions sufficient for binding to occur.

[0071] The term "therapeutic" as used herein means treatment and / or prophylaxis. The therapeutic effect is obtained by suppression, amelioration, or eradication of a pathological condition.

[0072] "Transplant" refers to the tissue, organ, or cells of the biocompatible lattice or donor that is transplanted. Examples of transplants may include, but are not limited to, skin cells or tissue, bone marrow, and solid organs such as, for example, the heart, pancreas, kidney, lung, and liver. Transplants may also refer to any material that is administered to a host. For example, transplants may refer to nucleic acids or proteins.

[0073] The terms "transfect" or "transformation" or "transduction" as used herein refer to the process by which foreign nucleic acid is transferred or introduced into a host cell. A "transfected" or "transformed" or "transduced" cell is one that has been transfected, transformed or transduced with foreign nucleic acid. The cell includes the primary cell of interest and its progeny.

[0074] "Treating" a disease, as the term is used herein, means reducing the frequency or severity of at least one sign or symptom of the disease or disorder experienced by a patient.

[0075] A "vector" is a composition that contains an isolated nucleic acid and can be used to deliver the isolated nucleic acid to the inside of a cell. Many vectors are known in the art, including, but not limited to, linear polynucleotides, polynucleotides associated with ionic or amphiphilic compounds, plasmids, and viruses. Thus, the term "vector" includes autonomously replicating plasmids or viruses. The term should also be construed to include non-plasmid and non-viral compounds that facilitate the transfer of nucleic acid into cells, such as polylysine compounds, liposomes, etc. Examples of viral vectors include, but are not limited to, Sendai virus vectors, adenovirus vectors, adeno-associated virus vectors, retrovirus vectors, lentivirus vectors, etc.

[0076] Ranges: Throughout this disclosure, various aspects of the invention may be expressed in the form of a range. It should be understood that descriptions in the form of a range are provided merely for convenience and brevity, and should not be construed as rigid limitations on the scope of the invention. Thus, the description of a range should be considered to have specifically disclosed all possible subranges and all possible individual numerical values ​​within that range. For example, the description of a range such as 1-6 should be considered to have specifically disclosed subranges within that range such as 1-3, 1-4, 1-5, 2-4, 2-6, 3-6, etc., and individual numbers such as 1, 2, 2.7, 3, 4, 5, 5.3, and 6. This applies regardless of the breadth of the range.

[0077] B. In vitro and in vivo methods of gene editing Provided herein is a method for gene editing (in vitro, ex vivo, and in vivo) using a novel CRISPR-Cas system, referred to as peptide-assisted genome editing (PAGE) system. The PAGE system includes a cell membrane-permeable Cas (e.g., Cas (e.g., Cas9 or Cas12a) linked to a cell membrane-permeable peptide (CPP)) and an endosomal escape peptide (e.g., dTAT-HA2) linked to the CPP. Using this method, Cas is introduced into cells (e.g., primary resting T cells) in a non-virus-dependent and non-electroporation-dependent manner. Then, one type of single-stranded guide RNA (sgRNA) or CRISPR RNA (crRNA); or multiple types of sgRNAs or crRNAs can be introduced into cells (e.g., by retroviral expression constructs or RNPs) to achieve in vitro, ex vivo, and in vivo editing of cells (e.g., primary CD8 T cells).

[0078] In one aspect, the present disclosure provides an in vitro method for gene editing, comprising: introducing a PAGE system comprising a cell-permeable Cas and an endosomal escape peptide, and at least one sgRNA or crRNA into a cell. The cell-permeable Cas comprises a Cas (e.g., Cas9, Cas12a) linked to a CPP. The endosomal escape peptide is linked to a CPP.

[0079] In another aspect, the present disclosure provides an ex vivo or in vivo method of gene editing, comprising: introducing a PAGE system comprising a cell-permeable Cas and an endosomal escape peptide, and at least one sgRNA or crRNA into a cell, and administering the cell to a subject. The cell-permeable Cas comprises a Cas (e.g., Cas9, Cas12a) linked to a CPP. The endosomal escape peptide is linked to a CPP.

[0080] In some embodiments, the Cas is Cas9. Exemplary Cas9 nucleases that can be used in the present invention include, but are not limited to, S. pyogenes Cas9 (SpCas9), S. aureus Cas9 (SaCas9), S. thermophilus Cas9 (StCas9), N. meningitidis Cas9 (NmCas9), C. jejuni Cas9 (CjCas9), and Geobacillus Cas9 (GeoCas9). In some embodiments, the Cas is Cas12a (Cpf1), including, but not limited to, Butyrivibrio sp. (BsCas12a), Thiomicrospira sp. XS5 (TsCas12a), Moraxella bovoculi (MbCas12a), Prevotella bryantii (PbCas12a), Bacteroidetes oral (BoCas12a), Lachnospiraceae bacteria (LbCas12a), and Acidaminococcus sp. (AsCas12a). In some embodiments, the Cas is Cas12a. In some embodiments, the Cas is selected from the group consisting of Cas12b, Cas12d, Cas12f, T7, Cas3, Cas8a, Cas8b, Cas10d, Cse1, Csy1, Csn2, Cas4, Cas10, Csm2, Cmr5, and Fok1.

[0081] In some embodiments, Cas is a Cas derivative. In some embodiments, Cas derivative is a Cas protein linked to another protein or catalytic domain. Cas protein can be linked to another protein or catalytic domain by any means known in the art, such as, but not limited to, chemical bond, fusion, or post-translational modification. In some embodiments, the protein or catalytic domain is selected from the group consisting of AID deaminase, APOBEC deaminase, TadA deaminase, TET enzyme, DNA methyltransferase, transactivation domain, reverse transcriptase, histone acetyltransferase, histone deacetylase, sirtuin, histone methyltransferase, histone demethylase, kinase, and phosphatase.

[0082] In some embodiments, the Cas comprises a nuclear localization signal (NLS) sequence. Any NLS known in the art or disclosed herein can be used. In some embodiments, the Cas comprises a Myc NLS sequence. In some embodiments, the Myc NLS sequence comprises or consists of the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). In some embodiments, the Cas comprises a 4xMyc NLS sequence or a 6xMyc NLS sequence. In some embodiments, the NLS (i.e., 4xMyc or 6xMyc) sequence further comprises a GGS linker.

[0083] In some embodiments, the cell membrane permeable Cas comprises a nucleotide sequence encoding a cell membrane permeable peptide or comprises an amino acid sequence comprising a cell membrane permeable peptide. A cell membrane permeable peptide (also known as CPP, protein transduction domain, PTD) is a carrier with a small peptide domain (generally less than 40 amino acids) that can easily pass through the cell membrane. Several types of cell membrane permeable peptides have been identified as promoting the cellular uptake of various molecular cargoes ranging from nano-sized particles to small chemical molecules. The cell membrane permeable sequence can be used to extend the peptide sequence, making it more permeable to the cell membrane, or the cell membrane permeable sequence can be linked to other cargo molecules, which enhances the uptake of the cargo molecule. The cell membrane permeable sequence can be either directly fused to the cargo molecule or chemically linked to the cargo molecule. Examples of such cell membrane penetrating peptides include, but are not limited to, transactivating transcription activator from HIV-1 (Tat), oligo-Arg, KALA, transportan, penetratin, penetratin-Arg, TAT-HA2, and dTAT-HA2E5. The PAGE system may include two different CPPs or may include two of the same CPP. The CPP may be linked to the Cas or endosomal escape peptide by any means known in the art, such as, but not limited to, chemical conjugation, fusion, or post-translational modification. In some embodiments, the CPP comprises a peptide listed in Table 2. In some embodiments, the Cas is linked to a CPP listed in Table 2. In some embodiments, the endosomal escape peptide is linked to a CPP listed in Table 2. In some embodiments, the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10-1422. In some embodiments, the Cas is linked to a CPP comprising any of the amino acid sequences set forth in SEQ ID NOs: 10-1422. In some embodiments, the endosomal escape peptide is linked to a CPP comprising any of the amino acid sequences set forth in SEQ ID NOs: 10-1422.

[0084] In some embodiments, the cell membrane permeable Cas comprises a sequence derived from the transactivating transcription activator (Tat) from HIV-1. In some embodiments, the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO: 2).

[0085] In some embodiments, the cell membrane permeable Cas is introduced into the cell at a concentration of 0.05 μM to 10 μM. In some embodiments, the cell membrane permeable Cas is introduced into the cell at a concentration of about 0.5 μM.

[0086] In some embodiments, the endosomal escape peptide comprises dTAT-HA2. Other endosomal escape peptides that may be used include, but are not limited to, EED, HA2-Penetratin, GALA, INF-7, and the like. In some embodiments, the endosomal escape peptide comprises any one of the peptides or sequences listed in Table 1. The endosomal escape peptide can include any of the chemical modifications to the peptide, or chemically modified derivatives of the peptide, or specific chemical linkers in the peptide, or D-forms of amino acids, with respect to those listed in Table 1. In some embodiments, the endosomal escape peptide comprises any one of the sequences set forth in SEQ ID NOs: 1434-1523. In some embodiments, the endosomal escape peptide comprises any one of the sequences set forth in SEQ ID NOs: 1434-1523 and chemical modifications and / or chemical linkers. Examples of chemical modifications include, but are not limited to, phosphoric acid (PO3), trifluoromethyl-bicyclopent-[1.1.1]-1-ylglycine (CF3-Bpg), aminoisobutyric acid (Aib), stearylated (stearyl), 6-aminohexanoic acid (Ahx), L-2-naphthylalanine (Φ), and 3-amino-3-carboxypropyl (acp).

[0087] In some embodiments, the endosomal escape peptide is introduced into the cell at a concentration of 10 μM to 100 μM. In some embodiments, the endosomal escape peptide is introduced into the cell at a concentration of about 75 μM.

[0088] In some embodiments, the cell is an immune cell. In some embodiments, the cell is a mouse primary CD8 T cell, a human primary T cell, or a human iPSC (induced pluripotent stem cell).

[0089] In some embodiments, the method does not require electroporation. In some embodiments, the PAGE system is introduced into cells in a medium that does not contain fetal bovine serum (FBS) or serum. In some embodiments, the PAGE system is introduced into cells in a medium that contains FBS or serum.

[0090] The method should be construed as targeting any gene / genomic region / nucleotide sequence in a cell (e.g., eukaryotic / human cell). Thus, for use with the methods herein, one sgRNA or crRNA, or multiple sgRNAs or crRNAs, can be designed to target any gene / genomic region / nucleotide sequence in a cell (e.g., eukaryotic / human cell). In an embodiment, the sgRNA targets Ano9 or Pdcd1. In an embodiment, the sgRNA targets human Ano9 or Pdcd1. In an embodiment, the sgRNA targets the nucleotide sequence In one embodiment, the sgRNA comprises or consists of the nucleotide sequence TIFF2024520644000002.tif4128. In some embodiments, the sgRNA comprises or consists of the nucleotide sequence: TIFF2024520644000003.tif5128. In some embodiments, the sgRNA targets Ptprc or Thy1. In some embodiments, the sgRNA comprises the nucleotide sequence: In one embodiment, the sgRNA comprises or consists of the nucleotide sequence TIFF2024520644000004.tif4128. In one embodiment, the sgRNA comprises or consists of the nucleotide sequence TIFF2024520644000005.tif5128. In one embodiment, the sgRNA comprises or consists of the nucleotide sequence: In one embodiment, the sgRNA comprises or consists of the nucleotide sequence: In one embodiment, the crRNA comprises or consists of the nucleotide sequence TIFF2024520644000008.tif4128. In one embodiment, the crRNA targets PTPRC or B2M. In one embodiment, the crRNA comprises the nucleotide sequence In one embodiment, the crRNA comprises or consists of the nucleotide sequence TIFF2024520644000009.tif5128. In one embodiment, the crRNA comprises or consists of the nucleotide sequence TIFF2024520644000010.tif4128. In one embodiment, the crRNA comprises or consists of the nucleotide sequence TIFF2024520644000011.tif5128. In one embodiment, the crRNA comprises or consists of the nucleotide sequence TIFF2024520644000012.tif4128. TIFF2024520644000013.tif5128 or consisting of said nucleotide sequence.

[0091] In some embodiments, the method disclosed herein is used to treat a subject for disease or disorder. The method includes introducing a PAGE system comprising cell membrane permeable Cas and endosomal escape peptide, and at least one sgRNA or crRNA into a cell, and then administering the cell to a subject. When the edited cell is administered to a subject, the disease or disorder is treated in the subject. In some embodiments, the disease or disorder to be treated in the subject is infection. In some embodiments, the disease or disorder is associated with T cell exhaustion.

[0092] In some embodiments, the PAGE system comprises a CRISPR / Cas9 system. The CRISPR / Cas9 system is an easy and efficient system for inducing targeted genetic changes. Target recognition by Cas9 protein requires a "seed" sequence in the guide RNA (gRNA) and also requires a protospacer adjacent motif (PAM) sequence containing a conserved dinucleotide upstream of the gRNA binding region. Therefore, the CRISPR / Cas9 system can be engineered to cleave virtually any DNA sequence in cell lines (such as 293T cells) and primary cells by redesigning the gRNA. The CRISPR / Cas9 system can simultaneously target multiple loci on the genome by co-expressing one Cas9 protein with two or more gRNAs, making this system suitable for editing multiple genes or synergistic activation of target genes.

[0093] The Cas9 protein and the guide RNA form a complex that identifies and cleaves the target sequence. Cas9 is composed of six domains: REC I domain, REC II domain, bridge helix domain, PAM interaction domain, HNH domain, and RuvC domain. The REC I domain binds to the guide RNA, while the bridge helix domain binds to the target DNA. The HNH domain and the RuvC domain are nuclease domains. The guide RNA is engineered to have a 5' end that is complementary to the target DNA sequence. When the guide RNA binds to the Cas9 protein, a conformational change occurs and the protein is activated. Once activated, Cas9 searches for the target DNA by binding to a sequence that matches its protospacer adjacent motif (PAM) sequence. The PAM is a two or three base sequence that is within one nucleotide downstream of the region that is complementary to the guide RNA. In one non-limiting example, the PAM sequence is 5'-NGG-3'. When the Cas9 protein finds its target sequence with the appropriate PAM, it unwinds the bases upstream of the PAM and pairs them with the complementary region on the guide RNA. The RuvC and HNH nuclease domains then cleave the target DNA after the third nucleotide base upstream of the PAM.

[0094] CRISPRi, a non-limiting example of a CRISPR / Cas system used to inhibit gene expression, is described in US Patent Publication No. 20140068797. CRISPRi induces permanent gene disruption, which utilizes RNA-guided Cas9 endonuclease to introduce double-stranded breaks in DNA and triggers error-prone repair pathways resulting in frameshift mutations. Catalytically inactive Cas9 lacks endonuclease activity. When co-expressed with guide RNA, a DNA recognition complex is produced that specifically interferes with transcription elongation, RNA polymerase binding, or transcription factor binding. This CRISPRi system efficiently suppresses the expression of target genes.

[0095] CRISPR / Cas-mediated gene disruption occurs when a guide nucleic acid sequence specific for a target gene and a Cas endonuclease are introduced into a cell and form a complex that allows the Cas endonuclease to introduce a double-strand break in the target gene.In some embodiments, the CRISPR / Cas system comprises an expression vector, such as, but not limited to, the pAd5F35-CRISPR vector.In other embodiments, the Cas expression vector induces the expression of Cas9 endonuclease.Other endonucleases may also be used, including, but not limited to, Cas12a (Cpf1), T7, Cas3, Cas8a, Cas8b, Cas10d, Cse1, Csy1, Csn2, Cas4, Cas10, Csm2, Cmr5, Fok1, other nucleases known in the art, and any combination thereof.

[0096] In some embodiments, inducing the Cas expression vector comprises exposing the cell to an agent that activates an inducible promoter in the Cas expression vector. In such embodiments, the Cas expression vector comprises an inducible promoter, such as one that is inducible by exposure to an antibiotic (e.g., tetracycline or a tetracycline derivative such as doxycycline). Other inducible promoters known to those of skill in the art can also be used. The inducing agent can be a selective condition that causes induction of the inducible promoter (e.g., exposure to an agent such as an antibiotic). This causes expression of the Cas expression vector.

[0097] As used herein, the term "guide RNA" or "gRNA" refers to any nucleic acid that facilitates the specific binding (or "targeting") of an RNA-guided nuclease, such as Cas9, to a target sequence (e.g., a genomic or episomal sequence) in a cell.

[0098] As used herein, a "modular" guide, or a "dual RNA" guide, comprises multiple, and typically two, separate RNA molecules, such as a CRISPR RNA (crRNA) and a transactivating crRNA (tracrRNA), which are typically linked together, e.g., by duplexing. gRNAs and their components are described in various publications (see, e.g., Briner et al. Mol. Cell, 56(2), 333-339 (2014), which is incorporated by reference).

[0099] As used herein, "unimolecular gRNA", "chimeric gRNA", or "single-stranded guide RNA (sgRNA)" includes one RNA molecule. The sgRNA can be a crRNA and a tracrRNA linked together. For example, the 3' end of the crRNA can be linked to the 5' end of the tracrRNA. The crRNA and the tracrRNA can be linked into one unimolecular gRNA or one chimeric gRNA, for example, by using a "tetraloop" or "linker" sequence of four nucleotides (e.g., GAAA) that bridges the complementary regions of the crRNA (at its 3' end) and the tracrRNA (at its 5' end).

[0100] As used herein, a "repeat" sequence or "repeat" region is a nucleotide sequence that is at or near the 3' end of the crRNA and is complementary to the anti-repeat sequence of the tracrRNA.

[0101] As used herein, an "anti-repeat" sequence or "anti-repeat" region is a nucleotide sequence that is at or near the 5' end of the tracrRNA and is complementary to the repeat sequence of the crRNA.

[0102] Further details regarding the structure and function of guide RNAs, including gRNA / Cas9 complexes, for genome editing can be found at least in: Mali et al. Science, 339(6121), 823-826 (2013); Jiang et al. Nat. Biotechnol. 31(3). 233-239 (2013); and Jinek et al. Science, 337(6096), 816-821 (2012); which are incorporated herein by reference.

[0103] As used herein, "guide sequence" or "targeting sequence" refers to a nucleotide sequence of a gRNA, whether unilamellar or modular, that is fully or partially complementary to a target domain or target polynucleotide in a DNA sequence on the genome of a cell where editing is desired. A guide sequence is typically 10-30 nucleotides in length, preferably 16-24 nucleotides in length (e.g., 16, 17, 18, 19, 20, 21, 22, 23, or 24 nucleotides in length), and is located at or near the 5' end of the Cas9 gRNA.

[0104] As used herein, a "target domain" or "target polynucleotide sequence" or "target sequence" is a DNA sequence on the genome of a cell that is complementary to the guide sequence of a gRNA.

[0105] In the context of forming CRISPR complex, "target sequence" refers to the sequence that guide sequence is designed to have some complementarity with, where hybridization between target sequence and guide sequence promotes the formation of CRISPR complex.Full complementarity is not necessarily required, as long as there is sufficient complementarity to cause hybridization and promote the formation of CRISPR complex.Target sequence may comprise any polynucleotide, such as DNA polynucleotide or RNA polynucleotide.In some embodiments, target sequence is located in the nucleus or cytoplasm of cell.In other embodiments, target sequence is located inside the organelle of eukaryotic cell, such as inside mitochondria or nucleus. Typically, in the context of CRISPR systems, formation of a CRISPR complex (including a guide sequence hybridized to a target sequence and complexed with one or more Cas proteins) causes cleavage of one or both strands at or near the target sequence (e.g., within about 1 base pair, within about 2 base pairs, within about 3 base pairs, within about 4 base pairs, within about 5 base pairs, within about 6 base pairs, within about 7 base pairs, within about 8 base pairs, within about 9 base pairs, within about 10 base pairs, within about 20 base pairs, within about 50 base pairs, or even further away). As with the target sequence, perfect complementarity is not believed to be required, provided it is sufficient to be functional.

[0106] In some embodiments, one or more vectors that drive the expression of one or more of the components of the CRISPR system are introduced into a host cell, resulting in the expression of the components of the CRISPR system and the formation of a CRISPR complex at one or more target sites.For example, Cas nuclease, crRNA, and tracrRNA may each be operably linked to separate regulatory elements on separate vectors.Alternatively, two or more of the components that are expressed from the same or different regulatory elements may be combined into one vector, with one or more additional vectors that provide any components of the CRISPR system that are not included in the first vector.The components of the CRISPR system combined into one vector may be arranged in any suitable orientation, such as, for example, one component is located 5' ("upstream") relative to the second component, or 3' ("downstream") relative to the second component. The coding sequence of one component may be located on the same strand as the coding sequence of the second component, or on the opposite strand, and they may be arranged in the same or opposite orientation. In one embodiment, one promoter drives the expression of a transcript encoding a CRISPR enzyme, and one or more of the following transcripts embedded in one or more intron sequences: a guide sequence, a tracr mate sequence (optionally operably linked to the guide sequence), and a tracr sequence (e.g., each embedded in a separate intron, two or more embedded in at least one intron, or all embedded in one intron).

[0107] In some embodiments, the CRISPR-associated (Cas) enzyme is part of a fusion protein, where the fusion protein comprises one or more heterologous protein domains (e.g., about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more domains in addition to the CRISPR enzyme, or more than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more domains). The CRISPR enzyme fusion protein may include any additional protein sequence and may optionally include a linker sequence between any two domains. Examples of protein domains that may be fused to the CRISPR enzyme include, but are not limited to, epitope tags, reporter gene sequences, and protein domains having one or more of the following activities: methylase activity, demethylase activity, transcriptional activation activity, transcriptional repression activity, transcriptional termination factor activity, histone modification activity, RNA cleavage activity, and nucleic acid binding activity. Additional domains that can form part of fusion proteins containing CRISPR enzymes are described in U.S. Patent Application Publication No. 20110059502, which is incorporated herein by reference. In some embodiments, tagged CRISPR enzymes are used to identify the location of the target sequence.

[0108] Conventional virus-based and non-virus-based gene transfer methods can be used to introduce nucleic acid into mammalian and non-mammalian cells or target tissues. Such methods can be used to administer nucleic acid encoding components of CRISPR system to cells in culture or cells in host organisms. Non-viral vector delivery systems include DNA plasmids, RNA (e.g., transcripts of vectors described herein), naked nucleic acid, and nucleic acid complexed with a delivery vehicle, such as liposome. Viral vector delivery systems include DNA and RNA viruses, which are either episomal or integrated into genome after delivery to cells (Anderson, 1992, Science 256:808-813; and Yu, et al., 1994, Gene Therapy 1:13-26).

[0109] In some embodiments, CRISPR / Cas is derived from type II CRISPR / Cas system.In other embodiments, CRISPR / Cas system is derived from Cas9 nuclease.The exemplary Cas9 nuclease that can be used in the present invention includes, but is not limited to, S. pyogenes Cas9 (SpCas9), S. aureus Cas9 (SaCas9), S. thermophilus Cas9 (StCas9), N. meningitidis Cas9 (NmCas9), C. jejuni Cas9 (CjCas9) and Geobacillus Cas9 (GeoCas9).

[0110] Generally, Cas proteins contain at least one RNA recognition and / or RNA binding domain. The RNA recognition and / or RNA binding domain interacts with the guide RNA. Cas proteins may also contain nuclease domains (i.e., DNase or RNase domains), DNA binding domains, helicase domains, RNAase domains, protein-protein interaction domains, dimerization domains, and other domains. Cas proteins may be modified to increase nucleic acid binding affinity and / or specificity, to alter enzymatic activity, and / or to alter another property of the protein. In some embodiments, the Cas-like protein of the fusion protein may be derived from a wild-type Cas9 protein or a fragment thereof. In other embodiments, Cas may be derived from a modified Cas9 protein. For example, the amino acid sequence of the Cas9 protein may be modified to alter one or more properties of the protein (e.g., nuclease activity, affinity, stability, etc.). Alternatively, the domains of Cas9 protein that are not involved in RNA-guided cleavage may be removed from Cas9 protein, so that modified Cas9 protein is smaller than wild-type Cas9 protein. Generally, Cas9 protein comprises at least two nuclease domains (i.e., DNase domains). For example, Cas9 protein may comprise RuvC-like nuclease domain and HNH-like nuclease domain. RuvC domain and HNH domain cooperate to break single strand in DNA to create double strand break (Jinek, et al., 2012, Science, 337:816-821). In some embodiments, protein derived from Cas9 may be modified to contain only one functional nuclease domain (either RuvC-like nuclease domain or HNH-like nuclease domain). For example, a protein derived from Cas9 may be modified to delete one of the nuclease domains or may be mutated such that one of the nuclease domains is no longer functional (i.e., there is no nuclease activity).In some embodiments in which one of the nuclease domains is inactive, the protein derived from Cas9 is capable of introducing nicks into double-stranded nucleic acids (such proteins are referred to as "nickases") but is unable to cleave double-stranded DNA. In any of the above embodiments, any or all of the nuclease domains may be inactivated by one or more of deletion, insertion, and / or substitution mutations using well-known methods, for example, site-directed mutagenesis, PCR-mediated mutagenesis, and total gene synthesis, as well as other methods known in the art.

[0111] In a non-limiting embodiment, the vector drives the expression of the CRISPR system. The art is rich in suitable vectors that are useful for the present invention. The vector used is suitable for replication in eukaryotic cells, and optionally suitable for integration. Typical vectors include transcription and translation terminators, initiation sequences, and promoters that are useful for regulating the expression of desired nucleic acid sequences. The vector of the present invention can also be used in standard gene delivery protocols for nucleic acids. Methods for gene delivery are known in the art (US Pat. Nos. 5,399,346, 5,580,859, and 5,589,466, which are incorporated herein by reference in their entirety).

[0112] Furthermore, the vector may be provided to the cell in the form of a viral vector. Viral vector technology is well known in the art and is described, for example, in Sambrook et al. (4th ed. "Molecular Cloning: A Laboratory Manual", Cold Spring Harbor Laboratory, New York, 2012) and in other manuals on virology and molecular biology. Viruses that are useful as vectors include, but are not limited to, retroviruses, adenoviruses, adeno-associated viruses, herpes viruses, Sindbis viruses, gamma retroviruses, and lentiviruses. In general, suitable vectors include a replication origin functional in at least one organism, a promoter sequence, a convenient restriction endonuclease site, and one or more selectable markers (e.g., WO 01 / 96584; WO 01 / 29058; and U.S. Patent No. 6,326,193).

[0113] Table 1. Exemplary endosomal escape peptide sequences TIFF2024520644000014.tif213170TIFF2024520644000015.tif165170

[0114] C. Cell Source Any type of cell can be edited using the methods disclosed herein. In some embodiments, the cell is an immune cell. An immune cell is a cell of the immune system, such as a cell of the innate or adaptive immune system, such as a myeloid or lymphoid cell, including, for example, lymphocytes, typically T cells and / or NK cells. Other exemplary cells include stem cells, such as multipotent and pluripotent stem cells, including induced pluripotent stem cells (iPSCs). In some aspects, the cell is a human cell. Immune cells can be obtained from a number of sources, including blood, peripheral blood mononuclear cells, bone marrow, lymph node tissue, spleen tissue, umbilical cord, lymph, and lymphoid organs.

[0115] In some embodiments, the immune cell is a T cell, such as, for example, a CD8+ T cell (e.g., a primary CD8+ T cell, a CD8+ naive T cell, a central memory T cell, or an effector memory T cell), a CD4+ T cell, a natural killer T cell (NKT cell), a regulatory T cell (Treg), a stem cell memory T cell, a lymphoid progenitor cell, a hematopoietic stem cell, a natural killer cell (NK cell), or a dendritic cell. In some embodiments, the cell is a monocyte or a granulocyte, such as, for example, a myeloid cell, a macrophage, a neutrophil, a dendritic cell, a mast cell, an eosinophil, and / or a basophil. In certain embodiments, the cell is an induced pluripotent stem (iPS) cell, or a cell derived from an iPS cell, such as, for example, an iPS cell generated from a subject and engineered to alter (e.g., induce mutations in) or manipulate expression of one or more target genes, and differentiated into, for example, a T cell, such as, for example, a CD8+ T cell (e.g., a primary CD8+ T cell, a CD8+ naive T cell, a central memory T cell, or an effector memory T cell), a CD4+ T cell, a stem cell memory T cell, a lymphoid progenitor cell, or a hematopoietic stem cell.

[0116] In some embodiments, the cells include one or more subsets of T cells or other cell types, such as the total T cell population, CD4+ cells, CD8+ cells, and subpopulations thereof, where the subpopulations are defined, for example, by function, activation state, maturity, differentiation potential, expansion potential, recirculation potential, localization potential, and / or persistence potential, antigen specificity, antigen receptor type, presence in a particular organ or compartment, marker profile or cytokine secretion profile, and / or degree of differentiation. Subtypes and subpopulations of T cells and / or subtypes and subpopulations of CD4+ T cells and / or CD8+ T cells include: naive T cells (TN), effector T cells (TEFF), memory T cells and their subtypes, such as stem cell memory T cells (TSCM), central memory T cells (TCM), effector memory T cells (TEM), or terminally differentiated effector memory T cells, tumor infiltrating lymphocytes (TIL), immature T cells, mature T cells, helper T cells, cytotoxic T cells, mucosal-associated invariant T cells (MAIT), intrinsic and adaptive regulatory T cells (Treg), helper T cells, such as TH1 cells, TH2 cells, TH3 cells, TH17 cells, TH9 cells, TH22 cells, follicular helper T cells, α / β T cells, and δ / γ T cells. In an embodiment, any kind of T cell line available in the art may be used.

[0117] In some embodiments, the cell comprises a chimeric antigen receptor (CAR). In some embodiments, the cell is a CAR T cell. Exemplary CARs include those disclosed herein, such as US10357514B2, US10221245B2, US10603378B2, US8916381B1, US9394368B2, US20140050708A1, US9598489B2, US9365641B2, US20210079059A1, US9783591B2, WO 2016028896A1, US9446105B2, WO2016014576A1, US20210284752A1, WO2016014565A2, WO2016014535A1, and US9272002B2, and also includes any other CARs generally disclosed in the art, but are not limited thereto. The present disclosure should be interpreted as including any CARs known in the art.

[0118] In some embodiments, the method includes isolating immune cells from a subject, preparing immune cells, treating immune cells, culturing immune cells, and / or manipulating immune cells. In some embodiments, preparing cells includes one or more culturing and / or preparation steps. Cells for manipulation as described may be isolated from a sample, such as a biological sample, for example, a biological sample obtained from or derived from a subject. In some embodiments, the subject from which the cells are isolated is a subject having a disease or disorder, or a subject in need of cell therapy, or a subject to be administered cell therapy. In some embodiments, the subject is a human in need of a particular therapeutic intervention, such as, for example, adoptive cell therapy, for which the cells are isolated, treated, and / or manipulated. Thus, in some embodiments, the cells are primary cells, such as, for example, primary human cells, such as, for example, primary human CD8+ cells. Samples include tissues, fluids, and other samples taken directly from subjects, and also include samples that have undergone one or more processing steps, such as separation, centrifugation, genetic manipulation (e.g., transduction with viral vectors), washing, and / or incubation. Biological samples may be samples obtained directly from biological sources or may be processed samples. Biological samples include body fluids, such as blood, plasma, serum, cerebrospinal fluid, synovial fluid, urine, and sweat, and also include, but are not limited to, tissue and organ samples, including processed samples derived from tissues and organs.

[0119] In some embodiments, the source of immune cells is obtained from a subject for ex vivo manipulation. The source of cells for ex vivo manipulation can also include blood, umbilical cord blood, or bone marrow, for example, from an autologous or heterologous donor. For example, the source of immune cells can be from a subject that is to be treated with the modified immune cells of the present invention, such as the subject's blood, the subject's umbilical cord blood, or the subject's bone marrow. Non-limiting examples of subjects include humans, dogs, cats, mice, rats, and transgenic species thereof. Preferably, the subject is a human.

[0120] In some embodiments, cells are modified using the methods contemplated herein; for example, by introducing a cell-permeable CRISPR-Cas9 system or a cell-permeable CRISPR-Cas12a system, which comprises a cell-permeable Cas9 or a cell-permeable Cas12a and an endosomal escape peptide, into the cells, and then the modified cells are administered to a subject. In some embodiments, the subject is in need of treatment for a disease or disorder. The cells can be allogeneic and / or autologous to the subject to be treated. The cells are typically primary cells, such as, for example, cells directly isolated from a subject and / or cells isolated from a subject and frozen.

[0121] In some aspects, the sample from which the cells are derived or isolated is blood or a sample derived from blood, or from the product of apheresis or leukapheresis.Exemplary samples include whole blood, peripheral blood mononuclear cells (PBMC), white blood cells, bone marrow, thymus, tissue biopsy, tumor, leukemia, lymphoma, lymph node, gut-associated lymphoid tissue, mucosa-associated lymphoid tissue, spleen, other lymphoid tissue, liver, lung, stomach, intestine, colon, kidney, pancreas, breast, bone, prostate, cervix, testis, ovary, tonsil, or other organ, and / or cells derived therefrom.In the context of cell therapy, such as adoptive cell therapy, samples include samples from autologous sources and samples from allogeneic sources.

[0122] In some embodiments, the cells are derived from a cell line, such as a T cell line. In some embodiments, the cells are obtained from a heterologous source, such as mouse, rat, non-human primate, and pig. In some embodiments, the isolation of cells includes one or more preparative and / or non-affinity-based cell separation steps. In some examples, cells are washed, centrifuged, and / or incubated in the presence of one or more reagents, such as to remove undesired components, to enrich for desired components, to lyse or remove cells that are sensitive to a particular reagent. In some examples, cells are separated based on one or more characteristics, such as density, adhesive properties, size, sensitivity and / or resistance to a particular component, etc.

[0123] In some examples, cells from the subject's circulating blood are obtained, for example, by apheresis or leukapheresis. In some aspects, the sample includes lymphocytes, including T cells, monocytes, granulocytes, B cells, other nucleated white blood cells, red blood cells, and / or platelets, and in some aspects, the sample includes cells that are not red blood cells or platelets. In some embodiments, blood cells collected from a subject are washed, for example, to remove the plasma fraction and to place the cells in a buffer or medium appropriate for subsequent processing steps. In some embodiments, the cells are washed with phosphate buffered saline (PBS). In some aspects, the washing step is accomplished by tangential flow filtration (TFF) according to the manufacturer's instructions. In some embodiments, the cells are resuspended in various buffers that are biocompatible after washing. In some embodiments, components in the blood cell sample are removed and the cells are resuspended directly in culture medium. In some embodiments, the methods include density-based cell separation methods, such as preparation of white blood cells from peripheral blood by lysing red blood cells and centrifugation through a Percoll or Ficoll gradient.

[0124] In one embodiment, immunity is obtained and cells from the individual's circulating blood are obtained by apheresis or leukapheresis. The apheresis product typically includes lymphocytes, including T cells, monocytes, granulocytes, B cells, other nucleated white blood cells, red blood cells, and platelets. The cells collected by apheresis may be washed to remove the plasma fraction and to place the cells in a buffer or medium suitable for subsequent processing steps, such as phosphate buffered saline (PBS) or a washing solution that may be calcium-free and magnesium-free, or may be free of many, if not all, divalent cations. After washing, the cells may be resuspended in a variety of biocompatible buffers, such as Ca-free, Mg-free PBS. Alternatively, undesirable components of the apheresis sample may be removed and the cells are resuspended directly in culture medium.

[0125] In some embodiments, the isolation method includes separating different cell types based on the expression or presence of one or more specific molecules, such as surface markers, such as surface proteins, intracellular markers, or nucleic acids, in cells. In some embodiments, any known method for separating based on such markers may be used. In some embodiments, the separation is affinity-based separation or immunoaffinity-based separation. For example, the isolation in some aspects includes the separation of cells and cell populations based on the expression or expression level of one or more markers, typically cell surface markers, for example by incubation with an antibody or binding partner that specifically binds to such marker, typically followed by a washing step and separation of cells that bind to the antibody or binding partner from cells that do not bind to the antibody or binding partner.

[0126] Such a separation step may be based on positive selection, which retains the cells that bind to the reagent for further use, and / or may be based on negative selection, which retains the cells that do not bind to the antibody or binding partner. In some examples, both fractions are retained for further use. In some aspects, negative selection is particularly useful when an antibody that specifically identifies a cell type in a heterogeneous population is not available, and therefore separation is best performed based on markers expressed by cells other than the desired population. Separation does not need to result in 100% enrichment or 100% removal of a certain cell population or cells that express a certain marker. For example, positive selection or enrichment of a certain type of cell, such as cells that express a marker, refers to increasing the number or percentage of such cells, but does not need to result in the complete absence of cells that do not express the marker. Similarly, negative selection, removal, or depletion of a particular type of cell, e.g., cells expressing a certain marker, refers to reducing the number or percentage of such cells, but does not necessarily result in the complete elimination of all such cells.

[0127] In some cases, multiple rounds of separation steps are performed, where the positively or negatively selected fraction from one step is subjected to another separation step, e.g., a subsequent positive or negative selection. In some cases, cells expressing multiple markers can be simultaneously depleted in one separation step, e.g., by incubating cells with multiple antibodies or binding partners, each specific for a marker that is the target of negative selection. Similarly, multiple cell types can be simultaneously positively selected by incubating cells with multiple antibodies or binding partners against markers expressed in various cell types.

[0128] In some embodiments, one or more of the T cell populations are positive for one or more particular markers, such as surface markers (markers + ) or express them at high levels (markers 高 ) enrichment or depletion for cells that are negative for one or more markers (marker - ) or express them at relatively low levels (markers 低For example, in some aspects, a particular subpopulation of T cells, such as cells that are positive for or express high levels of one or more surface markers, e.g., CD28+, CD62L+, CCR7+, CD27+, CD127+, CD4+, CD8+, CD45RA+, and / or CD45RO+ T cells, is isolated by positive or negative selection techniques. In some examples, such markers are absent or expressed at relatively low levels in some populations of T cells (e.g., populations of cells that are not memory cells) but are present or expressed at relatively high levels in other populations of T cells (e.g., memory cell populations). In one embodiment, cells (e.g., CD8+ cells or T cells, e.g., CD3+ cells) are enriched (i.e., positively selected) for cells that are positive for or express high surface levels of CD45RO, CCR7, CD28, CD27, CD44, CD127, and / or CD62L, and / or are depleted (e.g., negatively selected) for cells that are positive for or express high surface levels of CD45RA. In some embodiments, cells are enriched or depleted for cells that are positive for or express high surface levels of CD122, CD95, CD25, CD27, and / or IL7-Ra (CD127). In some examples, CD8+ T cells are enriched for cells that are positive for CD45RO (or negative for CD45RA) and positive for CD62L. For example, CD3+ and CD28+ T cells can be positively selected using CD3 / CD28 conjugated magnetic beads (e.g., DYNABEADS® M-450 CD3 / CD28 T Cell Expander).

[0129] In some embodiments, T cells are separated from the PBMC sample by negative selection for markers expressed in non-T cells, such as B cells, monocytes, or other leukocytes, such as CD14. In some aspects, a CD4+ or CD8+ selection step is used to separate CD4+ helper T cells and CD8+ cytotoxic T cells. Such CD4+ and CD8+ populations can be further sorted into subpopulations by positive or negative selection for markers expressed in or relatively highly expressed in one or more of naive T cell populations, memory T cell populations, and / or effector T cell populations. In some embodiments, CD8+ cells are further enriched or further depleted for naive cells, central memory cells, effector memory cells, and / or central memory stem cells, for example, by positive or negative selection based on surface antigens associated with each subpopulation. In some embodiments, enrichment of central memory T (TCM) cells is performed to increase efficacy, such as by improving long-term survival, expansion, and / or engraftment following administration, which in some aspects are particularly robust in such subpopulations. In some embodiments, combining TCM-enriched CD8+ T cells with CD4+ T cells further enhances efficacy.

[0130] In some embodiments, memory T cells are present in both CD62L+ and CD62L- subsets of CD8+ peripheral blood lymphocytes. PBMCs can be enriched or depleted for CD62L-CD8+ and / or CD62L+CD8+ fractions, for example, with anti-CD8 and anti-CD62L antibodies. In some embodiments, CD4+ T cell populations and CD8+ T cell subpopulations, such as subpopulations enriched for central memory (TCM) cells. In some embodiments, enrichment of central memory T (TCM) cells is based on positive or high surface expression of CD45RO, CD62L, CCR7, CD28, CD3, and / or CD127; in some aspects, the enrichment is based on negative selection of cells that express or highly express CD45RA and / or granzyme B. In some aspects, isolation of a CD8+ population enriched for TCM cells is performed by depletion of cells expressing CD4, CD14, CD45RA, and positive selection or enrichment of cells expressing CD62L. In one aspect, enrichment of central memory T (TCM) cells is performed by starting with a negative fraction of cells selected on the basis of CD4 expression, which is subjected to negative selection on the basis of CD14 and CD45RA expression, and positive selection on the basis of CD62L. Such selections are performed simultaneously in some aspects, and sequentially in either order in other aspects. In some aspects, the same selection step based on CD4 expression used in preparing the CD8+ cell population or subpopulation is also used to generate the CD4+ cell population or subpopulation, in which case both the positive and negative fractions from the CD4-based separation are retained and both fractions are used in subsequent steps of the method, optionally after one or more further positive or negative selection steps.

[0131] CD4+ T helper cells are sorted into naive cells, central memory cells, and effector cells by identifying cell populations with cell surface antigens. CD4+ lymphocytes can be obtained by standard methods. In some embodiments, naive CD4+ T lymphocytes are CD45RO-, CD45RA+, CD62L+, CD4+ T cells. In some embodiments, central memory CD4+ cells are CD62L+ and CD45RO+. In some embodiments, effector CD4+ cells are CD62L- and CD45RO. In one example, to enrich CD4+ cells by negative selection, the monoclonal antibody cocktail typically contains antibodies against CD14, CD20, CD11b, CD16, HLA-DR, and CD8. In some embodiments, the antibody or binding partner is bound to a solid support or matrix, such as magnetic or paramagnetic beads, which allows for the separation of cells by positive and / or negative selection.

[0132] In some embodiments, the cells are incubated and / or cultured prior to or in conjunction with genetic manipulation. The incubation step may include culturing, cultivating, stimulating, activating, and / or growing. In some embodiments, the composition or cells are incubated in the presence of stimulatory conditions or stimuli. Such conditions include conditions designed to induce proliferation, expansion, activation, and / or survival of cells in a population, mimic exposure to antigens, and / or prime cells for genetic manipulation, such as the introduction of recombinant antigen receptors. The conditions may include one or more of the following: a specific medium, temperature, oxygen content, carbon dioxide content, time, agents such as nutrients, amino acids, antibiotics, ions, and / or stimulatory factors such as cytokines, chemokines, antigens, binding partners, fusion proteins, recombinant soluble receptors, and other agents designed to activate cells. In some embodiments, the stimulatory conditions or stimuli include one or more agents, such as ligands capable of activating the intracellular signaling domain of the TCR complex. In some aspects, the agent activates or initiates the TCR / CD3 intracellular signaling cascade in the T cell. Such agents may include antibodies, such as, for example, antibodies specific for TCR components and / or costimulatory receptors, such as, for example, anti-CD3 antibodies, anti-CD28 antibodies, such as, for example, antibodies bound to a solid support, such as beads, and / or such agents may include one or more cytokines. Optionally, the expansion method may further include adding anti-CD3 antibodies and / or anti-CD28 antibodies to the culture medium (e.g., at a concentration of at least about 0.5 ng / ml). In some embodiments, the stimulatory agent includes IL-2 and / or IL-15, such as, for example, IL-2 at a concentration of at least about 10 units / mL.

[0133] In another embodiment, T cells are isolated from peripheral blood by lysing red blood cells and depleting monocytes, for example by centrifugation through a PERCOLL™ gradient. Alternatively, T cells can be isolated from umbilical cord. In either case, certain T cell subpopulations can be further isolated by positive or negative selection techniques.

[0134] The cord blood mononuclear cells so isolated may be depleted of cells expressing certain antigens, including, but not limited to, CD34, CD8, CD14, CD19, and CD56. Depletion of these cells can be accomplished using isolated antibodies, biological samples containing antibodies, such as ascites fluid, antibodies bound to solid supports, and antibodies bound to cells.

[0135] Enrichment of T cell population by negative selection can be achieved by using a combination of antibodies directed to surface markers specific to the cells to be negatively selected.The preferred method is cell sorting and / or selection by negative magnetic immunoadherence or flow cytometry using a cocktail of monoclonal antibodies directed to cell surface markers present on the cells to be negatively selected.For example, to enrich CD4+ cells by negative selection, the monoclonal antibody cocktail typically contains antibodies against CD14, CD20, CD11b, CD16, HLA-DR, and CD8.

[0136] For the isolation of desired cell populations by positive or negative selection, the concentration of cells and the concentration of surface-providing particles (e.g., particles such as beads) can be varied. In some embodiments, it may be desirable to significantly reduce the amount of beads and cells mixed together (i.e., increase the concentration of cells) to ensure maximum contact between cells and beads. For example, in one embodiment, a concentration of 2 billion cells / ml is used. In one embodiment, a concentration of 1 billion cells / ml is used. In a further embodiment, more than 100 million cells / ml is used. In a further embodiment, a cell concentration of 10 million cells / ml, 15 million cells / ml, 20 million cells / ml, 25 million cells / ml, 30 million cells / ml, 35 million cells / ml, 40 million cells / ml, 45 million cells / ml, or 50 million cells / ml is used. In yet another embodiment, a cell concentration of 75 million cells / ml to 80 million cells / ml, 85 million cells / ml, 90 million cells / ml, 95 million cells / ml, or 100 million cells / ml is used.In further embodiments, a concentration of 125 million cells / ml or 150 million cells / ml can be used.Using a high concentration can result in increased cell yield, increased cell activation, and increased cell expansion.

[0137] T cells can also be frozen after a washing step, which does not require a monocyte removal step. Without being bound by theory, the freezing and subsequent thawing steps provide a more homogenous product due to the removal of granulocytes and to some extent monocytes in the cell population. After a washing step to remove plasma and platelets, the cells may be suspended in a freezing solution. While many freezing solutions and freezing parameters are known in the art and are useful in this context, in one non-limiting example, one method involves using PBS containing 20% ​​DMSO and 8% human serum albumin, or other suitable cell freezing medium. The cells are then frozen down to -80°C at a rate of once per minute and stored in a vapor-phase liquid nitrogen cryopreservation tank. Other controlled freezing methods may be used, and uncontrolled rapid freezing at -20°C or in liquid nitrogen may be used as well.

[0138] In one embodiment, the T cell population is comprised among cells such as, for example, peripheral blood mononuclear cells, umbilical cord blood cells, purified populations of T cells, and T cell lines. In another embodiment, peripheral blood mononuclear cells comprise the T cell population. In yet another embodiment, purified T cells comprise the T cell population.

[0139] In some embodiments, regulatory T cells (Treg) can be isolated from the sample. The sample can include, but is not limited to, umbilical cord blood or peripheral blood. In some embodiments, Treg is isolated by flow cytometry sorting. The sample can be enriched for Treg before isolation by any means known in the art. The isolated Treg can be cryopreserved and / or expanded before use. Methods for isolating Treg are described in U.S. Patent Nos. 7,754,482, 8,722,400, and 9,555,105, and U.S. Patent Application No. 13 / 639,927, the contents of which are incorporated herein in their entirety.

[0140] D. composition In one aspect, the present disclosure provides a novel cell-permeable PAGE system capable of efficiently editing cells (e.g., primary CD8 T cells). The PAGE system includes a cell-permeable Cas (e.g., a Cas (e.g., Cas9 or Cas12a) linked to a CPP) and an endosomal escape peptide (e.g., dTAT-HA2) linked to the CPP.

[0141] In some embodiments, the Cas is Cas9. Exemplary Cas9 nucleases that can be used in the present invention include, but are not limited to, S. pyogenes Cas9 (SpCas9), S. aureus Cas9 (SaCas9), S. thermophilus Cas9 (StCas9), N. meningitidis Cas9 (NmCas9), C. jejuni Cas9 (CjCas9), and Geobacillus Cas9 (GeoCas9). In some embodiments, the Cas is Cas12a (Cpf1), including, but not limited to, Butyrivibrio spp. (BsCas12a), Thiomicrospira spp. XS5 (TsCas12a), Moraxella bovocri (MbCas12a), Prevotella briantii (PbCas12a), Bacteroides oralis (BoCas12a), Lachnospiraceae (LbCas12a), and Acidaminococcus spp. (AsCas12a). In some embodiments, the Cas is selected from the group consisting of Cas12b, Cas12d, Cas12f, T7, Cas3, Cas8a, Cas8b, Cas10d, Cse1, Csy1, Csn2, Cas4, Cas10, Csm2, Cmr5, and Fok1.

[0142] In some embodiments, the Cas protein (i.e., Cas9, Cas12a, Cas derivatives) is either fused to, chemically linked to, or post-translationally linked to a DNA modifier or its catalytic domain, including, but not limited to, AID deaminase, APOBEC deaminase, TadA deaminase, TET enzymes, DNA methyltransferases, transactivation domains, reverse transcriptases, histone acetyltransferases, histone deacetylases, sirtuins, histone methyltransferases, histone demethylases, kinases, phosphatases, and the like.

[0143] In some embodiments, the endosomal escape peptide comprises dTAT-HA2. Other endosomal escape peptides that may be used include, but are not limited to, EED, HA2-Penetratin, GALA, INF-7, and the like. In some embodiments, the endosomal escape peptide is any one of the peptides listed in Table 1. In some embodiments, the endosomal escape peptide comprises any one of the sequences set forth in SEQ ID NOs: 1434-1523. In some embodiments, the endosomal escape peptide is linked to any of the CPPs listed in Table 2. In some embodiments, the endosomal escape peptide is linked to a CPP comprising any of the amino acid sequences set forth in SEQ ID NOs: 10-1422.

[0144] In some embodiments, the Cas comprises a nuclear localization sequence (NLS). The NLS may include any NLS known in the art or disclosed herein. In some embodiments, the Cas comprises a 4xMyc NLS sequence or a 6xMyc NLS sequence. In some embodiments, the Myc NLS sequence comprises the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). In some embodiments, the NLS (i.e., 4xMyc NLS or 6xMyc NLS) sequence further comprises a GGS linker.

[0145] In some embodiments, the cell membrane permeable Cas comprises a nucleotide sequence encoding a cell membrane permeable peptide or comprises an amino acid sequence comprising a cell membrane permeable peptide. Examples of CPPs include, but are not limited to, transactivating transcription activator from HIV-1 (Tat), oligo-Arg, KALA, transportan, penetratin, penetratin-Arg, TAT-HA2, and dTAT-HA2E5. Examples of CPPs are also listed in Table 2 herein. In some embodiments, the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10-1422. In some embodiments, the cell membrane permeable Cas comprises a sequence derived from transactivating transcription activator from HIV-1 (Tat). In some embodiments, the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO: 2). Other truncated or modified Tat peptides that may be used include, but are not limited to, the following: Truncated Tat: TIFF2024520644000016.tif19163, as well as modified Tat: 2xTat, 3xTat, 4xTat, nxTat, etc.

[0146] The PAGE system may contain two different CPPs or may contain two of the same CPP. The CPPs may be linked to the Cas or endosomal escape peptide by any means known in the art, such as, but not limited to, chemical conjugation, fusion, or post-translational modification.

[0147] Kits are also provided that include the compositions of the invention described herein and / or for carrying out the methods of the invention described herein. For example, in some embodiments, kits for carrying out the methods of the invention include a composition that includes a cell-permeable PAGE system that includes a cell-permeable Cas and an endosomal escape peptide.

[0148] Additionally, additional reagents may also be present as required or desirable in the protocol to be performed with the kit components, including, but not limited to, sgRNA, nuclease-free water, carriers, and reagents (e.g., nucleotides, buffers, cations, etc.) The kit components may be in separate containers, or one or more of the components may be in the same container, which may be a storage container and / or, for kits designed for assays, a container utilized during the assay process.

[0149] In addition to the above-mentioned components, the kit may further include instructions for carrying out the methods described herein. The instructions may be present in the kit in various forms, and one or more of such instructions may be present in the kit. One form in which the instructions may be present is as information printed on a suitable medium or substrate, such as the kit's packaging, insert, or the like, such as one or more sheets of paper on which the information is printed. Yet another form of the instructions may include a computer-readable medium on which the information is recorded, such as a CD. Yet another form of the instructions may include a website address, which may be used via the Internet to access the information at a remote location. Any convenient means may be present in the kit.

[0150] The contents of the articles, patents, and patent applications, and the contents of all other literature and electronically available information mentioned or cited herein are incorporated herein by reference in their entirety to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference. Applicants reserve the right to substantially incorporate into this application any and all material and information from any such articles, patents, patent applications, or other literature, both physical and electronic.

[0151] Although the present invention has been described with reference to certain embodiments thereof, those skilled in the art will understand that various modifications may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. Other suitable modifications and adaptations of the methods described herein may be made with suitable equivalents without departing from the scope of the embodiments described herein, as will be apparent to those skilled in the art. In addition, many modifications may be made to adapt a particular situation, material, composition, process, process step or steps to the objective, spirit and scope of the present invention. All such modifications are intended to be within the scope of the claims appended hereto. Certain embodiments will now be described in detail, which will be more clearly understood by reference to the following examples, which are included for illustrative purposes only and are not intended to be limiting. EXAMPLES

[0152] Experimental Example The invention will now be described with reference to the following examples, which are provided for illustrative purposes only and the invention is not limited by these examples, but rather encompasses all variations that become evident as a result of the teachings provided herein.

[0153] Example 1: Purification of TAT-4xMyc NLS-Cas9 The TAT-4xMyc NLS-Cas9 expression construct was generated by replacing the 4xSV40 NLS (PKKKRKV (SEQ ID NO: 1423)) at the N-terminus of Cas9 (Staahl et al., (2017) Nat Biotechnol 35, 431-434) with the 4xMyc NLS (PAAKRVKLD (SEQ ID NO: 1)) with the linker "-GGS-" between the Myc NLS. The sequence of TAT (GRKKRRQRRRPQ (SEQ ID NO: 2)), a cell membrane permeable peptide derived from the transactivator of transcription (Tat) from HIV-1 (Frankel and Pabo, 1988; Green and Loewenstein, 1988), was added to the N-terminus, and TAT-4xMyc NLS-Cas9 was cloned into a bacterial recombinant protein expression vector (Gootenberg et al., 2017) together with Twin-Strep and SUMO tags (Figure 1A). The TAT-4xMyc NLS-Cas9 protein was then purified by Strep-Tactin affinity chromatography followed by in-column digestion with SUMO protease, ion exchange chromatography (IEC), and size exclusion chromatography (SEC) (Figure 1B) (Gootenberg et al., (2017) Science 356, 438-442). The purified TAT-4xMyc NLS-Cas9 protein efficiently cleaved DNA in an in vitro DNA cleavage assay (Figure 1C).

[0154] Example 2: Genome editing with TAT-4xMyc NLS-Cas9 in EL4 cells To determine whether TAT-4xMyc NLS-Cas9 has the ability to edit genomes, the EL4 thymoma cell line was used. A lentiviral reporter construct stably expressing mCherry and an sgRNA targeting mCherry was infected into EL4 cells. If TAT-4xMyc NLS-Cas9 penetrates the cell membrane and edits mCherry in the EL4 reporter cells, the loss of mCherry fluorescence, as measured by flow cytometry, would be due to the loss of mCherry fluorescence. - In this regard, when cells were incubated with 0.5 μM TAT-4xMyc NLS-Cas9 alone for 1 h, the frequency of mCherry expression was significantly increased compared to untreated cells (Figure 2A). - No increase in the frequency of cells was observed (Figure 2B). On the other hand, when the endosomal escape peptide dTAT-HA2 was added during incubation (up to 40 μM), mCherry - When cells were incubated with 4.0 μM TAT-4xMyc NLS-Cas9, the percentage of cells expressing mCherry increased to 44.1% (Figure 2B). - An even stronger increase in cells was observed, which was 62% at 40 μM dTAT-HA2 (FIG. 2B).

[0155] It was also tested whether the percentage of FBS during incubation had an effect on the editing efficiency of TAT-4xMyc NLS-Cas9. When the percentage of FBS was reduced from 10% to 0 and cells were co-treated with 10 μM dTAT-HA2 and 0.5 μM TAT-4xMyc NLS-Cas9, the mCherry - The percentage of cells expressing mCherry increased from 4.26% to 15.9% (Figure 2C, left panel). When the concentration of TAT-4xMyc NLS-Cas9 was increased to 4.0 μM, - The percentage of cells with mCherry increased from 44.3% to 69.1% (Figure 2C, left panel). Further increasing the concentration of dTAT-HA2 to 40 μM -The percentage of cells that expressed mCherry was also increased compared to treatment with 10 μM dTAT-HA2 (Figure 2C, right panel). To achieve maximum editing efficiency, we increased the concentration of TAT-4xMyc NLS-Cas9 to 5 μM, dTAT-HA2 to 75 μM, and decreased the incubation time to 30 min, and found that no FBS was added during incubation. - The percentage of cells reached 92.9% (Figure 2D).

[0156] Example 3: In vitro editing with TAT-4xMyc NLS-Cas9 in mouse primary T cells Prior to testing the in vitro editing of TAT-4xMyc NLS-Cas9 in mouse primary T cells, two kinds of sgRNAs were designed to target the cell surface marker CD45.2, and the editing efficiency of the sgRNAs was tested in RN2-Cas9 cells that stably express Cas9. RN2-Cas9 cells were infected with retroviruses that express sgRNA and mCherry, and 3 days after infection, the expression level of CD45.2 was measured by flow cytometry. Both sgRNAs that target CD45.2 knocked down CD45.2 efficiently compared with sgRNAs that target Rosa26 (Figure 3A). Next, it was tested whether TAT-4xMyc-Cas9 could edit genomes in mouse primary CD8 T cells. The schematic diagram of the experiment is shown in Figure 3B. Briefly, primary CD8 T cells were isolated from the spleens of 3-month-old mice on day -2 and activated with CD3, CD8, and IL-2 for 24 hours. On day -1, retroviruses expressing sgRNA and mCherry were infected into activated cells for 24 hours. Cells were then treated with 5 μM TAT-4xMyc NLS-Cas9 (GFP-tagged) and 75 μM dTAT-HA2 and incubated in RPMI 1640 supplemented with 1% FBS and 50 μM 2-mercaptoethanol in a 37° incubator for 40 minutes. Cells were washed twice with PBS, trypsinized for 10 min at 37°C to remove cell surface-bound TAT-4xMyc NLS-Cas9, treated with DNase I (400 U / ml) for 3 min at room temperature, neutralized, and washed once with complete RPMI 1640 medium. Immediately after washing, cells were resuspended in 100,000 sgRNA for in vitro culture. + Cas9 + (mCherry + GFP +) cells were sorted at 37°C (Figure 3C). CD45.2 expression levels were measured by flow cytometry from days 1 to 5. For cells infected with CD45.2 sgRNA_1, the percentage of CD45.2 knockdown cells increased after day 1 and reached a maximum of approximately 60% on day 4. No such increase was observed in cells infected with Rosa26 sgRNA or CD90.2 sgRNA (Figure 3D, left panel). For cells infected with CD90.2 sgRNA_2 or CD90.2 sgRNA_3, the percentage of CD90.2 knockdown cells dramatically increased after day 1 and reached a maximum on day 3 (approximately 70% for sgRNA_3 and approximately 90% for sgRNA_2). No increased knockdown of CD90.2 was observed in cells infected with Rosa26 sgRNA or CD45.2 sgRNA (Figure 3D, right panel). The stability of TAT-4xMyc NLS-Cas9 was assessed in cells by measuring the normalized mean fluorescence intensity (MFI) of GFP. The MFI of GFP decreased by approximately 75% on day 1 and by more than 90% on day 2 (Figure 3E), indicating the lower immunogenicity of TAT-4xMyc NLS-Cas9 compared to constitutively expressed Cas in other systems (Ajina et al., (2019) Oncoimmunology 8, e1577127; Chew et al., (2016) Nat Methods 13, 868-874; Wang et al., (2015) Hum Gene Ther 26, 432-442).

[0157] Example 4: In vivo editing with TAT-4xMyc NLS-Cas9 in mouse primary T cells A schematic workflow for testing the in vivo editing efficiency of TAT-4xMyc NLS-Cas9 is shown in Figure 4A. CD8 P14 cells from donor mice expressing T cell receptors (TCR) specific for the LCMV GP33-41 epitope were isolated and activated. On the same day (day -2), recipient mice were infected with LCMV clone 13 to induce chronic infection and T cell exhaustion. Twenty-four hours later (day -1), cells were infected with retroviral vectors (with VEX reporter) expressing sgRNAs targeting Ano9 or sgRNAs targeting Pdcd1 (encoding PD-1) for 24 hours. Cells were treated with TAT-4xMyc NLS-Cas9, dTAT-HA2, 0.25% trypsin, and DNase I as described herein, and sgRNAs were then transfected. + Cas9 + (VEX + GFP + ) P14 cells were sorted (Figure 4B). Fifty thousand sorted cells were adoptively transferred by tail vein injection into recipient mice infected with LCMV clone 13. Six days later, spleens and livers were harvested and analyzed by flow cytometry for PD-1 expression and expansion of P14 cells. A dramatic reduction in PD-1 expression was observed; down to approximately 20% in both spleen and liver in cells infected with both sgRNAs targeting Pdcd1 compared to cells infected with sgRNAs targeting Ano9 (Figure 4C). Importantly, the sgRNAs + Percentage of P14 T cell population, and sgRNA + Total numbers of P14 T cells were increased in both sgRNAs targeting Pdcd1 compared to sgRNAs targeting Ano9 in both spleen and liver (Figure 4D), consistent with enhanced expansion of antigen-specific CD8 T cells early during chronic infection as a result of genetic depletion of PD-1.

[0158] Example 5: In vitro editing with TAT-4xMyc NLS-Cas9 in human primary T cells A schematic workflow for testing the in vitro editing efficiency of TAT-4xMyc NLS-Cas9 in human primary T cells is shown in Figure 5A. Human total T cells were isolated by human T cell isolation kit from PBMCs of normal donors and activated by CD3 / CD28 Dynabeads, IL-7, and IL-15 in OpTmizer T cell expansion medium supplemented with 5% human serum and 1x Glutamax I on day 0. After 24 hours (day 1), cells were infected with lentiviral reporter constructs for 2 days as in Figure 2A. mCherry+ cells were selected by blasticidin on days 3-9, followed by treatment with 0.5 μM TAT-4xMyc NLS-Cas9 and 25-75 μM dTAT-HA2 in T cell expansion complete medium for 30 min at 37°C. The cells were washed once with PBS and cultured for an additional 5 days. - The frequency of mCherry T cells was measured by flow cytometry on days 12 to 14 (mCherry D3 to mCherry D5). - The frequency of cells increased from approximately 20% to approximately 35-70% (with 0.5 μM TAT-4xMyc NLS-Cas9 and 25 μM dTAT-HA2), and mCherry was not observed even when the concentration of dTAT-HA2 was increased from 25 μM to 50 μM or 75 μM. - The frequency of cells increased to 45–75% (Figure 5B, left panel). - The frequency of cells increased to approximately 70–90% (0.5 μM TAT-4xMyc NLS-Cas9, and 25 μM dTAT-HA2) (Figure 5B, right panel). - The frequency of mCherry-human T cells was not increased in T cells infected with sgRosa26 (Figure 5B). An example histogram of mCherry-human T cells on day 5 after treatment of cells with 0.5 μM TAT-4xMyc NLS-Cas9 and 50 μM dTAT-HA2 is shown in Figure 5C.

[0159] Example 6: In vitro editing with TAT-4xMyc NLS-Cas9 in iPSCs iPSCs were infected with the same lentiviral reporter construct as in Figure 2A and treated as in Figure 2A. When incubated with 0.5 μM TAT-4xMyc NLS-Cas9 and 75 μM dTAT-HA2, mCherry - The frequency of cells increased from approximately 20% to 60% on the fourth day after treatment. - The frequency of cells did not increase in iPSCs infected with sgRosa26 (Figure 6A). An example histogram of mCherry- iPSCs on day 4 after treatment of cells with 0.5 μM TAT-4xMyc NLS-Cas9 and 75 μM dTAT-HA2 is shown in Figure 6B.

[0160] The present disclosure provides a novel method for in vitro and in vivo CRISPR editing of mouse and human CD8 T cells, human primary T cells, and human iPSCs. The efficiency of the editing can reach up to 90% for in vitro editing of CD90.2 and in vivo editing of PD-1, which is much higher than other previously reported methods that use cell membrane-permeable Cas9 for genome editing (Staahl et al., (2017) Nat Biotechnol 35, 431-434). In addition, previously reported methods for editing the genome of mouse CD8 T cells require electroporation or Cas9 transgenic mice, whereas the present method does not, and thus genome editing can be achieved in a timely and economical manner. Thus, the present disclosure describes a simple, efficient, and economical approach for editing the genome of CD8 T cells both in vitro and in vivo.

[0161] Example 7: Peptide-assisted genome editing (PAGE) The PAGE system construct was made to contain cell membrane-permeable CRISPR-associated (Cas) proteins (Cas9, Cas12) and assisting / endosomal escape peptides (TAT, HA2) (Figure 7). The peptide-assisted cell membrane-permeable Cas9 system was optimized in EL4 reporter cells (Figures 8A-8E). EL4, a mouse T lymphoblast, was lentivirally transduced with a dual expression vector stably expressing mCherry (mChe) fluorescent reporter and sgRNA targeting the mCherry gene, or with a dual expression vector stably expressing mCherry (mChe) fluorescent reporter and sgRNA targeting the Ano9 gene as a negative control (Figure 8A). EL4-mChe cells were incubated with various Cas9-CPP proteins as well as various endosomal escape or cell membrane-permeable chemicals and peptides. Proteins, chemicals, and peptides were washed away after 30 min of incubation. Four days after treatment, gene editing efficiency was assessed based on the loss of mChe fluorescence using flow cytometry (Figure 8A).

[0162] Cas9-T6N was transfected with various endosomal escape or cell membrane permeable chemicals and peptides in EL4-mChe reporter cells. CPP (TAT-4xNLS MYC -Cas9-2xNLS SV40 The editing efficiency of Cas9-T6N (-sfGFP) was quantified (Figure 8B). EL4 mChe reporter cells were transfected with 0.5 μM Cas9-T6N in the presence of the chemicals 200 mM chloroquine or 1 mg / ml polybrene, or in the presence of 75 μM of the supporting peptides KALA, transportan, penetratin, penetratin-Arg, dTAT-HA2E5, or TH(dTAT-HA2). CPPTo measure the editing efficiency, the percentage of cells that lost mCherry was measured by flow cytometry on the fourth day after treatment. Among these chemicals and CPP peptides tested, the highest percentage of mCherryOFF (>90%) was shown by incubation with TH(dTAT-HA2), suggesting that incubation with TH strongly induced gene editing (Figure 8B).

[0163] EL4 cells were transfected with 5 μM of Cas9-T6N CPP and 75 μM TH at 37°C for 30 min, after which the cells were washed with PBS and the cell surface-bound Cas9-T6N CPP The cells were trypsinized to remove chromatin. Nuclear and cytoplasmic fractions were separated and subjected to immunoblotting analysis using antibodies against Cas9, the nuclear marker lamin B1, and the cytoplasmic marker α-tubulin. CPP Cas9-T6N in nuclear fractions, cytoplasmic fractions, and whole cell lysates prepared from EL4 cells treated with TH and CPP Western blots for levels of Cas9-T6N, lamin-B1, and α-tubulin are shown in Figure 8C. The data show that addition of TH increased the expression of Cas9-T6N compared to cells without TH treatment. CPP These results indicate increased translocation of Cas9-CPP into the cell, into the cytoplasmic fraction, and especially into the nuclear fraction (Figure 8C). Editing efficiency of 0.5 μM Cas9-CPP variants was quantified in EL4-mChe reporter cells with various concentrations of TH peptide (Figure 8D). The combination of cell membrane-permeable Cas proteins and endosomal escape peptides has been termed peptide-assisted genome editing (PAGE) (Figure 8E).

[0164] The Cas9-PAGE system was optimized in EL4 reporter cells (Figures 9A-9E). Gene editing efficiency was significantly improved with either TH or Cas9-T6N. CPPThe percentage of cells that had lost mCherry was measured by flow cytometry on the second day after treatment. EL4 mCherry reporter cells were quantified using a titration of either 0.5 μM Cas9-T6N CPP , and incubated with various concentrations of TH ranging from 5 to 100 μM. The concentration of TH was positively correlated with the increase in gene editing efficiency (Figure 9A). EL4 mCherry reporter cells were incubated with various concentrations of Cas9-T6N CPP , and 75 μM TH. CPP Increasing the concentration of TH resulted in increased gene editing efficiency (Figure 9B). Quantification of viable cell recovery of EL4 cells treated with increasing concentrations of TH is shown in Figure 9C. CPP Quantification of the GFP-positive cell population as a function of increasing doses of (FIG. 9D). The percentage of GFP-positive cells is a surrogate for the efficiency of cell membrane permeabilization.

[0165] TH (dTAT-HA2) is a trans-assisted PAGE system. Gene editing efficiency was quantified after truncation of TH. EL4 mCherry reporter cells were transfected with 0.5 μM Cas9-T6N in the presence of 75 μM T peptide, H peptide, or TH peptide. CPP The percentage of cells that had lost mCherry was measured by flow cytometry on the fourth day after treatment. The TH(dTAT-HA2) peptide upregulated the Cas9-T6N expression in EL4 mCherry reporter cells. CPP When dTAT-HA2(TH) was added in cis, it enhanced the editing efficiency of Cas9-T6N, whereas neither the T(dTAT) peptide alone nor the H(dHA2) peptide alone enhanced the editing efficiency (Figure 10A). CPP Gene editing efficiency of Cas9-TH6N CPPThe gene editing efficiency of Cas9-TH was quantified. The percentage of cells that had lost mCherry was measured by flow cytometry on day 4 after treatment. Regardless of whether the TH peptide was present in cis, TH was able to mediate the gene editing efficiency of Cas9-TH. CPP in trans (Fig. 10B).

[0166] The efficiency of gene editing mediated by the Cas9-PAGE system was quantified in various cell types (Figure 11). mCherry-positive reporters were established in the following cell types: MOLM-13, a human myeloid cell line model, NK-92, a human natural killer cell line, and primary human T cells isolated from PBMCs of three healthy donors. The mCherry reporter cells were expressed as Cas9-T6N CPP and TH for 30 min, and the percentage of cells that had lost mCherry was measured by flow cytometry on day 4 after treatment. The data demonstrated that the PAGE system can be used for gene editing in a variety of cell types (Figure 11).

[0167] The PAGE system was evaluated ex vivo in primary mouse CD8 T cells. Primary mouse T cells were activated with anti-CD3, anti-CD28, and IL-2, followed by retroviral transduction with an sgRNA expression vector linked to the mCherry fluorescent marker. FACS-sorted enriched mCherry-positive cells were stained for Cas9-T6N CPP and TH peptide, which was then washed off after 30 min of incubation. Gene editing was assessed at various time points by flow cytometry for the indicated gene products or by direct Sanger sequencing of the targeted genomic regions (Figure 12A). Primary CD8 T cells were transduced with either sgThy1_IG1 or sgNeg, followed by transduction with various concentrations of TH and 5 μM Cas9-T6N. CPPIncubation with TH was performed for 30 min. Flow cytometry analysis was performed on days 2, 4, and 6 after treatment. Time course analysis of CD90 protein expression in CD8 T cells treated with increasing concentrations of TH is shown in FIG. 12B. Quantification of flow cytometry analysis by mean fluorescence intensity (MFI) after 4 days of treatment is shown in FIG. 12C. Representative flow cytometry plots of CD90 after 4 days of treatment in cells transduced with either sgThy1_IG1 or sgNeg are shown in FIG. 12D. Quantification of viable cell recovery of CD8 T cells treated with increasing concentrations of TH is shown in FIG. 12E. Additional sgRNAs were tested, targeting the Thy1 gene (sgThy1_IG1, sgThy1_IG2, sgThy1_IG3: targeting the immunoglobulin domain of Thy1) and the Ptprc gene (sgPtprc_CAT1 and sgPtprc_TM1: targeting either the catalytic or transmembrane domain of Ptprc); and an sgRNA targeting the Ano9 gene was used as a negative control. A schematic bar graph of the gene editing efficiency of PAGE with additional sgRNAs targeting the Thy1 gene and additional sgRNAs targeting the Ptprc gene in mouse primary CD8 T cells at day 4 after treatment is shown in FIG. 12F. Tracking of Indels by DEcomposition (TIDE) mutagenesis assay was performed with the PAGE sgRNAs listed in FIG. 12F. Results are presented as dot plots showing the TIDE assay score (% of indels) for each sgRNA (Figure 12G). Genomic DNA was isolated on day 6 after PAGE and Sanger sequenced, followed by quantification with the online TIDE analysis tool. Results demonstrated that Cas9-PAGE with retroviral sgRNA mediated genome editing ex vivo in primary mouse CD8 T cells (Figures 12A-12G).

[0168] The cell membrane-permeable ribonucleoprotein (RNP) complexes for PAGE genome editing were tested in mouse primary T cells ex vivo (Figures 13A-13D). For RNP-PAGE experiments in mouse primary T cells, a series of Cas complexes including: CPP A variant was created: Cas9-T6N CPP (TAT-4xNLS MYC NLS-Cas9-2xNLS SV40 -sfGFP), Cas9-T8N CPP (TAT-6xNLS MYC NLS-Cas9-2xNLS SV40 -sfGFP), and opCas12a-T8N CPP (TAT-6xNLS MYC NLS-opCas12a-2x\NLS SV40 -sfGFP) (Figure 13A). Ex vivo editing by Cas9 / opCas12a-RNP-PAGE was performed in mouse primary T cells (Figure 13B). Mouse primary CD8 T cells, either naive or activated for 2 days, were incubated with 5 μM RNP complex and various concentrations of TH at 37 degrees for 30 minutes. Cells were washed once and cultured for 5 days with or without sorting GFP+ cells, and editing efficiency was measured by flow cytometry for expression of target genes (Figure 13B). Expression levels of CD90 were measured in either naive or activated CD8 T cells treated with various Cas9 / opCas12a-RNP-PAGE systems (Figure 13C). Naïve or activated mouse primary CD8 T cells were transfected with 5 μM Cas9-T6N with guide RNA targeting the IG domain of CD90 in combination with 25 μM TH as described in FIG. 13B. CPP RNP complex, Cas9-T8N CPP RNP complex, or opCas12a-T8N CPPThe cells were treated with RNP complexes. CD90 expression was measured by flow cytometry on the 5th day after treatment. The results showed that opCas12a-RNP-PAGE showed superior gene editing efficiency over Cas9-RNP-PAGE in mouse primary T cells (Figure 13C). The concentration of TH was optimized for the delivery of opCas12a-RNP-PAGE in primary mouse CD8 T cells (Figure 13D). Mouse primary CD8 T cells were activated for 2 days and then treated with 5 μM opCas12a-T8N targeting the IG domain of CD90 in the presence of various concentrations of TH from 25 to 50 μM. CPP The expression of CD90 was measured by flow cytometry on the 5th day after treatment.

[0169] Genome editing by opCas12a-RNP-PAGE was demonstrated ex vivo in human chimeric antigen receptor (CAR) T cells (Figures 14A-14C). CPP A schematic of the experiment demonstrating ex vivo editing with opCas12a-T8N is shown in Figure 14A. Human primary T cells from healthy donors were isolated and activated with anti-CD3, anti-CD28, and IL-2. Activated T cells were transduced with CAR19 lentivirus on day 1. On day 6, CAR19+ cells were FACS sorted and then transduced with 5 μM opCas12a-T8N. CPP Incubation with RNP and 25 μM TH was performed for 30 min. Cells were cultured for an additional 10 days after treatment, and expression of target genes was measured by flow cytometry. Human CAR T cells were transfected with 5 μM opCas12a-T8N targeting the catalytic domain of CD45 (encoded by PTPRC) or the immunoglobulin domain of beta-2-microglobulin (encoded by B2M) in the presence of 25 μM TH. CPP RNP (Figures 14B-14C). CD45 expression (Figure 14B) or B2M expression (Figure 14C) was measured by flow cytometry on day 6 after treatment.

[0170] Highly efficient in vivo editing of clinically relevant genes by the Cas9-PAGE system was demonstrated in primary mouse T cells (Figures 15A-15G). A schematic of the experimental workflow for evaluating the PAGE system in vivo in primary mouse CD8 T cells is shown in Figure 15A. Donor CD8 T cells from P14 transgenic (CD45.1+ or CD45.1 / 2+ congenic) mice were isolated and activated with anti-CD3, anti-CD28, and IL-2, followed by retroviral transduction with either a test or negative control sgRNA expression vector linked to a fluorescent marker. T cells transduced with sgRNA were transduced with 5 μM Cas9-T6N CPP and 25 μM TH peptide for 30 min, followed by FACS sorting to enrich for Cas9-positive and sgRNA-positive (double-positive) populations. P14 T cells transduced with test sgRNA and negative control sgRNA were mixed at a 1:1 ratio and subsequently adoptively transferred into CD45.2+ congenic recipient mice infected with LCMV clone 13 virus. Gene editing and P14 T cell populations were assessed over time for 30 days by flow cytometry. At day 8 post-infection, surface expression of CD90 was decreased after sgThy1_IG1-mediated editing (Figures 15B-15C), as was PD-1 after sgPdcd1_IG44-mediated editing (Figures 15D-15E). The proportion of P14 T cells transduced with the indicated sgRNAs and co-transferred in the blood over time is shown in Figure 15F. P14 T cells transduced with the indicated sgRNAs as a proportion of total CD8 T cells in the blood over a 30 day period is shown in Figure 15G.

[0171] Base editing by Cas9-BE PAGE was demonstrated in the K562 d2GFP reporter cell line (Figure 16A-16C). A Cas9-BE expression construct was generated (Figure 16A), and the base editing efficiency of the Cas9-BE PAGE system was evaluated in the K562 d2GFP reporter cell line (Figure 16B). K562 cells were lentivirally transduced with a dual expression vector stably expressing the d2GFP fluorescent reporter and a sgRNA targeting the d2GFP fluorescent reporter gene, or a dual expression vector stably expressing the d2GFP fluorescent reporter and a sgRNA targeting the Ano9 gene as a negative control. K562 d2GFP cells were transduced with Cas9-BE-T6N CPP and TH peptide for 30 min, after which the protein and peptide were washed away. Base editing was assessed 5 days after treatment based on the loss of fluorescence of the d2GFP reporter upon complete degradation of the Cas9-BE protein linked to GFP (Figure 16C).

[0172] Numbered Aspects Although numbered aspects are provided below, the numbering should not be construed as indicating any level of importance. Aspect 1 provides: A Peptide-Assisted Genome Editing (PAGE) system comprising: (a) a CRISPR-associated (Cas) protein linked to a cell-penetrating peptide (CPP); and (b) an endosomal escape peptide linked to the CPP. Aspect 2 provides: 2. The PAGE system of embodiment 1, wherein the Cas is Cas9, or Cas12a, or a Cas derivative. Aspect 3 provides: The PAGE system of embodiment 2, wherein the Cas derivative is a Cas protein linked to another protein or catalytic domain. Aspect 4 provides: The PAGE system of embodiment 3, wherein said protein or catalytic domain is selected from the group consisting of AID deaminase, APOBEC deaminase, TadA deaminase, TET enzymes, DNA methyltransferases, transactivation domains, reverse transcriptases, histone acetyltransferases, histone deacetylases, sirtuins, histone methyltransferases, histone demethylases, kinases, and phosphatases. Aspect 5 provides the following: 2. The PAGE system of any one of the preceding aspects, wherein the endosomal escape peptide comprises any of the amino acid sequences set forth in SEQ ID NOs: 1434-1523. Aspect 6 provides the following: 2. The PAGE system of any one of the preceding aspects, wherein the endosomal escape peptide comprises dTAT-HA2. Aspect 7 provides the following: 2. The PAGE system of any one of the preceding aspects, wherein the Cas comprises a nuclear localization signal (NLS) sequence. Aspect 8 provides the following: The PAGE system of embodiment 7, wherein the NLS sequence comprises the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). Aspect 9 provides the following: The PAGE system of embodiment 7 or 8, wherein the NLS sequence further comprises a GGS linker. Aspect 10 provides the following: 2. The PAGE system of any one of the preceding aspects, wherein the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10-1422. Aspect 11 provides the following: 2. The PAGE system of any one of the preceding embodiments, wherein the CPP comprises a sequence derived from the trans-activating transcription activator from HIV-1 (Tat). Aspect 12 provides the following: 12. The PAGE system of embodiment 11, wherein the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO:2). Aspect 13 provides the following: introducing a PAGE system and at least one sgRNA or crRNA into a cell, the PAGE system comprising a Cas protein linked to a CPP and an endosomal escape peptide linked to the CPP; An in vitro method of gene editing comprising: Aspect 14 provides the following: introducing a PAGE system and at least one sgRNA or crRNA into a cell, the PAGE system comprising a Cas protein linked to a CPP and an endosomal escape peptide linked to the CPP; Administering the cells to a subject. An in vivo method of gene editing comprising: Aspect 15 provides the following: The method of embodiment 13 or 14, wherein the Cas is Cas9, or Cas12a, or a Cas derivative. Aspect 16 provides the following: The method of embodiment 15, wherein the Cas derivative is a Cas protein linked to another protein or catalytic domain. Aspect 17 provides the following: 17. The method of embodiment 16, wherein said protein or catalytic domain is selected from the group consisting of AID deaminase, APOBEC deaminase, TadA deaminase, TET enzymes, DNA methyltransferases, transactivation domains, reverse transcriptases, histone acetyltransferases, histone deacetylases, sirtuins, histone methyltransferases, histone demethylases, kinases, and phosphatases. Aspect 18 provides the following: 18. The method of any one of aspects 13-17, wherein the endosomal escape peptide comprises any of the amino acid sequences set forth in SEQ ID NOs: 1434-1523. Aspect 19 provides the following: 19. The method of any one of embodiments 13-18, wherein the endosomal escape peptide comprises dTAT-HA2. Aspect 20 provides the following: 20. The method of any one of embodiments 13-19, wherein the Cas comprises an NLS sequence. Aspect 21 provides the following: The method of embodiment 20, wherein the NLS sequence comprises the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). Aspect 22 provides the following: 22. The method of embodiment 20 or 21, wherein the NLS sequence further comprises a GGS linker. Aspect 23 provides the following: 23. The method of any one of embodiments 13-22, wherein the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10-1422. Aspect 24 provides the following: The method of any one of embodiments 13-23, wherein the CPP comprises a sequence derived from the trans-activating transcription activator from HIV-1 (Tat). Aspect 25 provides the following: 25. The method of embodiment 24, wherein the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO:2). Aspect 26 provides the following: The method of any one of embodiments 13 to 25, wherein electroporation is not required. Aspect 27 provides the following: The method of any one of embodiments 13 to 26, wherein the PAGE system is introduced into the cells in a serum-free medium. Aspect 28 provides the following: The method of any one of embodiments 13 to 27, wherein the endosomal escape peptide is introduced into the cell at a concentration of about 25 to 75 μM. Aspect 29 provides the following: The method of any one of embodiments 13-28, wherein the Cas is introduced into the cell at a concentration of about 0.5-5 μM. Aspect 30 provides the following: The method of any one of embodiments 13 to 29, wherein the cell is an immune cell. Aspect 31 provides the following: The method of any one of embodiments 13-30, wherein the cells are selected from the group consisting of primary human CD8 T cells, human iPSCs, and CAR T cells. Aspect 32 provides the following: The method of any one of embodiments 13-30, wherein the sgRNA targets Ano9, Pdcd1, Thy1, Ptprc, PTPRC, or B2M. Aspect 33 provides the following: The method of any one of embodiments 13-32, wherein the subject is in need of treatment for a disease or disorder, and when the edited cells are administered to the subject, the disease or disorder is treated in the subject. Aspect 34 provides the following: The method of embodiment 33, wherein the disease or disorder is an infection. Embodiment 35 provides the following: The method of embodiment 34, wherein the disease or disorder is associated with T cell exhaustion.

[0173] The contents of the articles, patents, and patent applications, and the contents of all other literature and electronically available information mentioned or cited herein are incorporated herein by reference in their entirety to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference. Applicants reserve the right to substantially incorporate into this application any and all material and information from any such articles, patents, patent applications, or other literature, both physical and electronic.

[0174] While the present invention has been disclosed with reference to certain specific embodiments, it is apparent that others skilled in the art may devise other embodiments and variations of the present invention without departing from the true spirit and scope of the invention, and it is intended that the appended claims be construed to cover all such embodiments and equivalent variations.

[0175] Table 2: Cell-penetrating peptides (CPPs): exemplary sequences TIFF2024520644000017.tif255156TIFF2024520644000018.tif254168TIFF2024520644000019.tif246166TIFF2024520644000020.tif255166TIFF2024520644000021.tif253167TIFF2024520644000022.tif254168TIFF2024520644000023.tif254168TIFF2024520644000024.tif251168TIFF2024520644000025.tif247170TIFF2024520644000026.tif255166TIFF2024520644000027.tif255168TIFF2024520644000028.tif245170TIFF2024520644000029.tif230170TIFF2024520644000030.tif254170TIFF2024520644000031.tif253170TIFF2024520644000032.tif254170TIFF2024520644000033.tif253145

Claims

**Claim 1** A Peptide-Assisted Genome Editing (PAGE) system comprising: (a) a CRISPR-associated (Cas) protein linked to a cell-penetrating peptide (CPP); and (b) an endosomal escape peptide linked to the CPP. **Claim 2** The PAGE system according to claim 1, wherein the Cas is Cas9, or Cas12a, or a Cas derivative. **Claim 3** The PAGE system according to claim 2, wherein the Cas derivative is a Cas protein linked to another protein or catalytic domain. **Claim 4** The PAGE system according to claim 3, wherein the protein or catalytic domain is selected from the group consisting of AID deaminase, APOBEC deaminase, TadA deaminase, TET enzyme, DNA methyltransferase, transactivation domain, reverse transcriptase, histone acetyltransferase, histone deacetylase, sirtuin, histone methyltransferase, histone demethylase, kinase, and phosphatase. **Claim 5** The PAGE system according to claim 1, wherein the endosomal escape peptide comprises any of the amino acid sequences set forth in SEQ ID NOs: 1434 to 1523. **Claim 6** The PAGE system according to claim 1, wherein the endosomal escape peptide comprises dTAT-HA2. **Claim 7** The PAGE system according to claim 1, wherein the Cas comprises a nuclear localization signal (NLS) sequence. **Claim 8** The PAGE system according to claim 7, wherein the NLS sequence comprises the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). **Claim 9** The PAGE system according to claim 7 or 8, wherein the NLS sequence further comprises a GGS linker. **Claim 10** The PAGE system according to claim 1, wherein the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10 to 1422. **Claim 11** The PAGE system according to claim 1, wherein the CPP comprises a sequence derived from the trans-activating transcriptional activator (Tat) derived from HIV-1. **Claim 12** The PAGE system according to claim 11, wherein the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO: 2). **Claim 13**: A composition for gene editing in vivo, ex vivo, or in vitro, comprising a PAGE system and cells into which at least one type of sgRNA or crRNA has been introduced, wherein the PAGE system comprises a Cas protein linked to a CPP and an endosomal escape peptide linked to the CPP. **Claim 14**: A composition for gene editing in vivo, comprising a PAGE system and cells into which at least one type of sgRNA or crRNA has been introduced, wherein the PAGE system comprises a Cas protein linked to a CPP and an endosomal escape peptide linked to the CPP, and the composition is administered to a subject. **Claim 15** The composition according to claim 13 or 14, wherein Cas is Cas9, or Cas12a, or a Cas derivative. **Claim 16** The composition according to claim 15, wherein the Cas derivative is a Cas protein linked to another protein or catalytic domain. **Claim 17** The composition according to claim 16, wherein the protein or catalytic domain is selected from the group consisting of AID deaminase, APOBEC deaminase, TadA deaminase, TET enzyme, DNA methyltransferase, transactivation domain, reverse transcriptase, histone acetyltransferase, histone deacetylase, sirtuin, histone methyltransferase, histone demethylase, kinase, and phosphatase. **Claim 18** The composition according to claim 13 or 14, wherein the endosomal escape peptide comprises any of the amino acid sequences set forth in SEQ ID NOs: 1434 - 1523. **Claim 19** The composition according to claim 13 or 14, wherein the endosomal escape peptide comprises dTAT-HA2. **Claim 20** The composition according to claim 13 or 14, wherein Cas comprises an NLS sequence. **Claim 21** The composition according to claim 20, wherein the NLS sequence comprises the amino acid sequence PAAKRVKLD (SEQ ID NO: 1). **Claim 22** The composition according to claim 20, wherein the NLS sequence further comprises a GGS linker. **Claim 23** The composition according to claim 13 or 14, wherein the CPP comprises any of the amino acid sequences set forth in SEQ ID NOs: 10 - 1422. **Claim 24** The composition according to claim 13 or 14, wherein the CPP comprises a sequence derived from the trans-activating transcriptional activator (Tat) derived from HIV-1.

25. The composition according to claim 24, wherein the Tat sequence comprises the amino acid sequence GRKKRRQRRRPQ (SEQ ID NO: 2).

26. The composition according to claim 13 or 14, wherein the gene editing does not require electroporation.

27. The composition according to claim 13 or 14, wherein the PAGE system is introduced into cells in a serum-free medium.

28. The composition according to claim 13 or 14, wherein the endosomal escape peptide is introduced into cells at a concentration of about 25 - 75 μM.

29. The composition according to claim 13 or 14, wherein Cas is introduced into cells at a concentration of about 0.5 - 5 μM.

30. The composition according to claim 13 or 14, wherein the cells are immune cells.

31. The composition according to claim 13 or 14, wherein the cells are selected from the group consisting of primary human CD8 T cells, human iPSCs, and CAR T cells.

32. The composition according to claim 13 or 14, wherein the sgRNA targets Ano9, Pdcd1, Thy1, Ptprc, PTPRC, or B2M.

33. The composition according to claim 14, wherein the subject is in need of treatment for a disease or disorder, and when the edited cells are administered to the subject, the disease or disorder is treated in the subject.

34. The composition according to claim 33, wherein the disease or disorder is an infection.

35. The composition according to claim 33, wherein the disease or disorder is related to T cell exhaustion.

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