Engineered cells and uses thereof
A cell, immune cell technology, applied in the field of engineered cells and their uses, can solve problems such as off-target toxicity, release syndrome, and unwanted cytokines
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[0193] Various aspects of the present disclosure are further illustrated by the following non-limiting examples.
example 1
[0194] Example 1: Design of a TCR+ CAR construct containing only a co-stimulatory domain
[0195] This example describes the design of an exemplary TCR+ CAR construct comprising only a co-stimulatory domain. Twelve constructs were designed, each comprising a polynucleotide as follows:
[0196] Construct 1 (anti-CLL-1 TCRε+anti-CD33 co-stimulatory CAR): polynucleotide contains CD3ε leader peptide from N-terminus to C-terminus-anti-CLL-1 sdAb-(G4S) 3 -CD3ε-T2A-CD8 leader peptide-anti-CD33 sdAb-CD8 hinge-CD8 transmembrane-CD27 co-stimulatory domain;
[0197] Construct 2 (anti-CLL-1 TCRδ+anti-CD33 co-stimulatory CAR): polynucleotide contains CD3δ leader peptide from N-terminus to C-terminus-anti-CLL-1 sdAb-(G4S) 3 -CD3δ-T2A-CD8 leader peptide-anti-CD33 sdAb-CD8 hinge-CD8 transmembrane-CD27 co-stimulatory domain;
[0198] Construct 3 (anti-CLL-1 TCRγ + anti-CD33 co-stimulatory CAR): polynucleotide contains CD3γ leader peptide from N-terminus to C-terminus-anti-CLL-1 sdAb-(G4S) ...
example 2
[0222] Example 2: Viral transfection and virion production
[0223]To generate viral particles comprising polynucleic acids encoding any of the systems disclosed herein, a mixture of lentiviral packaging plasmids including pMDLg / pRRE (Addgene #12251), pRSV-Rev (Addgene #12253) and pMD2.G (Addgene #12259) was mixed with PLVX-EF1A (including target system) vector was premixed with polyetherimide (PEI) at a pre-optimized ratio, mixed well and incubated at room temperature for 5 minutes. Add the transfection mixture dropwise to 293-T cells and mix gently. Incubate the transfected 293-T cells at 37°C and 5% CO 2 Incubate overnight. Twenty-four hours after transfection, the supernatant was collected and centrifuged at 500 g for 10 min at 4°C to remove any cell debris. The centrifuged supernatant was filtered through a 0.45 μm PES filter, and the virus supernatant was concentrated after ultracentrifugation. After centrifugation, carefully discard the supernatant and wash the virus...
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