Ganglioside GM3-containing nanoparticles as immunomodulatory agents

Abstract

The present invention relates to a pharmaceutical composition having special characteristics regarding size, surface charge, and morphology associated with a nanoparticle system that contains an active ingredient comprising a membrane vesicle conjugate of Neisseria meningitidis in a protein-excess conjugation ratio and GM3 ganglioside, and that confers advantageous properties as an immunomodulator, since it induces a simple and significant reduction in myeloid-derived suppressor cells that affect lymphocyte T responses and tumor patient survival. The present invention further relates to the use of the disclosed pharmaceutical composition for the treatment of cancer, particularly cancer types with an increase in myeloid-derived suppressor cells (MDSCs); and to a method for treating cancer patients with this composition, and a method for selecting patients for this treatment.

Description

[Technical field]

[0001] The present invention relates to the field of immuno-nanotechnology and immuno-oncology, in particular to immunomodulatory agents for treating individuals with cancer and / or chronic infections. The present invention describes nanoparticulate immunomodulatory agents specifically tailored to specifically disrupt myeloid derived suppressor cells (MDSCs) and restore T cell responses in these individuals. [Background technology]

[0002] In recent years, important clinical results have been obtained using immune checkpoint inhibitor antibodies (Abs) with the ability to induce long-lasting objective responses with a significant impact on patient survival. These therapies, which modulate the immune system and restore the patient's ability to destroy tumor cells, have led to a renaissance of cancer immunotherapy with a particular focus on the design of new immunomodulatory agents.

[0003] However, there are other suppressive circuits of antitumor immune responses that are important targets for the development of new immunomodulatory agents (Malmberg KJ et al. (2004) Cancer Immunol Immunother 53(10):879-92). Myeloid-derived suppressor cells (MDSCs) constitute one of the main cell populations recruited by tumors with the ability to suppress immune responses (Mantovani A. et al. (2010) Curr Opin Immunol 22(2):231-7; Condamine T. et al. (2011) Trends Immunol 32(1):19-25). In particular, as proposed by Shipp et al. in a review article, the frequency of circulating MDSCs is a factor of poor prognosis in patients with tumors from a wide variety of locations. Moreover, high circulating levels of these populations are associated with less benefit from conventional therapies such as chemotherapy, radiotherapy, and even anti-checkpoint Abs (Shipp C. et al. (2016) Cell Mol Life Sci 73(21):4043-61). In humans, the general consensus is that LIN - CD11b + CD33 +HLA-DR - Early MDSC (eMDSC), defined as CD14 + HLA-DR 低 / - Monocytic MDSCs (mMDSCs), defined as CD11b + CD33 + CD14 - CD15 + (CD66b + Three populations of MDSCs have been described: granulocytic MDSCs (gMDSCs) with a phenotype of 12-fold increase in IL-16 expression (Bronte V. et al. (2016) Nat Commun 7:12150). All three populations are thought to be suppressors of tumor-specific immune responses (Shipp C. et al. (2016) Cell Mol Life, Sci 73(21):4043-61).

[0004] Research strategies currently being developed to counteract the immunosuppression induced by MDSCs focus on three approaches: (1) reducing their numbers, (2) influencing their function, and (3) influencing their differentiation. In these directions, promising results have already been reported for some of the drugs evaluated (Najjar YG et al. (2013) Frontiers in Oncology 3(49):1-9).

[0005] Of particular relevance to the present invention within therapeutic strategies targeting MDSCs are strategies based on nanoparticle systems. Nanoparticles offer a wide range of applications and are known to behave differently in vivo depending on their size and surface properties. For example, size determines the site of evacuation, while surface properties affect adhesion and capture mechanisms (Wilkerson A. et al. (2017) Current Topics in Medicinal Chemistry 17:1843-57). In this sense, as reported by Serda RE, particle systems with diameters in the range of 500-2000 nm are preferentially captured at the injection site and migrate to lymph nodes (LNs), while particles with diameters of 20-200 nm are passively evacuated into LNs where they interact with resident cells (Serda RE (2013) Int J of Nanomed 8:1683-1696).

[0006] So far, only six nanoparticle-based strategies with effects on MDSCs have been described, including gemcitabine-loaded nanoparticles, chemokine CCL21-loaded nanoparticles, CpG-loaded nanoparticles, all-trans retinoic acid-loaded liposomes, and glucan-designed nanoparticles (Wilkerson A. et al. (2017) Current Topics in Medicinal Chemistry 17:1843-57). These five strategies share three fundamental characteristics: the size of the nanoparticles falls within the range of 30-250 nm, their use is limited to mouse models, and they constitute particles that have no effect on MDSCs per se but are carrier systems for biological drugs.

[0007] The sixth strategy based on nanoparticle systems with effects on MDSCs is the use of very small proteoliposomes (VSSPs) containing GM3 ganglioside. These preparations can be considered as the closest technical solution to the present invention. First, Molina et al. in US Pat. No. 8,591,917 describe a method of using VSSPs administered subcutaneously (SC) to stimulate the immune response of subjects. Furthermore, studies by Fernandez et al. and Oliver et al. demonstrated that administration of VSSPs induces a significant increase in the spleen of cells with a phenotype similar to MDSCs but with a significantly reduced suppressive capacity in healthy tumor-bearing mice or mice with chemotherapy-induced leukopenia (Fernandez A. et al. (2011) J Immunol 186:264-74; Oliver L. et al. (2012) Vaccine 30:2963-72). Other studies have also described the use of VSSP in tumor-bearing mice, which prevents cross-presentation of antigens by tumor-induced MDSCs and induces their differentiation into antigen-presenting cells (Fernandez A. et al. (2014) J ImmunoTherapy of Cancer 2:5). A method for obtaining these VSSPs has been described by Rodriguez et al. in US Pat. No. 6,149,921, which emphasizes that conjugation of Neisseria meningitidis proteins is mixed with an excess of ganglioside GM3 in the presence of a detergent, which is then removed by dialysis. Furthermore, Estevez et al. describe that after dialysis, an ultracentrifugation step is performed to discard conjugates with larger mass and size (Estevez F. et al. (2000) Vaccine 18:190-7).

[0008] The novel active ingredient of the immunomodulatory preparation described in the present invention also comprises a conjugate of N. meningitidis membrane vesicles and GM3 ganglioside. This preparation has specific properties of size, surface charge and morphology related to nanoparticle systems that have never been described before in any technical solution or in previous scientific publications. These properties provide this new invention with advantageous and surprising properties in terms of its effect on MDSCs, compared to those previously described by Fernandez A. et al. and Oliver L. et al. The present invention is preferably administered by SC to treat patients with tumors and, in contrast to what the prior art teaches, induces a favorable and significant reduction of gMDSCs and mMDSCs, affecting the response of T lymphocytes and the survival of the treated patient. The novelty of the present invention therefore consists in providing a new immunomodulatory agent that has an effect on the reduction of MDSC levels in patients with tumors. Summary of the Invention [Means for solving the problem]

[0009] One embodiment of the present invention is a pharmaceutical composition for immunomodulating the immune response in cancer patients comprising nanoparticles formed by hydrophobic conjugation of outer membrane protein complex (OMPC) of Neisseria meningitidis bacteria with GM3 ganglioside, wherein the protein-ganglioside conjugation ratio ranges from 1.5:1 to 10:1.

[0010] In particular, the composition is characterized by a monomodal distribution of particle sizes in the range of 15-25 nm, a polydispersity index of 0.230, and a negative Z potential having a nominal value in the range of 25-45 mV.

[0011] In a particular embodiment, the present invention relates to the use of the pharmaceutical composition subject of the present invention in the treatment of cancer, particularly as an immunomodulator of MDSCs in patients with cancer that increases the presence of these cells.

[0012] In another embodiment, the present invention relates to a method of treating a subject in need thereof comprising administering a pharmaceutical composition described herein by SC route, intradermally, intramuscularly, intratumorally, or by direct application to a mucosa at a weekly frequency for a total of at least four administrations, followed by biweekly or monthly maintenance administrations for at least six months.

[0013] In a particular embodiment, the object of the present invention is a method for selecting a patient with cancer as a candidate for treatment with the described pharmaceutical composition, comprising: - extracting a blood and / or tumor tissue sample from a patient; - determining the level of MDSC in a blood and / or tumor tissue sample; The method includes:

[0014] Patients with a high frequency or absolute number of MDSC in the blood or who test positive for the degree of infiltration of MDSC in tumor tissue are considered candidates for such treatment. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] immunomodulatory composition The present invention provides an immunomodulatory system that significantly reduces circulating MDSCs in cancer patients with high levels of circulating or tumor MDSCs. An immunomodulatory system can be defined as one that is capable of eliminating or modulating any of the suppressive mediators of the immune response, such as in the case of MDSCs.

[0016] The immunomodulatory target claimed in the present invention consists of nanoparticles obtained from the outer membrane of Neisseria meningitidis, a Gram-negative bacterium related to GM3 ganglioside. The present invention establishes that OMPCs of Neisseria meningitidis are first dispersed in a Tris-HCl buffer solution containing a mixture of sodium deoxycholate (10-40 mM) and sodium dodecyl sulfate (1-10 mM) in a stirred reactor for a period of time ranging from 1 to 36 hours.

[0017] Then, GM3 ganglioside is added in a mass 0.6-10 times less than the added mass of OMPC to obtain a protein:ganglioside ratio of 1.5:1-10:1 and stirring is prolonged. Nanoparticle formation is achieved through the use of a tangential flow filtration system with a 10 kDa-100 kDa membrane and a transmembrane pressure of 1.15-1.75 bar to completely remove the surfactant. The ultrafiltered retentate solution is ultracentrifuged at 100000 g and concentrated to adjust its concentration to the desired dosage of 0.1-2 mg / ml of OMPC and sterilized by filtration through sterile 0.2 μm pore size capsules.

[0018] The conjugation of gangliosides to the protein mass in a ratio favorable to the amount of protein and the step of tangential flow ultrafiltration under controlled conditions results in a preparation with defined characteristics, named VSSP-iMod. Analysis of particle morphology, size and surface charge density shows the presence of a heterogeneous nanoparticle preparation with a size of 15-25 nm and a nominal negative Z potential ranging from 25 to 45 mV.

[0019] Methods for identifying and / or selecting patients for treatment with VSSP-iMod To select patients to be administered VSSP-iMod, the levels of gMDSC and mMDSC that can suppress T-specific responses against tumors are determined. The increase in MDSC due to the presence of tumors can be determined by evaluating different subpopulations of these cells in the circulation or in the tumor microenvironment. Furthermore, their presence implies an increase in certain plasma proteins and circulating DNA. Sources of samples for evaluation include both peripheral blood samples and tumor samples, including but not limited to tumor biopsies, circulating plasma proteins, ascites, and circulating DNA.

[0020] The increase in these cells can be determined by diagnostic or prognostic assays using flow cytometry, immunohistochemistry (IHC), ELISA, immunofluorescence or polymerase chain reaction.On the other hand, patients who do not have increased levels of MDSC due to disease stage or tumor location are those who have levels higher than normal healthy donors but do not reach the substantial levels observed in patients with the same disease state.

[0021] Determination of the levels of MDSCs in patient blood samples distinguishes both populations from FSCs. 中 / 高 / SSC 低 / 高 This is done by flow cytometry, analyzing within the field. In particular, for the gMDSC population, the CD11b and CD33 double positive population is selected, and within that the CD66b positive and CD14 negative subpopulation is selected. For mMDSC, the population with negative or low HLA-DR expression and positive CD14 is selected. Based on these results, and in relation to the same determination for age- and sex-matched healthy donors, the level of MDSC can be classified according to their frequency or absolute number as follows: - Negative: percentage and / or number values ​​within a range determined by the mean (M) + / - standard deviation of normal values ​​with 95% confidence. - Weak: for M, percentage and / or number value 2M≦MDSC<3M. -High: percentage and / or number value 3M≦MDSC.

[0022] Patients with a high frequency or absolute number of MDSCs in their blood are treated with VSSP-iMod.

[0023] To determine the level of MDSC in a sample of tumor tissue, the measurement by IHC technique of CD33+ cells can be used. For this purpose, the percentage of CD33+ cells in the tissue must be determined, which is expressed as follows: - Negative: <10% positive cells - Positive / lowly infiltrating MDSC: 10-19% of positive cells -Positive / highly infiltrating MDSC: >20% of positive cells

[0024] Depending on its histological type and stage, tumors can be considered to recruit MDSCs, as long as they are positive for the degree of infiltration by CD33+ cells.

[0025] Therapeutic Uses and Methods The present invention provides an immunomodulatory composition dedicated to reducing MDSCs, both gMDSC and mMDSC phenotypes, establishing a targeted solution specific to immuno-oncology, where MDSCs are known to constitute an essential inhibitory node of the anti-tumor immune response.

[0026] The progression of certain tumors is accompanied by the recruitment of MDSCs to the tumor site, for which specific mechanisms have been described that suppress the antitumor immune response of T and NK lymphocytes. The present invention proposes that in patients with elevated gMDSCs and / or mMDSCs in the circulation and / or in the tumor, the number of these cells can be significantly reduced by treatment with VSSP-iMod. This reduction allows these patients to avoid suppressing the natural antitumor immune response, or the immune response induced by some therapies, by MDSCs, which results in the survival of the treated patients.

[0027] The VSSP-iMod immunomodulators of the invention can be introduced into a patient by SC, intradermal, intramuscular, intratumoral routes, or by direct application to a mucosa.

[0028] Among the cancer types that can be treated with the VSSP-iMod immunomodulatory agent subject of the present invention are cancers that have been reported to recruit MDSCs as an immunosuppressive mechanism of anti-tumor immune responses. More specifically, examples of these cancers include melanoma, prostate cancer, head and neck cancer, ovarian cancer, bladder cancer, hepatocellular carcinoma, non-small cell lung cancer, chronic lymphocytic leukemia, squamous cell carcinoma of the esophagus, Hodgkin's lymphoma, renal carcinoma, and breast cancer.

[0029] The dose range of the VSSP-iMod immunomodulator for use in humans is 100 μg to 2 mg, preferably 200 μg to 1200 μg (depending on the OMPC content).

[0030] The immunomodulatory agent is administered to the subject on a weekly basis for a total of at least four doses to achieve a rapid reduction in MDSCs, followed by biweekly or monthly maintenance doses for at least six months. This treatment can be administered chronically for as long as the patient requires.

[0031] The present invention will be further described in the following examples and figures.However, these examples should not be interpreted as limiting the scope of the present invention.These examples include the experimental details that allow to verify the specific physicochemical properties of VSSP-iMod and its effectiveness in reducing the MDSC content of treated patients.Furthermore, these examples also show the effect of this reduction on T lymphocyte response and on the survival of treated patients. [Brief description of the drawings]

[0032] [Figure 1] FIG. 13. Photon correlation spectroscopy assessment of VSSP-iMod particle diameter. [Diagram 2] FIG. 13. Photon correlation spectroscopy assessment of the Z potential of VSSP-iMod particles. [Diagram 3] 13 is an atomic force microscopy image of the morphology of VSSP-iMod particles. [Figure 4A] FIG. 13 shows flow cytometric assessment of the effect of treatment with VSSP-iMod in patients with metastatic renal cell carcinoma (mRCC) on the frequency of gMDSCs. [Figure 4B] FIG. 13: Flow cytometric assessment of the effect of treatment with VSSP-iMod in patients with metastatic renal cell carcinoma (mRCC) with proportion of patients with gMDSC frequencies above and below the median. [Figure 5A] FIG. 1 shows flow cytometric assessment of the effect of VSSP-iMod treatment on the ability of MDSCs to suppress proliferation of TCD4+ lymphocytes. [Figure 5B]FIG. 13 shows flow cytometric assessment of the effect of VSSP-iMod treatment on the ability of MDSCs to suppress proliferation of TCD8+ lymphocytes. [Figure 6A] FIG. 13 shows flow cytometric assessment of the effect of treatment with VSSP-iMod in patients with breast cancer on frequency and % of patients with gMDSC frequency above and below the median. [Figure 6B] FIG. 13 shows flow cytometric assessment of the effect of treatment with VSSP-iMod on frequency and % of patients with mMDSC frequency above and below the median in patients with breast cancer. [Figure 7] FIG. 1 shows the effect of treatment with VSSP-iMod on the absolute number of TCD8+ lymphocytes in patients with breast cancer determined by flow cytometry.

[0033] example Example 1 VSSP-iMod has a defined size and surface charge. The size (nm) and Z potential of the particles constituting the VSSP-iMod were measured by photon correlation spectroscopy. Samples were evaluated in triplicate, and size and Z potential values ​​were obtained using the CONTIN and Smoluchowski algorithms, respectively. As shown in Figure 1, the VSSP-iMod exhibited a unimodal distribution in the volume distribution ranging from 15 to 25 nm with a polydispersity index (PDI) of 0.230, which means that there is a heterogeneous formulation of particles. Furthermore, as shown in Figure 2, the VSSP-iMod exhibited a negative Z potential, the nominal value of which ranged from 25 to 45 mV.

[0034] Example 2 Nanoparticle morphology of VSSP-iMod. Images of VSSP-iMod were acquired with a multimode atomic force microscope, using a silicon cantilever. 50 μL of sample was applied to mica previously functionalized with 50 mol / L nickel chloride solution. A 1 / 10 dilution of VSSP-iMod with a 10 mmol / L Tris buffer solution pH 8.5 was performed before application to the mica. The images in Figure 3 show a heterogeneous formulation composed of nanoparticle structures of spherical nature on the order of a few tens of nanometers, in full agreement with the results obtained by photon correlation spectroscopy.

[0035] Example 3 VSSP reduces the frequency and suppressive activity of MDSCs in patients with mRCC. The effect of VSSP-iMod on MDSCs in patients with mRCC was evaluated. For this purpose, 15 patients with this diagnosis were treated with 400 μg of VSSP-iMod administered by SC route in the deltoid muscle. A total of four doses of VSSP-iMod were administered weekly, followed by monthly maintenance doses until the completion of 6 months of treatment. In this assay, the frequency of gMDSCs was evaluated by flow cytometry. For this purpose, a total of 200,000 cells were analyzed, and CD11b + / CD66b + / CD14 -The percentage of gMDSC was determined by measuring the phenotype. As a control, the frequency of gMDSC in 15 age- and sex-matched healthy donors was evaluated. As can be seen in Figure 4A, VSSP-iMod reduced the frequency of circulating gMDSC in patients 21 days or after three doses after the start of treatment. The prior art teaches that patients showing gMDSC below the median established for patients at a certain position have a significantly higher survival than patients with a lower level (Shipp C. et al. (2016) Cell, Mol. Life, Sci. 73(21):4043-61). An analysis of the percentage of patients with gMDSC frequency above and below the median is shown in Figure 4B. As can be observed after treatment with VSSP-iMod, only about 20% of treated patients maintain a high MDSC. This result is maintained even after 147 days or 5 months, indicating that this effect of VSSP-iMod is maintained throughout the treatment.

[0036] In these patients, the effect of VSSP-iMod on MDSCs was also assessed in terms of T lymphocyte responses in a flow cytometric proliferation experiment. A total of 40 × 10 6 cells were used as starting material. CD11b+ cells were purified using magnetic beads conjugated to CD11b-specific Ab. - The negative fraction was labeled with CFSE and cultured alone or with CD11b+ cells at a 5:1 ratio for 96 hours. Figure 5 shows the relative proliferation rates of T lymphocytes at days 0 and 21 after VSSP-iMod administration in RCC patients. As seen in Figure 5A, the proliferation of TCD4+ lymphocytes increased at day 21, an effect similar to that observed in TCD8+ lymphocytes (Figure 5B), implying that VSSP-iMod can modulate MDSC-mediated suppression of T cell proliferation in RCC patients.

[0037] The majority of patients enrolled in the study showed a good quality of life at the end of treatment, and it was decided to continue monthly immunizations, as established in the protocol. With the extension of the treatment, gMDSCs remained below the median value on day 0, and the median survival time for all patients in this study was 37.5 months (Table 1). This value is much higher than the historical median of 6.6 months reported for similar patients treated with interferon, the current standard of care in Cuba. Furthermore, the National Comprehensive Cancer Network (NCCN) clinical practice guidelines for mRCC classify patients as having good, intermediate, and poor prognosis, according to the Memorial Sloan Kettering Cancer Center (MSKCC) model. These guidelines state that patients with mRCC treated with therapy against vascular endothelial growth factor have a median survival time of 27 months for those diagnosed with intermediate prognosis, while 75% of those diagnosed with good prognosis are alive at 24 months. A relative comparison of the values ​​obtained with VSSP-iMod to those stated in the guidelines indicates that the effect of VSSP-iMod on gMDSCs resulted in a higher survival than the standard defined in the NCCN guidelines. In the VSSP-iMod study, 100% of patients with a good prognosis were alive at 36 months, and patients with an intermediate prognosis had a median survival of 42 months. [Table 1]

[0038] Example 4 VSSP reduces the frequency of MDSCs of monocytic and granulocytic phenotype in patients with breast cancer. The effect of VSSP-iMod on MDSCs was also evaluated in patients with breast cancer. For this purpose, a phase 0 Window-of-Opportunity study was designed in which patients received 400 μg of VSSP-iMod by SC route in the deltoid muscle at a weekly frequency for 3 weeks. This treatment was administered at the traditional time established between diagnosis and the initiation of standard treatment of physician-indicated surgery or chemotherapy. In this study, the frequency of G-MDSCs, mMDSCs and CD8 T cells was measured by flow cytometry. A total of 200,000 cells were analyzed, each of which was of the phenotype CD11b in total PBMCs. + / CD66b + / CD14 - yCD11b + / CD14 + / HLA-DR 低 / 陰 Using VSSP-iMod, the percentage of gMDSC and mMDSC was determined. As can be seen in Figure 6A, VSSP-iMod reduced the frequency of circulating gMDSC, and this same behavior was observed in the circulating mMDSC of patients after 21 days of treatment (Figure 6B). Furthermore, analysis of the percentage of patients with gMDSC and mMDSC frequencies above and below the median shows that only 15% and 0% of treated patients maintained high gMDSC and mMDSC, respectively, after treatment with VSSP-iMod. The treatment also increased the frequency of CD8+ T cells in the blood of patients (Figure 7).

Claims

1. A pharmaceutical composition for the treatment of cancer comprising nanoparticles formed by hydrophobic conjugation of outer membrane protein complex (OMPC) of Neisseria meningitidis bacteria with GM3 ganglioside, wherein the mass ratio of protein-ganglioside conjugation is in the range of 1.5:1 to 10:

1.

2. 2. The pharmaceutical composition of claim 1, characterized by a monomodal distribution of particle size by volume in the range of 15-25 nm, a polydispersity index of 0.230, and a negative Z potential with a nominal value in the range of 25-45 mV.

3. The pharmaceutical composition according to claim 1 or 2 as an immunomodulator of myeloid derived suppressor cells (MDSCs) in patients with cancer.

4. 3. The pharmaceutical composition of claim 1 or 2, wherein the pharmaceutical composition is administered to a subject by SC, intradermal, intramuscular, intratumoral routes, or by direct application to a mucosal surface on a weekly basis for a total of at least four administrations, and thereafter with biweekly or monthly maintenance administrations for at least six months.

5. 3. A method for selecting a patient having cancer as a candidate for treatment with the pharmaceutical composition of claim 1 or 2, comprising: Determining the level of MDSCs in a sample of blood and / or tumor tissue extracted from the patient; and selecting patients with a high frequency or high absolute number of said MDSC levels; The above method.

6. The method of claim 5, wherein the selected patient is a patient positive for the degree of MDSC infiltration.

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