Specific t cell for preventing or treating cancer, and preparation method thereof
AssigneeSuzhou Ersheng Biomedical Co., Ltd.
InventorMi LIU
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AssigneeSuzhou Ersheng Biomedical Co., Ltd.
InventorMi LIU
Estimating the term…
The present disclosure relates to a method for preparing a cancer-specific T cell based on peripheral blood or a peripheral immune organ for preventing or treating cancer, specifically including steps of: first, isolating an immune cell from peripheral blood or the peripheral immune organ; then, co-incubating with a nanoparticle and/or a microparticle loaded with a tumor whole-cell antigen for a period of time to activate the cancer-specific T cell; then, isolating a cancer-specific T cell activated by the tumor antigen; and, reinfusing the cancer-specific T cell into the body to exert an anti-cancer effect after in vitro expansion. According to the nanoparticle or microparticle prepared by the present disclosure, a tumor antigen component is loaded onto the microparticle and/or the nanoparticle to activate the cancer-specific T cell, and then the cancer-specific T cell is expanded and reinfused into a patient for treating cancer or preventing recurrence or metastasis. The cancer-specific T cell isolated by a sorting method has high specificity, and may prevent or treat cancer by killing cancer cells after expansion.
A method for preparing a cancer-specific T cell derived from an autologous or allogeneic source for preventing or treating cancer, specifically comprising steps of:
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A cancer-specific T cell derived from an autologous or allogeneic source for preventing or treating cancer, the specific T cell comprising but not limited to any one of T cells such as CD3+ CD69+, CD3+ CD8+ CD69+, CD3+ CD4+ CD69+, CD3+ CD137+, CD3+ CD4+ CD137+, CD3+ CD8+ CD137+, CD3+ CD25+, CD3+ CD8+ CD25+, CD3+ CD4+ CD25+, CD3+ CD134+, CD3+ CD8+ CD134+, CD3+ CD4+ CD134+, CD3+ IL-2R+, CD3+ CD8+ IL-2R+, CD3+ CD4+ IL-2R+, CD3+ HLA-DR+, CD3+ CD8+ HLA-DR+, CD3+ CD4+ HLA-DR+, CD3+ FASL+ CD3+ CD8+ FASL+, CD3+ CD4+ FASL+, CD3+ OX40+, CD3+ CD8+ OX40+, CD3+ CD4+ OX40+, CD3+ TCF-1+, CD3+ CD8+ TCF-1+, CD3+ CD4+ TCF-1+, CD3+ PD-1+, CD3+ CD8+ PD-1+, CD3+ CD4+ PD-1+, CD3+ CD39+, CD3+ CD8+ CD39+, CD3+ CD4+ CD39+, CD3+ CD38+, CD3+ CD8+ CD38+, CD3+ CD4+ CD38+, CD3+ CD28+, CD3+ CD8+ CD28+, CD3+ CD4+ CD28+, CD3+ CD71+, CD3+ CD8+ CD71+, CD3+ CD4+ CD71+, CD3+ CD44+, CD3+ CD8+ CD44+, CD3+ CD4+ CD44+, CD3+ CXCR3+, CD3+ CD8+ CXCR3+, CD3+ CD4+ CXCR3+, CD3+ CXCR1+, CD3+ CD8+ CXCR1+, CD3+ CD4+ CXCR1+, CD3+ ICAM-1+, CD3+ CD8+ ICAM-1+, CD3+ CD4+ ICAM-1+, CD3+ CD70+, CD3+ CD8+ CD70+, CD3+ CD4+ CD70+, CD3+ CD154+, CD3+ CD8+ CD154+, CD3+ CD4+ CD154+, CD3+ CD62L+, CD3+ CD8+ CD62L+, CD3+ CD4+ CD62L+, CD3+ CD154+, CD3+ CD8+ CD154+, CD3+ CD4+ CD154+, CD3+ CD160+, CD3+ CD8+ CD160+, CD3+ CD4+ CD160+, CD3+ CD160+, CD3+ CD8+ CD160+, CD3+ CD4+ CD160+, CD3+ ICOS+, CD3+ CD8+ ICOS+, CD3+ CD4+ ICOS+, CD3+ CD27+, CD3+ CD8+ CD27+, CD3+ CD4+ CD27+, CD3+ CD107A+, CD3+ CD8+ CD107A+, CD3+ CD4+ CD107A+, etc., or a combination thereof, wherein viability of the specific T cell is greater than 60%, preferably greater than 70%, and more preferably greater than 80%;
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A method for preparing a pharmaceutical composition comprising the specific T cell of 97, comprising a step of adding a substance enhancing an innate immune system, such as albumin, an NK cell, a neutrophil, a γδ T cell, and an NK T cell, to the cancer-specific T cell before reinfusing the cancer-specific T cell into the patient, wherein
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Dependencies are inferred from the claim text.