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In vitro amplification method of self-specific T cell, prepared T cell system, pharmaceutical use of cell system and component monitoring method of cell system

An in vitro amplification and specific technology, applied in the fields of drug combination, animal cells, individual particle analysis, etc., can solve the problems that hinder the standardization and implementation of new technologies, insufficient cell expansion, lack of quality control monitoring and evaluation methods, etc. question

Inactive Publication Date: 2012-10-10
BEIJING AIGEN BIO TECH
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  • Abstract
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  • Application Information

AI Technical Summary

Problems solved by technology

[0006] 1. The in vitro cell culture system for autologous cells is not perfect, and there are many uncontrollable factors, which lead to insufficient or failed expansion of cells, and more importantly, the cultured cells lack the specificity of killing tumors;
[0007] 2. There is a lack of quality control monitoring and evaluation methods for in vitro cell culture preparation, and the curative effect cannot be accurately and timely evaluated after reinfusion into the patient's body, which hinders the implementation of the standardization and standardization of this new technology

Method used

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  • In vitro amplification method of self-specific T cell, prepared T cell system, pharmaceutical use of cell system and component monitoring method of cell system
  • In vitro amplification method of self-specific T cell, prepared T cell system, pharmaceutical use of cell system and component monitoring method of cell system
  • In vitro amplification method of self-specific T cell, prepared T cell system, pharmaceutical use of cell system and component monitoring method of cell system

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Embodiment Construction

[0063] see figure 2In the example shown, firstly, 50ml of EDTA anticoagulated blood is collected from the patient, and then the peripheral blood mononuclear cells (PBMCs) are separated by the density gradient method, and a certain amount of peripheral blood mononuclear cells (PBMCs) is retained according to the need for cell phenotype flow. Formula analysis and TCR polymorphism analysis, and then the remaining peripheral blood mononuclear cells were prepared with medium MEDO-A cell suspension 40ml, and then after adding the stimulating factors SUPF-31 and SUPF-5, SUPF-6, SUPF-7 Co-cultivate in the medium MEDO-A for 48-72 hours, then add SUPF-3 and SUPF-10 stimulating factors, continue to culture in the medium MEDO-A, and harvest the cells after 10-14 days (the specific culture time can be determined according to the number of cells) ), followed by cell phenotype flow analysis and TCR cloning analysis.

[0064] In order to better explain the present invention and understand i...

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Abstract

The invention relates to an in vitro amplification method of self-specific T cells, a T cell system prepared by the method, pharmaceutical use of the cell system, and a component monitoring method of the cell system. The in vitro amplification method comprises the steps of: (1) separating peripheral blood mononuclear cells from peripheral blood of a patient; (2) adding corresponding T cell stimulating factors as needed, adding or not adding corresponding cell growth factors, and amplifying T cells by cultivating the peripheral blood mononuclear cells separated in the step (1) in a corresponding culture medium. According to the invention, polyclonal immunocompetent cells with various functionalities can be prepared according to different clinical needs by adopting the amplification method of the invention in a GMP environment, and the prepared polyclonal immunocompetent cells can be used in immune system regeneration and immunotherapy of patients.

Description

technical field [0001] The present invention relates to an in vitro expansion method of autologous specific T cells, and also relates to the autologous specific T cell system obtained after the expansion by the method, the application of the cell system in medicine preparation and the components of the cell system monitoring method. Background technique [0002] Tumor treatment has been using three traditional treatment methods, namely radiotherapy, chemotherapy and surgery. Traditional surgical treatment can only solve local problems. Radiotherapy and chemotherapy can also damage normal tissues and cells of the human body while killing cancer cells, especially the immune function of T cells that dominate cellular immunity. tumor. Therefore, the three traditional treatment methods of radiotherapy, chemotherapy and surgery have always had disadvantages such as incompleteness, easy transfer, and large side effects. [0003] In recent years, a new tumor autologous cell immun...

Claims

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Application Information

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IPC IPC(8): C12N5/0783C12Q1/68A61K35/14A61P35/00A61P31/12A61P37/02G01N33/577G01N15/10A61K35/15
Inventor 寇中琛
Owner BEIJING AIGEN BIO TECH
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