Antigen sensitized dendritic cell preparing method

A technology of dendritic cells and antigens, applied in the field of cell engineering and biomedicine, can solve the problems such as poor preservation and application of culture medium, failure to eliminate potential safety hazards of serum, and complex composition.

Inactive Publication Date: 2015-12-09
MINZU UNIVERSITY OF CHINA
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Although the serum-free medium has many advantages that the traditional serum-containing medium cannot match, it still has the following deficiencies to be improved: a. Cells are susceptible to certain mechanical and chemical factors in the serum-free medium. The preservation and application of the medium are not as convenient as the traditional synthetic medium; b. Strong pertinence, different types of cells, even different cell lines or cell strains have different requirements for the nutrients in the medium; c. Use serum-free medium for original d. Cell function may be changed to cause cell dysfunction; e. At present, most of the insulin and transferrin necessary for serum-free medium are still derived from animals, and the serum band has not been eliminated. potential safety hazards; f. higher cost
[0008] In order to improve and solve the above problems, researchers are constantly exploring and improving the formulation of serum-free medium for immune cells. Patent CN201110081988.5 provides a human-derived serum-free medium, which is composed of human serum albumin for treatment, human Composed of recombinant insulin, human transferrin, human cholesterol, human catalase, 2-mercaptoethanol, ascorbic acid, linoleic acid, ethanolamine, human vitronectin, L-glutamine, the added protein and lipid All are derived from human plasma, serum or tissue, and are pharmaceutical-grade or highly purified human-derived proteins or human recombinant proteins, which do not contain animal-derived components. Although this invention avoids the safety hazards of animal-derived substances, the human-derived protein Or human recombinant protein is expensive, which is not conducive to large-scale promotion and use; patent CN201310082166.8 provides a serum-free medium for the cultivation and proliferation of lymphocytes with clear chemical composition and no animal origin. The composition is complex and contains IMEM basal medium, L-glutamine, sodium bicarbonate, recombinant human insulin, human transferrin, human serum albumin, 2-mercaptoethanol, N-acetyl-cysteine, lipids, amino acids, microorganisms, Trace Minerals, Hydrocortisone, Ethanolamine, Non-Essential Amino Acids & Ferric Citrate
However, this product is only suitable for the culture and proliferation of lymphocytes, and the human recombinant protein or human protein used is expensive, which has great limitations in use

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  • Antigen sensitized dendritic cell preparing method
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  • Antigen sensitized dendritic cell preparing method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] Example 1 Preparation of medium A for the preparation of antigen-sensitized dendritic cells

[0052] The medium used for the preparation of antigen-sensitized dendritic cells of the present invention consists of basic medium and other components. Preferably, the basal medium is RPMI1640 medium, and the other components are composed of formula A, wherein formula A is shown in Table 1.

[0053] Table 1 is used for formula A prepared by antigen-sensitized dendritic cells

[0054]

[0055]

[0056] Among them, pharmaceutical grade human albumin, recombinant human insulin, recombinant human fibronectin and rhIL-4 were purchased from R&Dsystem, and the other reagents were purchased from Sigma-Aldrich Company. Described formula A preparation method is as follows:

[0057] 1. Preparation of cholesterol solution: Weigh 50 mg of cholesterol powder, add it to 20 ml of RPMI1640 medium, shake it with an ultrasonic oscillator at 4°C for 1 hour to emulsify it completely, and obt...

Embodiment 2

[0061] Example 2 Utilizing HHP to Prepare Tumor Antigen with Strong Immunogenicity

[0062] 1. Human breast cancer cells T47-D and human non-small cell lung cancer cells H1299 were respectively selected to be treated with HHP (the tumor cell lines were all purchased from the Institute of Basic Medical Sciences, Peking Union Medical College, China), and the treatment conditions were HHP=250MPa, and the treatment temperature was 25 ℃, the treatment time is 20 minutes. After treatment, the cells were cultured with RPMI1640 containing 10% FBS for 48 hours at 37° C., 5% CO 2 , and saturated humidity.

[0063] 2. The cell density in the obtained cell sample is 10 6 / ml, the storage volume is 1ml, resuspended in serum-free freezing solution (CryostorCS10, Biolife Solutions, USA), and frozen in liquid nitrogen.

Embodiment 3

[0064] Example 3 Using medium A of the present invention to induce PBMC-derived iDC cells

[0065] 1. Add 5ml of cell separation medium (human mononuclear cell separation medium 1.077, product number 25710, Beijing Dongfang Huahui Biomedical Technology Co., Ltd.) into a 15ml centrifuge tube (SARSTEDT, Germany), and then add 5ml of PBS buffer Biomedical Technology Co., Ltd.) 1:1 diluted peripheral blood samples were carefully spread on the cell separation medium along the tube wall, and centrifuged for 15 minutes at a temperature of 20° C. and a centrifugation speed of 2000 rpm.

[0066] 2. After centrifugation is stopped, PBMCs form a relatively obvious cloud layer at the interface between the separation liquid and plasma. Use a pipette to suck out the serum layer and discard it, and then use a pipette to carefully suck out the cloudy cell strips and place them in another Into a centrifuge tube, add 5 times the volume of Hank'S solution (Beijing Dongfang Huahui Biomedical Tech...

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Abstract

The invention relates to an antigen sensitized dendritic cell (DC) preparing method. On one hand, a culture medium for preparing antigen sensitized DCs is provided and is composed of a basal culture medium and other ingredients, the basal culture medium and the other ingredients can be conveniently mixed into the culture medium for culturing the DCs before using, the other ingredients comprise pharmaceutical grade human albumin, recombinant human insulin and the like, and the culture medium has the advantages of being definite in ingredient, free of ingredients of animal origin and the like; on the other hand, the invention provides a method for preparing the antigen sensitized DCs through the culture medium, and the method includes the steps that a single karyocyte is cultured and induced through the culture medium to obtain immaturate DC cells; strong immunogenicity tumor antigens are prepared through high hydrostatic pressure, astragalus polysaccharide is united to serve as an immunologic adjuvant, antigen sensitization is conducted on the immaturate DCs, and the antigen sensitized DCs are obtained. The preparing method has the advantages of being safe, efficient, easy to implement and the like. The DC vaccines for specific therapy can be provided for clinic through the method.

Description

technical field [0001] The invention relates to a method for preparing antigen-sensitized dendritic cells, belonging to the technical fields of cell engineering and biomedicine. Background technique [0002] Somatic cell therapy refers to the treatment method of using human autologous, allogeneic or heterogeneous (non-human) somatic cells, which are reinfused (or implanted) into the human body after extracorporeal manipulation. This in vitro operation includes cell passage, expansion, screening, and drugs or other treatments that can change the biological behavior of cells. The somatic cells after in vitro operation can be used for the treatment of diseases, and can also be used for the diagnosis and prevention of diseases. There are many different types of somatic cell therapy, including in vivo reinfusion of mononuclear cells activated in vitro, such as lymphokine activated killer cells (Lymphokine Activated Killer Cells, LAK), tumor infiltrating lymphocytes (Tumor Infiltr...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N5/0784
Inventor 覃筱燕赵宇程勇曹畅刘婷婷
Owner MINZU UNIVERSITY OF CHINA
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