Application of Bacteroides fragilis in preparation of drugs to induce proliferation and/or accumulation of gamma delta T cells
A technology of Bacteroides fragilis and cell proliferation, applied in the field of immunology research, can solve the problem of unclear immunological function of γδT cells, and achieve the effect of improving immune function
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0052] Embodiment 1 Bacteroides fragilis culture
[0053] training method
[0054] Step 1: Take a freeze-dried strain of Bacteroides fragilis (Bacteroides fragilis), add 200 μL of BHI medium, redissolve, absorb 20 μl, draw a line on the blood plate, and put it in the biochemical incubator for 37 degree, anaerobic culture for 48 hours (h);
[0055] Step 2: Pick a single clonal colony and insert it into 10mL BHI medium, and culture it anaerobically at 37°C for 12h;
[0056] Step 3: Take a bottle of 500mL BHI medium, insert 1% (v / v) strains, and culture anaerobically at 37 degrees Celsius (°C) for 48 hours;
[0057] Step 4: Take the bacterial solution and centrifuge at 6000rpm for 10min. Wash twice with normal saline, and finally reconstitute the sludge with normal saline for use and count the viable bacteria.
Embodiment 2
[0058] Example 2 Bacteroides fragilis induces the expression of γδTCR, the proliferation and accumulation of γδT cells and the enhancement of effector function in mice immunized with Mycobacterium tuberculosis
[0059] 1. Training method
[0060] The culture method of Bacteroides fragilis is the same as in Example 1.
[0061] 2. Sample preparation
[0062] 1) Preparation of live Bacteroides fragilis ZY-312 cells
[0063] training method
[0064] Step 1: Take a freeze-dried strain of Bacteroides fragilis (Bacteroides fragilis), add 200 μL of BHI medium, redissolve, absorb 20 μl, draw a line on the blood plate, and put it in the biochemical incubator for 37 degree, anaerobic culture for 48h;
[0065] Step 2: Pick a monoclonal colony and insert it into 10mL of BHI medium, and culture it anaerobically at 37°C for 12 hours;
[0066] Step 3: Take a bottle of 500mL BHI medium, insert 1% (v / v) strains, and incubate anaerobically at 37 degrees Celsius for 48 hours;
[0067] Step ...
Embodiment 3
[0077] Example 3 Experiment of Bacteroides fragilis Inducing γδTCR Expression, γδT Cell Proliferation, Accumulation and Effector Function Enhancement in Melanoma Transplanted Mice
[0078] 1. Training method
[0079] The culture method of Bacteroides fragilis is the same as in Example 1.
[0080] 2. Sample preparation
[0081] Sample preparation method is the same as embodiment 2
[0082] 3. Bacteroides fragilis induces the expression of γδT and the enhancement of effector functions in melanoma transplanted mice figure 2 Schematic diagram of the experimental flow for detecting that B. fragilis enhances the proliferation and accumulation of γδT cells or promotes their effector functions in tumors.
[0083] Experimental animals: 36 3- to 4-week-old C57BL / 6 mice, in good mental state, were purchased from the Experimental Animal Center of Sun Yat-sen University. The mice were randomly divided into 3 groups, 12 in each group, and the 3 groups were respectively the control grou...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com