Antigen epitope polypeptide cd44-p3 based on prostate cancer stem cell marker cd44 and its application
A CD44-P3, antigen epitope technology, applied in the direction of CD44, receptor/cell surface antigen/cell surface determinant, application, etc., can solve the problem of limited killing effect, low specificity of anti-tumor treatment technology, easy tumor recurrence, etc. problem, to reduce recurrence, enhance clear effect, and enhance suppression effect
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Embodiment 1
[0075] Design and synthesis of embodiment 1 CD44 epitope short peptide
[0076] 1. Find the complete amino acid sequence (NP_000601.3) of human CD44 protein from the international open shared gene bank NCBI Genbank, a total of 742 amino acids. Its amino acid sequence is as follows:
[0077] MDKFWWHAAWGLCLVPLSLAQIDLNITCRFAGVFHVEKNGRYSISRTEAADLCKAFNSTLPTMAQMEKALSIGFETCRYGFIEGHVVIPRIHPNSICAANNTGVYILTSNTSQYDTYCFNASAPPEEDCTSVTDLPNAFDGPITITIVNRDGTRYVQKGEYRTNPEDIYPSNPTDDDVSSGSSSERSSTSGGYIFYTFSTVHPIPDEDSPWITDSTDRIPATTLMSTSATATETATKRQETWDWFSWLFLPSESKNHLHTTTQMAGTSSNTISAGWEPNEENEDERDRHLSFSGSGIDDDEDFISSTISTTPRAFDHTKQNQDWTQWNPSHSNPEVLLQTTTRMTDVDRNGTTAYEGNWNPEAHPPLIHHEHHEEEETPHSTSTIQATPSSTTEETATQKEQWFGNRWHEGYRQTPKEDSHSTTGTAAASAHTSHPMQGRTTPSPEDSSWTDFFNPISHPMGRGHQAGRRMDMDSSHSITLQPTANPNTGLVEDLDRTGPLSMTTQQSNSQSFSTSHEGLEEDKDHPTTSTLTSSNRNDVTGGRRDPNHSEGSTTLLEGYTSHYPHTKESRTFIPVTSAKTGSFGVTAVTVGDSNSNVNRSLSGDQDTFHPSGGSHTTHGSESDGHSHGSQEGGANTTSGPIRTPQIPEWLIILASLLALALILAVCIAVNSRRRCGQKKKLVINSGNGAVEDRKPSGLN...
Embodiment 2
[0086] The antigenic epitope polypeptide CD44-P3 of the CD44 protein antigenic epitope provided in Example 1 of the present invention was used to study the killing effect of CD44-induced effector T cells on human prostate cancer cell LNCAP-multicellular spheres. Specifically include the following steps:
[0087] 1. Separation and preparation of peripheral blood mononuclear cells: collect 10 mL of peripheral blood collected from HLA-A2 positive healthy volunteers into 2 centrifuge tubes, centrifuge at 2000 r / min for 5 min, discard the supernatant, mix the precipitated cells, add physiological Add saline to 25mL to fully suspend the precipitated cells to form a blood cell suspension. Take another centrifuge tube, add 20 mL of lymphocyte separation medium, and slowly transfer the blood cell suspension to the surface of the lymphocyte separation medium with a dropper, so that a clear interface is formed between the two.
[0088]2. After centrifuging the above-mentioned centrifuge...
Embodiment 3
[0101] The antigenic epitope polypeptide CD44-P3 of the CD44 protein antigenic epitope provided in Example 1 of the present invention was used to study the killing effect of CD44-induced effector T cells on human prostate cancer cell VCaP-multicellular spheres.
[0102] 1. The separation and preparation method of peripheral blood mononuclear cells is the same as in Example 2.
[0103] 2. The culture method of DC-CIK cells is the same as that in Example 2.
[0104] 3. The preparation of target cells VCaP-multicellular spheroid cells and the detection method of killing effect are the same as in Example 2.
[0105] Such as Figure 4A with Figure 4B As shown, the CIK cells induced by the CD44-P3 epitope peptide have a significant killing effect on the VCaP-tumor multicellular spheres enriched with human prostate cancer cell stem cells. When the effect-target ratio is 5:1, the average killing effect is from this 9.8% of the base increased to 27.2%; in the case of an effect-to-t...
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