| CPC G01N 33/57492 (2013.01) [A61K 40/11 (2025.01); A61K 40/42 (2025.01); C07K 16/18 (2013.01); C07K 16/2812 (2013.01); A61K 2239/31 (2023.05); A61K 2239/38 (2023.05); A61K 2239/57 (2023.05); G01N 2333/70514 (2013.01); G01N 2333/70564 (2013.01); G01N 2333/7155 (2013.01)] | 6 Claims |
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1. A method of predicting a response to cancer immunotherapy of a subject, the method comprising:
measuring an amount of CD4+CD62Llow T-cells of the subject (X);
comparing X with an ineffective group threshold value, wherein an amount of X that is higher than the ineffective group threshold value indicates that the subject is not a part of an ineffective group to the cancer immunotherapy; and
applying a cancer immunotherapy to the subject predicted to be not a part of an ineffective group;
wherein the cancer immunotherapy comprises administration of an immune checkpoint inhibitor; and
wherein X is a ratio of a CD62LlowCD4+ T-cell subpopulation in CD4+ T-cells.
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