Peripheral blood biomarker for evaluating anti-tumor immune effect of radiation therapy
AssigneeSaitama Medical University
InventorHiroshi Kagamu
Life of this patent
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Abstract
Provided is a peripheral blood biomarker for evaluating the antitumor immune effect of radiation therapy. Also provided is a method in which the composition of cell subpopulation in a sample obtained from a subject is used as an index for immune activation in the subject caused by a radiation therapy. By comparing, with a reference, the amount of CD4+ T cell subpopulation that correlates with dendritic cell stimulation in an antitumor immune response or the amount of dendritic cell subpopulation that correlates with the dendritic cell stimulation in an antitumor immune response, the presence or absence of, and/or the magnitude of, immune activation occurring in the subject as a result of a radiation therapy can be determined.
Claims18
A method of using a composition of a cell subpopulation in a sample obtained from a subject who has undergone radiation therapy as an indicator of radiation therapy-induced immune activation in the subject, comprising:
- analyzing the composition of the cell subpopulation in the sample obtained from the subject;
- wherein the presence/absence of immune activation in the subject is indicated by comparing an amount of a CD4+ T cell subpopulation correlated with dendritic cell stimulation in an antitumor immune response in the sample with a baseline, and the CD4+ T cell subpopulation correlated with dendritic cell stimulation in an antitumor immune response is a cell subpopulation within a CD62LlowCD4+ T cell population,
- wherein an increase in the amount of the cell subpopulation in the sample relative to the baseline indicates that immunity is activated by radiation therapy in the subject,
- wherein no increase in the amount of the cell subpopulation in the sample relative to the baseline indicates that immunity is not activated by radiation therapy in the subject,
- wherein radiation therapy-induced immune activation in the subject further indicates that cancer immunotherapy comprising one or more immune checkpoint inhibitors should be administered to the subject at that point in time,
- wherein the one or more immune checkpoint inhibitors comprise a PD-1 inhibitor, a PD-L1 inhibitor, and/or a CTLA-4 inhibitor, and
- wherein no radiation therapy-induced immune activation in the subject further indicates that radiation therapy should be re-administered to the subject.
Dependencies are inferred from the claim text.