Cyclophosphamide treatment regulates the balance of functional/exhausted tumor-specific CD8+ T cells

Hanoteau, Aurélie;Henin, Coralie;Svec, David;Bisilliat Donnet, Charlotte;Moser, Muriel;et.al.
(2017) OncoImmunology — Vol. 6, n° 8, p. e1318234 [1-10] (2017)

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Authors
  • Hanoteau, Aurélie
    Author
  • Henin, Coralie
    Author
  • Svec, David
    Author
  • Bisilliat Donnet, Charlotte
    Author
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  • Moser, Muriel
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Abstract
(en) An important question is how chemotherapy may (re-)activate tumor-specific immunity. In this study, we provide a phenotypic, functional and genomic analysis of tumor-specific CD8+ T cells in tumor (P815)-bearing mice, treated or not with cyclophosphamide. Our data show that chemotherapy favors the development of effector-type lymphocytes in tumor bed, characterized by higher KLRG-1 expression, lower PD-1 expression and increased cytotoxicity. This suggests re-engagement of T lymphocytes into the effector program. IFN-I appears involved in this remodeling. Our findings provide some insight into how cyclophosphamide regulates the amplitude and quality of tumor-specific immune responses.
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Citations

Hanoteau, A., Henin, C., Svec, D., Bisilliat Donnet, C., Denanglaire, S., Colau, D., Romero, P., Leo, O., Van den Eynde, B., & Moser, M. (2017). Cyclophosphamide treatment regulates the balance of functional/exhausted tumor-specific CD8+ T cells. OncoImmunology, 6(8), e1318234 [1-10]. https://doi.org/10.1080/2162402x.2017.1318234 (Original work published 2017)