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Modeling anti-tumor Th1 and Th2 immunity in the rejection of melanoma

Modeling anti-tumor Th1 and Th2 immunity in the rejection of melanoma

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Original languageEnglish
Pages467-480
Number of pages14
JournalJournal of Theoretical Biology
Journal publication date7 Aug 2010
Journal number3
Volume265
DOIs
StatePublished

Abstract

Recent experiments indicate that CD4(+) Th2 cells can reject skin tumors in mice, while CD4(+) Th1 cells cannot (Mattes et al., 2003; Zhang et al., 2009). These results are surprising because CD4(+) Th1 cells are typically considered to be capable of tumor rejection. We used mathematical models to investigate this unexpected outcome. We found that neither CD4(+) Th1 nor CD4(+) Th2 cells could eliminate the cancer cells when acting alone, but that tumor elimination could be induced by recruitment of eosinophils by the Th2 cells. These recruited eosinophils had unexpected indirect effects on the decay rate of type 2 cytokines and the rate at which Th2 cells are inactivated through interactions with cancer cells. Strikingly, the presence of eosinophils impacted tumor growth more significantly than the release of tumor-suppressing cytokines such as IFN-gamma and TNF-alpha. Our simulations suggest that novel strategies to enhance eosinophil recruitment into skin tumors may improve cancer immunotherapies. (C) 2010 Elsevier Ltd. All rights reserved.

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