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The Common γ Chain Cytokines Interleukin (IL)–2 and IL‐7 Indirectly Modulate Blood Fluke Development via Effects on CD4+T Cells
Author(s) -
Rebecca B. Blank,
Erika Lamb,
Anna S. Tocheva,
Emily T. Crow,
K. C. Lim,
James H. McKerrow,
Stephen J. Davies
Publication year - 2006
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/508896
Subject(s) - biology , immune system , schistosoma mansoni , cytokine , immunology , interleukin 15 , microbiology and biotechnology , t cell , interleukin 4 , interleukin , interleukin 13 , schistosoma , interleukin 10 , schistosomiasis , helminths
The human pathogen Schistosoma mansoni exhibits a highly evolved and intricate relationship with its host, evading immune destruction while co-opting CD4(+) T cell-driven mechanisms to facilitate parasite development and egg excretion. Because the common gamma ( gamma (c)) chain cytokine interleukin (IL)-7 is also implicated in modulating schistosome development, we investigated whether this effect is mediated indirectly through the essential role that IL-7 plays in CD4(+) T cell growth and survival. We demonstrate that attenuated schistosome development in the absence of IL-7 results from dysregulated T cell homeostasis and not from disruption of direct interactions between schistosomes and IL-7. We also identify an indirect role that another gamma (c) chain cytokine plays in schistosome development, demonstrating that IL-2 expression by CD4(+) T cells is essential for normal parasite development. Thus, cytokines critical for CD4(+) T cell survival and function can mediate indirect but potent effects on developing schistosomes and underscore the importance of CD4(+) T cells in facilitating schistosome development.

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