Abstract
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 γ (γc) 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 deregulated T cell homeostasis and not from disruption of direct interactions between schistosomes and IL-7. We also identify an indirect role that another γc 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. © 2006 by the Infectious Diseases Society of America. All rights reserved.
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CITATION STYLE
Blank, R. B., Lamb, E. W., Tocheva, A. S., Crow, E. T., Lim, K. C., McKerrow, J. H., & Davies, S. J. (2006). The common γ chain cytokines interleukin (IL)-2 and IL-7 indirectly modulate blood fluke development via effects on CD4+ T cells. Journal of Infectious Diseases, 194(11), 1609–1616. https://doi.org/10.1086/508896
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