The Differentiation of CD4(+) T-Helper Cell Subsets in the Context of Helminth Parasite Infection.

The Differentiation of CD4(+) T-Helper Cell Subsets in the Context of Helminth Parasite Infection.
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DOI:
10.3389/fimmu.2014.00487
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发表时间:
2014
影响因子:
7.3
通讯作者:
Le Gros G
Le Gros G
中科院分区:
医学2区
文献类型:
--
作者:
Bouchery T;Kyle R;Ronchese F;Le Gros G

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Helminths are credited with being the major selective force driving the evolution of the so-called “type 2” immune responses in vertebrate animals, with their size and infection strategies presenting unique challenges to the immune system. Originally, type 2 immune responses were defined by the presence and activities of the CD4+ T-helper 2 subset producing the canonical cytokines IL-4, IL-5, and IL-13. This picture is now being challenged by the discovery of a more complex pattern of CD4+ T-helper cell subsets that appear during infection, including Tregs, Th17, Tfh, and more recently, Th22, Th9, and ThGM. In addition, a clearer view of the mechanisms by which helminths and their products selectively prime the CD4+ T-cell subsets is emerging. In this review, we have focused on recent data concerning the selective priming, differentiation, and functional role of CD4+ T-helper cell subsets in the context of helminth infection. We argue for a re-evaluation of the original Th2 paradigm and discuss how the observed plasticity of the T-helper subsets may enable the parasitized host to achieve an appropriate compromise between elimination, tissue repair, containment, and pathology.
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