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白细胞介素-4和干扰素-γ在稳定1型和2型辅助性T细胞表型中的作用。

Roles of IL-4 and IFN-gamma in stabilizing the T helper cell type 1 and 2 phenotype.

作者信息

Nakamura T, Lee R K, Nam S Y, Podack E R, Bottomly K, Flavell R A

机构信息

Section of Immunobiology, Yale University School of Medicine, Howard Hughes Medical Institute, New Haven, CT 06520, USA.

出版信息

J Immunol. 1997 Mar 15;158(6):2648-53.

PMID:9058797
Abstract

It has previously been reported that Th1 CD4 T cell populations can be converted to IL-4 producers, whereas Th2 populations are refractory to IL-12-mediated IFN-gamma production. We have recently shown that CD30 is a marker for the IL-4 response and have therefore used CD30 here to study Th1 and Th2 commitment. We show that Th2 cell populations normally show a stable phenotype and fail to respond to IL-12 because of endogenous IL-4 production. IFN-gamma abrogates this antagonistic effect of IL-4 and permits the conversion of Th2 populations to IFN-gamma producers by IL-12. In the complete absence of IL-4, however, IFN-gamma is not required for this transformation, and Th1 cells generated by IL-12 become committed to the Th1 pathway and lose the ability to respond to IL-4. Thus, the balance between local IL-4 and IFN-gamma in an immune response is a key factor in determining the outcome of the CD4 effector T cell response.

摘要

此前有报道称,Th1 CD4 T细胞群体可转化为产生白细胞介素-4(IL-4)的细胞,而Th2细胞群体对IL-12介导的γ干扰素(IFN-γ)产生具有抗性。我们最近发现,CD30是IL-4反应的标志物,因此在此使用CD30来研究Th1和Th2的分化。我们发现,Th2细胞群体通常表现出稳定的表型,并且由于内源性IL-4的产生而对IL-12无反应。IFN-γ消除了IL-4的这种拮抗作用,并使Th2细胞群体通过IL-12转化为产生IFN-γ的细胞。然而,在完全缺乏IL-4的情况下,这种转化不需要IFN-γ,由IL-12产生的Th1细胞会定向分化为Th1途径,并失去对IL-4作出反应的能力。因此,免疫反应中局部IL-4和IFN-γ之间的平衡是决定CD4效应T细胞反应结果的关键因素。

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