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B7-H5 costimulates human T cells via CD28H

机译:B7-H5通过CD28H共刺激人类T细胞

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摘要

The B7/CD28 family has profound modulatory effects in immune responses and constitutes important targets for the development of novel therapeutic drugs against human diseases. Here we describe a new CD28 homolog (CD28H) that has unique functions in the regulation of the human immune response and is absent in mice. CD28H is constitutively expressed on all naive T cells. Repetitive antigenic exposure, however, induces a complete loss of CD28H on many T cells, and CD28H-negative T cells have a phenotype of terminal differentiation and senescence. After extensive screening in a receptor array, a B7-like molecule, B7 homolog 5 (B7-H5), was identified as a specific ligand for CD28H. B7-H5 is constitutively found in macrophages and could be induced on dendritic cells. The B7-H5/CD28H interaction co-stimulates human T cell growth and cytokine production, selectively via an AKT-dependent signaling cascade. Our study identifies a novel co-stimulatory pathway regulating human T cell responses.
机译:B7 / CD28家族在免疫反应中具有深远的调节作用,并构成开发针对人类疾病的新型治疗药物的重要目标。在这里,我们描述了一种新的CD28同源物(CD28H),在人类免疫应答的调节中具有独特的功能,并且在小鼠中不存在。 CD28H在所有幼稚T细胞上组成性表达。但是,重复性抗原暴露会在许多T细胞上引起CD28H的完全丧失,而CD28H阴性T细胞则具有终末分化和衰老的表型。在受体阵列中进行广泛筛选后,B7样分子B7同系物5(B7-H5)被鉴定为CD28H的特异性配体。 B7-H5组成性地存在于巨噬细胞中,并可在树突状细胞中被诱导。 B7-H5 / CD28H相互作用通过AKT依赖性信号传导级联选择性刺激人T细胞的生长和细胞因子的产生。我们的研究确定了调节人类T细胞反应的新型共刺激途径。

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