Nature communications · 2013
B7-H5 costimulates human T cells via CD28H.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Zhu Yuwen, Yao Sheng, Iliopoulou Bettina P, Han Xue, Augustine Mathew M, Xu Haiying, Phennicie Ryan T, Flies Sarah J, Broadwater Megan, Ruff William, Taube Janis M, Zheng Linghua, Luo Liqun, Zhu Gefeng, Chen Jianzhu, Chen Lieping
Аннотация
The B7/CD28 family has profound modulatory effects in immune responses and constitutes an important target for the development of novel therapeutic drugs against human diseases. Here we describe a new CD28 homologue (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 homologue 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 selectively costimulates human T-cell growth and cytokine production via an AKT-dependent signalling cascade. Our study identifies a novel costimulatory pathway regulating human T-cell responses.
Предметные рубрики MeSH
Amino Acid SequenceAnimalsB7 AntigensCD28 AntigensCoculture TechniquesEpitopesFluoresceinsGene Expression RegulationGenome, HumanHEK293 CellsHumansLigandsLymphocyte ActivationMembrane ProteinsMiceMolecular Sequence DataPhosphorylationPhosphotyrosineProtein BindingSignal TransductionSuccinimidesT-LymphocytesVanadates