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B7-H5 costimulates human T cells via CD28H

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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3698612/
https://www.ncbi.nlm.nih.gov/pubmed/23784006
http://dx.doi.org/10.1038/ncomms3043
Descripción
Sumario: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.