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HIV-1 infection depletes human CD34(+)CD38(-) hematopoietic progenitor cells via pDC-dependent mechanisms

Chronic human immunodeficiency virus-1 (HIV-1) infection in patients leads to multi-lineage hematopoietic abnormalities or pancytopenia. The deficiency in hematopoietic progenitor cells (HPCs) induced by HIV-1 infection has been proposed, but the relevant mechanisms are poorly understood. We report...

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Detalles Bibliográficos
Autores principales: Li, Guangming, Zhao, Juanjuan, Cheng, Liang, Jiang, Qi, Kan, Sheng, Qin, Enqiang, Tu, Bo, Zhang, Xin, Zhang, Liguo, Su, Lishan, Zhang, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552321/
https://www.ncbi.nlm.nih.gov/pubmed/28759657
http://dx.doi.org/10.1371/journal.ppat.1006505
Descripción
Sumario:Chronic human immunodeficiency virus-1 (HIV-1) infection in patients leads to multi-lineage hematopoietic abnormalities or pancytopenia. The deficiency in hematopoietic progenitor cells (HPCs) induced by HIV-1 infection has been proposed, but the relevant mechanisms are poorly understood. We report here that both human CD34(+)CD38(-) early and CD34(+)CD38(+) intermediate HPCs were maintained in the bone marrow (BM) of humanized mice. Chronic HIV-1 infection preferentially depleted CD34(+)CD38(-) early HPCs in the BM and reduced their proliferation potential in vivo in both HIV-1-infected patients and humanized mice, while CD34(+)CD38(+) intermediate HSCs were relatively unaffected. Strikingly, depletion of plasmacytoid dendritic cells (pDCs) prevented human CD34(+)CD38(-) early HPCs from HIV-1 infection-induced depletion and functional impairment and restored the gene expression profile of purified CD34(+) HPCs in humanized mice. These findings suggest that pDCs contribute to the early hematopoietic suppression induced by chronic HIV-1 infection and provide a novel therapeutic target for the hematopoiesis suppression in HIV-1 patients.