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Loss of CD103+ DCs and Mucosal IL-17+ and IL-22+ Lymphocytes is Associated with Mucosal Damage in SIV Infection
Journal article   Open access   Peer reviewed

Loss of CD103+ DCs and Mucosal IL-17+ and IL-22+ Lymphocytes is Associated with Mucosal Damage in SIV Infection

Nichole R. Klatt, Jacob D. Estes, Xiaoyong Sun, Alexandra M. Ortiz, John S. Barber, Levelle D. Harris, Barbara Cervasi, Lauren K. Yokomizo, Li Pan, Carol L. Vinton, …
Mucosal immunology, v 5(6), pp 646-657
30 May 2012
PMID: 22643849
url
https://www.nature.com/articles/mi201238.pdfView
Published, Version of Record (VoR) Open
url
https://doi.org/10.1038/mi.2012.38View
Published, Version of Record (VoR) Open

Abstract

HIV/SIV disease progression is associated with multifocal damage to the GI tract epithelial barrier that correlates with microbial translocation and persistent pathological immune activation but the underlying mechanisms remain unclear. Investigating alterations in mucosal immunity during SIV infection, we found that damage to the colonic epithelial barrier was associated with loss of multiple lineages of IL-17-producing lymphocytes, cells that microarray analysis showed express genes important for enterocyte homeostasis, including IL-22. IL-22-producing lymphocytes were also lost after SIV infection. Potentially explaining coordinate loss of these distinct populations, we also observed loss of CD103+ DCs after SIV infection which associated with loss of IL-17 and IL-22-producing lymphocytes. CD103+ DCs expressed genes associated with promotion of IL-17/IL-22+ cells, and co-culture of CD103+ DCs and naïve T-cells led to increased IL17A and RORc expression in differentiating T-cells. These results reveal complex interactions between mucosal immune cell subsets providing potential mechanistic insights into mechanisms of mucosal immune dysregulation during HIV/SIV infection, and offer hints for development of novel therapeutic strategies to address this aspect of AIDS virus pathogenesis.

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Web of Science research areas
Immunology
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