alexa Th17 Cells Coordinate with Th22 Cells in Maintaining Ho
ISSN 2155-6113

Journal of AIDS & Clinical Research
Open Access

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Research Article

Th17 Cells Coordinate with Th22 Cells in Maintaining Homeostasis of Intestinal Tissues and both are Depleted in SIV-Infected Macaques

Huanbin Xu, Xiaolei Wang and Ronald S. Veazey*

Tulane National Primate Research Center, Tulane University School of Medicine, 18703 Three Rivers Road Covington, LA 70433, USA

*Corresponding Author:
Ronald S. Veazey
Tulane National Primate Research Center
Division of Comparative Pathology
18703 Three Rivers Road, Covington, LA 70433 USA
Tel: (985) 871-6228
Fax: (985) 871-6510
E-mail: [email protected]

Received Date: March 05, 2014; Accepted Date: April 16, 2014; Published Date: April 27, 2014

Citation: Xu H, Wang X, Veazey RS (2014) Th17 Cells Coordinate with Th22 Cells in Maintaining Homeostasis of Intestinal Tissues and both are Depleted in SIVInfected Macaques. J AIDS Clin Res 5:302. doi:10.4172/2155-6113.1000302

Copyright: © 2014 Xu H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



Th17 and Th22 cells are thought to function as innate regulators of mucosal antimicrobial responses, tissue inflammation and mucosal integrity, yet their role in persistent SIV infection is still unclear. Here we compared Th17 and Th22 cells in their phenotype, effector/cytokine function, and frequency in blood and intestinal mucosal tissues, and correlate levels with mucosal damage in SIV-infected rhesus macaques. We found that Th17/Th22 cells share similar features in that both highly produce TNF-α and IL-2 and express CCR5 in intestinal tissues; yet very few show cytotoxic functions, as evidenced by lack of IFN-γ and granzyme B production. Further, Th17/Th22 cells display distinct tissue-specific distributions. Both Th17 and Th22 cells and cytokine secretion were significantly depleted in both blood and intestine in chronically SIV-infected macaques. The frequency of Th17 and Th22 cells in the intestine positively correlated with percentages of intestinal CD4+ T cells and negatively with damage to intestinal mucosa, and plasma viral loads in SIV infection. These findings indicate Th17 and Th22 cells share considerable functions, and may coordinate in innate mucosal immune responses, and their regional loss in the intestine may be associated with local mucosal immune dysfunction in persistent HIV/SIV infection.


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