The goal of this project is to elucidate the role of T-regulatory cells in the immunopathology of SIV disease. Abundant evidence suggests that generalized, chronic immune activation is an important cause of naive T-cell depletion and (immune dysfunction. Natural and adaptive T-regulatory cells can suppress immune activation in vitro and in vivo. We hypothesize that T-regulatory cells can slow the progression of SIV and HIV disease by moderating generalized, chronic immune activation. The following Specific Aims will be pursued: 1. Assess natural T-regulatory cells in the blood and lymphoid organs of fetal, infant, juvenile, and adult macaques. Candidate natural T-reg populations will be isolated from macaque blood and tissue samples, then characterized. The distribution of T-regs as a function of age will be described. 2. Assess T-regulatory cells in SIV-infected macaques. We test the number and function of natural T-regs in infected macaques, as well as the possibility that macaques develop adaptive T-regulatory responses to SIV. We hypothesize that more T-regs are correlated with a reduction in measures of immune activation. 3. Measure the influence of an expanded T-reg population on SIV disease progression. Natural T-regs will be expanded in vitro and then reinfused either before or after infection with SIVmac239. Markers of disease progression, immune responses to SIV, and inflammation will be studied for at least six months after infection. Successful completion of these Aims will provide a new understanding of T-reg biology in non-human primates and the possible importance of these cells in SIV disease progression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
7F32AI067088-02
Application #
7196310
Study Section
AIDS Molecular and Cellular Biology Study Section (AMCB)
Program Officer
Finzi, Diana
Project Start
2006-03-01
Project End
2008-10-31
Budget Start
2006-03-01
Budget End
2006-10-31
Support Year
2
Fiscal Year
2005
Total Cost
$30,817
Indirect Cost
Name
University of California San Francisco
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Hartigan-O'Connor, Dennis J; Abel, Kristina; Van Rompay, Koen K A et al. (2012) SIV replication in the infected rhesus macaque is limited by the size of the preexisting TH17 cell compartment. Sci Transl Med 4:136ra69
Hartigan-O'Connor, Dennis J; Poon, Chungkee; Sinclair, Elizabeth et al. (2007) Human CD4+ regulatory T cells express lower levels of the IL-7 receptor alpha chain (CD127), allowing consistent identification and sorting of live cells. J Immunol Methods 319:41-52
Hartigan-O'Connor, Dennis J; Abel, Kristina; McCune, Joseph M (2007) Suppression of SIV-specific CD4+ T cells by infant but not adult macaque regulatory T cells: implications for SIV disease progression. J Exp Med 204:2679-92