Abstract |
To define the possible impact of T-lymphocyte trafficking parameters on simian immunodeficiency virus (SIV) pathogenesis, we examined migratory profiles of carboxyfluorescein diacetate succinimidyl ester ( CFSE)-labeled T lymphocytes in acutely SIVmac251-infected and uninfected macaques within 48 h after autologous transfer. Despite significant upregulation of homeostatic chemokine CCL19/ macrophage inflammatory protein 3beta and proinflammatory chemokine CXCL9/monokine induced by gamma interferon in secondary lymphoid tissue in SIV infection, no differences in CFSE+ T-lymphocyte frequencies or cell compartmentalization in lymph nodes were identified between animal groups. By contrast, a higher frequency of CFSE+ T lymphocytes in the small intestine was detected in acute SIV infection. This result correlated with increased numbers of gut CD4 T lymphocytes expressing chemokine receptors CCR9, CCR7, and CXCR3 and high levels of their respective chemokine ligands in the small intestine. The changes in trafficking parameters in SIV-infected macaques occurred concomitantly with acute gut CD4 T-lymphocyte depletion. Here, we present the first in vivo T-lymphocyte trafficking study in SIV infection and a novel approach to delineate T-lymphocyte recruitment into tissues in the nonhuman primate animal model for AIDS. Such studies are likely to provide unique insights into T-lymphocyte sequestration in distinct tissue compartments and possible mechanisms of CD4 T-lymphocyte depletion and immune dysfunction in simian AIDS.
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Authors | Candice C Clay, Denise S Rodrigues, Danielle J Harvey, Christian M Leutenegger, Ursula Esser |
Journal | Journal of virology
(J Virol)
Vol. 79
Issue 21
Pg. 13759-68
(Nov 2005)
ISSN: 0022-538X [Print] United States |
PMID | 16227295
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- 5-(6)-carboxyfluorescein diacetate succinimidyl ester
- CC chemokine receptor 9
- CCL19 protein, human
- CCR7 protein, human
- CXCL9 protein, human
- CXCR3 protein, human
- Chemokine CCL19
- Chemokine CXCL9
- Chemokines, CC
- Chemokines, CXC
- Fluoresceins
- Intercellular Signaling Peptides and Proteins
- Receptors, CCR
- Receptors, CCR7
- Receptors, CXCR3
- Receptors, Chemokine
- Succinimides
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Topics |
- Animals
- CD4-Positive T-Lymphocytes
(immunology)
- Cell Movement
- Chemokine CCL19
- Chemokine CXCL9
- Chemokines, CC
(biosynthesis)
- Chemokines, CXC
(metabolism)
- Flow Cytometry
- Fluoresceins
- Immunity, Cellular
- Intercellular Signaling Peptides and Proteins
(metabolism)
- Intestinal Mucosa
(immunology)
- Lymph Nodes
(immunology)
- Lymphocyte Count
- Macaca
- Male
- Receptors, CCR
- Receptors, CCR7
- Receptors, CXCR3
- Receptors, Chemokine
- Simian Acquired Immunodeficiency Syndrome
(immunology)
- Simian Immunodeficiency Virus
- Succinimides
- T-Lymphocytes
(immunology)
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