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Distinct chemokine triggers and in vivo migratory paths of fluorescein dye-labeled T Lymphocytes in acutely simian immunodeficiency virus SIVmac251-infected and uninfected macaques.

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.
AuthorsCandice C Clay, Denise S Rodrigues, Danielle J Harvey, Christian M Leutenegger, Ursula Esser
JournalJournal of virology (J Virol) Vol. 79 Issue 21 Pg. 13759-68 (Nov 2005) ISSN: 0022-538X [Print] United States
PMID16227295 (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.)
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
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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