Elicitation of Simian Immunodeficiency Virus-Specific Cytotoxic T Lymphocytes in Mucosal Compartments of Rhesus Monkeys by Systemic Vaccination
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Published:2002-11-15
Issue:22
Volume:76
Page:11484-11490
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ISSN:0022-538X
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Container-title:Journal of Virology
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language:en
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Short-container-title:J Virol
Author:
Baig Jamal1, Levy Daniel B.1, McKay Paul F.1, Schmitz Joern E.1, Santra Sampa1, Subbramanian Ramu A.1, Kuroda Marcelo J.1, Lifton Michelle A.1, Gorgone Darci A.1, Wyatt Linda S.2, Moss Bernard2, Huang Yue3, Chakrabarti Bimal K.3, Xu Ling3, Kong Wing-Pui3, Yang Zhi-Yong3, Mascola John R.3, Nabel Gary J.3, Carville Angela4, Lackner Andrew A.5, Veazey Ronald S.5, Letvin Norman L.1
Affiliation:
1. Division of Viral Pathogenesis, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215 2. Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-0445 3. Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-3005 4. New England Regional Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772 5. Tulane Regional Primate Research Center, Covington, Louisiana 70433
Abstract
ABSTRACT
Since most human immunodeficiency virus (HIV) infections are initiated following mucosal exposure to the virus, the anatomic containment or abortion of an HIV infection is likely to require vaccine-elicited cellular immune responses in those mucosal sites. Studying vaccine-elicited mucosal immune responses has been problematic because of the difficulties associated with sampling T lymphocytes from those anatomic compartments. In the present study, we demonstrate that mucosal cytotoxic T lymphocytes (CTL) specific for simian immunodeficiency virus (SIV) and simian HIV can be reproducibly sampled from intestinal mucosal tissue of rhesus monkeys obtained under endoscopic guidance. These lymphocytes recognize peptide-major histocompatibility complex class I complexes and express gamma interferon on exposure to peptide antigen. Interestingly, systemic immunization of monkeys with plasmid DNA immunogens followed by live recombinant attenuated poxviruses or adenoviruses with genes deleted elicits high-frequency SIV-specific CTL responses in these mucosal tissues. These studies therefore suggest that systemic delivery of potent HIV immunogens may suffice to elicit substantial mucosal CTL responses.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Reference30 articles.
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