Distribution and functional analysis of memory antiviral CD8 T cell responses in HIV-1 and cytomegalovirus infections.

Details

Serval ID
serval:BIB_23749
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Distribution and functional analysis of memory antiviral CD8 T cell responses in HIV-1 and cytomegalovirus infections.
Journal
European Journal of Immunology
Author(s)
Ellefsen K., Harari A., Champagne P., Bart P.A., Sékaly R.P., Pantaleo G.
ISSN
0014-2980
Publication state
Published
Issued date
2002
Peer-reviewed
Oui
Volume
32
Number
12
Pages
3756-3764
Language
english
Notes
Publication types: In Vitro ; Journal Article ; Research Support, Non-U.S. Gov't - Publication Status: ppublish
Abstract
In the present study, we have investigated the anatomic distribution and the function of different populations of HIV-1- and cytomegalovirus (CMV)-specific memory CD8 T cells. The different populations of virus-specific memory CD8 T cells were distinguished on the basis of the expression of CD45RA and CCR7, and the composition of HIV-1- and CMV-specific memory CD8 T cell pools were compared in subjects with chronic HIV-1 and CMV co-infection. The distribution of HIV-1-specific CD8 T cells was similar between blood and lymph node. However, CMV-specific CD8 T cells were accumulated predominantly in the blood away from the lymphoid tissue. The majority (>70%) of HIV-1- and CMV-specific CD8 T cells in both blood and lymph node had a phenotype, e.g. CCR7-, typical of effector T cells. HIV-1-specific memory CD8 T cells were mostly (>80%) pre-terminally differentiated cells, e.g. CD45RA-CCR7-, in both blood and lymph node while 30-50% of CMV-specific CD8 T cells were terminally differentiated, e.g. CD45RA+CCR7-. Therefore, consistently with studies in mice, antigen-specific effector memory CD8 T cells accumulate predominantly in the target organ of the pathogen in humans, and the differences in the composition of HIV-1- and CMV-specific CD8 T cell pools were also present in the lymphoid tissue. A substantial proportion (30-40%) of virus-specific CD8+CCR7+ T cells produced IFN-gamma. Thus, indicating that the expression of CCR7 does not provide a clear-cut separation of memory CD8 T cells with distinct functional capacities. Taken together, these results provide further advances in the characterization of human memory CD8 T cells.
Keywords
Adult, Antigens, CD45/metabolism, CD8-Positive T-Lymphocytes/immunology, Cytomegalovirus/immunology, Cytomegalovirus Infections/immunology, HIV Infections/immunology, HIV-1/immunology, Humans, Immunologic Memory, Interferon-gamma/biosynthesis, Lymph Nodes/immunology, Receptors, CCR7, Receptors, Chemokine/metabolism, T-Lymphocyte Subsets/immunology
Pubmed
Web of science
Create date
19/11/2007 13:19
Last modification date
20/08/2019 14:01
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