Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (2)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Taupin, J.-L.
Right arrow Articles by Moreau, J.-F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Taupin, J.-L.
Right arrow Articles by Moreau, J.-F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

International Immunology, Vol. 11, No. 4, 545-552, April 1999
© 1999 Japanese Society for Immunology

An enlarged subpopulation of T lymphocytes bearing two distinct {gamma}{delta} TCR in an HIV-positive patient

Jean-Luc Taupin, Franck Halary1, Julie Déchanet, Marie-Alix Peyrat1, Jean-Marie Ragnaud2, Marc Bonneville1 and Jean-Franciois Moreau

CNRS UMR 5540, Université de Bordeaux II, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France
1 INSERM U463, Institut de Biologie, 9 Quai Moncousu, 44035 Nantes Cedex, France
2 Service de Médecine Interne et Maladies Infectieuses, Hôpital Pellegrin, Place Amélie Raba-Léon, 33076 Bordeaux Cedex, France

Correspondence to: J.-L. Taupin

Although T cell clone monospecificity is ensured by several allelic exclusion processes operating at either the genotypic or phenotypic levels, clones expressing two distinct {alpha}ß or {gamma}{delta} TCR have been described in several instances. Thus far, the origin of dual TCR-expressing cells and the homeostatic mechanisms controlling the size of this subset in the periphery remain poorly understood. In the course of a phenotypic analysis of {gamma}{delta} T cells in HIV-infected patients, we detected the presence of a T cell subset stained by both V{delta}2- and V{delta}3-specific mAb, which represented a large fraction (up to 16.5%) of {gamma}{delta} peripheral blood lymphocytes (PBL) in one HIV patient. The presence of two distinct functional {delta} chains on these cells was confirmed by phenotypic and molecular analysis of TCR transcripts expressed by V{delta}2+V{delta}3+ T cell clones derived from this patient. For 18 months, the absolute number of these cells varied similarly to the other PBL subsets, before becoming undetectable in blood samples. Moreover, most of these cells expressed CD8 receptors, which are classically found on activated, but not resting, {gamma}{delta} T cells. Taken together, these data suggest that dual TCR-expressing T cells are subjected to peripheral expansions and contractions presumably following antigen recognition, which would argue against a systematic counter-selection of these cells during peripheral antigen-driven responses.

Keywords: dual TCR, flow cytometry, {gamma}{delta} T lymphocytes

Transmitting editor: A. Fischer


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Virol.Home page
G. Alter, S. Rihn, H. Streeck, N. Teigen, A. Piechocka-Trocha, K. Moss, K. Cohen, A. Meier, F. Pereyra, B. Walker, et al.
Ligand-Independent Exhaustion of Killer Immunoglobulin-Like Receptor-Positive CD8+ T Cells in Human Immunodeficiency Virus Type 1 Infection
J. Virol., October 1, 2008; 82(19): 9668 - 9677.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.