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International Immunology, Vol. 12, No. 6, 797-805, June 2000
© 2000 Japanese Society for Immunology

High frequency of circulating {gamma}{delta} T cells with dominance of the V{delta}1 subset in a healthy population

Lars Hviid1, Bartholomew D. Akanmori2, Severine Loizon3, Jorgen A. L. Kurtzhals1,2, Christina H. Ricke1, Annick Lim4, Kwadwo A. Koram2, Francis K. Nkrumah2, Odile Mercereau-Puijalon3 and Charlotte Behr3

1 Centre for Medical Parasitology at Department of Infectious Diseases, Copenhagen University Hospital (Rigshospitalet) and Institute for Medical Microbiology and Immunology, University of Copenhagen, 2000 Copenhagen, Denmark
2 Immunology and Epidemiology Units, Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Ghana
3 Unité d'Immunologie Moléculaire des Parasites, CNRS URA 1960 and
4 Unité de Biologie Moleculaire du Gene, Institut Pastéur, 75724 Paris, France

Correspondence to: L. Hviid, Department of Infectious Diseases M7641, Rigshospitalet, Tagensvej 20, 2200 Copenhagen N, Denmark

TCR {gamma}{delta}+ cells constitute <5% of all circulating T cells in healthy, adult Caucasians, and V{delta}1+ cells constitute a minority of these cells. In contrast to TCR {alpha}ß+ cells, their repertoire is selected extrathymically by environmental antigens. Although increased frequencies of V{delta}1+ cells are found in several diseases, their function remains obscure. Here we show that the frequency of peripheral blood {gamma}{delta} T cells in healthy West Africans is about twice that of Caucasians, mainly due to a 5-fold increase in V{delta}1+ cells, which is consequently the dominant subset. No age dependency of V{delta}1 frequencies was identified and the V{delta}1+ cells in the African donors did not show preferential V{gamma} chain usage. Analysis of the CDR3 region size did not reveal any particular skewing of the V{delta}1 repertoire, although oligoclonality was more pronounced in adults compared to children. The proportions of CD8+, CD38+ and CD45RAhiCD45RO cells within the V{delta}1+ subset were higher in the African than in the European donors, without obvious differences in expression of activation markers. No significant correlations between levels of V{delta}1+ cells and environmental antigens or immunological parameters were identified. Taken together, the evidence argues against a CDR3-restricted, antigen-driven expansion of V{delta}1+ cells in the African study population. Our study shows that high frequencies of TCR {gamma}{delta}+ cells with dominance of the V{delta}1+ subset can occur at the population level in healthy people, raising questions about the physiological role of V{delta}1+ T cells in the function and regulation of the immune system.

Keywords: age, CDR3, Epstein-Barr virus, {gamma}{delta}, T cells, malaria, T cell repertoire, V{delta}1

Transmitting editor: S. Kaufmann


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