TY - JOUR
T1 - A novel human Vδ gene expressed predominantly in the TiγA fraction of γ/δ+ peripheral lymphocytes
AU - Triebel, Frédéric
AU - Faure, Florence
AU - Mami‐Chouaib, Fathia
AU - Jitsukawa, Setsuko
AU - Griscelli, Annelise
AU - Genevée, Catherine
AU - Roman‐Roman, Sergio
AU - Hercend, Thierry
PY - 1988/1/1
Y1 - 1988/1/1
N2 - We have characterized a functional T cell receptor (TcR) δ transcript in a TiγA+ human cloned cell line derived from peripheral blood. This cDNA includes a novel V gene (V‐AB12), whose expression was initially studied in a series of TcR γ/δ′ clones. Nine TiγA+ clones derived independently from distinct donors have been tested: each of them was found to possess a unique V‐AB12/J‐IDP2 5.5‐kb Eco RI rearrangement, which was constantly transcribed. Surface expression of the protein encoded by this unique rearranged gene was demonstrated by immunoprecipitations performed on three TiγA′ polyclonal cell lines using a specific rabbit heteroantiserum. Further analysis strongly suggested that a monoclonal antibody (mAb), designated anti‐BB3, detects a V‐ABl2‐encoded antigenic determinant on the cell surface. Double‐color immunofluorescence analysis of peripheral blood lymphocytes from ten donors indicated that most BB3+ cells are recognized by anti‐TiγA mAb. In previous studies, we have shown that a majority of TcR γ/δ+′ peripheral T cells expresses a γ chain including V9 (TiγA) and most frequently JP‐encoded peptides. Given the present results on the δ chain, it can be concluded that, in many individuals, a predominant fraction (Vγ9+/V‐AB12+) of circulating CD3+ TcRa/β− T lymphocytes expresses a receptor with little, if any, combinatorial diversity.
AB - We have characterized a functional T cell receptor (TcR) δ transcript in a TiγA+ human cloned cell line derived from peripheral blood. This cDNA includes a novel V gene (V‐AB12), whose expression was initially studied in a series of TcR γ/δ′ clones. Nine TiγA+ clones derived independently from distinct donors have been tested: each of them was found to possess a unique V‐AB12/J‐IDP2 5.5‐kb Eco RI rearrangement, which was constantly transcribed. Surface expression of the protein encoded by this unique rearranged gene was demonstrated by immunoprecipitations performed on three TiγA′ polyclonal cell lines using a specific rabbit heteroantiserum. Further analysis strongly suggested that a monoclonal antibody (mAb), designated anti‐BB3, detects a V‐ABl2‐encoded antigenic determinant on the cell surface. Double‐color immunofluorescence analysis of peripheral blood lymphocytes from ten donors indicated that most BB3+ cells are recognized by anti‐TiγA mAb. In previous studies, we have shown that a majority of TcR γ/δ+′ peripheral T cells expresses a γ chain including V9 (TiγA) and most frequently JP‐encoded peptides. Given the present results on the δ chain, it can be concluded that, in many individuals, a predominant fraction (Vγ9+/V‐AB12+) of circulating CD3+ TcRa/β− T lymphocytes expresses a receptor with little, if any, combinatorial diversity.
UR - http://www.scopus.com/inward/record.url?scp=0024245362&partnerID=8YFLogxK
U2 - 10.1002/eji.1830181223
DO - 10.1002/eji.1830181223
M3 - Article
C2 - 2975601
AN - SCOPUS:0024245362
SN - 0014-2980
VL - 18
SP - 2021
EP - 2027
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 12
ER -