A novel subset of human lymphocytes with a T cell receptor-gamma complex.

S Jitsukawa(Laboratoire d'études sur les monothéismes), Florence Faure(Laboratoire d'études sur les monothéismes), Marta M. Lipinski(Laboratoire d'études sur les monothéismes), Frédéric Triebel(Laboratoire d'études sur les monothéismes), Thierry Hercend(Laboratoire d'études sur les monothéismes)
The Journal of Experimental Medicine
October 1, 1987
Cited by 145Open Access
Full Text

Abstract

We have previously characterized a CD3+ T cell receptor (TCR) alpha/beta- human fetal cloned cell line, termed F6C7, which surface-expresses a CD3-associated gamma chain identified by anti-NKFi, an mAb with a restricted clonotypic reactivity. Here, we have produced an additional antibody, anti-Ti-gamma A, which recognizes a public epitope of the gamma molecule defined by anti-NKFi. Ti-gamma A is present on approximately 3% of circulating lymphocytes with a wide range (1-15%) among 30 healthy individuals tested. Two-color immunofluorescence experiments performed with anti-Ti-gamma A and BMA 031 mAb (a reagent specific for the TCR-alpha/beta receptor) showed that surface expression of Ti-alpha/beta and Ti-gamma A is mutually exclusive. Moreover, it was found that most Ti-gamma A+ cells are CD2+, CD3+, CD4-, CD5+, NKH1-, HLA class II-negative. In contrast, the expression of the CD8 molecule on these T lymphocytes appears to be variable from one individual to another. Finally, we found that Ti-gamma A+ cells represent a majority of peripheral lymphocytes that express CD3 proteins but not the TCR-alpha/beta heterodimer. The delineation of this unique lymphocyte subset should help further studies on the biology of cells with a CD3-associated gamma complex.


Related Papers

No related papers found

Powered by citation graph analysis