Open AccessT cell receptor (TCR) V gene segment use in HLA‐typed Japanese healthy subjects
Author(s) -
SHIGEMATSU M.,
NAGAI S.,
MIKUNIYA T.,
IZUMI T.,
WIGZELL H.,
EKLUND A. G.,
GRUNEWALD J.
Publication year - 1996
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1046/j.1365-2249.1996.d01-14.x
Subject(s) - t cell receptor , immunology , human leukocyte antigen , gene , receptor , immunogenetics , biology , t cell , genetics , medicine , antigen , immune system
The expression of 13 different α and β V gene segments of the T cell receptor for antigen (TCR) was examined, using V gene‐specific MoAbs, on human peripheral blood T lymphocytes from 32 healthy Japanese subjects. In addition, to examine associations between TCR V gene products and HLA alleles, the HLA class I and class II types of all subjects were serologically determined. The reactivities of the anti‐TCR V‐specific MoAbs were, with some significant exceptions, similar to those previously described in healthy Caucasian subjects. We found a non‐random V gene usage as well as a statistically significant bias of the expression of eight Vβ gene products towards the CD4 + subpopulation, and a significant skewness in the usage of Vα12 towards the CD8 + population. Some subjects showed increased reactivities (above 10%) of certain MoAbs, mainly in the CD8 + subpopulation. We found no distinct correlation between any certain HLA class I or II allele and TCR V gene usage in the CD8 + or CD4 + subpopulations, respectively. In conclusion, the pattern of anti‐TCR V‐specific MoAb reactivities found in CD4 + and CD8 + subsets of peripheral blood lymphocytes of healthy Japanese subjects was in general found to match that previously described in healthy Caucasian subjects.