V. Bonfert et al., PREFERENTIAL EXPRESSION OF V-BETA GENE FAMILIES IN CD8 MEMORY CELLS OF APPARENTLY HEALTHY DONORS, Cellular immunology, 166(2), 1995, pp. 165-171
Antigen stimulation may lead to expansion or deletion of T-cells expre
ssing T-cell receptors that belong to specific V beta gene families. S
ince such stimulation at the same time will lead to conversion from na
ive to memory T-cells, we have asked whether a bias in V beta families
can be observed when comparing these two populations. We have studied
the expression of V beta 3, 8, 13.3, 19, and 22 in peripheral blood T
-cells for 12 apparently healthy male donors. For how cytometry 100,00
0 CD4(+) or CD8+ cells each were analysed in three-colour immunofluore
scence for percentage of V beta families among CD45R0(-) naive and CD4
5R0(+) memory cells. Greater than twofold excess was found in the CD8(
+)CD45R0(+) cells in four cases (1x V beta 13.3, 2x V beta 19, 1x V be
ta 22) and a greater than twofold decrease in CD8(+)CD45R0(+) cells in
two cases (1x V beta 8, 1x V beta 22). In contrast, among CD4(+) cell
s no such bias was detected, The excess in CD8(+)CD45R0(+) memory cell
s showed no substantial fluctuation over time in that it was found to
be stable for 19 to 70 days. Finally, in vitro conversion of purified
CD8(+)CD45R0(-) cells to CD45R0(+) cells by polyclonal stimulation wit
h PHA did not result in the excess of V beta usage observed in vivo. T
hese data suggest that specific antigen stimulation during past infect
ion or allergy may be responsible for the excess of certain V beta gen
e families. Clinical studies looking for disease associations will hav
e to test CD4 and CD8 naive and memory subsets in order to precisely i
dentify a bias in V beta usage and these studies will have to consider
the pronounced changes observed in healthy controls. (C) 1995 Academi
c Press, Inc.