INFLUENCE OF HUMAN-LEUKOCYTE ANTIGEN GENES ON TCR-V GENE SEGMENT FREQUENCIES

Human leukocyte antigen (HLA)-dependent selection mechanisms exerted during thymic maturation are supposed to be main contributing factors to the genetic predetermination of the TCR repertoire and may have a detectable effect on adult peripheral blood lymphocyte V segment frequencies. Here, we analyzed whether polymorphic or non-polymorphic HLA determinants are associated with selected expression of some V gene segment specificities. We first examined the reactivity of 17 V segment specific mAb on purified CD4(+) and CD8(+) cell fractions in 10 unrelated people. We found a significant overexpression of only three V segment products (V(beta)2, V(beta)5.1 and V(beta)6.7) in CD4(+) and none in CD8(+) cell fractions in most individuals. Skewing of certain V-beta segments by non-polymorphic HLA determinants (i.e. class II for CD4(+) and class I for CD8(+) cells) is therefore more limited (3/17) than previously thought. Considering the effects of polymorphic HLA determinants, we compared TCR V segment frequencies in HLA-identical siblings to sibling pairs who differ at one or both HLA haplotypes, using 13 V-beta specific mAb. In pairwise comparisons, we found that the HLA complex had no detectable effect on TCR repertoire in five large families with multiple siblings. Together, these observations suggest that HLA-predicted selection mechanisms exerted during thymic maturation might not have a predominant influence shaping the TCR repertoire of normal adults.