The human T-cell antigen receptor (TCR) is the counter-receptor for the HLA
/peptide complex displayed on the surface of antigen-presenting cells. It c
onfers antigen specificity on T lymphocytes and therefore plays a central r
ole in pathogen recognition and host response. The most frequently used for
m of the TCR is a heterodimer composed of variable alpha and beta chains. W
e investigated allele frequencies for four variable-region gene segments of
the beta chain (2S1, 3S1, 8S3, and 15S1) in 146 Caucasians and 165 African
s. The results reveal significant unexpected differences between the two po
pulations for allele frequencies, phenotypes, genotypes, and haplotypes. Am
ong Caucasians. there are 43 phenotypes, whereas there are 31 among the Afr
icans studied. There are 17 haplotypes in the Caucasian sample but only 10
in Africans. This loss of diversity is largely due to the high frequency of
one haplotype in the African sample which represents 65% of the informativ
e chromosomes. At least one copy of this haplotype is present in 90% of inf
ormative individuals. As a result, 29% of Africans are homozygous for the c
ommon haplotype. Less genetic diversity at TCRBV is unexpected, since Afric
ans usually show greater genetic diversity than other ethnic groups. For ex
ample, there are approximately twice as many HLA haplotypes in Africans com
pared to Caucasians. Homozygosity is also unexpected because it reduces the
number of TCR variants available to recognize HLA pathogen-derived peptide
complexes.