Jr. Currier et al., Contributions of CD4(+), CD8(+), and CD4(+)CD8(+) T cells to skewing within the peripheral T cell receptor beta chain repertoire of healthy macaques, HUMAN IMMUN, 60(3), 1999, pp. 209-222
Diversity in the peripheral T cell receptor repertoire of rhesus (Macaca mu
latta) and pig-tailed macaques (Macaca nemestrina) has been studied by exam
ining the profile of CDR3 lengths in TCR beta chains. Expressed CDR3 length
distribution profiles for individual TCRBV families were obtained from tot
al peripheral blood mononuclear cells (PBMC) and T cell subsets isolated fr
om PBMC. These studies reveal that the T cell receptor repertoire of PBMC f
rom healthy macaques often exhibits skewing in TCRBV family CDR3 profiles.
The skewing of TCRBV family CDR3 profiles was evident as discrete expanded
length(s) and was detected in up to 50% of the PBMC profiles. Analyses of s
eparated T cell populations demonstrated that the CD8(+) T cell subset was
responsible for the majority of observed skewing in CDR3 length profiles. H
owever, CD4(+) T cells were also shown to contribute to the skewed peripher
al PBMC repertoire in these animals. While certain TCRBV families frequentl
y displayed skewed profiles, there was no concordance in the particular CDR
3 lengths expanded among the different animals. Furthermore, an additional
feature of the peripheral blood of the animals studied was the presence of
an unusual population of extrathymic CD4(+) and CD8(+) (double-positive)T c
ells (up to 9.6% in the PBMC of rhesus macaques). The double-positive T cel
ls could be differentiated from CD4 single-positive and CD8 single-positive
T cells by their increased surface expression of LFA-1 and decreased CD62L
expression. The percentage of the double-positive T cells was higher in rh
esus than pig-tailed macaques and contributed substantially to the peripher
al T cell repertoire. Human Immunology 60, 209-222 (1999). (C) American Soc
iety for Histocompatibility and Immunogenetics, 1999 Published by Elsevier
Science Inc.