Alterations in T-cell receptor Vbeta repertoire of CD4 and CD8 T lymphocytes in human immunodeficiency virus-infected children

Abstract

Perturbations in the T-cell receptor (TCR) Vbeta repertoire were assessed in the CD4 and CD8 T lymphocytes of human immunodeficiency virus (HIV)-infected children who were receiving therapy during the chronic phase of infection by flow cytometry (FC) and PCR analysis. By FC, representation of 21 TCR Vbeta subfamilies was assessed for an increased or decreased percentage in CD4 and CD8 T cells, and by PCR, 22 TCR Vbeta subfamilies of CD4 and CD8 T cells were analyzed by CDR3 spectratyping for perturbations and reduction in the number of peaks, loss of Gaussian distribution, or clonal dominance. The majority of the TCR Vbeta subfamilies were examined by both methods and assessed for deviation from the norm by comparison with cord blood samples. The CD8-T-lymphocyte population exhibited more perturbations than the CD4 subset, and clonal dominance was present exclusively in CD8 T cells. Of the 55 total CD8-TCR Vbeta families classified with clonal dominance by CDR3 spectratyping, only 18 of these exhibited increased expression by FC. Patients with high numbers of CD8-TCR Vbeta families with decreased percentages had reduced percentages of total CD4 T cells. Increases in the number of CD4-TCR Vbeta families with increased percentages showed a positive correlation with skewing. Overall, changes from normal were often discordant between the two methods. This study suggests that the assessment of HIV-induced alterations in TCR Vbeta families at cellular and molecular levels yields different information and that our understanding of the immune response to HIV is still evolving.

FIG. 1.

Greater disruption of the CD8-TCR Vβ repertoire as compared to CD4-TCR Vβ repertoire in HIV-infected study patients. TCR Vβ repertoire in study patients was analyzed in relation to that for normal cord blood T cells, which represent an unperturbed repertoire. The CD8-T-lymphocyte population exhibited more changes by both PCR (A) and FC (B) than the CD4 population. Box plots indicate the median value as well as 5th, 25th, 75th, and 95th percentiles. The two groups were compared using the Mann-Whitney rank sum test with a P of ≤0.05 considered significant.

FIG. 2.

Correlation of FC-based expression of TCR Vβ families with each other and with CD4 T cells. Decreases in the percent expression of CD8-TCR Vβ families correlate inversely with the percentage of CD4 T cells (A). Increases in the percent expression of CD8-TCR Vβ families correlate with increases in the percentages of CD4-TCR Vβ families (B).

FIG. 3.

Relation of FC-based changes in TCR Vβ families with skewing observed by CDR3 length analyses. Increases in the percent expression of CD4-TCR Vβ families correlate with CD4-TCR Vβ skewing (A), and decreases in the percent expression of CD8-TCR Vβ families are correlated with CD4-TCR Vβ skewing (B).