Rebai N, Pantaleo G, Demarest J F, Ciurli C, Soudeyns H, Adelsberger J W, Vaccarezza M, Walker R E, Sekaly R P, Fauci A S
Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1529-33. doi: 10.1073/pnas.91.4.1529.
We analyzed the T-cell receptor (TCR) V beta repertoire in human immunodeficiency virus type 1 (HIV-1)-infected individuals at different stages of disease. To circumvent the effect of HLA and other loci on the expressed TCR repertoire, we compared the TCR repertoire in nine pairs of monozygotic twins who were discordant for HIV infection. A semiquantitative polymerase chain reaction (PCR) assay and flow cytometry enabled us to show distinct differences in the V beta repertoire in the HIV-positive twin compared with the HIV-negative twin. By combining PCR and cytofluorometry, these differences were restricted to a specific set of TCR V beta segments, with members of the V beta 13 family perturbed in six out of seven cases and those of the V beta 21 family perturbed in four out of seven cases studied. Most of the other V beta families remained unchanged. Our results provide direct evidence for a skewed TCR repertoire in HIV infection.
我们分析了处于疾病不同阶段的1型人类免疫缺陷病毒(HIV-1)感染者的T细胞受体(TCR)Vβ谱。为规避HLA和其他基因座对表达的TCR谱的影响,我们比较了9对HIV感染情况不一致的同卵双胞胎的TCR谱。半定量聚合酶链反应(PCR)检测和流式细胞术使我们能够显示出HIV阳性双胞胎与HIV阴性双胞胎相比,其Vβ谱存在明显差异。通过将PCR和细胞荧光测定法相结合,这些差异局限于一组特定的TCR Vβ片段,在7例研究病例中,Vβ13家族的成员在6例中受到干扰,Vβ21家族的成员在4例中受到干扰。大多数其他Vβ家族保持不变。我们的结果为HIV感染中TCR谱的倾斜提供了直接证据。