Sala P, Tonutti E, Feruglio C, Florian F, Colombatti A
Istituto di Chimica Clinica, Ospedale S. Maria della Misericordia, Udine, Italy.
Blood. 1993 Sep 1;82(5):1546-52.
CD4+ CD8+ cells are present during T cell differentiation in the thymus. Less than 2% of normal T cells that coexpress CD4 and CD8 also are released in the circulation and are present in the peripheral blood. In this study, nine individuals are described that manifested persistent expansions (11% to 43%) of circulating CD4+ CD8+ T cells that in three cases had large granular lymphocyte (LGL) morphology in the absence of either lymphocytosis or overt lymphoproliferative disorders. Southern blot hybridization of enriched CD4+ CD8+ cells with T-cell receptor beta (TCR beta) and TCR gamma probes showed that most cases had the 12-kb Eco RI germinal band deleted or of decreased intensity. In several individuals new TCR beta-specific bands of different intensity and distinct from case to case suggested either monoclonal or oligoclonal and polyclonal expansions. Immunophenotypic analysis showed that in 7 out of 9 cases the CD4+ CD8+ T cells presented with CD8 dim expression. Furthermore, all the CD4+ CD8+ cells did not express many of the known activation antigens (low or absent CD25, CD38, CD71, HLA-DR), whereas they expressed high levels of CD2, CD29, CD56, and CD57. In addition, the CD4+ CD8+ cells of 5 out of 9 subjects coexpressed CD45RA and CD45RO suggesting that these cells might be "frozen" in an intermediate state between naive and memory T cells. In conclusion, the present CD4+ CD8+ cases fall within a larger spectrum of disorders ranging from apparently normal to reactive or proliferative situations and encompassing cells with LGL morphology or LGL-associated antigens expression either in the presence or in the absence of absolute lymphocytosis that deserve careful follow-up investigations.
CD4+CD8+细胞在胸腺中T细胞分化过程中存在。共表达CD4和CD8的正常T细胞中不到2%也会释放到循环中并存在于外周血中。在本研究中,描述了9名个体,他们表现出循环CD4+CD8+T细胞持续扩增(11%至43%),其中3例具有大颗粒淋巴细胞(LGL)形态,且无淋巴细胞增多症或明显的淋巴增殖性疾病。用T细胞受体β(TCRβ)和TCRγ探针对外周血中富集的CD4+CD8+细胞进行Southern印迹杂交显示,大多数病例中12kb的Eco RI生发带缺失或强度降低。在几个个体中,不同强度且因病例而异的新的TCRβ特异性条带提示存在单克隆、寡克隆或多克隆扩增。免疫表型分析显示,9例中有7例的CD4+CD8+T细胞呈现CD8低表达。此外,所有CD4+CD8+细胞均不表达许多已知的活化抗原(CD25、CD38、CD71、HLA-DR低表达或不表达),而它们表达高水平的CD2、CD29、CD56和CD57。另外,9名受试者中有5名的CD4+CD8+细胞共表达CD45RA和CD45RO,提示这些细胞可能“停滞”在幼稚T细胞和记忆T细胞之间的中间状态。总之,目前的CD4+CD8+病例属于一个更大的疾病谱,范围从看似正常到反应性或增殖性情况,包括存在或不存在绝对淋巴细胞增多症时具有LGL形态或LGL相关抗原表达的细胞,值得仔细随访研究。