Zaffaroni M, Rossini S, Ghezzi A, Parma R, Cazzullo C L
Centro Studi Sclerosis Multipla, Universita di Milano, Ospedale S. Antonio Abate, Gallarate, Italy.
J Neurol. 1990 Feb;237(1):1-4. doi: 10.1007/BF00319659.
Circulating lymphocyte subpopulations defined by anti-CD45 and other more common T-cell-specific monoclonal antibodies were analysed in 77 patients with multiple sclerosis and 38 healthy controls. A selective decrease of CD4+CD45+ cell percentages and absolute numbers in chronic-progressive patients was found; in 13 out of 26 patients this subpopulation was less than 11% CD4+CD45+ cells. Similarly, the whole CD45+ cell subset, as well as CD45+ cells expressed as percentages of CD4+ cells, were significantly reduced in chronic-progressive multiple sclerosis. CD4+CD45+ cells, commonly termed "inducer of suppression" T-lymphocytes, did not correlate with percentages or numbers of CD8+ cells. It is concluded that suppressor inducer T-cells act on the CD8+ subset function rather than reducing CD8+ cell numbers. Since CD4+CD45+ cells represent an early stage of lymphocyte maturation (naive T-cells), an under-representation of this subpopulation in active multiple sclerosis might reflect an increased conversion of naive cells into memory cells. This concept may be relevant for a better understanding of the disease pathogenesis.
采用抗CD45及其他更常用的T细胞特异性单克隆抗体对77例多发性硬化患者和38名健康对照者的循环淋巴细胞亚群进行了分析。发现慢性进展型患者的CD4+CD45+细胞百分比和绝对数量选择性降低;26例患者中有13例该亚群的CD4+CD45+细胞少于11%。同样,在慢性进展型多发性硬化中,整个CD45+细胞亚群以及以CD4+细胞百分比表示的CD45+细胞均显著减少。通常称为“抑制诱导物”的T淋巴细胞CD4+CD45+细胞与CD8+细胞的百分比或数量无关。得出的结论是,抑制诱导性T细胞作用于CD8+亚群功能,而非减少CD8+细胞数量。由于CD4+CD45+细胞代表淋巴细胞成熟的早期阶段(初始T细胞),该亚群在活动性多发性硬化中数量不足可能反映初始细胞向记忆细胞的转化增加。这一概念可能有助于更好地理解疾病发病机制。