Massaia M, Dianzani U, Bianchi A, Camponi A, Boccadoro M, Pileri A
Dipartimento di Medicina ed Oncologia Sperimentale, Universita' di Torino, Ospedale Maggiore S. Giovanni Battista, Italia.
Clin Exp Immunol. 1988 Aug;73(2):214-8.
The generation of cytotoxic T lymphocytes (CTL) towards allogeneic cells was investigated in 19 patients with monoclonal gammopathy of undetermined significance (MGUS) and 31 patients with multiple myeloma (MM). This function was significantly decreased in all patients. The cytotoxic deficiency was more pronounced in MM with poor prognosis than MM with good prognosis and MGUS patients. A phenotypic analysis of PBT lymphocytes showed that poor prognosis MM also had the highest proportions of activated cells (HLA-DR+) in CD8+ subpopulations. CTL were generated after depletion of CD11+ lymphocytes (including suppressor cells) or after inhibition of suppressor function with deoxyguanosine. No increase of cytotoxicity was detected under these conditions. Exogenous supplementation of recombinant interleukin 2 (rIL-2) was also ineffective. These data indicate that MG PBT lymphocytes are unable to fully differentiate into CTL following allogeneic stimulation. This deficiency is most evident in MM patients already showing the poorest prognosis and the most altered T cell phenotype.
在19例意义未明的单克隆丙种球蛋白病(MGUS)患者和31例多发性骨髓瘤(MM)患者中,研究了针对同种异体细胞的细胞毒性T淋巴细胞(CTL)的产生情况。所有患者的这一功能均显著降低。与预后良好的MM患者和MGUS患者相比,预后不良的MM患者的细胞毒性缺陷更为明显。对外周血T淋巴细胞(PBT)的表型分析表明,预后不良的MM患者的CD8 +亚群中活化细胞(HLA - DR +)的比例也最高。在去除CD11 +淋巴细胞(包括抑制细胞)后或用脱氧鸟苷抑制抑制功能后产生了CTL。在这些条件下未检测到细胞毒性增加。外源性补充重组白细胞介素2(rIL - 2)也无效。这些数据表明,MG PBT淋巴细胞在同种异体刺激后无法完全分化为CTL。这种缺陷在已经显示出最差预后和最改变的T细胞表型的MM患者中最为明显。