Lopez H M, Tanner M K, Kierszenbaum F, Sztein M B
Department of Microbiology and Public Health, Michigan State University, East Lansing 48823.
Parasite Immunol. 1993 May;15(5):273-80. doi: 10.1111/j.1365-3024.1993.tb00610.x.
Although a number of immunological anomalies have been shown to occur during the acute period of Trypanosoma cruzi infection, the contribution of the parasite has not been clarified. In this work, we co-cultured activated splenic mononuclear cells (SMC) from normal outbred (CD1) or inbred (CBA/J) mice with purified T. cruzi trypomastigotes and studied ensuing T- and B-lymphocyte alterations. In the presence of parasites, phytohaemagglutinin-stimulated SMC from either mouse background manifested a marked reduction in both lymphoproliferative capacity (i.e., 3H-thymidine incorporation) and cell membrane level of interleukin-2 receptors (IL-2R; determined by flow cytometry) relative to SMC from parasite-free cultures. Thus, substantial proportions of activated SMC either became unable to express detectable levels of IL-2R or expressed this receptor in significantly lower numbers than control SMC. Supernatants from T. cruzi suspensions reproduced these suppressive effects on phytohaemagglutinin-stimulated SMC from normal or chronically infected CD1 or CBA/J mice. Similar results were obtained with SMC activated with a bacterial lipopolysaccharide. Since IL-2R expression is required for activated lymphocytes to progress through the cell cycle and multiply to mount effective immune responses, impaired IL-2R expression by T. cruzi provides a plausible hypothesis for the wide-ranged immunosuppression that occurs in the infected host.
尽管已证实在克氏锥虫感染急性期会出现一些免疫异常,但寄生虫的作用尚未阐明。在本研究中,我们将来自正常远交(CD1)或近交(CBA/J)小鼠的活化脾单核细胞(SMC)与纯化的克氏锥虫滋养体进行共培养,并研究随后的T淋巴细胞和B淋巴细胞变化。在有寄生虫存在的情况下,无论何种小鼠背景,经植物血凝素刺激的SMC相对于无寄生虫培养的SMC,其淋巴细胞增殖能力(即3H-胸腺嘧啶核苷掺入)和白细胞介素-2受体(IL-2R;通过流式细胞术测定)的细胞膜水平均显著降低。因此,相当一部分活化的SMC要么无法表达可检测水平的IL-2R,要么表达该受体的数量明显低于对照SMC。克氏锥虫悬浮液的上清液对来自正常或慢性感染的CD1或CBA/J小鼠经植物血凝素刺激的SMC产生了同样的抑制作用。用细菌脂多糖激活的SMC也得到了类似结果。由于活化淋巴细胞要完成细胞周期并增殖以产生有效的免疫反应需要表达IL-2R,克氏锥虫导致IL-2R表达受损为受感染宿主中发生的广泛免疫抑制提供了一个合理的假设。