Kierszenbaum F
Immunology. 1981 Nov;44(3):641-8.
The ability of spleen cells taken from mice infected with Trypanosoma cruzi to proliferate after stimulation with specific trypanosomal antigens was investigated during the acute and chronic phases of the disease. Lymphoproliferation was minimal or undetectable during the acute period whereas the chronic phase was characterized by significant responses over a wide range of antigen concentration. Transfer of infected mouse spleen cells to cultures of splenocytes from chronically infected animals failed to modify the response of the latter to antigenic stimulation as measured by DNA synthesis. Furthermore, the responses of infected mouse spleen cells collected during the acute period and freed of Lyt 2.1-bearing lymphocytes, a subclass known to contain the suppressor T cells, did not differ significantly from those of untreated aliquots of the same cell suspensions. These results, together with the fact that the T-cell compartment of the spleen was severely depleted during the acute but not the chronic stage of the infection, suggest that the impaired immunological responsiveness of acutely infected mice may be due in part to the absence or marked reduction of responder and/or accessory T lymphocytes. An active role for suppressor T cells in the reduced response to trypanosomal antigens by lymphocytes from mice in the early, acute phase of T. cruzi infection is not supported by the present observations.
在克氏锥虫感染小鼠疾病的急性期和慢性期,研究了取自感染克氏锥虫小鼠的脾细胞在用特定锥虫抗原刺激后增殖的能力。在急性期,淋巴细胞增殖极少或无法检测到,而慢性期的特征是在广泛的抗原浓度范围内有显著反应。将感染小鼠的脾细胞转移至慢性感染动物的脾细胞培养物中,通过DNA合成测量,未能改变后者对抗原刺激的反应。此外,在急性期收集的感染小鼠脾细胞,去除携带Lyt 2.1的淋巴细胞(已知该亚类包含抑制性T细胞)后,与相同细胞悬液未处理的等分试样相比,其反应无显著差异。这些结果,连同感染急性期而非慢性期脾的T细胞区室严重耗竭这一事实,表明急性感染小鼠免疫反应性受损可能部分归因于反应性和/或辅助性T淋巴细胞的缺失或显著减少。目前的观察结果不支持抑制性T细胞在克氏锥虫感染早期急性期小鼠淋巴细胞对锥虫抗原反应降低中起积极作用。