Russo M, Starobinas N, Marcondes M C, Minoprio P, Honteyberie-Joskowicz M
Departamento de Imunologia, Universidade de São Paulo, Brazil.
Immunol Lett. 1996 Mar;49(3):163-8. doi: 10.1016/0165-2478(96)02498-4.
Several studies in mice have strengthened the active role played either by CD4+, CD8+ or both T cell subsets in conferring resistance to Trypanosoma cruzi infection. To date, no studies reported the role played by T cell subsets on parasite multiplication in different organs. In the present work, mice were infected with CL strain of T. cruzi and T cell subset activities were blocked by i.p. injection of monoclonal antibody (mAb) directed against CD4, or IAk, or CD8 molecules. The effect of these treatments was determined by counting the number of parasite nests in heart and liver sections 16 days after infection. Our results showed that mice treated with anti-CD4 or anti-IAk mAbs presented a significant increase in the parasite load in the hearts and in the livers. Conversely, the number of parasites in hearts of anti-CD8 treated mice did not increase significantly. This treatment, however, resulted in a 20-fold increase in the number of parasites found in the liver. Simultaneous depletion of both T cell subsets by treatment of mice with anti-CD4/CD8 mAbs had, in the heart, the same effect as the CD4 depletion. Interestingly, this treatment caused a dramatic increase (200-fold) in the T. cruzi parasitism of the liver. These results indicate that the activity of T cell subsets against T. cruzi varies according to the infected organ.
多项针对小鼠的研究强化了CD4+、CD8+或这两个T细胞亚群在赋予抵抗克氏锥虫感染能力方面所发挥的积极作用。迄今为止,尚无研究报道T细胞亚群在不同器官中对寄生虫增殖所起的作用。在本研究中,用克氏锥虫CL株感染小鼠,并通过腹腔注射针对CD4、IAk或CD8分子的单克隆抗体(mAb)来阻断T细胞亚群的活性。在感染后16天,通过计数心脏和肝脏切片中寄生虫巢的数量来确定这些处理的效果。我们的结果表明,用抗CD4或抗IAk单克隆抗体处理的小鼠,其心脏和肝脏中的寄生虫负荷显著增加。相反,用抗CD8单克隆抗体处理的小鼠心脏中的寄生虫数量没有显著增加。然而,这种处理导致肝脏中发现的寄生虫数量增加了20倍。用抗CD4/CD8单克隆抗体同时耗尽两个T细胞亚群,在心脏中的效果与耗尽CD4相同。有趣的是,这种处理导致肝脏中克氏锥虫的寄生率急剧增加(200倍)。这些结果表明,T细胞亚群针对克氏锥虫的活性因感染器官而异。