Cabeza Meckert P, Chambó J G, Laguens R P
Cátedra de Patología II, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, Argentina.
Antimicrob Agents Chemother. 1988 Feb;32(2):241-5. doi: 10.1128/AAC.32.2.241.
Reinfection of chronic chagasic mice after treatment with nifurtimox resulted in different outcomes according to the number of parasites used for inoculation. Nifurtimox-treated chagasic animals injected with 2,500 trypomastigotes developed higher parasitemia and increased mortality compared with nontreated chagasic mice. When reinfection was done with 25 trypomastigotes, treated and nontreated animals showed similar parasitemias and mortalities, which were significantly higher in nonchagasic controls infected for the first time. Immunological studies showed that treatment with nifurtimox led to a decrease in anti-Trypanosoma cruzi antibodies engaged in parasite destruction, inducing either complement-dependent lysis or antibody-dependent cytotoxicity, but no difference in anti-T. cruzi cell-mediated immunity was found between treated and nontreated chagasic animals. It is concluded that treatment with nifurtimox leads to a loss of resistance to reinfection with a large number of trypanosomes, which is maintained with challenge with a few parasites, and that these two thresholds of premunition are probably associated with humoral and cell-mediated anti-T. cruzi immune responses, respectively.
用硝呋替莫治疗后的慢性恰加斯病小鼠再次感染,根据接种寄生虫的数量会产生不同的结果。与未治疗的恰加斯病小鼠相比,注射2500个锥鞭毛体的经硝呋替莫治疗的恰加斯病动物出现了更高的寄生虫血症和死亡率。当用25个锥鞭毛体进行再次感染时,治疗组和未治疗组动物的寄生虫血症和死亡率相似,而首次感染的非恰加斯病对照组的则明显更高。免疫学研究表明,硝呋替莫治疗导致参与寄生虫破坏的抗克氏锥虫抗体减少,诱导补体依赖性裂解或抗体依赖性细胞毒性,但在治疗组和未治疗组的恰加斯病动物之间未发现抗克氏锥虫细胞介导免疫的差异。得出的结论是,硝呋替莫治疗会导致对大量锥虫再次感染的抵抗力丧失,而少量寄生虫攻击时这种抵抗力仍会维持,并且这两个免疫阈可能分别与体液和细胞介导的抗克氏锥虫免疫反应有关。