Didoli G, Revelli S, Davila H, Ferro M E, Romero-Piffiguer M, Bottasso O
Instituto de Inmunologia, Facultad de Ciencias Médicas, Universidad Nacional de Rosario, Santa Fe, Argentina.
Braz J Med Biol Res. 1999 Jun;32(6):753-60. doi: 10.1590/s0100-879x1999000600011.
We demonstrated that administration of interferon gamma (IFN-gamma) to the inbred "I" strain of pregnant rats conferred partial resistance on their offspring to challenge with Trypanosoma cruzi. We now examine if this intervention also modifies the reportedly immunodepressed cellular responses which occur during chronic infection. Offspring were born to mothers undergoing one of the following procedures during gestation: subcutaneous injections of recombinant rat IFN-gamma, 50,000 IU/rat, five times/week for 3 weeks, which was started on the day of mating (IFN-Mo); infection with 10(6) trypomastigotes of T. cruzi at 7, 14, and 21 days after mating plus IFN-gamma treatment as given to the former group (TcIFN-Mo); the same protocol except that physiological saline was injected instead of IFN-gamma (Te-Mo); injection of physiological saline only (control-Mo). All offspring groups (N = 8-10/group) were infected at weaning and were assessed 90 days later for their adjuvant-induced arthritic response or levels of major T cell subsets in spleen and lymph nodes. TcIFN-Mo and IFN-Mo offspring showed a reestablished arthritic response, which remained within the range seen in controls. Immunolabeling studies on parallel groups of 90-day-infected offspring showed that the inverse CD4/CD8 cell ratio that is usually seen in lymphoid organs from these chronically infected rats (median 0.61) appeared to have recovered in the TcIFN-Mo and IFN-Mo groups (median 1.66 and 1.78, respectively) and was not different from uninfected controls (1.96). These studies indicate that early stimulation with IFN-gamma is able to reverse the immunosuppressive state that is usually present during the chronic period of the experimental infection.
我们证明,给近交“ I”系妊娠大鼠注射干扰素γ(IFN-γ)可使其后代对克氏锥虫的攻击产生部分抗性。我们现在研究这种干预是否也能改变慢性感染期间据报道出现的免疫抑制细胞反应。在妊娠期间接受以下程序之一的母亲所生的后代:皮下注射重组大鼠IFN-γ,50,000 IU /只大鼠,每周5次,共3周,从交配日开始(IFN-Mo);在交配后第7、14和21天感染10⁶个克氏锥虫的锥鞭毛体,并给予与前一组相同的IFN-γ治疗(TcIFN-Mo);除注射生理盐水而非IFN-γ外,采用相同方案(Te-Mo);仅注射生理盐水(对照-Mo)。所有后代组(每组N = 8-10)在断奶时感染,并在90天后评估其佐剂诱导的关节炎反应或脾脏和淋巴结中主要T细胞亚群的水平。TcIFN-Mo和IFN-Mo后代显示出重新建立的关节炎反应,该反应仍在对照组所见范围内。对90天感染后代的平行组进行的免疫标记研究表明,这些慢性感染大鼠的淋巴器官中通常出现的CD4 / CD8细胞比例倒置(中位数0.61)在TcIFN-Mo和IFN-Mo组中似乎已恢复(分别为中位数1.66和1.78),且与未感染对照组(1.96)无差异。这些研究表明,早期用IFN-γ刺激能够逆转实验性感染慢性期通常存在的免疫抑制状态。