Goes A M, Gazzinelli G, Rocha R, Katz N, Doughty B L
Department of Veterinary Microbiology and Parasitology, College of Veterinary Medicine, Texas A & M University, College Station.
Am J Trop Med Hyg. 1991 Apr;44(4):434-43. doi: 10.4269/ajtmh.1991.44.434.
Granulomatous hypersensitivity to parasite eggs of Schistosoma mansoni is an important factor in the development of morbidity in chronic schistosomiasis. It has been demonstrated previously that the chronic, well-tolerated, intestinal form of schistosomiasis is associated with the establishment and maintenance of a variety of immunoregulatory mechanisms. We have used an in vitro model of granuloma formation for the purpose of studying the regulation of granulomatous hypersensitivity to S. mansoni egg antigens, mediated by immune complexes (IC). Our results show that the peripheral blood mononuclear cells (PBMCs) from patients with active schistosome infections, when treated with sera from chronic schistosomiasis patients, were able to induce an inhibitory activity on in vitro granuloma formation. Significant modulation of the in vitro granuloma reaction remained after treatment of PBMCs with isolated IC or manufactured IC with soluble egg antigen (SEA) and purified IgG from pooled chronic schistosomiasis sera. In contrast to granuloma modulation stimulated with whole molecule IgG-SEA IC, the incubation of PBMCs with F(ab')2 IgG-SEA IC did not induce any suppression of the granulomatous hypersensitivity to SEA. It appears in this model system that IC may inhibit the activity of granuloma formation by stimulating macrophages to release suppressive mediators. We have demonstrated this possibility by inhibition of prostaglandin activity using indomethacin. The addition of indomethacin to the granuloma culture significantly reduced in vitro granulomatous hypersensitivity to S. mansoni eggs in patients with chronic intestinal schistosomiasis and do so by inducing macrophages to secrete prostaglandins.
对曼氏血吸虫寄生虫卵的肉芽肿性超敏反应是慢性血吸虫病发病机制中的一个重要因素。先前已经证明,慢性、耐受性良好的肠道型血吸虫病与多种免疫调节机制的建立和维持有关。我们使用了一种肉芽肿形成的体外模型,以研究由免疫复合物(IC)介导的对曼氏血吸虫卵抗原的肉芽肿性超敏反应的调节。我们的结果表明,来自活动性血吸虫感染患者的外周血单核细胞(PBMC),在用慢性血吸虫病患者的血清处理后,能够诱导对体外肉芽肿形成的抑制活性。用分离的IC或用可溶性卵抗原(SEA)和来自合并的慢性血吸虫病血清的纯化IgG制备的IC处理PBMC后,体外肉芽肿反应仍有显著调节。与用全分子IgG-SEA IC刺激的肉芽肿调节相反,用F(ab')2 IgG-SEA IC孵育PBMC不会诱导对SEA的肉芽肿性超敏反应的任何抑制。在这个模型系统中,IC似乎可能通过刺激巨噬细胞释放抑制性介质来抑制肉芽肿形成的活性。我们通过使用吲哚美辛抑制前列腺素活性证明了这种可能性。在肉芽肿培养物中添加吲哚美辛可显著降低慢性肠道血吸虫病患者对曼氏血吸虫卵的体外肉芽肿性超敏反应,并且通过诱导巨噬细胞分泌前列腺素来实现。