Souza-Lemos C, de-Campos S N, Teva A, Côrte-Real S, Fonseca E C, Porrozzi R, Grimaldi G
Laboratório de Pesquisa em Leishmaniose, Instituto Oswaldo Cruz/Fiocruz, Rio de Janeiro, Brazil.
J Pathol. 2008 Nov;216(3):375-86. doi: 10.1002/path.2403.
In order to unravel the physiopathology of leishmaniasis in humans, it is necessary to better understand how Leishmania are able to survive for years within immunologically active granulomas. In the present study, we used a macaque (Macaca mulatta) model of infection with Leishmania braziliensis as a means of assessing the usefulness of this primate system. This model more closely mirrors human protective immunity to Leishmania than the murine model; therefore, we used it to study the host inflammatory granulomatous response involved in the control of cutaneous leishmaniasis. Infected primates developed localized long-term skin ulcerations, but complete spontaneous clinical healing occurred in all infected animals. The infection induced the recruitment and activation of inflammatory mast cells, granulocytes, mononuclear phagocytes, and lymphocytes at the site of infection. During the acute reaction, polymorphonuclear leukocytes were more prominent than other cell types and apparently destroyed many parasites; macrophages then rapidly engulfed dying neutrophils together with their parasitic cargo. In the chronic phase, persisting parasites induced a typical T helper (Th) cytokine, type 1-mediated, immunity-induced granulomatous reaction. By this time, more or less differentiated macrophage accumulations were found, and these evolved to become mature tissue granulomas consisting of all the specific cell types found within human granulomas. In the healing stage, fibroblasts proliferated at the periphery and finally invaded the granulomas with fibrotic substitution. These findings point to the feasibility of using this model to elucidate the potentially disabling Th1-cell mechanisms that may eventually render the host granulomatous response inadequate for fighting L. braziliensis infections.
为了阐明人类利什曼病的病理生理学,有必要更好地了解利什曼原虫如何能够在免疫活性肉芽肿内存活数年。在本研究中,我们使用巴西利什曼原虫感染的猕猴(恒河猴)模型来评估这个灵长类动物系统的实用性。该模型比小鼠模型更能准确反映人类对利什曼原虫的保护性免疫;因此,我们用它来研究参与控制皮肤利什曼病的宿主炎症性肉芽肿反应。受感染的灵长类动物出现了局部长期皮肤溃疡,但所有受感染动物均实现了完全自发临床愈合。感染在感染部位诱导了炎性肥大细胞、粒细胞、单核吞噬细胞和淋巴细胞的募集和激活。在急性反应期间,多形核白细胞比其他细胞类型更突出,显然破坏了许多寄生虫;然后巨噬细胞迅速吞噬死亡的中性粒细胞及其携带的寄生虫。在慢性期,持续存在的寄生虫诱导了典型的1型辅助性T(Th)细胞因子介导的免疫诱导性肉芽肿反应。此时,发现了或多或少分化的巨噬细胞聚集,这些聚集逐渐演变成由人类肉芽肿中发现的所有特定细胞类型组成的成熟组织肉芽肿。在愈合阶段,成纤维细胞在周边增殖,最终通过纤维化替代侵入肉芽肿。这些发现表明,使用该模型来阐明可能最终导致宿主肉芽肿反应不足以对抗巴西利什曼原虫感染的潜在致残性Th1细胞机制是可行的。