Leopoldo Paulo T G, Machado Paulo R L, Almeida Roque P, Schriefer Albert, Giudice Angela, de Jesus Amélia Ribeiro, Ho John L, Guimarães Luiz Henrique, Bacellar Olívia, Carvalho Edgar M
Departamento de Fisiologia, Universidade Federal de Sergipe, Aracaju, Sergipe, Brazil.
BMC Infect Dis. 2006 Apr 25;6:75. doi: 10.1186/1471-2334-6-75.
Disseminated leishmaniasis is an emerging infectious disease, mostly due to L. braziliensis, which has clinical and histopathological features distinct from cutaneous leishmaniasis.
In the current study we evaluated the in vitro production of the cytokines IFN-gamma, TNF-alpha, IL-5 and IL-10 by peripheral blood mononuclear cells (PBMC) from 15 disseminated leishmaniasis and 24 cutaneous leishmaniasis patients upon stimulation with L. braziliensis antigens genotyped as disseminated leishmaniasis or cutaneous leishmaniasis isolates.
Regardless of the source of L. braziliensis antigens, PBMC from cutaneous leishmaniasis patients produced significantly higher IFN-gamma than PBMC from disseminated leishmaniasis patients. Levels of TNF-alpha by PBMC from cutaneous leishmaniasis patients were significantly higher than disseminated leishmaniasis patients only when stimulated by genotyped cutaneous leishmaniasis antigens. The levels of IL-5 and IL-10 production by PBMC were very low and similar in PBMCs from both disseminated leishmaniasis and cutaneous leishmaniasis patients. The immune response of each patient evaluated by the two L. braziliensis antigens was assessed in a paired analysis in which we showed that L. braziliensis genotyped as disseminated leishmaniasis isolate was more potent than L. braziliensis genotyped as cutaneous leishmaniasis isolate in triggering IFN-gamma and TNF-alpha production in both diseases and IL-5 only in cutaneous leishmaniasis patients.
This study provides evidence that antigens prepared from genotypically distinct strains of L. braziliensis induce different degrees of immune response. It also indicates that both parasite and host play a role in the outcome of L. braziliensis infection.
播散性利什曼病是一种新发传染病,主要由巴西利什曼原虫引起,其临床和组织病理学特征与皮肤利什曼病不同。
在本研究中,我们评估了15例播散性利什曼病患者和24例皮肤利什曼病患者的外周血单核细胞(PBMC)在受到基因型为播散性利什曼病或皮肤利什曼病分离株的巴西利什曼原虫抗原刺激后,体外产生细胞因子IFN-γ、TNF-α、IL-5和IL-10的情况。
无论巴西利什曼原虫抗原的来源如何,皮肤利什曼病患者的PBMC产生的IFN-γ显著高于播散性利什曼病患者的PBMC。仅在受到基因型为皮肤利什曼病的抗原刺激时,皮肤利什曼病患者PBMC产生的TNF-α水平显著高于播散性利什曼病患者。PBMC产生IL-5和IL-10的水平非常低,且在播散性利什曼病患者和皮肤利什曼病患者的PBMC中相似。通过对两种巴西利什曼原虫抗原评估的每位患者的免疫反应进行配对分析,我们发现基因型为播散性利什曼病分离株的巴西利什曼原虫在引发两种疾病的IFN-γ和TNF-α产生以及仅在皮肤利什曼病患者中引发IL-5产生方面比基因型为皮肤利什曼病分离株的巴西利什曼原虫更有效。
本研究提供了证据表明,由基因型不同的巴西利什曼原虫菌株制备的抗原可诱导不同程度的免疫反应。这也表明寄生虫和宿主在巴西利什曼原虫感染的结果中都起作用。