Research and Innovation Division, Armauer Hansen Research Institute, P.O. Box 1005, Addis Ababa, Ethiopia.
Research and Innovation Division, Armauer Hansen Research Institute, P.O. Box 1005, Addis Ababa, Ethiopia.
Acta Trop. 2021 Aug;220:105967. doi: 10.1016/j.actatropica.2021.105967. Epub 2021 May 21.
Recent studies suggest an essential role of the innate immune effector cells neutrophils and monocytes in protection or disease progression in the early course of Leishmania infection. In areas endemic for cutaneous leishmaniasis in Ethiopia most individuals are exposed to bites of infected sandflies. Still only a minor ratio of the inhabitants develops symptomatic disease. Neutrophils, followed by monocytes, are the first cells to be recruited to the site of Leishmania infection, the initial response of neutrophils to parasites appears to be crucial for the protective response and disease outcome. Our working hypothesis is that neutrophils and/or monocytes in localized cutaneous leishmaniasis (LCL) patients may have defects in function of innate immune cell that contribute to failure to parasite clearance that lead to establishment of infection. The response of cells in Ethiopian LCL patients and healthy controls to Leishmania aethiopica and to the Toll like receptor (TLR) agonists lipopolysaccharide (LPS) and macrophage activating lipopeptide-2 (MALP-2) was investigated by assessing the cell surface expression of CD62L (on neutrophil and monocyte) and CD66b (only on neutrophil), as well as reactive oxygen species (ROS) production by using whole blood-based assays in vitro. No impaired response of neutrophils and monocytes to the microbial constituents LPS and MALP-2 was observed. Neutrophils and monocytes from LCL patients responded stronger to Leishmania aethiopica in the applied whole blood assays than cells from healthy individuals. These experimental findings do not support the hypothesis regarding a possible dysfunction of neutrophils and monocytes in cutaneous leishmaniasis. On the contrary, these cells react stronger in LCL patients as compared to healthy controls. The differential response to L. aethiopica observed between LCL patients and healthy controls have the potential to serve as biomarker to develop FACS based diagnostic/ prognostic techniques for LCL.
最近的研究表明,固有免疫效应细胞中性粒细胞和单核细胞在利什曼原虫感染早期的保护或疾病进展中起着重要作用。在埃塞俄比亚皮肤利什曼病流行地区,大多数人都曾被感染的沙蝇叮咬过。尽管如此,只有少数居民会出现症状性疾病。中性粒细胞和单核细胞是最早被招募到利什曼原虫感染部位的细胞,中性粒细胞对寄生虫的初始反应似乎对保护性反应和疾病结局至关重要。我们的工作假设是,局限性皮肤利什曼病(LCL)患者的中性粒细胞和/或单核细胞可能存在固有免疫细胞功能缺陷,导致寄生虫清除失败,从而导致感染的建立。通过评估中性粒细胞和单核细胞表面 CD62L(中性粒细胞和单核细胞)和 CD66b(仅中性粒细胞)的表达以及使用体外全血测定法评估活性氧物质(ROS)的产生,研究了埃塞俄比亚 LCL 患者和健康对照者对利什曼原虫埃塞俄比亚亚种和 Toll 样受体(TLR)激动剂脂多糖(LPS)和巨噬细胞激活肽-2(MALP-2)的细胞反应。未观察到中性粒细胞和单核细胞对微生物成分 LPS 和 MALP-2 的反应受损。与健康个体的细胞相比,LCL 患者的中性粒细胞和单核细胞在应用的全血测定中对利什曼原虫埃塞俄比亚亚种的反应更强。这些实验结果不支持关于中性粒细胞和单核细胞在皮肤利什曼病中可能功能失调的假设。相反,这些细胞在 LCL 患者中的反应比健康对照者更强。LCL 患者和健康对照者之间对 L. aethiopica 的差异反应有可能成为开发基于 FACS 的 LCL 诊断/预后技术的生物标志物。