Laboratory of Pathology of Infectious Diseases, Medical School, São Paulo University, São Paulo, Brazil.
Microbiology Research Institute, National Autonomous University of Honduras, Tegucigalpa, Honduras.
Parasite Immunol. 2020 Nov;42(11):e12772. doi: 10.1111/pim.12772. Epub 2020 Jul 15.
Skin lesions in nonulcerated cutaneous leishmaniasis (NUCL) caused by Leishmania (L.) infantum chagasi are characterized by a mononuclear inflammatory infiltrate in the dermis, which is composed mainly of lymphocytes, followed by macrophages, few plasma cells and epithelioid granulomas with mild tissue parasitism. Previous studies have shown that the main population of lymphocytes present in the dermal infiltrate is CD8 T cells, followed by CD4 T cells, which are correlated with IFN-γ cells. To improve the knowledge of cellular immune responses in NUCL, skin biopsies were submitted to immunohistochemistry using anti-ROR-γt, anti-IL-17, anti-IL-6, anti-TGF-β, and anti-IL-23 antibodies to characterize the involvement of Th17 cells in the skin lesions of patients affected by NUCL. ROR-γt , IL-17 , IL-6 , TGF-β and IL-23 cells were observed in the dermal inflammatory infiltrate of NUCL skin lesions. A positive correlation between CD4 T-lymphocytes and ROR-γt and IL-17 cells suggests that some of the CD4 T-lymphocytes in NUCL could be Th17 lymphocytes. Moreover, a positive correlation between ROR-γt cells and TGF-β , IL-6 , IL-17 and IL-23 cells could indicate the role of these cytokines in the differentiation and maintenance of Th17 lymphocytes. Our findings improve knowledge of the pathogenesis of this rare and atypical clinical form of leishmaniasis.
无溃疡皮肤利什曼病(NUCL)所致的皮肤损害表现为真皮内单核炎性浸润,主要由淋巴细胞组成,其次为巨噬细胞、少量浆细胞和具有轻度组织寄生的上皮样肉芽肿。先前的研究表明,真皮浸润中存在的主要淋巴细胞群是 CD8 T 细胞,其次是 CD4 T 细胞,这与 IFN-γ 细胞相关。为了提高对 NUCL 细胞免疫反应的认识,对皮肤活检进行了免疫组织化学分析,使用抗 ROR-γt、抗 IL-17、抗 IL-6、抗 TGF-β 和抗 IL-23 抗体,以确定 Th17 细胞在 NUCL 患者皮肤损害中的参与情况。在 NUCL 皮肤损害的真皮炎症浸润中观察到 ROR-γt、IL-17、IL-6、TGF-β 和 IL-23 细胞。CD4 T 淋巴细胞与 ROR-γt 和 IL-17 细胞之间存在正相关,表明 NUCL 中的一些 CD4 T 淋巴细胞可能是 Th17 淋巴细胞。此外,ROR-γt 细胞与 TGF-β、IL-6、IL-17 和 IL-23 细胞之间的正相关可能表明这些细胞因子在 Th17 淋巴细胞的分化和维持中发挥作用。我们的研究结果提高了对这种罕见和非典型临床形式利什曼病发病机制的认识。