Luciana Polaco Covre, Carlos Henrique Fantecelle, Ariadne Mendes Queiroz, Julia Miranda Fardin, Pedro Henrique Miranda, Sian Henson, Alessandra Marcia da Fonseca-Martins, Herbert Leonel de Matos Guedes, David Mosser, Aloisio Falqueto, Arne Akbar, Daniel Claudio Oliveira Gomes
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引用次数: 0
摘要
自然杀伤(NK)细胞包括具有不同效应能力的不同亚群,而这些亚群在寄生虫病中的作用却鲜为人知。在这里,我们研究了皮肤利什曼病(CL)患者 NK 细胞上抑制性和激活性受体的表达,并根据 CD57 和 NKG2C 的表达探讨了它们的表型和功能异质性。CD57 的表达确定了在 CL 患者中积累并表现出衰老特征的 NK 细胞。CD57+细胞的活化受体NKG2C水平升高,而抑制受体NKG2A表达减少。基于 NKG2C 转录组的 RNA 测序分析显示,CL 患者有两种不同的细胞毒性基因和功能基因。CD57+NKG2C+ 亚群在患者血液中积累,并呈现出明显的衰老特征,包括 p16、yH2ax 和 p38 等标记物的表达,以及增殖能力的降低。此外,它们还与病变消退的天数呈正相关。这项研究让人们对利什曼病感染期间的 NK 细胞生物学有了广泛的了解,并加强了衰老细胞在皮肤利什曼病不良临床结果中的作用。
NKG2C+CD57+ natural killer with senescent features cells are induced in cutaneous leishmaniasis and accumulate in patients with lesional healing impairment
Natural killer (NK) cells include different subsets with diverse effector capacities that are poorly understood in the context of parasitic diseases. Here, we investigated inhibitory and activating receptor expression on NK cells in patients with cutaneous leishmaniasis (CL) and explored their phenotypic and functional heterogeneity based on CD57 and NKG2C expression. The expression of CD57 identified NK cells that accumulated in CL patients and exhibited features of senescence. The CD57+ cells exhibited heightened levels of the activating receptor NKG2C and diminished expression of the inhibitory receptor NKG2A. RNA sequencing analyses based on NKG2C transcriptome have revealed two distinct profiles among CL patients associated with cytotoxic and functional genes. The CD57+NKG2C+ subset accumulated in the blood of patients and presented conspicuous features of senescence, including the expression of markers such as p16, yH2ax, and p38, as well as reduced proliferative capacity. In addition, they positively correlated with the number of days until lesion resolution. This study provides a broad understanding of the NK cell biology during Leishmania infection and reinforces the role of senescent cells in the adverse clinical outcomes of cutaneous leishmaniasis.