Cunha C F, Ferraz R, Pimentel M I F, Lyra M R, Schubach A O, Da-Cruz A M, Bertho A L
Laboratory of Immunoparasitology, Oswaldo Cruz Institute (IOC), FIOCRUZ, Rio de Janeiro, RJ, Brazil.
Flow Cytometry Sorting Core, Oswaldo Cruz Institute (IOC), FIOCRUZ, Rio de Janeiro, RJ, Brazil.
Parasite Immunol. 2016 Apr;38(4):244-54. doi: 10.1111/pim.12312.
Cutaneous leishmaniasis (CL) is an important public health issue worldwide. The control of Leishmania infection depends on cellular immune mechanisms, and the inflammatory response may contribute to pathogenesis. A beneficial role of CD8(+) T lymphocytes has been proposed; nevertheless, other studies suggest a cytotoxic role of CD8(+) T lymphocytes involved in tissue damage, showing controversial role of these cells. The goal of the current study was to understand the immunopathology of CL and determine the profile of cytotoxic cells--such as CD4(+) T, natural killer and natural killer T cells--that might be involved in triggering immunological mechanisms, and may lead to cure or disease progression. The frequencies of cytotoxic cell populations in peripheral blood, obtained from patients with active disease, during treatment and after clinical healing, were assessed by flow cytometry. Cytotoxicity could not be related to a deleterious role in Leishmania braziliensis infection, as patients with active CL showed similar percentages of degranulation to healthy individuals (HI). Cured patients exhibited a lower percentage of degranulating cells, which may be due to a downregulation of the immune response. The understanding of the immunopathological mechanisms involved in CL and the commitment of cytotoxic cells enables improvements in therapeutic strategies.
皮肤利什曼病(CL)是全球重要的公共卫生问题。利什曼原虫感染的控制依赖于细胞免疫机制,炎症反应可能参与发病过程。有研究提出CD8(+) T淋巴细胞具有有益作用;然而,其他研究表明CD8(+) T淋巴细胞在组织损伤中具有细胞毒性作用,这显示出这些细胞的作用存在争议。本研究的目的是了解CL的免疫病理学,并确定可能参与触发免疫机制、可能导致治愈或疾病进展的细胞毒性细胞(如CD4(+) T细胞、自然杀伤细胞和自然杀伤T细胞)的特征。通过流式细胞术评估了从患有活动性疾病的患者、治疗期间和临床治愈后的外周血中细胞毒性细胞群体的频率。细胞毒性与巴西利什曼原虫感染中的有害作用无关,因为活动性CL患者与健康个体(HI)的脱颗粒百分比相似。治愈的患者脱颗粒细胞百分比更低,这可能是由于免疫反应下调所致。对CL中涉及的免疫病理机制以及细胞毒性细胞作用的了解有助于改进治疗策略。