Laboratório de Imunologia Celular e Bioquímica de Fungos e Protozoários, Departamento de Ciências Farmacêuticas, Universidade Federal de São Paulo, Campus Diadema, Diadema, Brazil.
Pós Graduação em Patologia Ambiental e Experimental, Universidade Paulista, São Paulo, Brazil.
J Immunol Res. 2021 Dec 24;2021:7809637. doi: 10.1155/2021/7809637. eCollection 2021.
Depending on species and the presence/absence of virulence factors, extracellular vesicles (EVs) can differently stimulate host immune cells. This work is aimed at characterizing and evaluating the protective role of EVs released by promastigotes under different maintenance conditions. Initially, using a control strain, we standardized 26°C as the best release temperature to obtain EVs with a potential protective role in the experimental leishmaniasis model. Then, long-term (LT-P) promastigotes of were obtained after long-term culture (100 passages). -derived (IVD-P) promastigotes of were selected after 3 consecutive experimental infections in BALB/c mice. Those strains developed similar lesion sizes except for IVD-P at 8 weeks post infection. No differences in EV production were detected in both strains. However, the presence of LPG between LT-P and IVD-P EVs was different. Groups of mice immunized with EVs emulsified in the adjuvant and challenged with IVD-P parasites showed decreased lesion size and parasitic load compared with the nonimmunized groups. The immunization regimen with two doses showed high IFN- and IgG2a titers in challenged mice with either IVD-P or LT-P EVs. IL-4 and IL-10 were detected in immunized mice, suggesting a mixed Th1/Th2 profile. EVs released by either IVD-P or LT-P induced a partial protective effect in an immunization model. Thus, our results uncover a potential protective role of EVs from for cutaneous leishmaniasis. Moreover, long-term maintenance under conditions did not seem to affect EV release and their immunization properties in mice.
根据物种以及毒力因子的存在与否,细胞外囊泡(EVs)可以不同程度地刺激宿主免疫细胞。本研究旨在对不同维持条件下由前鞭毛体释放的 EVs 进行表征和评估其保护作用。最初,我们使用对照株,将 26°C 标准化为最佳释放温度,以获得在实验性利什曼病模型中具有潜在保护作用的 EVs。然后,通过长期培养(100 代)获得了长期(LT-P)前鞭毛体。在 BALB/c 小鼠中连续进行 3 次实验感染后,选择了 的衍生(IVD-P)前鞭毛体。除了感染后 8 周的 IVD-P 外,这两种菌株的病变大小相似。两种菌株的 EV 产量均无差异。然而,LT-P 和 IVD-P EV 中 LPG 的存在不同。用佐剂乳化 EV 免疫的小鼠组与未免疫组相比,感染 IVD-P 寄生虫的小鼠病变大小和寄生虫载量均降低。用两剂免疫方案免疫的感染 IVD-P 或 LT-P EV 的小鼠表现出高 IFN-和 IgG2a 滴度。在免疫的小鼠中检测到 IL-4 和 IL-10,表明存在混合 Th1/Th2 表型。IVD-P 或 LT-P 释放的 EV 在免疫模型中诱导了部分保护作用。因此,我们的结果揭示了 的 EV 在皮肤利什曼病中的潜在保护作用。此外,在 条件下长期维持似乎不会影响 EV 的释放及其在小鼠中的免疫特性。