Departamento de Biología Molecular, Facultad de Ciencias, Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas (CSIC)-Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Departamento de Bioquímica-Investigación, Hospital Ramón y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain.
Front Cell Infect Microbiol. 2018 Apr 5;8:112. doi: 10.3389/fcimb.2018.00112. eCollection 2018.
Different members of intracellular protein families are recognized by the immune system of the vertebrate host infected by parasites of the genus . Here, we have analyzed the antigenic and immunogenic properties of the eIF2 and eIF2B translation initiation factors. An in silico search in sequence databases allowed the identification of the genes encoding the α, β, and γ subunits and the α, β, and δ subunits of the putative orthologs of the eukaryotic initiation factors F2 (LieIF2) or F2B (LieIF2B), respectively. The antigenicity of these factors was analyzed by ELISA using recombinant versions of the different subunits. Antibodies against the different LieIF2 and LieIF2B subunits were found in the sera from human and canine visceral leishmaniasis patients, and also in the sera from hamsters experimentally infected with . In (BALB/c) and (BALB/c or C57BL/6) challenged mice, a moderate humoral response against these protein factors was detected. Remarkably, these proteins elicited an IL-10 production by splenocytes derived from infected mice independently of the species employed for experimental challenge. When DNA vaccines based on the expression of the LieIF2 or LieIF2B subunit encoding genes were administered in mice, an antigen-specific secretion of IFN-γ and IL-10 cytokines was observed. Furthermore, a partial protection against murine CL development due to infection was generated in the vaccinated mice. Also, in this work we show that the LieIF2α subunit and the LieIF2Bβ and δ subunits have the capacity to stimulate IL-10 secretion by spleen cells from naïve mice. B-lymphocytes were identified as the major producers of this anti-inflammatory cytokine. Taking into account the data found in this study, it may be hypothesized that these proteins act as virulence factors implicated in the induction of humoral responses as well as in the production of the down-regulatory IL-10 cytokine, favoring a pathological outcome. Therefore, these proteins might be considered markers of disease.
不同的细胞内蛋白家族成员被感染寄生虫属的脊椎动物宿主的免疫系统识别。在这里,我们分析了 eIF2 和 eIF2B 翻译起始因子的抗原性和免疫原性。在 序列数据库中的计算机搜索允许鉴定编码假定真核起始因子 F2 (LieIF2)或 F2B (LieIF2B)的α、β和γ亚基以及α、β和δ亚基的基因。通过使用不同亚基的重组版本进行 ELISA 分析了这些因子的抗原性。在人类和犬内脏利什曼病患者的血清以及用 实验感染的仓鼠血清中发现了针对这些 LieIF2 和 LieIF2B 亚基的抗体。在 (BALB/c)和 (BALB/c 或 C57BL/6) challenged 小鼠中,检测到针对这些蛋白因子的中度体液反应。值得注意的是,这些蛋白因子在感染小鼠的脾细胞中独立于用于实验挑战的 物种诱导产生了 IL-10 产生。当在小鼠中给予基于 LieIF2 或 LieIF2B 亚基编码基因表达的 DNA 疫苗时,观察到针对抗原的 IFN-γ和 IL-10 细胞因子的特异性分泌。此外,在接种疫苗的小鼠中,由于 感染导致对小鼠 CL 发育产生了部分保护。此外,在这项工作中,我们表明 LieIF2α 亚基和 LieIF2Bβ和δ 亚基具有刺激来自幼稚小鼠脾细胞的 IL-10 分泌的能力。B 淋巴细胞被鉴定为这种抗炎细胞因子的主要产生者。考虑到本研究中发现的数据,可以假设这些蛋白作为毒力因子起作用,诱导体液反应以及产生下调的 IL-10 细胞因子,有利于病理结果。因此,这些蛋白可能被视为疾病的标志物。