Department of Microbiology and Immunology, Faculty of Pharmacy, Sinai University, Ismailia 41611, Egypt.
Cell Biology, Histology & Genetics Division, Zoology Department, Faculty of Science, Zagazig University, Zagazig 44519, Egypt.
Cells. 2021 Nov 4;10(11):3014. doi: 10.3390/cells10113014.
During the current era of the COVID-19 pandemic, the dissemination of Mucorales has been reported globally, with elevated rates of infection in India, and because of the high rate of mortality and morbidity, designing an effective vaccine against mucormycosis is a major health priority, especially for immunocompromised patients. In the current study, we studied shared Mucorales proteins, which have been reported as virulence factors, and after analysis of several virulent proteins for their antigenicity and subcellular localization, we selected spore coat (CotH) and serine protease (SP) proteins as the targets of epitope mapping. The current study proposes a vaccine constructed based on top-ranking cytotoxic T lymphocyte (CTL), helper T lymphocyte (HTL), and B cell lymphocyte (BCL) epitopes from filtered proteins. In addition to the selected epitopes, β-defensins adjuvant and PADRE peptide were included in the constructed vaccine to improve the stimulated immune response. Computational tools were used to estimate the physicochemical and immunological features of the proposed vaccine and validate its binding with TLR-2, where the output data of these assessments potentiate the probability of the constructed vaccine to stimulate a specific immune response against mucormycosis. Here, we demonstrate the approach of potential vaccine construction and assessment through computational tools, and to the best of our knowledge, this is the first study of a proposed vaccine against mucormycosis based on the immunoinformatics approach.
在当前 COVID-19 大流行时代,毛霉目真菌在全球范围内传播,印度的感染率较高,由于死亡率和发病率高,因此针对毛霉病设计有效的疫苗是一个主要的健康优先事项,尤其是对于免疫功能低下的患者。在本研究中,我们研究了已报道为毒力因子的共享毛霉目蛋白,经过对几种毒力蛋白的抗原性和亚细胞定位分析,我们选择孢子壳(CotH)和丝氨酸蛋白酶(SP)蛋白作为表位作图的靶标。本研究提出了一种基于过滤蛋白的细胞毒性 T 淋巴细胞(CTL)、辅助性 T 淋巴细胞(HTL)和 B 细胞淋巴细胞(BCL)优势表位构建的疫苗。除了选择的表位外,β-防御素佐剂和 PADRE 肽也被包含在构建的疫苗中,以提高刺激的免疫反应。计算工具用于估计所提出疫苗的物理化学和免疫学特性,并验证其与 TLR-2 的结合,这些评估的输出数据增强了构建疫苗刺激针对毛霉病的特异性免疫反应的可能性。在这里,我们通过计算工具展示了潜在疫苗构建和评估的方法,据我们所知,这是首次基于免疫信息学方法研究针对毛霉病的拟议疫苗。