Development of a vaccine construct against Pneumocystis jirovecii pneumonia using computational tools.

IF 2.8 Q1 GENETICS & HEREDITY
NAR Genomics and Bioinformatics Pub Date : 2025-12-31 eCollection Date: 2025-12-01 DOI:10.1093/nargab/lqaf199
Ragini Mishra, Nahid Akhtar, Jorge Samuel Leon Magdeleno, Abdul Rajjak Shaikh, Manik Prabhu Narsing Rao, Neeta Raj Sharma, Luigi Cavallo, Mohit Chawla
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Abstract

Pneumocystis jirovecii poses a significant threat to immunocompromised individuals, necessitating the development of an effective vaccine. This study employs an immunoinformatics approach to design a promising vaccine candidate against P. jirovecii. Utilizing various computational tools, the study identified potential antigenic epitopes capable of eliciting immune responses within the P. jirovecii major surface glycoprotein C. The chosen epitopes were evaluated using computational tools for their allergenicity, interferon-γ and interleukin activation ability, and toxicity, ensuring the selection of immunogenic and safe candidates. These analyses led to the selection of 10 epitopes, which were then linked with adjuvants to model a potential vaccine candidate. Molecular docking and molecular dynamics simulations were performed in a solvent environment to investigate the binding interactions between the vaccine candidate and toll-like receptors, along with calculations of thermodynamic properties. Finally, in silico immune simulations were performed to analyze the immunogenic potential of the vaccine candidate. Future prospects include in vitro and in vivo validation of the vaccine candidate and the exploration of novel adjuvants to enhance its immunogenicity. This study contributes to the ongoing efforts to develop a preventive solution against P. jirovecii infections, addressing a critical gap in the protection of immunocompromised individuals.

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利用计算工具开发一种抗吉罗氏肺囊虫肺炎的疫苗结构。
吉罗氏肺囊虫对免疫功能低下的个体构成重大威胁,需要开发有效的疫苗。本研究采用免疫信息学方法设计了一种有前途的疫苗候选物。利用各种计算工具,该研究确定了能够在p.j rovecii主要表面糖蛋白c中引发免疫应答的潜在抗原表位。选择的表位使用计算工具评估其致敏性,干扰素-γ和白细胞介素活化能力以及毒性,确保选择免疫原性和安全的候选物。这些分析导致了10个表位的选择,然后将其与佐剂连接以模拟潜在的候选疫苗。在溶剂环境中进行分子对接和分子动力学模拟,以研究候选疫苗与toll样受体之间的结合相互作用,并计算热力学性质。最后,进行了计算机免疫模拟,分析了候选疫苗的免疫原性潜力。未来的前景包括在体外和体内验证候选疫苗和探索新的佐剂,以增强其免疫原性。这项研究有助于正在进行的努力,以开发一种预防方案,以防止p.j roveci感染,解决一个关键的差距,在保护免疫功能低下的个体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
2.20%
发文量
95
审稿时长
15 weeks
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