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在小鼠模型中对一种设计的FepA肽疫苗针对[具体疾病未提及]的疫苗潜力进行研究。

Investigation of the vaccine potential of an designed FepA peptide vaccine against in mice model.

作者信息

Ali Md Rayhan, Mahmud Shahin, Faruque Md Omar, Hossain Md Imam, Hossain Mohammed Akhter, Kibria K M Kaderi

机构信息

Department of Biotechnology and Genetic Engineering, Mawlana Bhashani Science and Technology University, Tangail-1902, Bangladesh.

Florey Institute of Neuroscience and Mental Health, University of Melbourne, Victoria 3052, Australia.

出版信息

Vaccine X. 2024 May 8;18:100493. doi: 10.1016/j.jvacx.2024.100493. eCollection 2024 Jun.

Abstract

BACKGROUND

Shigellosis is one of the significant causes of diarrhea in Bangladesh. It is a global health problem; approximately 1.3 million people die yearly from Shigellosis. The current treatment method, using different antibiotics against Shigellosis is ineffective. Moreover, it becomes a worrying situation due to the emergence of antibiotic-resistant pathogenic microbes responsible for these diarrheal diseases.

METHODOLOGY

Previous immunoinformatics study predicted a potential peptide from the Ferric enterobactin protein (FepA) of spp. In this study, we have chemically synthesized the FepA peptide. As a highly immunogenic, FepA peptide conjugated with KLH has been tested in mice model with complete and incomplete adjuvants as a vaccine candidate.

RESULTS

Immunological analysis showed that all vaccinated mice were immunologically boosted, which was statistically significant (value 0.0325) compared to control mice. Immunological analysis for bacterial neutralization test result was also statistically significant (-value 0.0468), where each ELISA plate was coated with 1 × 10 cells. The Challenge test with 1 × 10 cells to each vaccinated and controlled mice showed that 37.5 % of control (non-vaccinated) mice died within seven days after the challenge was given while 100 % of vaccinated mice remained strong and stout. The analyses of the post-challenge weight loss of the mice were also significant (-value 0.0367) as the weight loss percentage in control mice was much higher than in the vaccinated mice. The pathological and phenotypic appearances of vaccinated mice were also clearly differentiable compared with control mice. Thus all these immunological analysis and pathological appearances directly supported our FepA peptide as a potential immune booster.

CONCLUSION

This study provides evidence that the FepA peptide is a highly immunogenic vaccine candidate against . Therefore, these findings inspire future trials for the evaluation of the suitability of this vaccine candidate against Shigellosis.

摘要

背景

志贺氏菌病是孟加拉国腹泻的重要病因之一。它是一个全球性的健康问题;每年约有130万人死于志贺氏菌病。目前使用不同抗生素治疗志贺氏菌病的方法无效。此外,由于导致这些腹泻疾病的耐药性致病微生物的出现,情况令人担忧。

方法

先前的免疫信息学研究预测了一种来自 spp. 的铁肠杆菌素蛋白(FepA)的潜在肽段。在本研究中,我们化学合成了FepA肽段。作为一种高度免疫原性的物质,与钥孔血蓝蛋白(KLH)偶联的FepA肽段已在小鼠模型中作为候选疫苗,分别与完全佐剂和不完全佐剂一起进行了测试。

结果

免疫学分析表明,所有接种疫苗的小鼠免疫功能均得到增强,与对照小鼠相比具有统计学意义(值为0.0325)。细菌中和试验结果的免疫学分析也具有统计学意义(-值为0.0468),每个酶联免疫吸附测定(ELISA)板包被1×10个细胞。对每组接种疫苗和对照小鼠注射1×10个细胞进行攻毒试验,结果显示,37.5%的对照(未接种疫苗)小鼠在攻毒后7天内死亡,而100%的接种疫苗小鼠保持健康强壮。小鼠攻毒后体重减轻的分析也具有显著性(-值为0.0367),因为对照小鼠的体重减轻百分比远高于接种疫苗的小鼠。与对照小鼠相比,接种疫苗小鼠的病理和表型外观也有明显差异。因此,所有这些免疫学分析和病理表现都直接支持我们的FepA肽段作为一种潜在的免疫增强剂。

结论

本研究提供了证据表明FepA肽段是一种针对 的高度免疫原性候选疫苗。因此,这些发现激发了未来对该候选疫苗针对志贺氏菌病适用性评估的试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20cb/11134883/868282c95a36/gr1.jpg

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