Amir Namvar Vansofla, Abbas Hajizade, Shahram Nazarian, Yousof Tarverdizadeh, Ahad Shahmaleki
{"title":"一种硅片设计的多表位候选疫苗能有效地保护小鼠免受致病性志贺氏菌的侵袭","authors":"Amir Namvar Vansofla, Abbas Hajizade, Shahram Nazarian, Yousof Tarverdizadeh, Ahad Shahmaleki","doi":"10.1016/j.jim.2025.113905","DOIUrl":null,"url":null,"abstract":"<div><div><em>Shigella</em> species remain a major global health concern, causing gastrointestinal infections with significant morbidity and mortality. The rise of antibiotic-resistant <em>Shigella</em> strains underscores the urgent need for effective vaccines. This study evaluated the immunogenicity and protective efficacy of a novel multi-epitope recombinant protein vaccine against pathogenic <em>Shigella</em> species in a murine model. The multi-epitope antigen was expressed in <em>E. coli</em> and purified for immunization. BALB/c mice were subcutaneously immunized, and immune responses were assessed through serum IgG quantification (ELISA) and challenge studies. Immunized mice exhibited significantly higher antigen-specific IgG titers compared to controls (<em>p < 0.05</em>). Subsequent challenge with 10LD<sub>50</sub> of virulent <em>Shigella flexneri</em> and <em>Shigella boydii</em> demonstrated robust protection, with vaccinated mice surviving lethal infections. Our findings indicate that this in silico-designed multi-epitope vaccine elicits potent humoral immunity and confers cross-species protection against clinically relevant <em>Shigella</em> pathogens. These results support its potential as a promising candidate for further vaccine development against shigellosis.</div></div>","PeriodicalId":16000,"journal":{"name":"Journal of immunological methods","volume":"542 ","pages":"Article 113905"},"PeriodicalIF":1.6000,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An in-silico-designed multiepitope vaccine candidate can efficiently protect mice against pathogenic species of Shigella\",\"authors\":\"Amir Namvar Vansofla, Abbas Hajizade, Shahram Nazarian, Yousof Tarverdizadeh, Ahad Shahmaleki\",\"doi\":\"10.1016/j.jim.2025.113905\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Shigella</em> species remain a major global health concern, causing gastrointestinal infections with significant morbidity and mortality. The rise of antibiotic-resistant <em>Shigella</em> strains underscores the urgent need for effective vaccines. This study evaluated the immunogenicity and protective efficacy of a novel multi-epitope recombinant protein vaccine against pathogenic <em>Shigella</em> species in a murine model. The multi-epitope antigen was expressed in <em>E. coli</em> and purified for immunization. BALB/c mice were subcutaneously immunized, and immune responses were assessed through serum IgG quantification (ELISA) and challenge studies. Immunized mice exhibited significantly higher antigen-specific IgG titers compared to controls (<em>p < 0.05</em>). Subsequent challenge with 10LD<sub>50</sub> of virulent <em>Shigella flexneri</em> and <em>Shigella boydii</em> demonstrated robust protection, with vaccinated mice surviving lethal infections. Our findings indicate that this in silico-designed multi-epitope vaccine elicits potent humoral immunity and confers cross-species protection against clinically relevant <em>Shigella</em> pathogens. These results support its potential as a promising candidate for further vaccine development against shigellosis.</div></div>\",\"PeriodicalId\":16000,\"journal\":{\"name\":\"Journal of immunological methods\",\"volume\":\"542 \",\"pages\":\"Article 113905\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-07-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of immunological methods\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S002217592500105X\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of immunological methods","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002217592500105X","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
An in-silico-designed multiepitope vaccine candidate can efficiently protect mice against pathogenic species of Shigella
Shigella species remain a major global health concern, causing gastrointestinal infections with significant morbidity and mortality. The rise of antibiotic-resistant Shigella strains underscores the urgent need for effective vaccines. This study evaluated the immunogenicity and protective efficacy of a novel multi-epitope recombinant protein vaccine against pathogenic Shigella species in a murine model. The multi-epitope antigen was expressed in E. coli and purified for immunization. BALB/c mice were subcutaneously immunized, and immune responses were assessed through serum IgG quantification (ELISA) and challenge studies. Immunized mice exhibited significantly higher antigen-specific IgG titers compared to controls (p < 0.05). Subsequent challenge with 10LD50 of virulent Shigella flexneri and Shigella boydii demonstrated robust protection, with vaccinated mice surviving lethal infections. Our findings indicate that this in silico-designed multi-epitope vaccine elicits potent humoral immunity and confers cross-species protection against clinically relevant Shigella pathogens. These results support its potential as a promising candidate for further vaccine development against shigellosis.
期刊介绍:
The Journal of Immunological Methods is devoted to covering techniques for: (1) Quantitating and detecting antibodies and/or antigens. (2) Purifying immunoglobulins, lymphokines and other molecules of the immune system. (3) Isolating antigens and other substances important in immunological processes. (4) Labelling antigens and antibodies. (5) Localizing antigens and/or antibodies in tissues and cells. (6) Detecting, and fractionating immunocompetent cells. (7) Assaying for cellular immunity. (8) Documenting cell-cell interactions. (9) Initiating immunity and unresponsiveness. (10) Transplanting tissues. (11) Studying items closely related to immunity such as complement, reticuloendothelial system and others. (12) Molecular techniques for studying immune cells and their receptors. (13) Imaging of the immune system. (14) Methods for production or their fragments in eukaryotic and prokaryotic cells.
In addition the journal will publish articles on novel methods for analysing the organization, structure and expression of genes for immunologically important molecules such as immunoglobulins, T cell receptors and accessory molecules involved in antigen recognition, processing and presentation. Submitted full length manuscripts should describe new methods of broad applicability to immunology and not simply the application of an established method to a particular substance - although papers describing such applications may be considered for publication as a short Technical Note. Review articles will also be published by the Journal of Immunological Methods. In general these manuscripts are by solicitation however anyone interested in submitting a review can contact the Reviews Editor and provide an outline of the proposed review.