MAIT激活配体5-OP-RU作为粘膜佐剂在O1霍乱弧菌疫苗接种小鼠模型中的应用。

Q1 Medicine Pathogens and Immunity Pub Date : 2022-08-24 eCollection Date: 2022-01-01 DOI:10.20411/pai.v7i1.525
Owen Jensen, Shubhanshi Trivedi, Kelin Li, Jeffrey Aubé, J Scott Hale, Edward T Ryan, Daniel T Leung
{"title":"MAIT激活配体5-OP-RU作为粘膜佐剂在O1霍乱弧菌疫苗接种小鼠模型中的应用。","authors":"Owen Jensen, Shubhanshi Trivedi, Kelin Li, Jeffrey Aubé, J Scott Hale, Edward T Ryan, Daniel T Leung","doi":"10.20411/pai.v7i1.525","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Mucosal-associated invariant T (MAIT) cells are innate-like T cells enriched in the mucosa with capacity for B-cell help. We hypothesize that targeting MAIT cells, using a MAIT-activating ligand as an adjuvant, could improve mucosal vaccine responses to bacterial pathogens such as <i>Vibrio cholerae</i>.</p><p><strong>Methods: </strong>We utilized murine models of <i>V. cholerae</i> vaccination to test the adjuvant potential of the MAIT-activating ligand, 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil (5-OP-RU). We measured <i>V. cholerae</i>-specific antibody and antibody-secreting cell responses and used flow cytometry to examine MAIT-cell and B-cell phenotype, in blood, bronchoalveolar lavage fluid (BALF), and mucosal tissues, following intranasal vaccination with live <i>V. cholerae</i> O1 or a <i>V. cholerae</i> O1 polysaccharide conjugate vaccine.</p><p><strong>Results: </strong>We report significant expansion of MAIT cells in the lungs (<i>P</i> < 0.001) and BALF (<i>P</i> < 0.001) of 5-OP-RU treated mice, and higher mucosal (BALF, <i>P</i> = 0.045) but not systemic (serum, <i>P</i> = 0.21) <i>V. cholerae</i> O-specific-polysaccharide IgG responses in our conjugate vaccine model when adjuvanted with low-dose 5-OP-RU. In contrast, despite significant MAIT cell expansion, no significant differences in <i>V. cholerae</i>-specific humoral responses were found in our live <i>V. cholerae</i> vaccination model.</p><p><strong>Conclusions: </strong>Using a murine model, we demonstrate the potential, as well as the limitations, of targeting MAIT cells to improve antibody responses to mucosal cholera vaccines. Our study highlights the need for future research optimizing MAIT-cell targeting for improving mucosal vaccines.</p>","PeriodicalId":36419,"journal":{"name":"Pathogens and Immunity","volume":"7 1","pages":"122-144"},"PeriodicalIF":0.0000,"publicationDate":"2022-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438945/pdf/","citationCount":"0","resultStr":"{\"title\":\"Use of a MAIT-Activating Ligand, 5-OP-RU, as a Mucosal Adjuvant in a Murine Model of <i>Vibrio cholerae</i> O1 Vaccination.\",\"authors\":\"Owen Jensen, Shubhanshi Trivedi, Kelin Li, Jeffrey Aubé, J Scott Hale, Edward T Ryan, Daniel T Leung\",\"doi\":\"10.20411/pai.v7i1.525\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Mucosal-associated invariant T (MAIT) cells are innate-like T cells enriched in the mucosa with capacity for B-cell help. We hypothesize that targeting MAIT cells, using a MAIT-activating ligand as an adjuvant, could improve mucosal vaccine responses to bacterial pathogens such as <i>Vibrio cholerae</i>.</p><p><strong>Methods: </strong>We utilized murine models of <i>V. cholerae</i> vaccination to test the adjuvant potential of the MAIT-activating ligand, 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil (5-OP-RU). We measured <i>V. cholerae</i>-specific antibody and antibody-secreting cell responses and used flow cytometry to examine MAIT-cell and B-cell phenotype, in blood, bronchoalveolar lavage fluid (BALF), and mucosal tissues, following intranasal vaccination with live <i>V. cholerae</i> O1 or a <i>V. cholerae</i> O1 polysaccharide conjugate vaccine.</p><p><strong>Results: </strong>We report significant expansion of MAIT cells in the lungs (<i>P</i> < 0.001) and BALF (<i>P</i> < 0.001) of 5-OP-RU treated mice, and higher mucosal (BALF, <i>P</i> = 0.045) but not systemic (serum, <i>P</i> = 0.21) <i>V. cholerae</i> O-specific-polysaccharide IgG responses in our conjugate vaccine model when adjuvanted with low-dose 5-OP-RU. In contrast, despite significant MAIT cell expansion, no significant differences in <i>V. cholerae</i>-specific humoral responses were found in our live <i>V. cholerae</i> vaccination model.</p><p><strong>Conclusions: </strong>Using a murine model, we demonstrate the potential, as well as the limitations, of targeting MAIT cells to improve antibody responses to mucosal cholera vaccines. Our study highlights the need for future research optimizing MAIT-cell targeting for improving mucosal vaccines.</p>\",\"PeriodicalId\":36419,\"journal\":{\"name\":\"Pathogens and Immunity\",\"volume\":\"7 1\",\"pages\":\"122-144\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-08-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9438945/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pathogens and Immunity\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20411/pai.v7i1.525\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pathogens and Immunity","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20411/pai.v7i1.525","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

背景:粘膜相关不变T细胞(MAIT)是在粘膜中富集的具有B细胞帮助能力的先天性T细胞。我们假设,使用MAIT激活配体作为佐剂靶向MAIT细胞,可以改善粘膜疫苗对霍乱弧菌等细菌病原体的反应。方法:我们利用霍乱弧菌疫苗接种小鼠模型来测试MAIT激活配体5-(2-氧代亚丙基氨基)-6-脱氧核糖核酸(5-OP-RU)的佐剂潜力。我们测量了霍乱弧菌特异性抗体和分泌抗体的细胞反应,并使用流式细胞术检测了O1活霍乱弧菌或O1霍乱弧菌多糖偶联疫苗鼻内接种后血液、支气管肺泡灌洗液(BALF)和粘膜组织中的MAIT细胞和B细胞表型。结果:我们报告了5-OP-RU治疗小鼠肺部(P<0.001)和BALF(P<0.001。相反,尽管MAIT细胞显著扩增,但在我们的霍乱弧菌活疫苗接种模型中,没有发现霍乱弧菌特异性体液反应的显著差异。结论:使用小鼠模型,我们证明了靶向MAIT细胞改善对粘膜霍乱疫苗的抗体反应的潜力和局限性。我们的研究强调了未来研究优化MAIT细胞靶向以改进粘膜疫苗的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Use of a MAIT-Activating Ligand, 5-OP-RU, as a Mucosal Adjuvant in a Murine Model of Vibrio cholerae O1 Vaccination.

Background: Mucosal-associated invariant T (MAIT) cells are innate-like T cells enriched in the mucosa with capacity for B-cell help. We hypothesize that targeting MAIT cells, using a MAIT-activating ligand as an adjuvant, could improve mucosal vaccine responses to bacterial pathogens such as Vibrio cholerae.

Methods: We utilized murine models of V. cholerae vaccination to test the adjuvant potential of the MAIT-activating ligand, 5-(2-oxopropylideneamino)-6-D-ribitylaminouracil (5-OP-RU). We measured V. cholerae-specific antibody and antibody-secreting cell responses and used flow cytometry to examine MAIT-cell and B-cell phenotype, in blood, bronchoalveolar lavage fluid (BALF), and mucosal tissues, following intranasal vaccination with live V. cholerae O1 or a V. cholerae O1 polysaccharide conjugate vaccine.

Results: We report significant expansion of MAIT cells in the lungs (P < 0.001) and BALF (P < 0.001) of 5-OP-RU treated mice, and higher mucosal (BALF, P = 0.045) but not systemic (serum, P = 0.21) V. cholerae O-specific-polysaccharide IgG responses in our conjugate vaccine model when adjuvanted with low-dose 5-OP-RU. In contrast, despite significant MAIT cell expansion, no significant differences in V. cholerae-specific humoral responses were found in our live V. cholerae vaccination model.

Conclusions: Using a murine model, we demonstrate the potential, as well as the limitations, of targeting MAIT cells to improve antibody responses to mucosal cholera vaccines. Our study highlights the need for future research optimizing MAIT-cell targeting for improving mucosal vaccines.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Pathogens and Immunity
Pathogens and Immunity Medicine-Infectious Diseases
CiteScore
10.60
自引率
0.00%
发文量
16
审稿时长
10 weeks
期刊最新文献
Historical Highlight: The Luria-Delbrück Fluctuation Test - A Study of the Nature of Bacterial Mutations Conferring Resistance to Infection by Bacteriophage. Escape of SARS-CoV-2 Variants KP.1.1, LB.1, and KP3.3 From Approved Monoclonal Antibodies. Jonathan Yewdell Discusses Viral Immunology, Vaccine Development, Navigating a Scientific Career, and Offers Perspectives on Transforming Scientific Publishing and Research Education. Effect of Ceftaroline, Ceftazidime/Avibactam, Ceftolozane/Tazobactam, and Meropenem/Vaborbactam on Establishment of Colonization by Vancomycin-Resistant Enterococci and Klebsiella pneumoniae in Mice. People Living With HIV Have More Intact HIV DNA in Circulating CD4+ T Cells if They Have History of Pulmonary Tuberculosis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1