Use of a MAIT-Activating Ligand, 5-OP-RU, as a Mucosal Adjuvant in a Murine Model of Vibrio cholerae O1 Vaccination.

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
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Abstract

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.

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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。
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。
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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
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