Mechanisms of superior respiratory IgA responses against SARS-CoV-2 after mucosal vaccination 2158

Abstract Description Mucosal immunization and respiratory IgA responses offer significant promise in protecting against airborne pathogens, including SARS-CoV-2. However, However, the conditions and mechanisms that lead to the robust induction of respiratory IgA responses following mucosal vaccination remain poorly understood. It is also currently debatable whether mucosal vaccination is still warranted given that most individuals in developed countries have established a hybrid immunity from vaccination and infection. Here, we analyzed respiratory immune responses in humans following SARS-CoV-2 infection, vaccination, or both. We found that hybrid immunity resulted in moderately increased respiratory IgA and neutralizing antibody responses compared to infection or vaccination alone. However, a direct comparison of hybrid immunity and a mucosal adenovirus-based booster vaccination in animal models revealed that respiratory booster immunization elicited markedly stronger and more durable respiratory IgA, T cell response and protective immunity, supporting the promise of respiratory vaccination. Mechanistically, mucosal boosters prompted IgA-secreting cells in the respiratory mucosa with help from local IL-21-producing Blimp1+ Th1 cells. Furthermore, lung macrophages were important for this respiratory IgA response via TGF-β. Our findings highlight a local network for robust respiratory IgA responses, supporting mucosal vaccination strategies against SARS-CoV-2 and other respiratory pathogens. Funding Sources AI147394, AG069264, AI112844, HL170961, and AI154598 to J.S, AI176171 to W.G.T. and J.S.; U54CA260582 to S.L.L; R01AI168684 to G. Z. Topic Categories Vaccines and Immunotherapy (VAC)

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Publication Details

Journal
The Journal of Immunology
Published
2025-11-01
DOI
https://doi.org/10.1093/jimmun/vkaf283.117
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
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article

Mechanisms of superior respiratory IgA responses against SARS-CoV-2 after mucosal vaccination 2158

Zihai Li, Jin‐Tai Yu, Nu Zhang, Wei Qian et al.
The Journal of Immunology
SARS-CoV-2 and COVID-19 Research
article

Mechanisms of superior respiratory IgA responses against SARS-CoV-2 after mucosal vaccination 2158

Zihai Li, Jin‐Tai Yu, Nu Zhang, Wei Qian, Mark H. Kaplan, Guizhi Zhu, In Su Cheon, Hirohito Kita, Takao Kobayashi, Justin J. Taylor, Kristin Wavell, Maria Velegraki, Yue Wu, Gislane de Almeida Santos, Harish Narasimhan, Feng Zhu, Marthajoy Spano, Mohd Arish, W. Gerald Teague, Panke Qu, Haitao Hu, Jie Sun, Yajie Liu, Hui Hu, Pei Li, Chaofan Li, Samuel Young, Jinyi Tang, Anika Agarwal, Arka Sen Chaudhuri, Shan-Lu Liu
article en

Abstract

Abstract Description Mucosal immunization and respiratory IgA responses offer significant promise in protecting against airborne pathogens, including SARS-CoV-2. However, However, the conditions and mechanisms that lead to the robust induction of respiratory IgA responses following mucosal vaccination remain poorly understood. It is also currently debatable whether mucosal vaccination is still warranted given that most individuals in developed countries have established a hybrid immunity from vaccination and infection. Here, we analyzed respiratory immune responses in humans following SARS-CoV-2 infection, vaccination, or both. We found that hybrid immunity resulted in moderately increased respiratory IgA and neutralizing antibody responses compared to infection or vaccination alone. However, a direct comparison of hybrid immunity and a mucosal adenovirus-based booster vaccination in animal models revealed that respiratory booster immunization elicited markedly stronger and more durable respiratory IgA, T cell response and protective immunity, supporting the promise of respiratory vaccination. Mechanistically, mucosal boosters prompted IgA-secreting cells in the respiratory mucosa with help from local IL-21-producing Blimp1+ Th1 cells. Furthermore, lung macrophages were important for this respiratory IgA response via TGF-β. Our findings highlight a local network for robust respiratory IgA responses, supporting mucosal vaccination strategies against SARS-CoV-2 and other respiratory pathogens. Funding Sources AI147394, AG069264, AI112844, HL170961, and AI154598 to J.S, AI176171 to W.G.T. and J.S.; U54CA260582 to S.L.L; R01AI168684 to G. Z. Topic Categories Vaccines and Immunotherapy (VAC)

The Journal of ImmunologyVol. 214(Supplement_1)
University of Virginia (US)
Openalex Percentile: Top 58%
SARS-CoV-2 and COVID-19 Research
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