Heterologous mucosal vaccine boosting enhances mucosal and systemic immunity by distinct mechanisms

Seasonal booster vaccination is the primary intervention for protection from respiratory viral infections, such as influenza virus or SARS-CoV-2. However, efficacy is often limited because immune exposure to prior strains impairs development of new responses. In this study, we sought to determine how this issue could be overcome in a mouse model of heterologous immunization against WT and omicron strains of SARS-CoV-2. Intranasal booster immunization circumvented the shortcomings of intramuscular immunization, resulting in superior systemic and mucosal T and B cell immunity and better viral control following SARS-CoV-2 challenge in hamsters. Mechanistically, an intranasal omicron booster immunization bypassed deleterious immune imprinting following intramuscular ancestral strain prime, which allowed for induction of de novo lung B cell and antibody responses against the omicron strain. Cross-reactive memory T cells were also efficiently recruited into the lungs. These findings support further testing of mucosal booster vaccines against respiratory viruses, particularly as a means of simultaneously overcoming deleterious immunological imprinting and enhancing mucosal responses.

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Publication Details

Journal
The Journal of Experimental Medicine
Published
2025-09-25
DOI
https://doi.org/10.1084/jem.20241529
Citations
2
Primary Topic
Immune responses and vaccinations
Type
article
Field-Weighted Citation Impact
1.59
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article

Heterologous mucosal vaccine boosting enhances mucosal and systemic immunity by distinct mechanisms

Teresa Lambe, Reshma Kailath, Neeltje van Doremalen, Nicholas M. Provine et al.
2 citations
The Journal of Experimental Medicine
Immune responses and vaccinations
1.59
article

Heterologous mucosal vaccine boosting enhances mucosal and systemic immunity by distinct mechanisms

Teresa Lambe, Reshma Kailath, Neeltje van Doremalen, Nicholas M. Provine, Vincent J. Munster, Reshma Koolaparambil Mukesh, Cameron Bissett, Marta Ulaszewska, Alexandra J. Spencer, Sandra Belij‐Rammerstorfer, Alex Sampson, Freda Lam, Lyn Yong, Susan Morris, Claire Powers, Ethan A. Courchesne, Marie Lucienne
article en
2 citations

Abstract

Seasonal booster vaccination is the primary intervention for protection from respiratory viral infections, such as influenza virus or SARS-CoV-2. However, efficacy is often limited because immune exposure to prior strains impairs development of new responses. In this study, we sought to determine how this issue could be overcome in a mouse model of heterologous immunization against WT and omicron strains of SARS-CoV-2. Intranasal booster immunization circumvented the shortcomings of intramuscular immunization, resulting in superior systemic and mucosal T and B cell immunity and better viral control following SARS-CoV-2 challenge in hamsters. Mechanistically, an intranasal omicron booster immunization bypassed deleterious immune imprinting following intramuscular ancestral strain prime, which allowed for induction of de novo lung B cell and antibody responses against the omicron strain. Cross-reactive memory T cells were also efficiently recruited into the lungs. These findings support further testing of mucosal booster vaccines against respiratory viruses, particularly as a means of simultaneously overcoming deleterious immunological imprinting and enhancing mucosal responses.

The Journal of Experimental MedicineVol. 223(1)
Centre for Human Genetics (GB), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Oxford Research Group (GB), University of Oxford (GB), National Institute of Allergy and Infectious Diseases (US), Science Oxford (GB), University of Newcastle Australia (AU)
Openalex Percentile: Top 14%
Immune responses and vaccinations
1.59
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