Optimizing COVID-19 vaccination strategies for high-risk populations: potential and challenges of combining heterologous boosting with respiratory mucosal delivery.

Publication date: Apr 07, 2026

Despite the decline of the global peak of COVID-19, SARS-CoV-2 continues to circulate, evolve, and undergo immune escape, posing persistent threats, particularly to older adults, individuals with comorbidities, and immunocompromised populations. Although existing vaccination strategies have substantially reduced the risks of severe disease, hospitalization, and death, their ability to block infection and transmission remains limited, and protection wanes over time. Current heterologous booster strategies still rely largely on combinations of different parenteral vaccine platforms. Although these regimens can enhance systemic humoral and cellular immunity, they are insufficient to robustly induce upper respiratory mucosal immunity, thereby limiting their role in early infection control and interruption of transmission. Because respiratory mucosal vaccines target the natural entry site of SARS-CoV-2, they have the potential to induce secretory IgA, tissue-resident memory immune cells, and local immune memory, offering distinct advantages in compensating for the shortcomings of conventional heterologous boosting. Combining heterologous boosting with respiratory mucosal delivery may further enhance the control of viral infection, early replication, and subsequent transmission while preserving systemic immunity, thereby providing more comprehensive immune protection for high-risk populations. However, this strategy still faces challenges related to mucosal barriers, delivery efficiency, adjuvant safety, manufacturing scale-up, and incomplete clinical evaluation frameworks. Future high-quality studies focusing on high-risk populations are needed to clarify its value in preventing infection, protecting against severe disease, and providing long-term protection.

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Concepts Keywords
Global COVID-19
Hospitalization COVID-19 Vaccines
Mucosal COVID-19 Vaccines
Older heterologous boosting
Vaccine high-risk populations
Humans
Immunity, Mucosal
Immunization, Secondary
mucosal immunity
Respiratory Mucosa
respiratory mucosal delivery
SARS-CoV-2
SARS-CoV-2
Vaccination

Semantics

Type Source Name
disease MESH COVID-19
disease MESH death
disease MESH infection
disease MESH viral infection
drug DRUGBANK Coenzyme M
pathway REACTOME Reproduction
disease MESH reinfection
disease MESH face
disease MESH chronic kidney disease
disease MESH breakthrough infection
disease MESH strain
pathway KEGG Viral replication
disease MESH Ad5
disease MESH lung inflammation
disease MESH chronic diseases
disease MESH long COVID
disease MESH STING
disease MESH APC
pathway REACTOME Translation
disease MESH Bell’s palsy
disease MESH inflammation
disease MESH CMC
drug DRUGBANK Fosfomycin
disease MESH FCM
disease MESH Dis
drug DRUGBANK Guanosine
disease MESH Allergy
drug DRUGBANK Carboxyamidotriazole

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