As Plain as the Nose on Your Face: The Case for A Nasal (Mucosal) Route of Vaccine Administration for Covid-19 Disease Prevention

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SARS-CoV-2 Reverse Genetics Reveals a Variable Infection Gradient in the Respiratory Tract

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Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein

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Inflammasomes and Pyroptosis as Therapeutic Targets for COVID-19

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Longitudinal analyses reveal immunological misfiring in severe COVID-19

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Vasculopathy and Coagulopathy Associated with SARS-CoV-2 Infection

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The receptor binding domain of the viral spike protein is an immunodominant and highly specific target of antibodies in SARS-CoV-2 patients

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Immunogenicity and Toxicity of Different Adjuvants Can Be Characterized by Profiling Lung Biomarker Genes After Nasal Immunization

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Superior immune responses induced by intranasal immunization with recombinant adenovirus-based vaccine expressing full-length Spike protein of Middle East respiratory syndrome coronavirus

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Defective lung function following influenza virus is due to prolonged, reversible hyaluronan synthesis

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IgA polymerization contributes to efficient virus neutralization on human upper respiratory mucosa after intranasal inactivated influenza vaccine administration

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Nasal-associated lymphoid tissues (NALTs) support the recall but not priming of influenza virus-specific cytotoxic T cells

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Parenteral Vaccination Can Be an Effective Means of Inducing Protective Mucosal Responses

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Induction of mucosal immunity through systemic immunization: Phantom or reality?

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Prior Immunization with Severe Acute Respiratory Syndrome (SARS)-Associated Coronavirus (SARS-CoV) Nucleocapsid Protein Causes Severe Pneumonia in Mice Infected with SARS-CoV

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Intranasal Vaccination of Recombinant Adeno-Associated Virus Encoding Receptor-Binding Domain of Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) Spike Protein Induces Strong Mucosal Immune Responses and Provides Long-Term Protection against SARS-CoV Infection

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Virus-Specific Memory CD8 T Cells Provide Substantial Protection from Lethal Severe Acute Respiratory Syndrome Coronavirus Infection

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Secretory immunity with special reference to the oral cavity

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Potential of Nasopharynx-associated Lymphoid Tissue for Vaccine Responses in the Airways

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Anti-Severe Acute Respiratory Syndrome Coronavirus Spike Antibodies Trigger Infection of Human Immune Cells via a pH- and Cysteine Protease-Independent Fc R Pathway

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Epithelial Cells Lining Salivary Gland Ducts Are Early Target Cells of Severe Acute Respiratory Syndrome Coronavirus Infection in the Upper Respiratory Tracts of Rhesus Macaques

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Prevalence of Antibodies to Four Human Coronaviruses Is Lower in Nasal Secretions than in Serum

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Robust IgA and IgG-producing antibody forming cells in the diffuse-NALT and lungs of Sendai virus-vaccinated cotton rats associate with rapid protection against human parainfluenza virus-type 1

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The recycling and transcytotic pathways for IgG transport by FcRn are distinct and display an inherent polarity

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