Related Experiment Video
Updated: Jun 15, 2026

Intranasal Administration of Recombinant Influenza Vaccines in Chimeric Mouse Models to Study Mucosal Immunity
Published on: June 25, 2015
mRNA booster vaccination protects aged mice against the SARS-CoV-2 Omicron variant
Etsuro Nanishi1,2, Marisa E McGrath3, Timothy R O'Meara1
1Precision Vaccines Program, Division of Infectious Diseases, Boston Children's Hospital, Boston, MA, USA.
Abstract:
The SARS-CoV-2 Omicron variant evades vaccine-induced immunity. While a booster dose of ancestral mRNA vaccines effectively elicits neutralizing antibodies against variants, its efficacy against Omicron in older adults, who are at the greatest risk of severe disease, is not fully elucidated. Here, we evaluate multiple longitudinal immunization regimens of mRNA BNT162b2 to assess the effects of a booster dose provided >8 months after the primary immunization series across the murine lifespan, including in aged 21-month-old mice. Boosting dramatically enhances humoral and cell-mediated responses with evidence of Omicron cross-recognition. Furthermore, while younger mice are protected without a booster dose, boosting provides sterilizing immunity against Omicron-induced lung infection in aged 21-month-old mice. Correlational analyses reveal that neutralizing activity against Omicron is strongly associated with protection. Overall, our findings indicate age-dependent vaccine efficacy and demonstrate the potential benefit of mRNA booster immunization to protect vulnerable older populations against SARS-CoV-2 variants.
Insights
Booster doses of mRNA vaccines enhance immune responses against SARS-CoV-2 Omicron variants. This boosting is crucial for protecting older adults, who are more vulnerable to severe disease, by providing sterilizing immunity.
Area of Science:
- Immunology
- Virology
- Gerontology
Background:
- The SARS-CoV-2 Omicron variant exhibits immune evasion properties, potentially reducing the efficacy of existing vaccine-induced immunity.
- While mRNA vaccine boosters enhance neutralizing antibodies against variants, their specific impact on older adults, a high-risk group for severe COVID-19, requires further investigation.
Purpose of the Study:
- To evaluate the longitudinal effects of mRNA-1273 booster immunization in a murine model across different age groups, including aged mice.
- To assess the efficacy of a booster dose administered over 8 months after primary immunization against the Omicron variant.
Main Methods:
- Longitudinal immunization regimens using mRNA-1273 were administered to mice of varying ages, including aged (21-month-old) mice.
- Humoral and cell-mediated immune responses were analyzed, alongside assessments of protection against Omicron-induced lung infection.
- Correlational analyses were performed to link neutralizing antibody activity with protection.
Main Results:
- Boosting significantly enhanced both humoral and cell-mediated immune responses, demonstrating cross-recognition of the Omicron variant.
- While younger mice showed protection without a booster, aged mice required a booster dose to achieve sterilizing immunity against Omicron-induced lung infection.
- A strong correlation was observed between neutralizing activity against Omicron and protection from infection.
Conclusions:
- Vaccine efficacy against SARS-CoV-2 variants is age-dependent.
- mRNA booster immunizations offer significant potential benefits for protecting vulnerable older populations against emerging variants like Omicron.
Related Concept Videos
Mouse Models of Cancer Study
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...

