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Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
The Quest for a Respiratory Syncytial Virus Vaccine for Older Adults: Thinking beyond the F Protein
Victoria A Jenkins1, Bernard Hoet1, Hubertus Hochrein2
1Bavarian Nordic AG, 6301 Zug, Switzerland.
Insights
Older adults are susceptible to severe respiratory syncytial virus (RSV) due to incomplete immunity. Research is exploring RSV vaccine candidates targeting specific antigens to improve protection in this vulnerable population.
Area of Science:
- Immunology
- Vaccinology
- Gerontology
Background:
- Respiratory syncytial virus (RSV) causes significant respiratory illness in both children and older adults.
- Natural immunity to RSV is incomplete, leading to recurrent infections throughout life.
- Older adults experience increased susceptibility to severe RSV disease due to immunosenescence.
Purpose of the Study:
- To address the unmet need for RSV vaccines in older adults.
- To explore the complex immune response to RSV in the context of aging.
- To identify effective antigenic targets for RSV vaccine development in older populations.
Main Methods:
- Review of Phase 3 clinical trial data for RSV vaccine candidates in older adults.
- Analysis of immune responses, including neutralising IgG and cellular immunity, to various RSV antigens (pre-F, F, G, M2-1, N).
- Investigation into the relationship between antigenic targets and vaccine effectiveness.
Main Results:
- Several RSV vaccine candidates targeting different antigens have demonstrated efficacy in older adults during clinical trials.
- Vaccine candidates have induced robust neutralising IgG and cellular immune responses.
- Understanding the nuances of the RSV immune response is crucial for optimizing vaccine effectiveness.
Conclusions:
- Older adults are a key target population for RSV vaccine development due to their vulnerability.
- Ongoing research is vital to understand RSV-host interactions and refine vaccine strategies.
- Further investigation into antigenic targets is necessary to achieve optimal protection against RSV in older adults.
Abstract:
Respiratory syncytial virus (RSV) is a common cause of paediatric respiratory tract infection and causes a significant health burden in older adults. Natural immunity to RSV is incomplete, permitting recurrent symptomatic infection over an individual's lifespan. When combined with immunosenescence, this increases older adults' susceptibility to more severe disease symptoms. As RSV prophylaxis is currently limited to infants, older adults represent an important target population for RSV vaccine development. The relationship between RSV and our immune systems is complex, and these interactions require deeper understanding to tailor an effective vaccine candidate towards older adults. To date, vaccine candidates targeting RSV antigens, including pre-F, F, G (A), G (B), M2-1, and N, have shown efficacy against RSV infection in older adults in clinical trial settings. Although vaccine candidates have demonstrated robust neutralising IgG and cellular responses, it is important that research continues to investigate the RSV immune response in order to further understand how the choice of antigenic target site may impact vaccine effectiveness. In this article, we discuss the Phase 3 vaccine candidates being tested in older adults and review the hurdles that must be overcome to achieve effective protection against RSV.
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