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An Improved and High Throughput Respiratory Syncytial Virus RSV Micro-neutralization Assay
Published on: January 26, 2019
The long road to protect infants against severe RSV lower respiratory tract illness
Sofia Jares Baglivo1, Fernando P Polack1
1Fundacion INFANT, Buenos Aires, Argentina.
Insights
Preventing severe respiratory syncytial virus (RSV) lower respiratory tract illness (LRTI) in infants remains a challenge. While past vaccine strategies have failed, monoclonal antibodies and maternal immunization show promise for RSV prevention.
Area of Science:
- Pediatrics
- Immunology
- Vaccinology
Background:
- Severe lower respiratory tract illness (LRTI) caused by respiratory syncytial virus (RSV) in infants is a significant global health issue.
- Despite extensive research over 50 years, effective preventive strategies for RSV LRTI have been limited, with several vaccine and antibody approaches failing due to safety or efficacy concerns.
Purpose of the Study:
- To review the historical development of respiratory syncytial virus (RSV) vaccines.
- To discuss past and current RSV vaccine strategies, including challenges and recent advancements.
- To highlight the implications of RSV disease burden and the potential impact of successful prevention.
Main Methods:
- Literature review of historical and ongoing RSV vaccine and antibody development.
- Analysis of clinical trial outcomes for various preventive strategies.
- Examination of RSV disease burden data.
Main Results:
- Previous RSV vaccine candidates, including inactivated vaccines and early F protein approaches, have failed or caused adverse events.
- Monoclonal antibodies like palivizumab and motavizumab have shown some efficacy, but with limitations.
- Recent maternal immunization trials (e.g., Novavax ResVax) and extended half-life mAbs demonstrate potential for preventing severe RSV LRTI.
Conclusions:
- Successful prevention of severe RSV LRTI is achievable through monoclonal antibodies and maternal immunization.
- Effective RSV prevention may also reduce subsequent risks of recurrent wheezing and pneumonia.
- Continued research and development are crucial for addressing the ongoing challenge of RSV disease prevention.
Abstract:
Severe respiratory syncytial virus (RSV) lower respiratory tract illness (LRTI) in infants has proven challenging to prevent. In the last 50 years, conceptually different approaches failed to evolve into viable preventive alternatives for routine use. Inactivated RSV vaccine (that is, formalin-inactivated RSV) elicited severe LRTI in RSV-infected toddlers pre-immunized as infants; early purified F protein approaches in pregnant women failed to elicit sufficient immunity more than a decade ago; a second-generation monoclonal antibody (mAb) of high potency against the virus (that is, motavizumab) caused severe adverse reactions in the skin, and owing to lack of efficacy against RSV subgroup B, an extended half-life mAb targeting site V in the RSV fusion protein (that is, REG2222) did not meet its primary endpoint. In the meantime, two protein F vaccines failed to prevent medically attended LRTI in the elderly. However, palivizumab and the recent results of the Novavax maternal immunization trial with ResVax demonstrate that severe RSV LRTI can be prevented by mAb and by maternal immunization (at least to a certain extent). In fact, disease prevention may also decrease the rates of recurrent wheezing and all-cause pneumonia for at least 180 days. In this review, we discuss the history of RSV vaccine development, previous and current vaccine strategies undergoing evaluation, and recent information about disease burden and its implications for the effects of successful preventive strategies.
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