Respiratory syncytial virus vaccine
Vaccine description | |
---|---|
Target | RSVPreF3 antigen |
Vaccine type | Protein subunit |
Clinical data | |
Trade names | Arexvy, Abrysvo |
Other names | GSK3844766A,[1][2] respiratory syncytial virus vaccine, adjuvanted[3][4] |
License data | |
Pregnancy category |
|
Intramuscular | |
ATC code | |
Legal status | |
Legal status | |
Identifiers | |
KEGG |
A respiratory syncytial virus vaccine, or RSV vaccine, is a vaccine that protects against respiratory syncytial virus.[11] RSV affects an estimated 64 million people and causes 160,000 deaths worldwide each year.[14]
The RSV vaccines Arexvy (GSK),[3] and Abrysvo (Pfizer),[8] are approved for medical use in the United States.[4][9][15] Arexvy is approved for medical use in the European Union[10][11] and in Canada for adults aged 60 or older.[16]
Research to develop an RSV vaccine continued for decades; a 2013 study led to the approved vaccines.[17][18] Work on RSV vaccines also supported the rapid development of COVID-19 vaccines.[18][19]
Abrysvo is also approved in the US for use in pregnant women at 32 through 36 weeks gestational age to protect infants from birth through six months of age.[20] Abrysvo is approved for use in pregnant women at 24 through 36 weeks and older adults in the European Union.[21][22] and between 28 through 36 weeks and older adults in the UK.
Infant-specific issues include the immature infant immune system and the presence of maternal antibodies, which make infantile immunization difficult.[23]
Medical uses
History
Development
Attempts to develop an RSV vaccine began in the 1960s with an unsuccessful
A 1998 paper reported that research had advanced greatly over the previous 10 years.
A 2013 study detailed the crystal structure of the
In February 2023, results of a phase III study of around 25,000 participants age 60+ were published. One dose of the Arexvy vaccine provided 94% efficacy against severe RSV pneumonia and 72% efficacy against RSV acute respiratory infection.[31] An advisory panel to the FDA recommended approval of the vaccine in February 2023.[32][33]
In April 2023, the Committee for Medicinal Products for Human Use of the European Medicines Agency (EMA) recommended to grant a marketing authorization for Arexvy for the prevention of RSV lower respiratory tract disease in adults 60 years of age or older[34][35] after review under EMA's accelerated assessment program.[34]
In May 2023, Arexvy was approved for adults aged 60 and older, making it the first FDA-approved RSV vaccine.[36][37]
In May 2023, the FDA's expert panel unanimously recommended Abrysvo for approval in pregnant women.[38] The panel was split on the safety of the vaccine in respect of preterm births.[39]
In June 2023, Arexvy was approved for medical use in the European Union.[40]
Clinical trials
As of October 2022[update], Phase III trials by multiple companies were ongoing to test RSV vaccines with adults aged 60 and above. These included vaccines by GSK, Pfizer, Johnson & Johnson, Moderna, and Bavarian Nordic.[41][42][43] As of April 2023[update], other vaccines were in development, including vaccines for pregnant women to immunize their fetuses by passing maternal antibodies to them, and vaccines for children.[18][41]
GSK
In November 2020, GSK's vaccine, GSK3888550A, entered Phase III trials for pregnant women.[44] The vaccine's antigen is a stabilized version of the RSV F protein, which was developed using structure-based vaccine design.[45][46] This trial was terminated in February 2022, on the advice of an external Data Monitoring Committee, because of an excess of premature births in the trial arm.[47]
The FDA analyzed data from an ongoing, randomized, placebo-controlled clinical study conducted in the US and internationally in individuals 60 years of age and older.[36] The main clinical study was designed to assess the safety and effectiveness of a single dose administered to individuals 60 years of age and older.[36] Participants agreed to remain in the study through three RSV seasons to assess the duration of effectiveness and the safety and effectiveness of repeat vaccination.[36] Data from the first RSV season of the study were available for the FDA's analysis.[36] In this study, approximately 12,500 participants received vaccine and 12,500 participants received a placebo.[36] The vaccine reduced the risk of developing RSV-associated lower respiratory tract disease (LRTD) by 82.6% and reduced the risk of developing severe RSV-associated LRTD by 94.1%.[36] The FDA granted the application priority review designation and granted approval of Arexvy to GlaxoSmithKline Biologicals.[36]
Pfizer
RSVpreF (Abrysvo) is a bivalent recombinant protein subunit vaccine which consists of equal amounts of stabilized prefusion F antigens from the two major RSV subgroups: RSV A and RSV B.[48]
In April 2023, Pfizer published their interim results of their Phase III study of a RSV vaccine for adults age 60 and above in over 34,000 participants. One dose of the vaccine was 67% efficacious in preventing infections with at least two symptoms and it was 86% effective against more severe disease, in people with three related symptoms. The vaccine's protection was consistent across different subgroups, and was 62% effective in preventing acute respiratory illness caused by RSV infection.[49][50]
In April 2023, Pfizer published interim results of their double blind Phase III study in about 3,600 pregnant women, with another 3,600 women receiving a placebo. One dose of the vaccine provided 81% efficacy in preventing severe infection within three months after birth and 69% in six months after birth.[51] The most common side effects were pain at the injection site, headache, muscle pain and nausea.[20]
In a subgroup of pregnant individuals who were 32 through 36 weeks gestational age, of whom about 1,500 received Abrysvo and 1,500 received placebo, Abrysvo reduced the risk of lower respiratory tract disease by 34.7%, and reduced the risk of severe lower respiratory tract disease by 91.1% within 90 days after birth when compared to placebo. Within 180 days after birth, Abrysvo reduced the risk of lower respiratory tract disease by 57.3% and by 76.5% for severe lower respiratory tract disease, when compared to placebo. In a second study, about 100 pregnant individuals received Abrysvo and approximately 100 pregnant women received placebo.[20]
References
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External links
- Clinical trial number NCT04886596 for "Efficacy Study of GSK's Investigational Respiratory Syncytial Virus (RSV) Vaccine in Adults Aged 60 Years and Above" at ClinicalTrials.gov
- Clinical trial number NCT04732871 for "Immunogenicity, Safety, Reactogenicity and Persistence of an Investigational Respiratory Syncytial Virus (RSV) Vaccine in Adults Aged 60 Years and Above" at ClinicalTrials.gov
- Clinical trial number NCT04841577 for "A Study on the Immune Response and Safety Elicited by a Vaccine Against Respiratory Syncytial Virus (RSV) When Given Alone and Together With a Vaccine Against Influenza in Adults Aged 60 Years and Above" at ClinicalTrials.gov
- Clinical trial number NCT05035212 for "Study to Evaluate the Efficacy, Immunogenicity, and Safety of RSVpreF in Adults. (RENOIR)" at ClinicalTrials.gov
- Clinical trial number NCT04424316 for "A Trial to Evaluate the Efficacy and Safety of RSVpreF in Infants Born to Women Vaccinated During Pregnancy" at ClinicalTrials.gov