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This article, originally published on July 21, 2023, has been updated to include Moderna's new RSV vaccine, mRESVIA, to note that Arexvy is approved for those ages 50-59 at high risk of lower respiratory tract disease from RSV, and to reflect changes to vaccine recommendations.
Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract infections in babies and young children. It also causes infections in older adults and adults with chronic conditions. Until recently, respiratory virus hygiene, including handwashing, was the most effective RSV prevention for the general public. But, the U.S. Food and Drug Administration (FDA) has approved four preventative products for RSV in less than a year:
In the U.S., RSV season typically lasts from October through April, with a peak in December or January. Symptoms include runny nose, coughing, sneezing, fever, and difficulty breathing. RSV has two subtypes, A and B, that differ genetically, but there is no difference in disease severity between them.
The U.S. Centers for Disease Control and Prevention (CDC) estimates that between 58,000-80,000 children under age 5 and 60,000-160,000 adults 65 and over are hospitalized with RSV each year, mainly for breathing difficulty and dehydration. While most people recover, 100-300 children and 6,000-10,000 adults ultimately die from the infection or its complications. Along with chronic heart and lung disease, being immunocompromised is a risk factor for developing severe RSV.
Research on RSV in those with primary immunodeficiency (PI) has primarily focused on infants and children. A 2012 paper found that children with PI are 3.8 times more likely to be hospitalized for an RSV infection than children without a chronic condition. Studies in Japan and Spain found that, in particular, children with PIs that affect T cells (for example, combined immunodeficiencies) are at the greatest risk of hospitalization for RSV.
Prior to May 2023, the only FDA-approved product for the prevention of lower respiratory tract infections from RSV was palivizumab, a monoclonal antibody manufactured by Swedish Orphan Biovitrum under the trade name Synagis. Monoclonal antibodies provide passive immunity and work by binding to and blocking germs so they can’t infect cells. However, palivizumab is only approved for certain high-risk infants and is typically given as a monthly injection for up to five consecutive months during RSV season.
Technological breakthroughs have led to an explosion of clinical research on new prevention and treatment products for RSV over the last decade. As of June 2024, there are three approved RSV vaccines for adults and a long-lasting monoclonal antibody for infants.
Abrysvo, Arexvy, and mRESVIA are all vaccines, which means they rely on a person’s immune system to generate antibodies and/or T cells that will protect that person from RSV infection. All three are approved for people who are 60 years old and older. Arexvy is also approved for people 50-59 years of age who are at high risk, including those who are immunocompromised.
Importantly, none of the three vaccines contain live virus (or even whole virus), so they cannot cause RSV infections in individuals with PI. Likewise, household members and other close contacts who have been vaccinated cannot spread RSV to individuals with PI.
There are key differences between the three vaccines. Abrysvo and Arexvy are protein subunit vaccines that contain a piece of RSV meant to stimulate an immune response—in this case, a protein found on the virus surface that helps RSV infect human cells. Arexvy also contains an adjuvant, which is a substance added to vaccines that boosts a person’s immune response, whereas Abrysvo does not. In phase III clinical trials, Arexvy was 82.6% effective at preventing lower respiratory tract infections from RSV in adults aged 60 and older during their first RSV season after vaccination. Unpublished data submitted to the FDA to expand approval of Arexvy in younger individuals found that those 50-59 years old with certain chronic conditions produced similar antibody responses as the older individuals in the phase III trial. Abrysvo was 66.7% effective in a similar phase III clinical trial in adults aged 60 and older. Note that because each trial was done independently with different criteria, the efficacy of the vaccines cannot be compared directly.
In contrast, mRESVIA is an mRNA vaccine similar to the mRNA COVID-19 vaccines. It contains instructions (mRNA) that code for the same RSV surface protein Abrysvo and Arexvy contain. mRESVIA relies on your cells to use the mRNA to make the surface protein, which then stimulates an immune response. mRESVIA was 83.7% effective in preventing lower respiratory tract infections from RSV in older adults during the first RSV season after vaccination.
Recently, GlaxoSmithKline published additional analysis of Arexvy in those 60 and older with at least one chronic condition placing them at high risk of severe RSV. These conditions included any chronic respiratory or pulmonary disease (including COPD and asthma), chronic heart failure, diabetes mellitus type 1 or type 2, and advanced liver or renal disease. Among this population, Arexvy was 94.6% effective in preventing lower respiratory tract disease from RSV.
Based on these trials, the CDC’s Advisory Committee on Immunization Practices (ACIP) recommends that everyone 75 and older receive an RSV vaccine in late summer or early fall before RSV season begins. ACIP also recommends that those 60-74 years old who are at high risk from RSV speak with their healthcare provider about getting an RSV vaccine
At this time, whether individuals with PI produce a protective response to the RSV vaccines is unknown. Experience with COVID-19 vaccines suggests that vaccination against RSV may protect at least some individuals with PI. IDF’s Medical Advisory Committee agrees with ACIP’s recommendations and encourages those with PI who are age 60 or older to speak with their healthcare provider about the vaccines, particularly if they have chronic lung or heart disease.
Young children are also at risk for severe RSV. Two passive forms of immunity, which do not rely on an individual’s immune response, are now available to protect infants: maternal vaccination with Abrysvo and nirsevimab, a long-lasting monoclonal antibody made by AstraZeneca and Sanofi under the trade name Beyfortus.
For maternal vaccination, pregnant individuals are vaccinated so that they pass protective antibodies through the placenta to their babies. In the Abrysvo maternal vaccination trial, vaccination at 24-36 weeks of pregnancy was 81.8% effective in preventing severe RSV in newborns from birth through 6 months of age.
Nirsevimab is a monoclonal antibody that targets the same RSV surface protein as palivizumab and all three vaccines, blocking RSV’s ability to infect human cells. In phase IIb and phase III clinical trials in premature and term infants, a single shot of nirsevimab was 70.1-74.9% effective over five months in preventing RSV lower respiratory tract infections that required medical attention.
Interestingly, nirsevimab uses the same YTE technology as AstraZeneca’s Evusheld to stabilize the antibody and prevent it from breaking down in the bloodstream. This modification allows it to be given as a single intramuscular shot that lasts for the duration of a single RSV season.
To protect infants born during RSV season, the CDC recommends either maternal vaccination at 32-36 weeks gestation or immunization with nirsevimab within the first week after birth. Babies born between RSV seasons whose mothers were not vaccinated should receive nirsevimab if they are 8 months old or younger at the start of the next RSV season. In addition, high-risk babies up to 24 months old, including those who are severely immunocompromised, entering their second RSV season should also receive nirsevimab. Talk to your doctor to see if your child should receive the antibody prior to their second RSV season.
This page contains general medical and/or legal information that cannot be applied safely to any individual case. Medical and/or legal knowledge and practice can change rapidly. Therefore, this page should not be used as a substitute for professional medical and/or legal advice. Additionally, links to other resources and websites are shared for informational purposes only and should not be considered an endorsement by the Immune Deficiency Foundation.
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