Our representatives are available to schedule your appointment Monday through Friday from 9am to 5pm.
For a Northwell ambulance, call
(833) 259-2367.
Respiratory syncytial virus (RSV) has made a fair amount of news in recent years as a cause of several nationwide outbreaks, but the development of a vaccine for this strange-sounding virus has been in the works for decades. Thankfully, as of 2024, the approval of three vaccines and a new monoclonal antibody treatment have signaled a new era of RSV protection.
Experts say the suite of new options could significantly decrease the rate of severe infection in children. “The rate of hospitalization of children due to RSV should fall by at least 50%,” says Lorry Rubin, MD, director of pediatric infectious disease at Northwell. “And when the immunization program is mature, I would expect a 90% decrease in RSV hospitalization rate.”
For most people, this common respiratory virus causes nothing worse than a mild cold. But it’s the No. 1 reason for hospitalization among babies, says Cohen Children’s Medical Center infectious disease specialist Mundeep Kainth, DO, MPH. The pediatric immune system is still underdeveloped and inexperienced at fighting infection. This means trouble in the case of highly contagious viruses like RSV, which can cause inflammation of their tiny airways and leave them struggling to breathe.
Each year, as many as 80,000 children under age 5 are hospitalized because of RSV. Much of that has to do with the way the highly contagious virus spreads: direct contact with the virus, whether through respiratory droplets from an infected individual or by touching something a patient previously touched. This means that younger children, who tend to experience the world through touch and taste, are particularly susceptible to RSV infection.
Because RSV thrives in weaker immune systems, it’s also a problem for older populations; immunity tends to decline as we age. The Centers for Disease Control and Prevention (CDC) estimates that RSV sends between 60,000 and 160,000 older American adults to the hospital each year.
Infection rates typically peak around “RSV season”, or the period of time spanning from the beginning of October to the end of March.
Three RSV vaccines are FDA-approved for use. The Food and Drug Administration approved two RSV vaccines in 2023, starting in May with the vaccine AREXVY. This vaccine is adjuvanted — meaning it offers a stronger immune response — and it is recommended for all persons age 75 years and older. It is also recommended for those 60-74 with underlying conditions that put them at increased risk for serious RSV disease.
Then, in August 2023, the FDA approved bivalent RSVpreF (ABRYSVO). While ABRYSVO, like AREXVY, is recommended for older adults as noted above, it's also approved for pregnant women as a way of boosting their immunity levels, thereby conferring that immunity to the fetus — making it the only RSV vaccine approved for such use. ABRYSVO will help protect newborns from serious RSV infection through their first months of life.
May 2024 saw the FDA approval of mRESVIA, a Moderna vaccine for 60-and-older patients. Unlike AREXVY and ABRYSVO, mRESVIA is an mRNA vaccine.
The vaccines have hit the ground running, with each of the vaccines reducing the risk of lower respiratory tract infection, such as pneumonia, from RSV. The CDC reported the level of efficacy for each based on reviews by its Advisory Committee on Immunization Practices (ACIP):
In each case, ACIP reviewed the available body of evidence (such as clinical trial results) and performed a Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) review to determine the benefits and harms of each vaccine.
Evidence for AREXVY was presented to ACIP June 21, 2023 and included two complete RSV seasons for Northern Hemisphere participants and one complete RSV season for Southern Hemisphere participants. Evidence for ABRYSVO was presented June 21, 2023 and spanned one complete RSV season and part of a second. Lastly, data for mRESVIA was collected from November 2021 to March 2024 and presented to ACIP on June 26, 2024.
Both AREXVY and ABRYSVO belong to a class of vaccines known as recombinant protein vaccines. To make them, genetic material of the virus that codes for certain RSV virus proteins is cloned into a cell. In turn, these cells produce the protein which is then used as the active ingredient in the vaccine. The injected protein triggers an immune response, but because only a part of the virus is present, it can’t replicate inside your body. This makes recombinant protein vaccines both safe and effective.
Other recombinant vaccines include the Hepatitis B and HPV vaccines.
mRESVIA, by contrast, is a messenger RNA (mRNA) vaccine. This means that it teaches your body how to make a protein that is on the surface of RSV. Your body then produces antibodies for this RSV protein — and remembers how it did it — so it’s prepared to fight a real case of RSV.
Researchers first attempted to develop an RSV vaccine in 1967. In the following decades, virologists began to better understand RSV’s structure and pathology by identifying the types of cells the immune system activates to fight it. By 2015, the World Health Organization predicted — correctly — that an RSV vaccine would be commercially available within 10 years.
The good news is that one vaccine dose will protect you — or, for pregnant women, your child — for one or more RSV seasons, according to the CDC. At present there are no indications for a booster dose of vaccine, Dr. Rubin says.
Here’s when each group can and should get the RSV vaccine.
The RSV vaccine for pregnant women (ABRYSVO) is recommended for use between 32 and 36 weeks of pregnancy from September to January to help protect their newborn infant from serious RSV disease. While vaccines are available year-round, it’s ideal to get vaccinated in late summer and early fall so you’re protected in time for RSV season. This is particularly true, Dr. Kainth explains, for pregnant women. She recommends this group get vaccinated up to a month prior to the start of RSV season in October; this is because their bodies typically need at least two weeks to mount a sufficient antibody response in the event of exposure to RSV.
If you’re 60 or older, you may be eligible for vaccination and can receive any of the RSV vaccines. Experts recommend that you do so ahead of RSV season in late summer or early fall and that you first speak with your doctor.
Current CDC recommendations call for one dose of the vaccine for all adults 75 and older, as well as adults ages 60-74 at an increased risk of severe RSV. For the purposes of these guidelines, the CDC considers the following to be risk factors:
Studies have found that one vaccine dose is enough to protect older adults for up to two years. Ongoing research seeks to determine whether booster shots beyond this period could offer additional protection.
Dr. Rubin added that none of the vaccines are approved for people under 60 except in the case of ABRYSVO for pregnant women. If you’re feeling moderately or severely ill, the CDC recommends waiting until you’ve recovered to receive an RSV vaccine.
Another recently approved preventive treatment can also provide protection for infants against serious RSV disease. Called nirsevimab (Beyfortus), it’s a monoclonal antibody. “It’s a kind of passive immunization,” Dr. Kainth says. “It provides temporary protection for babies until their immune system matures enough for them to create antibodies on their own.” Dr. Rubin adds that, when they lack protective antibodies for RSV, babies are likelier to be hospitalized if they contract RSV; nirsevimab is meant to prevent this.
The new drug replaces an earlier form of prevention called palivuzumab (Synagis), which had to be given every month. “Nirsevimab is easy because it is one shot and it lasts the entire RSV season,” says Dr. Kainth.
During the 2023-2024 RSV season, nirsevimab was found to be 90% effective at preventing hospitalization for children in their first RSV season, according to a CDC study released in March 2024. Analyzing data from nearly 700 pediatric patients treated between October 2023 and February 2024, these results show promise for the long-acting monoclonal antibody. The CDC recommends that children in their first RSV season receive nirsevimab if the mother did not get the vaccine ABRYSVO during their pregnancy.
Nirsevimab is only given to infants under 8 months between October 1 and March 31, coinciding with RSV season. As with the vaccines, one dose will, in most cases, be all your child needs. However, Dr. Rubin explains that infants who qualify for nirsevimab up to 20 months may need an additional dose in their second RSV season if they have one of the following conditions:
Keep in mind that these treatments are a preventive measure; once RSV kicks in, the vaccines and monoclonal antibody won’t be able to help. Instead, infants are managed with supportive care including ensuring adequate fluid intake, or a trip to the emergency room in the event of severe symptoms like blue skin or trouble breathing.
Dr. Kainth says that nirsevimab will likely be given to babies along with their routine vaccinations. “Although there was limited availability of nirsevimab for high-risk children last season, we are currently anticipating that it will be available for everyone in the 2024-25 season,” she noted.
Overall, Dr. Kainth considers the RSV treatments revolutionary and is confident that they will leave hospitals well-equipped to handle the upcoming season: “We think they’ll lead to a massive reduction in the number of cases of RSV. They’re going to change the winter season for babies everywhere.”
Our representatives are available to schedule your appointment Monday through Friday from 9am to 5pm.
For a Northwell ambulance, call
(833) 259-2367.