Immunize.org summarizes ACIP meeting recommending RSV vaccine during pregnancy to prevent illness in infants
The Advisory Committee on Immunization Practices (ACIP) met on September 22, 2023, to review Abrysvo, Pfizer’s respiratory syncytial virus (RSV) vaccine (“RSVpreF"). Because only one of two RSV vaccines is licensed and recommended for use during pregnancy, this summary will refer to it by its brand name. Abrysvo is licensed for use during pregnancy from 32 through 36 weeks gestation to prevent lower respiratory tract disease (LRTD) in infants. ACIP voted 11—1 to recommend seasonal (generally, September through January) use of the vaccine. All infants younger than 8 months are now recommended to receive either nirsevimab (monoclonal antibody) before or during their first RSV season or to be protected through RSV vaccination of their mother during pregnancy. In rare cases, both forms of protection may be appropriate. Presentation slides from the meeting are available online. Immunize.org describes the meeting’s highlights below. Following the meeting, the CDC director officially accepted the recommendations.
Separately, CDC announced that it will issue updated U.S. Recommended Immunization Schedules for adults and for children and adolescents, publishing an addendum to each schedule in the first week of October 2023. These schedules will incorporate updated ACIP recommendations since CDC published the 2023 schedules in February. Publishing the updated official schedules will reduce the time required to initiate insurance coverage of newly recommended immunizations, and help clinicians implement new recommendations. Updated schedules will have changes highlighted in red and include an additional page that summarizes new recommendations for COVID-19, RSV, poliovirus, and influenza published since February.
RSV background
RSV is a highly contagious virus that causes respiratory infections in people of all ages. RSV is the leading cause of hospitalization of infants in the United States; 2–3% of young infants are hospitalized with RSV, resulting in 58,000 to 80,000 hospitalizations and 100 to 300 childhood deaths per year. RSV circulation in the United States is seasonal, typically starting in the fall and peaking in the winter, although seasonality was temporarily disrupted during the COVID-19 pandemic.
The September 22 meeting focused on preventing RSV illness in early infancy through vaccination with the Abrysvo brand of RSV vaccine during pregnancy. The Arexvy (GSK) brand of adjuvanted RSVpreF vaccine is not licensed for use during pregnancy and was not discussed. This is the third set of RSV prevention recommendations made by ACIP in recent weeks. Earlier recommendations include:
Abrysvo given during pregnancy at least 14 days before delivery was shown in clinical trials to reduce the risk of a medical visit due to RSV LRTD by about half in the first 6 months of life and to reduce the risk of severe LRTD by about 70%.
Vaccine safety and coadministration during pregnancy
Abrysvo is licensed only for use during pregnancy between 32 and 36 weeks gestation. Clinical trials demonstrated possible associations between RSVpreF and prematurity and hypertension during pregnancy. However, the number of cases were too few to know whether the vaccine caused these issues or they occurred by chance. By limiting vaccination to no earlier than a gestational age of 32 weeks, any risk of premature delivery is minimized. Vaccine safety monitoring (including updated v-safe voluntary smartphone monitoring, adapted from the COVID-19 v-safe system) will enhance safety surveillance as widespread use of the vaccine begins.
When Abrysvo and Tdap were administered at the same time, studies found a decreased immune response to pertussis. The clinical significance of this finding is not known. Additional experience will be needed to decide if this is a meaningful issue. Since Tdap is recommended during pregnancy beginning at 27 weeks gestation, this interaction can be avoided by giving Tdap and Abrysvo at different prenatal visits.
Cost effectiveness
Although it is safe to administer RSV vaccine to a mother and then nirsevimab to the infant, the use of both products for the same infant increased costs without providing much additional benefit over choosing either timely vaccination or administration of monoclonal antibody. Because protection from maternal vaccination wanes over 6 months from birth, economic analysis showed that the most valuable strategy would be to restrict maternal RSVpreF vaccination to specific months of the year when infants would benefit from immediate protection during RSV season. For infants born outside RSV season (e.g., April through September), administration of nirsevimab immediately before the RSV season is the most effective and practical option for RSV protection.
Vote
ACIP voted 11-1 to adopt the following recommendation: “Maternal RSV vaccine is recommended for pregnant people during 32 through 36 weeks gestation, using seasonal administration, to prevent RSV lower respiratory tract infection in infants.” One member opposed the motion due to its complexity and preferred a simpler recommendation.
Seasonal timing of vaccination
ACIP recommended that Abrysvo be administered during pregnancy, in general, only from September through January to protect infants born during the RSV season. In jurisdictions where timing of the RSV season may differ (e.g., Alaska, Hawaii, Puerto Rico, U.S. Virgin Islands, Guam, parts of Florida), ACIP recommends flexibility and that timing of vaccination be directed by public health officials based on local conditions.
Use of either Abrysvo during pregnancy or nirsevimab after delivery
Pregnant people should be counseled about both options and be able to choose whether to be vaccinated during pregnancy (if the timing is appropriate) or to have the infant receive nirsevimab after delivery. ACIP expresses no preference during months where vaccination during pregnancy is an option (e.g., September through January). Because both products are new in fall 2023, it will take some time before there is widespread availability of both options.
Mothers and healthcare providers must weigh several considerations:
- Maternal RSV vaccination at least 14 days before birth results in protection immediately at birth, which wanes over the next 6 months; however, protection is not optimal if the infant is born sooner than 14 days after vaccination or if the mother’s immune system fails to produce sufficient antibodies.
- Nirsevimab lasts longer, provides direct protection as soon as administered to the baby, and has no effect on the pregnancy. However, if the infant’s healthcare provider does not yet stock nirsevimab, the family could have difficulty accessing the product.
Mothers who should receive RSV vaccination meet all three of these criteria:
- The time of year is between September and the end of January (unless public health authorities recommend different timing based on local RSV circulation), and
- The mother is between 32 and 36 weeks gestation, and
- The mother does not prefer to have the infant receive nirsevimab (or the infant will not have access to nirsevimab)
In the context of the maternal vaccination option, infants younger than 8 months who need nirsevimab should meet all three of these criteria:
- The time of year is between October and March, and
- The infant’s mother did not receive RSVpreF vaccine, or the vaccination status cannot be confirmed, or the mother received RSVpreF vaccine sooner than 14 days before delivery, and
- The infant has not previously received nirsevimab
Consistent with these criteria, nirsevimab is indicated for all infants born before 34 weeks gestational age (because Abrysvo cannot be given earlier than 32 weeks) and for all infants born in April through September (whose mothers will not be offered vaccine).
In rare situations, nirsevimab should be given to certain infants born 2 weeks or more after maternal vaccination. Examples include:
- Conditions in pregnant people resulting in an inadequate immune response to vaccine or decrease in transplacental antibody transfer (e.g., people living with HIV infection)
- Infants who have undergone cardiopulmonary bypass, leading to loss of maternal antibodies
- Infants at high risk for severe RSV disease (e.g., hemodynamically significant congenital heart disease, intensive care admission and requiring oxygen at discharge)
Additional clinical considerations
- Simultaneous vaccinations: it is acceptable to give Abrysvo at the same visit with other vaccinations
- Subsequent pregnancies: ACIP currently recommends only one dose of RSV vaccine during a single pregnancy. ACIP will consider whether to recommend RSV vaccination during subsequent pregnancies as more data become available
Implementation
- Communication challenges: ACIP members noted that the success of this complex recommendation requires effective documentation and communication between obstetric teams and pediatric teams about the mother’s RSV vaccination status or need for nirsevimab. It is not possible to document maternal vaccination on an infant’s record in state immunization information systems (IIS). Some state privacy laws may prevent a pediatrician from reviewing the mother’s vaccination record in an IIS (because the mother is not their patient). In cases where the mother’s vaccination status cannot be confirmed by the pediatric care provider, nirsevimab should be administered if otherwise indicated.
- Supply: Abrysvo for mothers is the same vaccine used for adults age 60 years or older, so it is already commercially available. Nirsevimab will begin shipping in early October, but may not be available in all pediatric settings this season.
Future ACIP meetings
The next scheduled ACIP meeting will be held on October 25–27, although additional emergency meetings may be announced before that time. Information about past and future ACIP meetings appear at the ACIP website.
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