CDC Statement on LAIV Effectiveness and Vaccination of Children
CDC conducts vaccine effectiveness (VE) studies with the U.S. Influenza Vaccine Effectiveness (Flu VE) Network each season to estimate flu vaccine VE. Mid-season VE estimates for the 2013-2014 season were published on February 20, 2014, in a Morbidity and Mortality Weekly Report entitled: “Interim Estimates of 2013-14 Seasonal Influenza Vaccine Effectiveness—United States.” Final overall VE estimates were similar to the interim published estimates. However, end of season data evaluated during the summer by the Flu VE Network also allowed separate estimates for the live attenuated influenza vaccine (LAIV, or the “nasal spray vaccine”) and inactivated influenza vaccine (IIV or “the flu shot). During 2013-2014 there was no measurable effectiveness for LAIV against influenza A (H1N1) among children enrolled in the study.
While it is well-known that VE can vary by age group, season, circulating influenza viruses and by vaccine, this finding is unexpected and different from some previous studies, which suggested that LAIV may be more effective for younger children. Since 2008, ACIP and CDC have recommended that all children 6 months and older (with rare exceptions) receive influenza vaccine annually, using any licensed age-appropriate vaccine. During the summer of 2014, however, ACIP and CDC recommended that beginning during the 2014-2015 influenza season, LAIV should be used for healthy children 2 through 8 years of age when immediately available and when there are no contraindications or precautions against getting that vaccine. This decision was based on previous data showing that LAIV offered superior protection against influenza virus infection compared to IIV in young children.
The reasons behind the lack of effectiveness against H1N1infections for LAIV during the 2013-14 season are not fully understood. It is possible that results may be specific to the H1N1 component of LAIV. Influenza H1N1 viruses predominated during the 2013-2014 season for the first time since their emergence in 2009 when they caused a pandemic. It also is possible – though less likely – that there is an unidentified issue with the study methods or analysis plan.
CDC is working with ACIP and other partners to collect more information to better understand these data and to determine what actions might be appropriate.
The 2013-2014 season LAIV VE estimates against H1N1 for children suggest that LAIV may not protect against H1N1 viruses during the 2014-2015 season because the same H1N1 vaccine virus from 2013-2014 is included in the 2014-2015 vaccine. All LAIV is designed to protect against four different influenza viruses: Influenza A (H1N1), A (H3N2) and two influenza B viruses.
CDC has been monitoring surveillance data closely. So far, U.S. seasonal surveillance data as reported in FluView indicate substantially greater circulation of H3N2 and B viruses and little circulation of H1N1 viruses. (Of the subtyped viruses reported to CDC from the week ending October 5 through the week ending October 25, 2014, 387 (31%) have been H3N2 viruses, 387 (31%) have been influenza B viruses and 16 (1%) have been H1N1 viruses. Another 466 influenza A viruses were not subtyped.)
In addition, some of the influenza A (H3N2) viruses have been drifted from the H3N2 vaccine virus used in this season’s vaccine. (An October 3 Morbidity and Mortality Weekly Report “Influenza Update” reported that CDC antigenically characterized 391 viruses collected worldwide during May 18 through September 20, 2014, including 70 A (H1N1) viruses, 141 influenza A (H3N2) viruses, and 180 influenza B viruses. Of the 141 influenza A (H3N2) viruses characterized 69 (49%) were antigenically similar to A/Texas/50/2012, the influenza A (H3N2) component of the 2014-2015 influenza vaccine for the Northern Hemisphere. Only 10 A (H3N2) viruses collected in the United States since October 1 have been characterized so far this season. Seven of these (70%) are like the A (H3N2) vaccine virus, 3 (30%) have been characterized as A/Switzerland/9715293/2013, an antigenic variant virus which has been selected for the 2015 Southern Hemisphere influenza vaccine.) It is important to note that there are some data to suggest that LAIV may offer better protection than IIV against antigenically drifted viruses.
As of October 31, manufacturers reported having distributed more than 132 million doses of the 151 million to 156 million total doses projected to be available for the U.S. market this season. (The manufacturer of LAIV projected that as many as 18 million doses of LAIV would be produced for the U.S. market this season.) Vaccine uptake data for this season are not yet available, however, past trends suggest that more than half of flu vaccines given to children are administered by the end of October, suggesting that many children may have already gotten vaccinated.
1. Surveillance shows that there is substantially more circulation of influenza A (H3N2) and B viruses and very little circulating H1N1 so far;
2. LAIV has been shown to offer good protection against influenza A (H3N2) and influenza B viruses in the past;
3. LAIV may offer better protection than IIV against antigenically drifted viruses that may circulate this season; and,
4. Vaccine providers have received their vaccine for the 2014-2015 season and have likely administered a good proportion of it;
ACIP and CDC have not changed the current influenza vaccination recommendations.
People who have not been vaccinated yet this season should get vaccinated now. Parents should seek to get their children immunized with whatever vaccine is immediately available and indicated. Influenza vaccination should not be delayed to procure a specific vaccine preparation. The HealthMap Vaccine Finderexternal icon can be used to locate vaccine.
CDC is in discussions with the manufacturer of LAIV, the Department of Defense, the Food and Drug Administration, and other partners to better understand the data from last season, and to determine causes and ways to address the low VE of LAIV against H1N1. For the current season, the U.S. Flu VE Network has expanded enrollment of children and will continue ongoing studies of serologic outcomes after vaccination in children getting IIV and LAIV. This additional data collected during 2014-2015 will help inform discussion about this matter further.