Differences in antibody responses between trivalent inactivated influenza vaccine and live attenuated influenza vaccine correlate with the kinetics and magnitude of interferon signaling in children.
Document Type
Article
Publication Date
7-15-2014
JAX Location
Reprint Collection
JAX Source
J Infect Dis 2014 Jul 15; 210(2):224-33.
Volume
210
Issue
2
First Page
224
Last Page
233
ISSN
1537-6613
PMID
24495909
Abstract
BACKGROUND: Live attenuated influenza vaccine (LAIV) and trivalent inactivated influenza vaccine (TIV) are effective for prevention of influenza virus infection in children, but the mechanisms associated with protection are not well defined.
METHODS: We analyzed the differences in B-cell responses and transcriptional profiles in children aged 6 months to 14 years immunized with these 2 vaccines.
RESULTS: LAIV elicited a significant increase in naive, memory, and transitional B cells on day 30 after vaccination, whereas TIV elicited an increased number of plasmablasts on day 7. Antibody titers against the 3 vaccine strains (H1N1, H3N2, and B) were significantly higher in the TIV group and correlated with number of antibody-secreting cells. Both vaccines induced overexpression of interferon (IFN)-signaling genes but with different kinetics. TIV induced expression of IFN genes on day 1 after vaccination in all age groups, and LAIV induced expression of IFN genes on day 7 after vaccination but only in childrentiters.
CONCLUSIONS: These results suggest that LAIV and TIV induced significantly different B-cell responses in vaccinated children. Early induction of IFN appears to be important for development of antibody responses.
J Infect Dis 2014 Jul 15; 210(2):224-33.
Recommended Citation
Cao R,
Suarez N,
Obermoser G,
Lopez S,
Flano E,
Mertz S,
Albrecht R,
García-Sastre A,
Mejias A,
Xu H,
Qin H,
Blankenship D,
Palucka K,
Pascual V,
Ramilo O.
Differences in antibody responses between trivalent inactivated influenza vaccine and live attenuated influenza vaccine correlate with the kinetics and magnitude of interferon signaling in children. J Infect Dis 2014 Jul 15; 210(2):224-33.