Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Mar 4;14(3):571-578.
doi: 10.1080/21645515.2017.1377376. Epub 2018 Jan 3.

Immune responses after live attenuated influenza vaccination

Affiliations
Review

Immune responses after live attenuated influenza vaccination

Kristin G-I Mohn et al. Hum Vaccin Immunother. .

Abstract

Since 2003 (US) and 2012 (Europe) the live attenuated influenza vaccine (LAIV) has been used as an alternative to the traditional inactivated influenza vaccines (IIV). The immune responses elicted by LAIV mimic natural infection and have been found to provide broader clinical protection in children compared to the IIVs. However, our knowledge of the detailed immunological mechanisims induced by LAIV remain to be fully elucidated, and despite 14 years on the global market, there exists no correlate of protection. Recently, matters are further complicated by differing efficacy data from the US and Europe which are not understood. Better understanding of the immune responses after LAIV may aid in achieving the ultimate goal of a future "universal influenza vaccine". In this review we aim to cover the current understanding of the immune responses induced after LAIV.

Keywords: Antibody; T-cell; immune response; live attenuated influenza vaccine (LAIV).

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
A suggested working model of how live attenuated influenza vaccine (LAIV) elicits immune response. The numbers in the figure refer to 1. adminstration of the LAIV intranasally as a nasal spray; 2. Limited virus replication (IFN-γ) by LAIV; 3. Viral influenza antigen is transported to the tonsils by dendritic cells (DCs); 4. Activation and proliferation of T cells (IL-2); 5. Activation and proliferation of B cells, affinity maturation and isotype switching; 6. Activated B and T cells homes to site of infection (vaccination); 7. Plasma cells secrete specific mucosal antibodies and 8. Plasma cells secrete specific antibodies into circulation. Adapted from.

Similar articles

Cited by

References

    1. WHO Fact sheet about seasonal influenza. 2017. http://www.who.int/mediacentre/factsheets/fs211/en/
    1. Stohr K. Influenza–WHO cares. Lancet Infect Dis. 2002;2:517. doi:10.1016/S1473-3099(02)00366-3. PMID:12206966. - DOI - PubMed
    1. Thompson WW, Shay DK, Weintraub E, et al.. Influenza-associated hospitalizations in the United States. JAMA. 2004;292:1333-40. doi:10.1001/jama.292.11.1333. PMID:15367555. - DOI - PubMed
    1. Molinari NA, Ortega-Sanchez IR, Messonnier ML, et al.. The annual impact of seasonal influenza in the US: Measuring disease burden and costs. Vaccine. 2007;25:5086-96. doi:10.1016/j.vaccine.2007.03.046. PMID:17544181. - DOI - PubMed
    1. WHO Vaccines against influenza WHo position paper – November 2012. Weekly Epidemiological Record. 2012;87(47):461-476. PMID:23210147. - PubMed

Publication types

MeSH terms