The Quest for a Truly Universal Influenza Vaccine

There is an unmet public health need for a universal influenza vaccine (UIV) to provide broad and durable protection from influenza virus infections. The identification of broadly protective antibodies and cross-reactive T cells directed to influenza viral targets present a promising prospect for th...

Full description

Bibliographic Details
Main Authors: Yo Han Jang, Baik Lin Seong
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-10-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
M2e
Online Access:https://www.frontiersin.org/article/10.3389/fcimb.2019.00344/full
id doaj-f67d2c00cb3744aab61ff7cd694c18d2
record_format Article
spelling doaj-f67d2c00cb3744aab61ff7cd694c18d22020-11-24T23:59:51ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882019-10-01910.3389/fcimb.2019.00344474292The Quest for a Truly Universal Influenza VaccineYo Han Jang0Baik Lin Seong1Baik Lin Seong2Molecular Medicine Laboratory, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, South KoreaMolecular Medicine Laboratory, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, South KoreaVaccine Translational Research Center, Yonsei University, Seoul, South KoreaThere is an unmet public health need for a universal influenza vaccine (UIV) to provide broad and durable protection from influenza virus infections. The identification of broadly protective antibodies and cross-reactive T cells directed to influenza viral targets present a promising prospect for the development of a UIV. Multiple targets for cross-protection have been identified in the stalk and head of hemagglutinin (HA) to develop a UIV. Recently, neuraminidase (NA) has received significant attention as a critical component for increasing the breadth of protection. The HA stalk-based approaches have shown promising results of broader protection in animal studies, and their feasibility in humans are being evaluated in clinical trials. Mucosal immune responses and cross-reactive T cell immunity across influenza A and B viruses intrinsic to live attenuated influenza vaccine (LAIV) have emerged as essential features to be incorporated into a UIV. Complementing the weakness of the stand-alone approaches, prime-boost vaccination combining HA stalk, and LAIV is under clinical evaluation, with the aim to increase the efficacy and broaden the spectrum of protection. Preexisting immunity in humans established by prior exposure to influenza viruses may affect the hierarchy and magnitude of immune responses elicited by an influenza vaccine, limiting the interpretation of preclinical data based on naive animals, necessitating human challenge studies. A consensus is yet to be achieved on the spectrum of protection, efficacy, target population, and duration of protection to define a “universal” vaccine. This review discusses the recent advancements in the development of UIVs, rationales behind cross-protection and vaccine designs, and challenges faced in obtaining balanced protection potency, a wide spectrum of protection, and safety relevant to UIVs.https://www.frontiersin.org/article/10.3389/fcimb.2019.00344/fullinfluenza virusuniversal influenza vaccinecross-protectionHA stalkM2eT cell
collection DOAJ
language English
format Article
sources DOAJ
author Yo Han Jang
Baik Lin Seong
Baik Lin Seong
spellingShingle Yo Han Jang
Baik Lin Seong
Baik Lin Seong
The Quest for a Truly Universal Influenza Vaccine
Frontiers in Cellular and Infection Microbiology
influenza virus
universal influenza vaccine
cross-protection
HA stalk
M2e
T cell
author_facet Yo Han Jang
Baik Lin Seong
Baik Lin Seong
author_sort Yo Han Jang
title The Quest for a Truly Universal Influenza Vaccine
title_short The Quest for a Truly Universal Influenza Vaccine
title_full The Quest for a Truly Universal Influenza Vaccine
title_fullStr The Quest for a Truly Universal Influenza Vaccine
title_full_unstemmed The Quest for a Truly Universal Influenza Vaccine
title_sort quest for a truly universal influenza vaccine
publisher Frontiers Media S.A.
series Frontiers in Cellular and Infection Microbiology
issn 2235-2988
publishDate 2019-10-01
description There is an unmet public health need for a universal influenza vaccine (UIV) to provide broad and durable protection from influenza virus infections. The identification of broadly protective antibodies and cross-reactive T cells directed to influenza viral targets present a promising prospect for the development of a UIV. Multiple targets for cross-protection have been identified in the stalk and head of hemagglutinin (HA) to develop a UIV. Recently, neuraminidase (NA) has received significant attention as a critical component for increasing the breadth of protection. The HA stalk-based approaches have shown promising results of broader protection in animal studies, and their feasibility in humans are being evaluated in clinical trials. Mucosal immune responses and cross-reactive T cell immunity across influenza A and B viruses intrinsic to live attenuated influenza vaccine (LAIV) have emerged as essential features to be incorporated into a UIV. Complementing the weakness of the stand-alone approaches, prime-boost vaccination combining HA stalk, and LAIV is under clinical evaluation, with the aim to increase the efficacy and broaden the spectrum of protection. Preexisting immunity in humans established by prior exposure to influenza viruses may affect the hierarchy and magnitude of immune responses elicited by an influenza vaccine, limiting the interpretation of preclinical data based on naive animals, necessitating human challenge studies. A consensus is yet to be achieved on the spectrum of protection, efficacy, target population, and duration of protection to define a “universal” vaccine. This review discusses the recent advancements in the development of UIVs, rationales behind cross-protection and vaccine designs, and challenges faced in obtaining balanced protection potency, a wide spectrum of protection, and safety relevant to UIVs.
topic influenza virus
universal influenza vaccine
cross-protection
HA stalk
M2e
T cell
url https://www.frontiersin.org/article/10.3389/fcimb.2019.00344/full
work_keys_str_mv AT yohanjang thequestforatrulyuniversalinfluenzavaccine
AT baiklinseong thequestforatrulyuniversalinfluenzavaccine
AT baiklinseong thequestforatrulyuniversalinfluenzavaccine
AT yohanjang questforatrulyuniversalinfluenzavaccine
AT baiklinseong questforatrulyuniversalinfluenzavaccine
AT baiklinseong questforatrulyuniversalinfluenzavaccine
_version_ 1725445888408551424