Chimeric hemagglutinin vaccine elicits broadly protective CD4 and CD8 T cell responses against multiple influenza strains and subtypes
Author(s) -
Hsin-Yu Liao,
Shih-Chi Wang,
YiAn Ko,
KuoI Lin,
Che Ma,
Ting-Jen Rachel Cheng,
ChiHuey Wong
Publication year - 2020
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2004783117
Subject(s) - virology , hemagglutinin (influenza) , influenza a virus subtype h5n1 , biology , immunization , influenza vaccine , immunity , pandemic , antibody , vaccination , virus , immunology , immune system , covid-19 , medicine , disease , infectious disease (medical specialty) , pathology
Significance Pandemic influenza continues to threaten public health across the world. Cross-species transmission of avian H5N1, H7N9, and H10N8 subtypes represent a potential threat to human as the viruses may acquire the ability to pass efficiently from human to human. In order to develop an effective influenza vaccine with protective immunity against a broad range of human and avian influenza viruses, we generated a monoglycosylated consensus cHA (cHAmg ) from human H1N1 and avian H5N1 HAs. After immunization with the monoglycosylated consensus cHA vaccine, mice were found to generate a high level of antibodies with broader cross-reactive neutralizing activities, higher ADCC responses, and more memory CD8+ T cell response. This strategy may facilitate the development of a universal vaccine against influenza viruses.
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