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A Method to Assess Fc-mediated Effector Functions Induced by Influenza Hemagglutinin Specific Antibodies
Published on: February 23, 2018
GC B Cells, Tfh Cells, and Influenza bnAbs: Insights for Improving Universal Vaccine Design
Takeshi Inoue1,2, Wataru Ise3,4,5, Tomohiro Kurosaki3,6
1Department of Molecular Systems Immunology, The University of Tokyo Pandemic Preparedness, Infection, and Advanced Research Center (UTOPIA), The University of Tokyo, Tokyo, Japan.
Abstract:
Antibodies are crucial for providing protection against influenza virus infection; however, protective humoral immunity is limited by antigenic drift and shift. Hence, the discovery of broadly neutralizing antibodies (bnAbs) targeting conserved epitopes on hemagglutinin protein evokes the hope of developing a universal influenza vaccine. Because of such historical reasons, much of the effort in universal vaccine design has focused on B cell epitopes. In contrast, despite the critical role of T follicular helper cells in bnAb induction, T cell epitopes have received far less attention. In this review, we summarize the cellular and molecular factors that impact the bnAb development and discuss key limitation factors that restrict their efficient induction.
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