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• W2991526660 abstract "The pneumoviruses respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) are two widespread human pathogens that can cause severe disease in the young, the elderly, and the immunocompromised. Despite the discovery of RSV over sixty years ago, and hMPV nearly 20 years ago, there are no approved vaccines for either virus. Antibody-mediated immunity is critical for RSV and hMPV, and, until recently, knowledge of the antibody epitopes on the surface glycoproteins of RSV and hMPV was very limited. However, recent breakthroughs in the recombinant expression and stabilization of pneumovirus fusion proteins have facilitated in-depth characterization of antibody responses and structural epitopes, and have provided an enormous diversity of new monoclonal antibody candidates for therapeutic development. These new data have primarily focused on the RSV F protein, and have led to a wealth of new vaccine candidates in preclinical and clinical trials. In contrast, the major structural antibody epitopes remain unclear for the hMPV F protein. Overall, this review will cover recent advances in characterizing the antigenic sites on the RSV and hMPV F proteins." @default.
• W2991526660 created "2019-12-05" @default.
• W2991526660 creator A5002706508 @default.
• W2991526660 creator A5029400285 @default.
• W2991526660 creator A5042643001 @default.
• W2991526660 date "2019-11-29" @default.
• W2991526660 modified "2023-09-28" @default.
• W2991526660 title "Antibody Epitopes of Pneumovirus Fusion Proteins" @default.
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• W2991526660 doi "https://doi.org/10.3389/fimmu.2019.02778" @default.
• W2991526660 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6895023" @default.
• W2991526660 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31849961" @default.
• W2991526660 hasPublicationYear "2019" @default.
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