| Literature DB >> 28903503 |
Lindsay Kim1, Brian Rha1, Jon S Abramson2, Larry J Anderson3, Carrie L Byington4, Grace L Chen5, John DeVincenzo6,7,8, Kathryn M Edwards9, Janet A Englund10, Ann R Falsey11, Marie R Griffin12,13,14, Ruth A Karron15, Karen G Martin16,17, H Cody Meissner18, Flor M Munoz19, Andrew T Pavia20, Pedro A Piedra19, William Schaffner21, Eric A F Simões22,23, Rosalyn Singleton24,25, H Keipp Talbot26, Edward E Walsh11, Jane R Zucker27,28, Susan I Gerber1.
Abstract
Respiratory syncytial virus (RSV) causes lower respiratory tract illness frequently. No effective antivirals or vaccines for RSV are approved for use in the United States; however, there are at least 50 vaccines and monoclonal antibody products in development, with those targeting older adults and pregnant women (to protect young infants) in phase 2 and 3 clinical trials. Unanswered questions regarding RSV epidemiology need to be identified and addressed prior to RSV vaccine introduction to guide the measurement of impact and future recommendations. The Centers for Disease Control and Prevention (CDC) convened a technical consultation to gather input from external subject matter experts on their individual perspectives regarding evidence gaps in current RSV epidemiology in the United States, potential studies and surveillance platforms needed to fill these gaps, and prioritizing efforts. Participants articulated their individual views, and CDC staff synthesized individuals' input into this report. Published by Oxford University Press for the Infectious Diseases Society of America 2017. This work is written by (a) US Government employee(s) and is in the public domain in the US.Entities:
Keywords: epidemiology; monoclonal antibody; respiratory syncytial virus; vaccine; vaccine impact
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Year: 2017 PMID: 28903503 PMCID: PMC5850021 DOI: 10.1093/cid/cix432
Source DB: PubMed Journal: Clin Infect Dis ISSN: 1058-4838 Impact factor: 9.079