4.7 Article

Genotype-specific features reduce the susceptibility of South American yellow fever virus strains to vaccine-induced antibodies

Journal

CELL HOST & MICROBE
Volume 30, Issue 2, Pages 248-+

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2021.12.009

Keywords

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Funding

  1. U.S. National Institutes of Health [R01AI132633, 440865/2016-6]
  2. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [312446/2018]
  3. CNPq fellowship for Productivity in Technological Development and Innovative Extension [309471/2016-8]
  4. Leukemia Research Foundation (Hollis Brownstein New Investigator Research Grant)
  5. AFAR
  6. NIH Office of the Director [1S10OD030286-01]
  7. NIH [2T32GM0 07288-45]
  8. Coordenacao de Aperfeicoamento de Pessoal de Ni'vel Superior Brasil (CAPES)
  9. (Medical Scientist Training Program) at Albert Einstein College of Medicine
  10. Deerfield (Xseed award)

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The reduced sensitivity of an emergent Brazilian strain of yellow fever virus to antibodies induced by current vaccines calls for a reevaluation of immunological surveillance and suggests the need for updating vaccines in South America.
The resurgence of yellow fever in South America has prompted vaccination against the etiologic agent, yellow fever virus (YFV). Current vaccines are based on a live-attenuated YF-17D virus derived from a virulent African isolate. The capacity of these vaccines to induce neutralizing antibodies against the vaccine strain is used as a surrogate for protection. However, the sensitivity of genetically distinct South American strains to vaccine induced antibodies is unknown. We show that antiviral potency of the polyclonal antibody response in vaccinees is attenuated against an emergent Brazilian strain. This reduction was attributable to amino acid changes at two sites in central domain II of the glycoprotein E, including multiple changes at the domain I-domain II hinge, which are unique to and shared among most South American YFV strains. Our findings call for a reevaluation of current approaches to YFV immunological surveillance in South America and suggest approaches for updating vaccines.

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