AI Article Synopsis

  • The live attenuated virus vaccine Dengvaxia has led to interest in subunit vaccines, particularly targeting nonstructural protein 1 (NS1), but recent studies show NS1 may not provide protection against high-virulence dengue strains in mouse models.
  • Findings suggest that the role of NS1 in disease varies by dengue virus strains, indicating the need to reconsider NS1's viability as a universal vaccine candidate.

Article Abstract

Dengue is a major public health concern in the tropical and subtropical world, with no effective treatment. The controversial live attenuated virus vaccine Dengvaxia has boosted the pursuit of subunit vaccine approaches, and nonstructural protein 1 (NS1) has recently emerged as a promising candidate. However, we found that NS1 immunization or passive transfer of NS1 antibodies failed to confer protection in symptomatic dengue mouse models using two non-mouse-adapted DENV2 strains that are highly virulent. Exogenous administration of purified NS1 also failed to worsen in vivo vascular leakage in sublethally infected mice. Neither method of NS1 immune neutralization changed the disease outcome of a chimeric strain expressing a vascular leak-potent NS1. Instead, virus chimerization involving the prME structural region indicated that these proteins play a critical role in driving in vivo fitness and virulence of the virus, through induction of key proinflammatory cytokines. This work highlights that the pathogenic role of NS1 is DENV strain dependent, which warrants reevaluation of NS1 as a universal dengue vaccine candidate.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478733PMC
http://dx.doi.org/10.1084/jem.20191548DOI Listing

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