AI Article Synopsis

  • The Zika virus outbreak in 2015 led to increased instances of microcephaly in infants and Guillain-Barré Syndrome (GBS) in adults.
  • Research focused on the specificity of antibodies in individuals with Zika-associated GBS, using specially mutated Zika virus particles for analysis.
  • Findings showed that GBS-positive individuals had more stable neutralizing antibodies over time and possibly targeted different virus components compared to GBS-negative individuals.

Article Abstract

The Zika virus (ZIKV) was responsible for a major outbreak in 2015 in the Americas. Infections were associated with increased cases of microcephaly in infants and Guillain-Barré Syndrome (GBS) in adults. Our group previously demonstrated that Zika-associated GBS correlated with the increased neutralization of ZIKV and DENV2, but the antibody specificity was not analyzed. Here, we generated reporter virus particles (RVPs) of ZIKV with specific-point mutations that allowed us to investigate the specificity of circulating plasma antibodies at two different timepoints from individuals with Zika-associated GBS. We found that neutralizing antibody titers to ZIKV waned between one and two years post-ZIKV infection in GBS-negative but not GBS-positive individuals. Interestingly, plasma neutralization by GBS-negative individuals was more sensitive to a mutation at position N154A than plasma from GBS-positive individuals. To determine if waning was associated with different levels of B-cell activation at the time of infection, pro-inflammatory cytokines were measured, but no differences were observed in people with or without GBS. These data suggest subtle differences between GBS-positive and-negative individuals' circulating antibodies, where antibodies from GBS-positive individuals may target different epitopes and remain in circulation longer as compared to GBS-negative individuals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11598927PMC
http://dx.doi.org/10.3390/v16111704DOI Listing

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