Ontology highlight
ABSTRACT: Background
Development of high avidity, broadly neutralizing antibodies (Abs) is a priority after vaccination against rapidly evolving, widely disseminated viruses like human norovirus. After vaccination with a multivalent GI.1 and GII.4c norovirus virus-like particle (VLP) vaccine candidate adjuvanted with alum and monophosphoryl lipid A (MPL), blockade Ab titers peaked early, with no increase in titer following a second vaccine dose.Methods
Blockade Ab relative avidity was evaluated by measuring the slope of blockade Ab neutralization curves.Results
Blockade Ab avidity to the GI.1 vaccine component peaked at day 35 (7 days after dose 2). Avidities to heterotypic genogroup I VLPs were not sustained at day 35 after vaccination or GI.1 infection, as measured from archived sera. Only secretor-positive participants maintained high avidity blockade Ab to GI.1 at day 180. Avidity to the GII.4c vaccine component peaked at day 7, remained elevated through day 180, and was not secretor dependent. Avidity to an immunologically novel GII.4 strain VLP correlated with preexisting Ab titer to an ancestral strain Epitope A.Conclusions
Host genetics and pre-exposure history shape norovirus vaccine Ab responses, including blockade Ab avidity. Avidity of potentially neutralizing Ab may be an important metric for evaluating vaccine responses to highly penetrant viruses with cross-reactive serotypes.
SUBMITTER: Lindesmith LC
PROVIDER: S-EPMC5853323 | biostudies-literature | 2017 Mar
REPOSITORIES: biostudies-literature
Lindesmith Lisa C LC Mallory Michael L ML Jones Taylor A TA Richardson Charles C Goodwin Robert R RR Baehner Frank F Mendelman Paul M PM Bargatze Robert F RF Baric Ralph S RS
The Journal of infectious diseases 20170301 6
<h4>Background</h4>Development of high avidity, broadly neutralizing antibodies (Abs) is a priority after vaccination against rapidly evolving, widely disseminated viruses like human norovirus. After vaccination with a multivalent GI.1 and GII.4c norovirus virus-like particle (VLP) vaccine candidate adjuvanted with alum and monophosphoryl lipid A (MPL), blockade Ab titers peaked early, with no increase in titer following a second vaccine dose.<h4>Methods</h4>Blockade Ab relative avidity was eval ...[more]