Quick Search:

Serological correlate of protection against norovirus-induced gastroenteritis.

Reeck, Amanda, Kavanagh, Owen ORCID logoORCID: https://orcid.org/0000-0002-2599-8511, Estes, Mary K, Opekun, Antone R, Gilger, Mark A, Graham, David Y and Atmar, Robert L (2010) Serological correlate of protection against norovirus-induced gastroenteritis. The Journal of infectious diseases, 202 (8). pp. 1212-8.

Full text not available from this repository.

Abstract

BACKGROUND

Norovirus infection is the leading cause of acute nonbacterial gastroenteritis. Histoblood group antigens (HBGAs) are host susceptibility determinants for Norwalk virus (NV) infection. We hypothesized that antibodies that block NV-HBGA binding are associated with protection from clinical illness following NV exposure.

METHODS

We developed an HBGA blocking assay to examine the ability of human serum to block the interaction of NV viruslike particles with H type 1 and H type 3 glycans. Serum samples from persons who were experimentally challenged with NV were evaluated.

RESULTS

There was a high correlation between the H type 1 and H type 3 synthetic glycan assays (r = 0.977; P < .001); the H type 1 assay had higher quantitative sensitivity (P < .001). Among 18 infected secretor-positive individuals, blocking titers peaked by day 28 after challenge and were higher for individuals who did not develop gastroenteritis than for those who developed gastroenteritis on days 0, 14, 28, and 180 (P < .05 for each). In addition, 6 of 6 subjects without gastroenteritis had measurable prechallenge blocking titers (>25), compared with 2 of 12 subjects with gastroenteritis (P = .002).

CONCLUSIONS

Blocking antibodies correlate with protection against clinical NV gastroenteritis. This knowledge will help guide the evaluation of new vaccine strategies and the elucidation of the nature of immunity to the virus. Trial registration. ClinicalTrials.gov identifier: NCT00138476.

Item Type: Article
Status: Published
DOI: 10.1086/656364
Subjects: Q Science > QR Microbiology > QR180 Immunology
Q Science > QR Microbiology > QR355 Virology
R Medicine > RM Therapeutics. Pharmacology
School/Department: School of Science, Technology and Health
URI: https://ray.yorksj.ac.uk/id/eprint/864

University Staff: Request a correction | RaY Editors: Update this record