4.7 Article

Antigenic Maps of Influenza A(H3N2) Produced With Human Antisera Obtained After Primary Infection

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 213, 期 1, 页码 31-38

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiv367

关键词

primary infection; influenza; human antisera; antigenic cartography; antibody landscapes

资金

  1. Medical Research Council UK [MR/K021885/1, MR/K50127X/1]
  2. Homerton College Cambridge
  3. European Union [602525, 602604]
  4. National Institute of Allergy and Infectious Diseases, National Institutes of Health [HHSN272201400008C]
  5. National Institute of Allergy and Infectious Diseases, National Institutes of Health (Centre for Pathogen Evolution)
  6. Medical Research Council [1544100, MR/K021885/1] Funding Source: researchfish
  7. MRC [MR/K021885/1] Funding Source: UKRI

向作者/读者索取更多资源

Antigenic characterization of influenza viruses is typically based on hemagglutination inhibition (HI) assay data for viral isolates tested against strain-specific postinfection ferret antisera. Here, similar virus characterizations were performed using serological data from humans with primary influenza A(H3N2) infection. We screened sera collected between 1995 and 2011 from children between 9 and 24 months of age for influenza virus antibodies, performed HI tests for the positive sera against 23 influenza viruses isolated between 1989 and 2011, and measured HI titers of antisera against influenza A(H3N2) from 24 ferrets against the same panel of viruses. Of the 17 positive human sera, 6 had a high response, showing HI patterns that would be expected from primary infection antisera, while 11 sera had lower, more dispersed patterns of reactivity that are not easily explained. The antigenic map based on the high-response human HI data was similar to the map created using ferret data. Although the overall structure of the ferret and human antigenic maps is similar, local differences in virus positions indicate that the human and ferret immune system might see antigenic properties of viruses differently. Further studies are needed to establish the degree of similarity between serological patterns in ferret and human data.

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