4.7 Article

An Egg-Derived Sulfated N-Acetyllactosamine Glycan Is an Antigenic Decoy of Influenza Virus Vaccines

Journal

MBIO
Volume 12, Issue 3, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/mBio.00838-21

Keywords

LacNAc; anti-glycan antibodies; antibody repertoire; influenza vaccines; vaccine platform

Categories

Funding

  1. National Institute of Allergy and Infectious Diseases through National Institutes of Health [U19AI082724, U19AI109946, U19AI057266, P01 AI097092, R01AI145870-01]
  2. NIAID Centers of Excellence for Influenza Research and Surveillance (CEIRS) [HHSN272201400005C, HHSN272201400008C]
  3. National Institute of Allergy and Infectious Diseases (NIAID) Collaborative Influenza Vaccine Innovation Centers (CIVIC) [75N93019C00051]
  4. National Center for Functional Glycomics (NCFG) at Beth Israel Deaconess Medical Center, Harvard Medical School [R24 GM137763]

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Seasonal influenza virus vaccines produced in eggs can induce antibody responses against egg-associated antigens, which have specific antibody features and may impact the host immune response.
Influenza viruses grown in eggs for the purposes of vaccine generation often acquire mutations during egg adaptation or possess different glycosylation patterns than viruses circulating among humans. Here, we report that seasonal influenza virus vaccines possess an egg-derived glycan that is an antigenic decoy, with eggbinding MAbs reacting with a sulfated N-acetyllactosamine (LacNAc). Half of subjects that received an egg-grown vaccine mounted an antibody response against this eggderived antigen. Egg-binding monoclonal antibodies specifically bind viruses grown in eggs, but not viruses grown in other chicken-derived cells, suggesting that only egggrown vaccines can induce antiegg antibodies. Notably, antibodies against the egg antigen utilized a restricted antibody repertoire and possessed features of natural antibodies, as most antibodies were IgM and had a simple heavy-chain complementaritydetermining region 3. By analyzing a public data set of influenza virus vaccine-induced plasmablasts, we discovered egg-binding public clonotypes that were shared across studies. Together, this study shows that egg-grown vaccines can induce antibodies against an egg-associated glycan, which may divert the host immune response away from protective epitopes.

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