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Influenza vaccination in the elderly boosts antibodies against conserved viral proteins and egg-produced glycans
Jiwon Jung, … , Jiwon Lee, George Georgiou
Jiwon Jung, … , Jiwon Lee, George Georgiou
Published July 1, 2021
Citation Information: J Clin Invest. 2021;131(13):e148763. https://doi.org/10.1172/JCI148763.
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Research Article Infectious disease

Influenza vaccination in the elderly boosts antibodies against conserved viral proteins and egg-produced glycans

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Abstract

Seasonal influenza vaccination elicits a diminished adaptive immune response in the elderly, and the mechanisms of immunosenescence are not fully understood. Using Ig-Seq, we found a marked increase with age in the prevalence of cross-reactive (CR) serum antibodies that recognize both the H1N1 (vaccine-H1) and H3N2 (vaccine-H3) components of an egg-produced split influenza vaccine. CR antibodies accounted for 73% ± 18% of the serum vaccine responses in a cohort of elderly donors, 65% ± 15% in late middle-aged donors, and only 13% ± 5% in persons under 35 years of age. The antibody response to non-HA antigens was boosted by vaccination. Recombinant expression of 19 vaccine-H1+H3 CR serum monoclonal antibodies (s-mAbs) revealed that they predominantly bound to non-HA influenza proteins. A sizable fraction of vaccine-H1+H3 CR s-mAbs recognized with high affinity the sulfated glycans, in particular sulfated type 2 N-acetyllactosamine (Galβ1-4GalNAcβ), which is found on egg-produced proteins and thus unlikely to contribute to protection against influenza infection in humans. Antibodies against sulfated glycans in egg-produced vaccine had been identified in animals but were not previously characterized in humans. Collectively, our results provide a quantitative basis for how repeated exposure to split influenza vaccine correlates with unintended focusing of serum antibody responses to non-HA antigens that may result in suboptimal immunity against influenza.

Authors

Jiwon Jung, Sophia T. Mundle, Irina V. Ustyugova, Andrew P. Horton, Daniel R. Boutz, Svetlana Pougatcheva, Ponraj Prabakaran, Jonathan R. McDaniel, Gregory R. King, Daechan Park, Maria D. Person, Congxi Ye, Bing Tan, Yuri Tanno, Jin Eyun Kim, Nicholas C. Curtis, Joshua DiNapoli, Simon Delagrave, Ted M. Ross, Gregory C. Ippolito, Harry Kleanthous, Jiwon Lee, George Georgiou

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Figure 2

Age-dependent increase in the vaccine-H1+H3 CR serological repertoire.

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Age-dependent increase in the vaccine-H1+H3 CR serological repertoire.
(...
(A) Clonal composition of the anti–vaccine-H1 serum antibody repertoire (rep.) in a representative young donor and a representative elderly donor. Vaccine-H1+H3 CR: antibody clonotypes were detected in both the anti–vaccine-H1 and anti–vaccine-H3 repertoires. Vaccine-H1 specific: antibody clonotypes were detected only in the anti–vaccine-H1 repertoire. (B) Vaccine-H1+H3 CR and monovalent vaccine-specific serum response in all donors. Inner wheel: percentage of the serum repertoire of vaccine-H1+H3 CR (green) and vaccine-H1 specific-antibody clonotypes (blue) or vaccine-H3 specific-antibody clonotypes (orange). Outer wheel: relative abundance of each clonotype estimated from the LC-MS/MS peak area. (C) Scatter plot showing Spearman’s correlation coefficient (and 95% CI of the regression line) between the fraction of the vaccine-H1+H3 CR serum repertoire and age.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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