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Limited efficacy of inactivated influenza vaccine in elderly individuals is associated with decreased production of vaccine-specific antibodies
Sanae Sasaki, … , Harry B. Greenberg, Xiao-Song He
Sanae Sasaki, … , Harry B. Greenberg, Xiao-Song He
Published July 25, 2011
Citation Information: J Clin Invest. 2011;121(8):3109-3119. https://doi.org/10.1172/JCI57834.
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Research Article Article has an altmetric score of 34

Limited efficacy of inactivated influenza vaccine in elderly individuals is associated with decreased production of vaccine-specific antibodies

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Abstract

During seasonal influenza epidemics, disease burden is shouldered predominantly by the very young and the elderly. Elderly individuals are particularly affected, in part because vaccine efficacy wanes with age. This has been linked to a reduced ability to induce a robust serum antibody response. Here, we show that this is due to reduced quantities of vaccine-specific antibodies, rather than a lack of antibody avidity or affinity. We measured levels of vaccine-specific plasmablasts by ELISPOT 1 week after immunization of young and elderly adults with inactivated seasonal influenza vaccine. Plasmablast-derived polyclonal antibodies (PPAbs) were generated from bulk-cultured B cells, while recombinant monoclonal antibodies (re-mAbs) were produced from single plasmablasts. The frequency of vaccine-specific plasmablasts and the concentration of PPAbs were lower in the elderly than in young adults, whereas the yields of secreted IgG per plasmablast were not different. Differences were not detected in the overall vaccine-specific avidity or affinity of PPAbs and re-mAbs between the 2 age groups. In contrast, reactivity of the antibodies induced by the inactivated seasonal influenza vaccine toward the 2009 pandemic H1N1 virus, which was not present in the vaccine, was higher in the elderly than in the young. These results indicate that the inferior antibody response to influenza vaccination in the elderly is primarily due to reduced quantities of vaccine-specific antibodies. They also suggest that exposure history affects the cross-reactivity of vaccination-induced antibodies.

Authors

Sanae Sasaki, Meghan Sullivan, Carlos F. Narvaez, Tyson H. Holmes, David Furman, Nai-Ying Zheng, Madhuri Nishtala, Jens Wrammert, Kenneth Smith, Judith A. James, Cornelia L. Dekker, Mark M. Davis, Patrick C. Wilson, Harry B. Greenberg, Xiao-Song He

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Figure 4

Yield of IgG and IgA per ASC in young and aged vaccinees.

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Yield of IgG and IgA per ASC in young and aged vaccinees.
(A) Yield of s...
(A) Yield of secreted Ig was estimated via RMA regression, using the concentration of total IgA or IgG in PPAb (ng/ml) and the total IgA or IgG ASCs in the B cell culture (cell count/ml) for each donor. Fitted RMA regression line is shown for each Ig isotype and age group, along with estimated mean yield per cell and 95% CI. (B) 95% CI of the difference between the estimated mean yield per cell in the 2 age groups. Because the 95% CI for IgG clearly includes 0, no difference in mean yield per cell between groups is indicated. For IgA, since the 95% CI does not include 0, the results suggest that mean yield per cell was significantly greater (P < 0.05) in the elderly. However, given that the lower confidence bound fell just above 0, this finding should be interpreted with some caution.

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

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