Tracking antibody profiles for influenza exposures across the lifespan

Seasonal influenza remains a ubiquitous threat to human health. Each infection leaves a mark on a person's immune system, and the accumulation of antibody responses over a lifetime leads to complex individual antibody profiles reflecting past exposures. A growing body of evidence suggests that the order and timing of influenza exposures shape the immune response in ways that may affect morbidity and mortality, particularly when encountering novel (i.e., pandemic or potentially pandemic) strains. But it has not been clear how past exposures to multiple strains vary across individuals and time and determine future infection risk and subsequent immune responses. To address this gap in knowledge, the researchers developed several novel metrics to define the key features of antibody profiles.

Specifically, they characterized antibody profiles at two time points (baseline from 2009 to 2011 and follow-up from 2014 to 2015), roughly four years apart, in a large sample of individuals, aged 2 to 86, in Guangzhou, Guangdong Province, China. They measured immune responses to 21 H3N2 influenza strains that represent the history of H3N2 circulation in humans since its emergence in 1968. Using these metrics, they found that immunity accumulates during the first twenty years of life and then declines until 40 to 50 years of age. These age patterns in antibody profiles are likely driven by continual exposure to influenza and the effects of existing immunity on immune responses to newly encountered strains. In addition, individuals with higher immunity to older, previously exposed strains show increased antibody production to recent strains. According to the authors, this study provides quantitative tools to analyze complex antibody profiles and to improve the understanding of heterogeneity in antibody responses and vaccine efficacy across age groups.

"We found antibody profiles to provide more information than homologous titers in predicting temporal changes in influenza immunity," the authors conclude.