AI Article Synopsis

  • Several studies highlight that the initial exposure to the influenza virus significantly influences the body's immune response to subsequent infections or vaccines.
  • Research on the antibody response immediately following primary influenza infection is limited, especially in humans, prompting a study using H1N1-infected macaques to analyze specific antibody responses.
  • The findings indicate that HA-stem antibodies are produced early but decrease rapidly, while HA-head antibodies are generated later and have a stronger tendency to mature and improve their effectiveness over time.

Article Abstract

Several studies have shown that the first encounter with influenza virus shapes the immune response to future infections or vaccinations. However, a detailed analysis of the primary antibody response is lacking as this is difficult to study in humans. It is therefore not known what the frequency and dynamics of the strain-specific hemagglutinin (HA) head- and stem-directed antibody responses are directly after primary influenza virus infection. Here, sera of twelve H1N1 influenza virus-infected cynomolgus macaques were evaluated for HA-head and HA-stem domain antibody responses. We observed an early induction of HA-stem antibody responses, which was already decreased by day 56. In contrast, responses against the HA-head domain were low early after infection and increased at later timepoint. The HA-specific B cell repertoires in each animal showed diverse VH-gene usage with preferred VH-gene and JH-gene family usage for HA-head or HA-stem B cells but a highly diverse allelic variation within the VH-usage. HA-head B cells had shorter CDRH3s and higher VH-gene somatic hyper mutation levels relative to HA-stem B cells. In conclusion, our data suggest that HA-stem antibodies are the first to react to the infection while HA-head antibodies show a delayed response, but a greater propensity to enter the germinal center and undergo affinity maturation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9670313PMC
http://dx.doi.org/10.3389/fimmu.2022.1026951DOI Listing

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