Influenza vaccines are updated regularly to provide protection against circulating strains, but responses to vaccination can vary between individuals.

H5N1_Avian_Influenza_A_Virus

Source: NIAID

Colorized transmission electron micrograph of avian influenza A H5N1 virus particles (green), grown in Madin-Darby Canine Kidney (MDCK) epithelial cells.

Previous exposure to influenza viruses and vaccines can leave behind pre-existing antibodies, which may influence how the immune system responds to later vaccination. However, how these antibodies are associated with subsequent B-cell responses remains incompletely understood.

B-cell responses to vaccination

In a study published in Virologica Sinica, a team of researchers followed 21 adults before and after seasonal influenza vaccination. Using flow cytometry, B-cell receptor sequencing, and monoclonal antibody characterization, they examined how baseline antibody levels were associated with B-cell responses after vaccination.

The study improves understanding of how pre-existing immunity relates to vaccine-induced immune responses and may provide insights for future influenza vaccine development.

“We found that individuals with different pre-vaccination antibody levels showed distinct patterns of HA-binding B-cell responses,” shares senior and co-corresponding Yong Gao. “Participants with higher baseline antibody titers showed increased frequencies of HA⁺CD27⁻IgD⁺ naive-phenotype B cells and B-cell receptor features associated with less maturation.”

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In contrast, B-cell receptors and antibodies from lower-titer groups showed greater mutation levels, broader class switching, and broader neutralizing activity against historical influenza strains.

“Our findings highlight that pre-existing antibody levels are associated with different patterns of B-cell maturation and antibody breadth following influenza vaccination,” Gao says.