Functional Immune Cell Differences Associated With Low Vaccine Responses in Infants

Michael E Pichichero1, Janet R Casey2, Anthony Almudevar3

  • 1Center for Infectious Disease and Vaccine Immunology, Research Institute, Rochester General Hospital.

Insights

Eleven percent of infants show poor vaccine responses due to a distinct immunologic profile. Low vaccine responders had fewer memory B cells and reduced T-cell activation, impacting antibody levels.

Area of Science:

  • Immunology
  • Pediatrics
  • Vaccinology

Background:

  • Understanding infant immune responses to vaccination is crucial for public health.
  • Some children exhibit suboptimal antibody levels after routine immunizations.

Purpose of the Study:

  • To investigate the immunological factors associated with poor vaccine responses in young children.
  • To identify distinct immune profiles in low vaccine responders.

Main Methods:

  • Serum and peripheral blood mononuclear cells were collected from 499 children (6-36 months) post-vaccination.
  • Enzyme-linked immunosorbent assay measured antibody levels; flow cytometry assessed B cell, T cell, and antigen-presenting cell responses.

Main Results:

  • Eleven percent of children were classified as low vaccine responders (subprotective IgG to ≥66% of vaccines).
  • Low responders exhibited reduced memory B cell generation and impaired CD4(+) and CD8(+) T cell activation.
  • Antigen-presenting cells in low responders showed lower major histocompatibility complex II expression.

Conclusions:

  • Suboptimal vaccine responses in infants are linked to a specific immunological signature.
  • This profile involves deficiencies in B cell memory, T cell function, and antigen presentation.
  • Further research may elucidate targeted strategies to improve infant vaccine efficacy.
Abstract

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