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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.
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.
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