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Somatic mutation of immunoglobulin VH6 genes in human infants
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SUMMARY: Infants respond to antigen by making antibody that is generally of low affinity for antigen. Somatic hypermutation of immunoglobulin genes, and selection of cells expressing mutations with improved affinity for antigen, are the molecular and cellular processes underlying the maturation of antibody affinity. We have reported previously that neonates and infants up to 2 months of age, including individuals undergoing strong immunological challenge, show very few mutated VH6 sequences, with low mutation frequencies in mutated sequences, and little evidence of selection. We have now examined immunoglobulin genes from healthy infants between 2 and 10 months old for mutation and evidence of selection. In this age group, the proportion of VH6 sequences which are mutated and the mutation frequency in mutated sequences increase with age. There is evidence of selection from 6 months old. These results indicate that the process of affinity maturation, which depends on cognate T–B cell interaction and functional germinal centres, is approaching maturity from 6 months old.
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B cells from neonates and infants aged less than 2 months show decreased somatic hypermutation compared with adults, limiting affinity maturation of antibodies.
“B cells from neonates and infants aged less than 2 months show decreased somatic hypermutation compared with adults, limiting affinity maturation of antibodies [37].”
From Evolution of the immune system in humans from infancy to old age (2015) · cites this paper as [37]
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Metadata
- Authors
- Ridings, J., Dinan, L., Williams, R., Roberton, D., & Zola, H.
- Affiliations
- The University of Adelaide (AU)
- Flinders University (AU)
- Corresponding author
- Zola, H
- ORCID
- Venue
- Clinical and Experimental Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 1998-10
- Volume
- 114
- Issue
- 1
- Pages
- 33-39
- ISSN
- 0009-9104 (ISSN-L)
- 1365-2249
- PMC
- PMC1905087
- OpenAlex
- W2032014294
- Cited by
- 53
- References
- 26
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 2 · 2022: 1 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 4 · 2017: 1 · 2016: 3 · 2015: 4 · 2014: 2 · 2013: 4 · 2012: 2
- FWCI
- 0.72
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Clinical & Experimental Immunology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
- Funders
- National Health and Medical Research Council
- National Medical Research Council
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
- Keywords
- somatic hypermutation, immunoglobulin variable heavy chain, affinity maturation, infants, mutation frequency, germinal center, T cell-B cell interaction
- MeSH terms
- Adult, Humans, Immunoglobulin Variable Region, Immunoglobulin alpha-Chains, Immunoglobulin Heavy Chains, Infant, Mutation, Genetic Variation, Complementarity Determining Regions
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