Cited by 53T-cell and B-cell ImmunologyMonoclonal and Polyclonal Antibodies ResearchImmunodeficiency and Autoimmune Disorders

The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.

Somatic mutation of immunoglobulin VH6 genes in human infants

Open access
Ridings, J, Dinan, L, Williams, R, Roberton, D, Zola, H·2001·Clinical and Experimental Immunology

Abstract

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.

Overview

Integrity signals

Registry

Crossref · 10.1046/j.1365-2249.1998.00694.x

Cites

26 of 26 references verified0 citation errors · 0 not checkable

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Claims the paper makes

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Claims other papers make about this one

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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].”

Citations

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Research works printed but not linked: 2

  1. Rijkers GT, 1993, Immunodeficiency, 5, 1
  2. 23 M Kaartinen, S Kulp, and O Makela . Characteristics of selection-free mutations and effects of subsequent selection. In: Steele EJ, ed. Somatic mutations in V-regions. Boca Raton: CRC Press, 1991 :105, 14 .

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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
Venue
Clinical and Experimental Immunology
Published
1998-10
Volume
114
Issue
1
Pages
33-39
ISSN
  • 0009-9104 (ISSN-L)
  • 1365-2249
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
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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