Cited by 205T-cell and B-cell ImmunologyImmunodeficiency and Autoimmune DisordersLymphoma Diagnosis and Treatment

The Effect of Age on the B-Cell Repertoire

Weksler, Marc E., Szabo, Paul·2000·Journal of Clinical Immunology

Abstract

The antibody repertoire changes with age. This change reflects, in part, the age-associated impairment in the production of a diverse population of naive B cells in the bone marrow and, in part, by the decreased diversification of B cells in the germinal center where affinity maturation and isotype switching takes place. B cell number is strictly regulated and despite the decreased output of B cells by the bone marrow does not decline during aging. Self-renewal of peripheral B cells is sufficient to assure the stability of peripheral B cell number. However, when B cell production is stressed as, for example, following drug-induced lymphopenia, the rate of recovery of B cell number as well as of B cell diversity is compromised in old compared to young mice. Finally, aging is associated with the appearance of B cell clonal expansions which not only limit the diversity of the B cell repertoire but very likely give rise to monoclonal serum immunoglobulins and B cell neoplasms.

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Crossref · 10.1023/a:1006659401385

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  • Advancing age is accompanied by profound qualitative changes in the peripheral B cell repertoire with reduced clonotypic diversity and a shift towards autoreactive specificities.

    “Advancing age is accompanied by profound qualitative changes in the peripheral B cell repertoire with reduced clonotypic diversity and a shift towards autoreactive specificities [65 -68].”

    From Is there a role for B cells in Alzheimer's disease? (2026) · cites this paper as [68]

  • During ageing, remodelling of peripheral B cell subsets occurs with a decline in B cell production in the bone marrow and expansion of atypical B cell subsets such as ABCs and DN B cells.

    “During ageing, a remodelling of peripheral B cell subsets occurs with a decline in B cell production in the bone marrow and the expansion of atypical B cell subsets, such as age-associated B cells (ABCs) and double-negative (DN) B cells.”

    From Is there a role for B cells in Alzheimer's disease? (2026) · cites this paper as [68]

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References 45 · Cited by 205

Authors
Weksler, M. E., & Szabo, P.
Affiliations
Cornell University (US)
Venue
Journal of Clinical Immunology
Published
2000-07
Volume
20
Issue
4
Pages
240-249
ISSN
  • 0271-9142 (ISSN-L)
  • 1573-2592
OpenAlex
W1512900561
Cited by
205
References
45
Citations by year
2026: 6 · 2025: 4 · 2024: 3 · 2023: 6 · 2022: 2 · 2021: 7 · 2020: 2 · 2019: 9 · 2018: 4 · 2017: 14 · 2016: 6 · 2015: 6 · 2014: 9 · 2013: 11 · 2012: 15
FWCI
0.64
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Clinical Immunology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5p01ag014669-03)
  • National Institute on Aging (AG-14669)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Lymphoma Diagnosis and Treatment
Keywords
B cell receptor repertoire, aging, naive B cells, bone marrow, germinal center, affinity maturation, class switch recombination, lymphopenia, B cell clonal expansion, M protein, B-cell malignancies, antibody diversity
MeSH terms
Adjuvants, Immunologic, Aged, Aging, Animals, Antibodies, Anti-Idiotypic, Antibody Formation, Antigens, Bacterial, Autoantibodies, Bone Marrow, Cell Division, Clone Cells, Disease Susceptibility, Hematopoiesis, Humans, Lymphopenia, Lymphoproliferative Disorders, Gene Rearrangement, B-Lymphocyte, Autoimmunity, B-Lymphocyte Subsets, Mice, SCID, Lymphocyte Count, Germinal Center, Mice

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