The Effect of Age on the B-Cell Repertoire
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.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
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]
The citation lists haven’t been fetched yet
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
- Licence
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review