Evidence map›Paper›PMID 2507726›Full record

ArticleThe Journal of experimental medicine1989

Evolution of antibody structure during the immune response. The differentiative potential of a single B lymphocyte.

T Manser

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1989. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Large-scale sequence and structural comparisons of human naive and antigen-experienced antibody repertoires.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  3. Article
  4. Silent development of memory progenitor B cells.Journal of immunology (Baltimore, Md. : 1950) · 2007
    Article
  5. Article
  6. A role for RAD51 in the generation of immunoglobulin gene diversity in rabbits.Journal of immunology (Baltimore, Md. : 1950) · 1999
    Article
  7. Homing behaviour of the malignant cell clone in multiple myeloma.Medical oncology (Northwood, London, England) · 1998
    Review
  8. The promotion of V region hypermutation.The Journal of experimental medicine · 1997
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Somatic recombination of heavy chain variable region transgenes with the endogenous immunoglobulin heavy chain locus in mice.Proceedings of the National Academy of Sciences of the United States of America · 1992
    Article
  20. Sequencing heavy- and light-chain variable genes of single B-hybridoma cells by total enzymatic amplification.Proceedings of the National Academy of Sciences of the United States of America · 1992
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

T ManserDepartment of Biology, Princeton University, New Jersey 08544.
Princeton University · US

Funding

EXPRESSION OF ANTIBODY DIVERSITY DURING IMMUNE RESPONSESR01AI023739 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI MANSER, TIMOTHY L · 1986 to 2001
$481k
NIAID NIH HHS AI-23739
6 · The paper itself

Abstract

Changes in the structure and function of antibodies occur during the course of an immune response due to variable (V) region gene somatic mutation and isotype switch recombination. While the end products of both these processes are now well documented, their mechanisms, timing, and regulation during clonal expansion remain unclear. Here I describe the characterization of antibodies expressed by a large number of hybridomas derived from single B cell clones at an intermediate stage of an immune response. These data provide new insights into the mechanism, relative timing, and potential of V gene mutation and isotype switching. The data suggest that somatic mutation and isotype switching are completely independent processes that may, but need not, occur simultaneously during clonal expansion. In addition, the results of this analysis demonstrate that individual B cell clones are far more efficient than previously imagined at generating and fixing particular V region somatic mutations that result in increased affinity for the eliciting epitope. Models to account for this high efficiency are discussed. Taken together with previous data, the results of this analysis also suggest that the "somatic evolution" of V region structure to a single epitope takes place in two stages; the first in which particular mutations are sustained and fixed by antigen selection in the CDR regions of the V region genes expressed in a clone over a short period of clonal expansion, and the second in which these selected CDR mutations are maintained in the growing clone, deleterious mutations are lost, and selectively neutral mutations accumulate throughout the length of V genes over long periods of clonal expansion.

Indexed as

Antibody DiversityAntibody FormationGenes, ImmunoglobulinAmino Acid SequenceAnimalsAntibodies, MonoclonalAntibody AffinityBase SequenceB-LymphocytesCell DifferentiationGene Rearrangement, B-LymphocyteGenes, SwitchImmunoglobulin Heavy ChainsImmunoglobulin IsotypesImmunoglobulin Light ChainsImmunoglobulin Variable RegionAntibodies, MonoclonalImmunoglobulin Heavy ChainsImmunoglobulin IsotypesImmunoglobulin Light ChainsImmunoglobulin Variable Regionp-Azobenzenearsonate

Identifiers

PMID2507726
PMCPMC2189475
OpenAlexW2109661366

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.