Evidence map›Paper›PMID 10051629›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Predominant VH genes expressed in innate antibodies are associated with distinctive antigen-binding sites.

K J Seidl, J A Wilshire, J D MacKenzie, A B Kantor, L A Herzenberg, L A Herzenberg

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

19 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. T-betJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  4. Article
  5. Article
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  7. Article
  8. A Hard(y) Look at B-1 Cell Development and Function.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Selection of individual VH genes occurs at the pro-B to pre-B cell transition.Journal of immunology (Baltimore, Md. : 1950) · 2011
    Article
  15. Progenitor cell origin plays a role in fate choices of mature B cells.Journal of immunology (Baltimore, Md. : 1950) · 2010
    Article
  16. Article
  17. Article
  18. Review
  19. 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

6 authors at 1 institution in 1 country.

K J SeidlDepartment of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
J A Wilshire
J D MacKenzie
A B Kantor
L A Herzenberg
L A Herzenberg
Stanford University · US

Funding

GENETICS OF IMMUNOGLOBULINS AND LYMPHOCYTE MOLECULESR35CA042509 · NCI · STANFORD UNIVERSITY · PI HERZENBERG, LEONARD A · 1986 to 2000
$71k
FETAL-MATERNAL IMMUNOLOGICAL INTERACTIONSR01AI034762 · NIAID · STANFORD UNIVERSITY · PI HERZENBERG, LEONORE A. · 1993 to 1997
–
GENETICS TRAINING PROGRAM FOR PHD CANDIDATEST32EY007106 · NEI · STANFORD UNIVERSITY · PI BOTSTEIN, DAVID · 1988 to 1999
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NCI NIH HHS CA 42509NEI NIH HHS EY 07106NEI NIH HHS T32 EY007106NIAID NIH HHS AI 34762
6 · The paper itself

Abstract

Antibodies to phosphatidylcholine (PtC), a common constituent of mammalian and bacterial cell membranes, represent a large proportion of the natural antibody repertoire in mice. Previous studies of several mouse strains (e.g., C57BL/6) have shown that anti-PtC antibodies are mainly encoded by the VH11 and VH12 immunoglobulin heavy chain variable region gene families. We show here, however, that VH11 and VH12 encode only a small proportion of the anti-PtC antibodies in BALB/c mice. Instead, VHQ52-encoded antibodies predominate in this strain. In addition, two-thirds of the cells expressing VHQ52 family genes use a single gene (which, interestingly, has been previously shown to predominate in the anti-oxazolone response). We also show here that in anti-PtC antibodies from all strains, the distinctive antigen-binding sites associated with VHQ52 differ substantially from those associated with VH11 and VH12. That is, VHQ52-containing transcripts preferentially use the joining region JH4 rather than JH1 and exhibit more diverse complementarity-determining region 3 (CDR3) junctions with more N-region nucleotide additions at the gene segment junctions. Thus, the VH gene family that predominates in the anti-PtC repertoire differs among mouse strains, whereas the distinctive VHDJH rearrangements (CDR3, JH) associated with each VH gene family are similar in all strains. We discuss these findings in the context of a recent hypothesis suggesting that CDR3 structure, independent of VH framework, is sufficient to define the specificity of an antibody.

Indexed as

Gene Rearrangement, B-Lymphocyte, Heavy ChainGenes, ImmunoglobulinAnimalsAntibody SpecificityAntigensBinding SitesFemaleImmunoglobulin Heavy ChainsImmunoglobulin Joining RegionImmunoglobulin Variable RegionMiceMice, Inbred BALB CMice, Inbred C57BLMolecular Sequence DataMultigene FamilyOxazoloneAntigensImmunoglobulin Heavy ChainsImmunoglobulin Joining RegionImmunoglobulin Variable RegionOxazolonePhosphatidylcholines

Identifiers

PMID10051629
PMCPMC26771
OpenAlexW2160512289

What OpenQuestion holds

Texttitle and abstract
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.