Evidence map›Paper›PMID 9396769›Full record

ArticleThe Journal of experimental medicine1997

Self-reactive B cells are not eliminated or inactivated by autoantigen expressed on thyroid epithelial cells.

S Akkaraju, K Canaan, C C Goodnow

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 72 citations in OpenAlex.

  1. Mechanisms of B Cell Tolerance in Health and Autoimmunity.Arthritis & rheumatology (Hoboken, N.J.) · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
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  8. Article
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  10. Article
  11. Characterization of pathogenic human monoclonal autoantibodies against GM-CSF.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  12. Article
  13. Peripheral deletion of mature alloreactive B cells induced by costimulation blockade.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  14. Article
  15. Maintenance and loss of self-tolerance in B cells.Springer seminars in immunopathology · 2001
    Review
  16. Article
  17. Article
  18. 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

3 authors at 2 institutions in 1 country.

S AkkarajuProgram in Immunology, Department of Microbiology and Immunology, and The Howard Hughes Medical Institute, Beckman Center, Stanford University School of Medicine, Stanford, California 94305-5428, USA.
K Canaan
C C Goodnow
Howard Hughes Medical Institute · USStanford University · US

Funding

THE ROLE OF TNF-ALPHA IN LYMPHOCYTE DEVELOPMENT IN NOD MICEP01AI036535 · NIAID · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 1994 to 2008
$6.6M
TRANSGENIC MOUSE MODELS FOR B LYMPHOCYTE TOLERANCE AND AUTOIMMUNITYP01AI019512 · NIAID · STANFORD UNIVERSITY · PI MCDEVITT, HUGH O · 1985 to 1998
–
NIAID NIH HHS AI19512NIAID NIH HHS AI36535NIAID NIH HHS P01 AI036535
6 · The paper itself

Abstract

Graves' Disease results from the production of autoantibodies against receptors for thyroid stimulating hormone (TSH) on thyroid epithelial cells, and represents the prototype for numerous autoimmune diseases caused by autoantibodies that bind to organ-specific cell membrane antigens. To study how humoral tolerance is normally maintained to organ-specific membrane antigens, transgenic mice were generated selectively expressing membrane-bound hen egg lysozyme (mHEL) on the thyroid epithelium. In contrast to the deletion of autoreactive B cells triggered by systemic mHEL (Hartley, S.B., J. Crosbie, R. Brink, A.B. Kantor, A. Basten, and C.C. Goodnow. 1991. Nature. 353:765-769), selective expression of mHEL autoantigen on thyroid cells did not trigger elimination or inactivation of circulating HEL-reactive B cells. These results provide evidence that tolerance is not actively acquired to organ-specific antigens in the preimmune B cell repertoire, underscoring the importance of maintaining tolerance to such antigens by other mechanisms. The role of an intact endothelial barrier in sequestering organ-specific antigens from circulating preimmune B cells is discussed.

Indexed as

Immune ToleranceAdoptive TransferAnimalsAutoantigensB-LymphocytesEpithelial CellsMiceMice, Inbred C57BLMice, TransgenicMuramidaseThyroid GlandThyroiditis, AutoimmuneAutoantigensMuramidase

Identifiers

PMID9396769
PMCPMC2199176
OpenAlexW2037723422

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.