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The repertoire of T cells shaped by a single MHC/peptide ligand

  • Leszek Ignatowicz(corresponding author)
    ,
  • John Kappler
    ,
  • Philippa Marrack
*Corresponding author for this work
  • University of Colorado Anschutz Medical Campus
    ,
  • Howard Hughes Medical Institute
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Although the thymus produces many immature thymocytes, few of these cells mature. Positive selection has been thought to limit thymocyte development. In thymuses expressing a single MHC/peptide combination, however, surprisingly large numbers of thymocytes are selected to mature. Many of these react with the selecting MHC, bound to other self-peptides. Therefore, the number of thymocytes that mature is limited by the fact that positively selected cells die because they react too well with MHC bound to self- peptides that are not identical to those involved in positive selection. T cells that mature in thymuses expressing a single MHC/peptide ligand react frequently with foreign MHC, suggesting that the repertoire of αβ receptors may be more biased toward reaction with MHC than was previously thought.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 521-529 (9 pages)

Journal (Volume, Issue Number)

Cell (Volume 84, Issue 4)

Publication milestones

  • Published - 02/23/1996

Publication status

Published - 02/23/1996

ISSN

0092-8674

Publication IDs

  • Scopus: 0030058657
  • PubMed: 8598039

Publication metrics

Metrics

Scopus
citations
SciVal
citations
373
SciVal
FWCI
14.07
SciVal
Author count
3
SciVal
Paper percentile
99
SciVal
Top percentile
1
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1

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Citation count
377
Captures
120

Funding Details

The authors are very grateful to Drs. Donal Murphy and Charles A. Janeway, Jr., for the B cell hybridomas Y3P and YAe; Drs. Diane Mathis, Christophe Benoist, Ronald Germain, and Jerry Bill for class II promoter and structural genes; and Drs. Elizabeth Bikoff and Ronald Germain for the invariant chain knockout mice. The authors would like to thank Dr. David Parker for many helpful discussions; Drs. Mark Scherer and Tony Vella for their comments on the manuscript; and Helena Gognat, Christopher Brown, and Ella Kushnir for breeding the mice used in these experiments. This work was supported in part by United States Public Health Service grants AI-18785, AI-17134, and AI-22295.
FunderFunding numbers
USPHS
AI-18785, AI-22295, AI-17134