Literature DB >> 3490311

The T cell repertoire may be biased in favor of MHC recognition.

M Blackman, J Yagüe, R Kubo, D Gay, C Coleclough, E Palmer, J Kappler, P Marrack.   

Abstract

The receptors of two T cell hybridomas that recognize class I and class II major histocompatibility complex (MHC) molecules, respectively, have been compared. In both cases these receptors are hybrid molecules formed as a result of cellular fusion. The receptors contain the same alpha chain, contributed by the tumor cell fusion partner, and related beta chains, contributed by the normal T cell component. Thus, surprisingly, the same alpha chain can contribute to recognition of class I and class II MHC molecules. Moreover, the finding that in two independent examples hybrid receptor molecules created randomly by in vitro cell fusion recognize MHC supports the theory that the T cell repertoire has an intrinsic affinity for MHC.

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Year:  1986        PMID: 3490311     DOI: 10.1016/0092-8674(86)90591-x

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  41 in total

1.  MHC restriction is imposed on a diverse T cell receptor repertoire by CD4 and CD8 co-receptors during thymic selection.

Authors:  François Van Laethem; Anastasia N Tikhonova; Alfred Singer
Journal:  Trends Immunol       Date:  2012-07-06       Impact factor: 16.687

2.  Functional evidence for TCR-intrinsic specificity for MHCII.

Authors:  Heather L Parrish; Neha R Deshpande; Jelena Vasic; Michael S Kuhns
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-01       Impact factor: 11.205

3.  Antigen/major histocompatibility complex-specific activation of murine T cells transfected with functionally rearranged T-cell receptor genes.

Authors:  C L Kuo; L Hood
Journal:  Proc Natl Acad Sci U S A       Date:  1987-11       Impact factor: 11.205

4.  Coevolution of TCR-MHC interactions: conserved MHC tertiary structure is not sufficient for interactions with the TCR.

Authors:  Hye-Jung Kim; Donglin Guo; Derek B Sant'Angelo
Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-09       Impact factor: 11.205

Review 5.  gammadelta T lymphocytes-selectable cells within the innate system?

Authors:  Willi K Born; Niyun Jin; M Kemal Aydintug; J M Wands; Jena D French; Christina L Roark; Rebecca L O'Brien
Journal:  J Clin Immunol       Date:  2007-02-14       Impact factor: 8.317

6.  Many different Vbeta CDR3s can reveal the inherent MHC reactivity of germline-encoded TCR V regions.

Authors:  Kira Rubtsova; James P Scott-Browne; Frances Crawford; Shaodong Dai; Philippa Marrack; John W Kappler
Journal:  Proc Natl Acad Sci U S A       Date:  2009-04-28       Impact factor: 11.205

Review 7.  Development of T cell receptor expression: studies using T cell hybridomas.

Authors:  W Born; J White; R O'Brien; R Kubo
Journal:  Immunol Res       Date:  1988       Impact factor: 2.829

8.  Effect of CDR3 sequences and distal V gene residues in regulating TCR-MHC contacts and ligand specificity.

Authors:  Brian D Stadinski; Peter Trenh; Brian Duke; Priya G Huseby; Guoqi Li; Lawrence J Stern; Eric S Huseby
Journal:  J Immunol       Date:  2014-05-09       Impact factor: 5.422

Review 9.  The molecular basis of TCR germline bias for MHC is surprisingly simple.

Authors:  K Christopher Garcia; Jarrett J Adams; Dan Feng; Lauren K Ely
Journal:  Nat Immunol       Date:  2009-02       Impact factor: 25.606

10.  Negative selection imparts peptide specificity to the mature T cell repertoire.

Authors:  Eric S Huseby; Frances Crawford; Janice White; John Kappler; Philippa Marrack
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-22       Impact factor: 11.205

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