The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Related articles in The JI
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ferreira, C.
Right arrow Articles by Dyson, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ferreira, C.
Right arrow Articles by Dyson, J.
The Journal of Immunology, 2006, 177: 2477-2485.
Copyright © 2006 by The American Association of Immunologists

TCR-{alpha} CDR3 Loop Audition Regulates Positive Selection1

Cristina Ferreira*, Anna Furmanski*, Maggie Millrain*, Istvan Bartok*, Philippe Guillaume{dagger}, Rosemary Lees{dagger}, Elizabeth Simpson*, H. Robson MacDonald{dagger} and Julian Dyson2,*

* Transplantation Biology Group, Department of Immunology, Imperial College, Hammersmith Hospital, London, United Kingdom; and {dagger} Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Switzerland

How positive selection molds the T cell repertoire has been difficult to examine. In this study, we use TCR-beta-transgenic mice in which MHC shapes TCR-{alpha} use. Differential AV segment use is directly related to the constraints placed on the composition of the CDR3 loops. Where these constraints are low, efficient selection of {alpha}beta pairs follows. This mode of selection preferentially uses favored AV-AJ rearrangements and promotes diversity. Increased constraint on the {alpha} CDR3 loops leads to inefficient selection associated with uncommon recombination events and limited diversity. Further, the two modes of selection favor alternate sets of AJ segments. We discuss the relevance of these findings to the imprint of self-MHC restriction and peripheral T cell activation.


Related articles in The JI:

IN THIS ISSUE

The JI 2006 177: 2033-2034. [Full Text]  



This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Ferreira, Y. Singh, A. L. Furmanski, F. S. Wong, O. A. Garden, and J. Dyson
Non-obese diabetic mice select a low-diversity repertoire of natural regulatory T cells
PNAS, May 19, 2009; 106(20): 8320 - 8325.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
A. L. Furmanski, C. Ferreira, I. Bartok, S. Dimakou, J. Rice, F. K. Stevenson, M. M. Millrain, E. Simpson, and J. Dyson
Public T Cell Receptor -Chains Are Not Advantaged during Positive Selection
J. Immunol., January 15, 2008; 180(2): 1029 - 1039.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 2006 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 2006 by The American Association of Immunologists, Inc. All rights reserved.