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


     
 


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fuller, B
Right arrow Articles by Lefrancois, L
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fuller, B
Right arrow Articles by Lefrancois, L

The Journal of Immunology, Vol 155, Issue 6 2808-2811, Copyright © 1995 by American Association of Immunologists


CUTTING EDGE

Requirement for extrathymic class I histocompatibility antigens for positive selection of thymus-derived T lymphocytes

B Fuller and L Lefrancois
Division of Rheumatic Diseases, University of Connecticut Health Center, Farmington 06030, USA.

We have examined whether the thymus can produce immature T cell precursors for subsequent positive selection in the periphery. Using the intestine as a model system, we demonstrate that extrathymic MHC class I molecules positively select thymus-derived TCR-alpha beta CD8+ intestinal intraepithelial lymphocytes. Grafting of MHC class I+ thymus onto MHC class I- hosts resulted in the generation of donor and host- derived CD4-CD8+ T cells in lymph node, but few TCR-alpha beta CD4-CD8+ intraepithelial lymphocytes. The results indicate that the intestine can act as a site of positive selection for thymus-derived T cells. Bone marrow reconstitution studies demonstrated that non-hematopoietic, radiation-resistant cells, perhaps intestinal epithelial cells, were responsible for extrathymic positive selection of thymus-derived T cells. These findings demonstrate that the thymus can support organ- specific immunity via provision of targeted precursor populations.


This article has been cited by other articles:


Home page
J. Immunol.Home page
F. Rharbaoui, D. Bruder, M. Vidakovic, T. Ebensen, J. Buer, and C. A. Guzman
Characterization of a B220+ Lymphoid Cell Subpopulation with Immune Modulatory Functions in Nasal-Associated Lymphoid Tissues
J. Immunol., February 1, 2005; 174(3): 1317 - 1324.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. N. Levelt, Y. P. de Jong, E. Mizoguchi, C. O'Farrelly, A. K. Bhan, S. Tonegawa, C. Terhorst, and S. J. Simpson
High- and low-affinity single-peptide/MHC ligands have distinct effects on the development of mucosal CD8alpha alpha and CD8alpha beta T lymphocytes
PNAS, May 11, 1999; 96(10): 5628 - 5633.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
K. Laky, L. Lefrancois, U. von Freeden-Jeffry, R. Murray, and L. Puddington
The Role of IL-7 in Thymic and Extrathymic Development of TCR{gamma}{delta} Cells
J. Immunol., July 15, 1998; 161(2): 707 - 713.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1995 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1995 by The American Association of Immunologists, Inc. All rights reserved.