help button home button Am J Pathol ASIP WHAT IS IT?
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dornmair, K.
Right arrow Articles by Hohlfeld, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dornmair, K.
Right arrow Articles by Hohlfeld, R.
(American Journal of Pathology. 2003;163:1215-1226.)
© 2003 American Society for Investigative Pathology


Review

T-Cell-Mediated Autoimmunity

Novel Techniques to Characterize Autoreactive T-Cell Receptors

Klaus Dornmair*{dagger}, Norbert Goebels{dagger}, Hans-Ulrich Weltzien{ddagger}, Hartmut Wekerle* and Reinhard Hohlfeld*{dagger}

From the Max-Planck Institute of Neurobiology,* Martinsried; the Institute for Clinical Neuroimmunology,{dagger} Klinikum Großhadern, Ludwig Maximilians University, Munich; Max-Planck-Institute for Immunobiology,{ddagger} Freiburg, Germany

Abstract

Histological samples of autopsy or biopsy tissue provide the best available evidence that autoreactive T cells are involved in the immunopathogenesis of many autoimmune diseases. However, morphology alone does not provide information on the antigen-specific T-cell receptor (TCR) of these cells, let alone on their antigen specificity. In this review article we discuss a number of emerging possibilities for identifying TCR sequences directly from biopsy tissue. We also review the methods for expressing presumably autoreactive TCR molecules and speculate on how the expressed TCR might be used to identify target antigens. Such information should eventually provide new insights into disease pathogenesis which lead to better therapies.





This article has been cited by other articles:


Home page
BrainHome page
A. Junker, J. Ivanidze, J. Malotka, I. Eiglmeier, H. Lassmann, H. Wekerle, E. Meinl, R. Hohlfeld, and K. Dornmair
Multiple sclerosis: T-cell receptor expression in distinct brain regions
Brain, November 1, 2007; 130(11): 2789 - 2799.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
R. Hohlfeld and H. Wekerle
Autoimmune concepts of multiple sclerosis as a basis for selective immunotherapy: From pipe dreams to (therapeutic) pipelines
PNAS, October 5, 2004; 101(suppl_2): 14599 - 14606.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Skulina, S. Schmidt, K. Dornmair, H. Babbe, A. Roers, K. Rajewsky, H. Wekerle, R. Hohlfeld, and N. Goebels
Multiple sclerosis: Brain-infiltrating CD8+ T cells persist as clonal expansions in the cerebrospinal fluid and blood
PNAS, February 24, 2004; 101(8): 2428 - 2433.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the American Society for Investigative Pathology.