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*
Howard Hughes Medical Institute, Department of Microbiology and Immunology, Vanderbilt University School of Medicine, Nashville, TN 37232; and
Institute of Molecular Medicine and Genetics, Medical College of Georgia, Augusta, GA 30912
The cellular basis for allograft rejection derives from the strong
T cell response to cells bearing foreign MHC. While it was originally
assumed that alloreactive T cells focus their recognition on the
polymorphic residues that differ between syngeneic and allogeneic MHC
molecules, studies with MHC class I-restricted CTL have shown that
MHC-bound peptides play a critical role in allorecognition. It has been
suggested that alloreactive T cells depend more strongly on
interactions with the MHC molecule than with the associated peptide,
but there is little evidence to support this idea. Here we have studied
the alloreactive and self-restricted response directed against the
class II H2-Ab molecule bound with a single peptide, Ep,
derived from the H2-E
chain. This MHC class II-peptide combination
was a poor target and stimulator of alloreactive CD4+ T
cell responses, indicating that MHC-bound peptides are as important for
alloreactive CD4+ T cells as they are for alloreactive CTL.
We also generated alloreactive T cells with exquisite specificity for
the Ab/Ep complex, and compared their reactivity with
self-restricted T cells specific for the same Ab/Ep
complex. Our results showed that peptide-specific alloreactive T cells,
as compared with self-restricted T cells, were more sensitive to
peptide stimulation, but equally sensitive to amino acid substitutions
in the peptide. These findings indicate that alloreactive and
self-restricted T cells interact similarly with their
MHC/peptide ligand.
This article has been cited by other articles:
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N. J. Felix, A. Suri, J. J. Walters, S. Horvath, M. L. Gross, and P. M. Allen I-Ep-Bound Self-Peptides: Identification, Characterization, and Role in Alloreactivity J. Immunol., January 15, 2006; 176(2): 1062 - 1071. [Abstract] [Full Text] [PDF] |
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