International Immunology, Vol 10, 1725-1732, Copyright © 1998 by Oxford University Press
R Friedl-Hajek, H Breiteneder, B Bohle, G Fischer, C Ebner and O Scheiner
We analyzed the cDNA sequence data of complementarity determining regions
(CDR3) of epitope mapped alphabeta TCR of T cell clones (TCC). The TCC were
specific for the major timothy grass (Phleum pratense) pollen allergen Phl
p 1 and were derived from the peripheral blood of seven unrelated grass
pollen-allergic individuals. Each TCR recognized one of two immunodominant
T cell epitopes, PP73 or PP103, of Phl p 1. Although a diversity of
recombined V and J segments was observed, amino acid motifs as long as five
residues were conserved among CDR3 loops of TCR from TCC of different
atopic individuals specific for the same peptide. The conserved sequences
could comprise as much as 60% of the CDR3. All amino acid residues of the
motifs of the CDR3beta and most of the CDR3alpha of all TCR used in this
study were encoded by randomly added nucleotides. This indicates that they
were specifically selected for by the peptide bound to the MHC class II
molecule. For one selected patient, a larger number of TCC, specific for
PP103, was analyzed. The TCR repertoire was limited to three different TCR.
The same MHC class II molecule, DRB1*1301, was identified to present PP103
to each of the three TCR.
ARTICLES
Conserved sequence motifs of CDR3 loops of TCR specific for two major epitopes of the grass pollen allergen PhI p 1
Department of General and Experimental Pathology, University of Vienna, Australia.
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