TY - JOUR
T1 - T cells are not as degenerate as you think, once you get to know them
AU - Shih, Fei F.
AU - Allen, Paul M.
N1 - Funding Information:
We thank M. Miley for help with Fig. 1 , E. Hailman for critical review of the manuscript, D. Kreamalmeyer for technical assistance, and J. Smith for administrative assistance. This work is supported by grants from the National Institutes of Health. F.F.S. is supported by a grant from the Pediatric Scientist Development Program (National Institute of Child Health and Human Development).
PY - 2004/2
Y1 - 2004/2
N2 - In this review, we dissect two different antigen systems which represent the apparent extremes of T cell receptor (TCR) recognition. In the hemoglobin (Hb) system, a minor change in a single MHC anchor residue disrupts TCR recognition. In the KRN system, a single TCR shows strong reactivity to two peptides from unrelated proteins, presented by different MHC molecules. Upon closer analysis, both turn out to be specific recognition events, following set rules of engagement. Thus, although a TCR can recognize multiple ligands sharing minimal sequence homology, this recognition is still highly specific and is constrained by the same structural requirements. TCR degeneracy is therefore limited and is unlikely to be a major mechanism for autoimmunity.
AB - In this review, we dissect two different antigen systems which represent the apparent extremes of T cell receptor (TCR) recognition. In the hemoglobin (Hb) system, a minor change in a single MHC anchor residue disrupts TCR recognition. In the KRN system, a single TCR shows strong reactivity to two peptides from unrelated proteins, presented by different MHC molecules. Upon closer analysis, both turn out to be specific recognition events, following set rules of engagement. Thus, although a TCR can recognize multiple ligands sharing minimal sequence homology, this recognition is still highly specific and is constrained by the same structural requirements. TCR degeneracy is therefore limited and is unlikely to be a major mechanism for autoimmunity.
KW - Autoimmunity
KW - Molecular mimicry
KW - T cell receptor degeneracy
UR - http://www.scopus.com/inward/record.url?scp=1242293084&partnerID=8YFLogxK
U2 - 10.1016/j.molimm.2003.11.008
DO - 10.1016/j.molimm.2003.11.008
M3 - Article
C2 - 15036908
AN - SCOPUS:1242293084
SN - 0161-5890
VL - 40
SP - 1041
EP - 1046
JO - Molecular Immunology
JF - Molecular Immunology
IS - 14-15
ER -