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|2wbj, resolution 3.00Å ()|
|Ligands:||, , ,|
|Related:||1kg0, 1d6e, 1bx2, 1d5m, 1lo5, 1hxy, 1seb, 1jws, 1h15, 1hqr, 2seb, 1fv1, 1sjh, 1jwm, 1fyt, 1klu, 1ymm, 1j8h, 1zgl, 1t5w, 1d5x, 1klg, 2g9h, 1aqd, 1dlh, 1sje, 1d5z, 1jwu, 1t5x, 1a6a|
Environmental factors account for 75% of the risk of developing multiple sclerosis (MS). Numerous infections have been suspected as environmental disease triggers, but none of them has consistently been incriminated, and it is unclear how so many different infections may play a role. We show that a microbial peptide, common to several major classes of bacteria, can induce MS-like disease in humanized mice by crossreacting with a T cell receptor (TCR) that also recognizes a peptide from myelin basic protein, a candidate MS autoantigen. Structural analysis demonstrates this crossreactivity is due to structural mimicry of a binding hotspot shared by self and microbial antigens, rather than to degenerate TCR recognition. Biophysical studies reveal that the autoreactive TCR binding affinity is markedly lower for the microbial (mimicry) peptide than for the autoantigenic peptide. Thus, these data suggest a possible explanation for the difficulty in incriminating individual infections in the development of MS.
T cell-mediated autoimmune disease due to low-affinity crossreactivity to common microbial peptides., Harkiolaki M, Holmes SL, Svendsen P, Gregersen JW, Jensen LT, McMahon R, Friese MA, van Boxel G, Etzensperger R, Tzartos JS, Kranc K, Sainsbury S, Harlos K, Mellins ED, Palace J, Esiri MM, van der Merwe PA, Jones EY, Fugger L, Immunity. 2009 Mar 20;30(3):348-57. PMID:19303388
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
About this Structure
- Harkiolaki M, Holmes SL, Svendsen P, Gregersen JW, Jensen LT, McMahon R, Friese MA, van Boxel G, Etzensperger R, Tzartos JS, Kranc K, Sainsbury S, Harlos K, Mellins ED, Palace J, Esiri MM, van der Merwe PA, Jones EY, Fugger L. T cell-mediated autoimmune disease due to low-affinity crossreactivity to common microbial peptides. Immunity. 2009 Mar 20;30(3):348-57. PMID:19303388 doi:10.1016/j.immuni.2009.01.009