Electrostatic modifications of the human leukocyte antigen‐DR P9 peptide‐binding pocket and susceptibility to primary sclerosing cholangitis
Johannes R. Hov, Vasilis Kosmoliaptsis, James A. Traherne, Marita Olsson, Kirsten M. Boberg, Annika Bergquist, Erik Schrumpf, J. Andrew Bradley, Craig J. Taylor, Benedicte A. Lie, John Trowsdale, Tom H. Karlsen – 16 March 2011 – The strongest genetic risk factors for primary sclerosing cholangitis (PSC) are found in the human leukocyte antigen (HLA) complex at chromosome 6p21. Genes in the HLA class II region encode molecules that present antigen to T lymphocytes.