Tumour necrosis factor receptor type II 196M/R genotype correlates with circulating soluble receptor levels in normal subjects and with graft-versus-host disease after sibling allogeneic bone marrow transplantation1

Autor: Stark, Gail L., Dickinson, Anne M., Jackson, Graham H., Taylor, Penelope R., Proctor, Stephen J., Middleton, Peter G.
Zdroj: Transplantation; December 2003, Vol. 76 Issue: 12 p1742-1749, 8p
Abstrakt: A single nucleotide polymorphism in the tumor necrosis factor type II receptor (TNFRII) gene, codon 196, results in the substitution of arginine (R allele) for methionine (M allele). The 196R allele is reportedly associated with an increased susceptibility to autoimmune disease, and donor 196R allele carriage correlates with increased severity of acute graft-versus-host disease (GVHD) after matched unrelated bone marrow transplantation (BMT).
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