| Literature DB >> 25323824 |
Effie W Petersdorf1, Theodore A Gooley2, Mari Malkki2, Andrea P Bacigalupo3, Anne Cesbron4, Ernette Du Toit5, Gerhard Ehninger6, Torstein Egeland7, Gottfried F Fischer8, Thibaut Gervais9, Michael D Haagenson10, Mary M Horowitz11, Katharine Hsu12, Pavel Jindra13, Alejandro Madrigal14, Machteld Oudshoorn15, Olle Ringdén16, Marlis L Schroeder17, Stephen R Spellman10, Jean-Marie Tiercy18, Andrea Velardi19, Campbell S Witt20, Colm O'Huigin21, Richard Apps22, Mary Carrington22.
Abstract
Life-threatening graft-versus-host disease (GVHD) limits the use of HLA-C-mismatched unrelated donors in transplantation. Clinicians lack criteria for donor selection when HLA-C-mismatched donors are a patient's only option for cure. We examined the role for HLA-C expression levels to identify permissible HLA-C mismatches. The median fluorescence intensity, a proxy of HLA-C expression, was assigned to each HLA-C allotype in 1975 patients and their HLA-C-mismatched unrelated transplant donors. The association of outcome with the level of expression of patients' and donors' HLA-C allotypes was evaluated in multivariable models. Increasing expression level of the patient's mismatched HLA-C allotype was associated with increased risks of grades III to IV acute GVHD, nonrelapse mortality, and mortality. Increasing expression level among HLA-C mismatches with residue 116 or residue 77/80 mismatching was associated with increased nonrelapse mortality. The immunogenicity of HLA-C mismatches in unrelated donor transplantation is influenced by the expression level of the patient's mismatched HLA-C allotype. HLA-C expression levels provide new information on mismatches that should be avoided and extend understanding of HLA-C-mediated immune responses in human disease.Entities:
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Year: 2014 PMID: 25323824 PMCID: PMC4271183 DOI: 10.1182/blood-2014-09-599969
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113