Projects per year
Abstract
Background. Chronic graft-versus-host disease (cGVHD) is a major complication of allogeneic bone marrow transplantation (BMT) the immunopathogenesis of which is not well understood. Humoral and cellular immunity are both implicated, patients express a range of autoantibodies, but the targets of cellular immunity are not well defined. Autologous human leukocyte antigen (HLA)-derived peptides constitute a significant proportion of the repertoire.
Methods. We have investigated the response to HLA-derived peptides after allogeneic BMT using gamma-interferon enzyme-linked immunospot assay (ELISPOT). We also studied the release of this gamma-interferon by flow cytometry in a subgroup of responsive patients.
Results. The peripheral blood mononuclear cell response was assessed by gamma-interferon ELISPOT in 42 BMT recipients (21 with cGVHD) and 30 healthy donors. Thirteen of 21 patients diagnosed with cGVHD responded to at least one HLA-derived peptide compared with 1 of 21 patients without cGVHD (62% vs. 5%, P <10(-4)) and 1 of 30 healthy donors. In all but one patient these peptides correspond with the sequences of autologous HLA. The median single peptide-specific response in ELISPOT was 43/10(6) peripheral blood mononuclear cells. In a subgroup studied by flow cytometry, gamma-interferon production to individual peptides occurred in 0.04% to 0.18% of CD4(+) T lymphocytes.
Conclusion. These observations identify HLA-derived peptides as targets of a cellular immune response in cGVHD.
Original language | English |
---|---|
Pages (from-to) | 555-563 |
Number of pages | 9 |
Journal | Transplantation |
Volume | 90 |
Issue number | 5 |
DOIs | |
Publication status | Published - 1 Sept 2010 |
Keywords
- HLA
- cGVHD
- Peptide
Fingerprint
Dive into the research topics of 'Chronic Graft Versus Host Disease Is Associated With an Immune Response to Autologous Human Leukocyte Antigen-Derived Peptides'. Together they form a unique fingerprint.Projects
- 1 Finished
-
Cellular Immunity to Herpesvirus Infection: Studies with Epstein-Barr Virus and Human Cytomegalovirus
1/09/05 → 31/08/10
Project: Research Councils