Chronic rejection of a lung transplant is characterized by a profile of specific autoantibodies
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Chronic rejection of a lung transplant is characterized by a profile of specific autoantibodies. / Hagedorn, Peter; Burton, Christopher Malcolm; Carlsen, Jørn; Steinbrüchel, Daniel; Andersen, Claus B; Sahar, Eli; Domany, Eytan; Cohen, Irun R; Flyvbjerg, Henrik; Iversen, Martin.
I: Immunology, Bind 130, Nr. 3, 01.07.2010, s. 427-35.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Chronic rejection of a lung transplant is characterized by a profile of specific autoantibodies
AU - Hagedorn, Peter
AU - Burton, Christopher Malcolm
AU - Carlsen, Jørn
AU - Steinbrüchel, Daniel
AU - Andersen, Claus B
AU - Sahar, Eli
AU - Domany, Eytan
AU - Cohen, Irun R
AU - Flyvbjerg, Henrik
AU - Iversen, Martin
PY - 2010/7/1
Y1 - 2010/7/1
N2 - SUMMARY: Obliterative bronchiolitis (OB) continues to be the major limitation to long-term survival after lung transplantation. The specific aetiology and pathogenesis of OB are not well understood. To explore the role of autoreactivity in OB, we spotted 751 different self molecules onto glass slides, and used these antigen microarrays to profile 48 human serum samples for immunoglobulin G (IgG) and IgM autoantibodies; 27 patients showed no or mild bronchiolitis obliterans syndrome (BOS; a clinical correlate of OB) and 15 patients showed medium to severe BOS. We now report that these BOS grades could be differentiated by a profile of autoantibodies binding to 28 proteins or their peptides. The informative autoantibody profile included down-regulation as well as up-regulation of both IgM and IgG specific reactivities. This profile was evaluated for robustness using a panel of six independent test patients. Analysis of the functions of the 28 informative self antigens showed that eight of them are connected in an interaction network involved in apoptosis and protein metabolism. Thus, a profile of autoantibodies may reflect pathological processes in the lung allograft, suggesting a role for autoimmunity in chronic rejection leading to OB.
AB - SUMMARY: Obliterative bronchiolitis (OB) continues to be the major limitation to long-term survival after lung transplantation. The specific aetiology and pathogenesis of OB are not well understood. To explore the role of autoreactivity in OB, we spotted 751 different self molecules onto glass slides, and used these antigen microarrays to profile 48 human serum samples for immunoglobulin G (IgG) and IgM autoantibodies; 27 patients showed no or mild bronchiolitis obliterans syndrome (BOS; a clinical correlate of OB) and 15 patients showed medium to severe BOS. We now report that these BOS grades could be differentiated by a profile of autoantibodies binding to 28 proteins or their peptides. The informative autoantibody profile included down-regulation as well as up-regulation of both IgM and IgG specific reactivities. This profile was evaluated for robustness using a panel of six independent test patients. Analysis of the functions of the 28 informative self antigens showed that eight of them are connected in an interaction network involved in apoptosis and protein metabolism. Thus, a profile of autoantibodies may reflect pathological processes in the lung allograft, suggesting a role for autoimmunity in chronic rejection leading to OB.
U2 - http://dx.doi.org/10.1111/j.1365-2567.2010.03246.x
DO - http://dx.doi.org/10.1111/j.1365-2567.2010.03246.x
M3 - Journal article
VL - 130
SP - 427
EP - 435
JO - Immunology
JF - Immunology
SN - 0019-2805
IS - 3
ER -
ID: 34138318