Anti-Angiotensin Type 1 Receptor Antibodies in Chronic Graft-Versus-Host Disease

被引:15
作者
Chiron, Andrada [1 ,2 ,3 ,4 ]
Bouaziz, Jean-David [1 ,2 ,3 ,5 ,6 ]
Carmagnat, Maryvonnick [1 ,2 ,3 ,4 ]
de Latour, Regis Peffault [1 ,2 ,3 ,7 ]
Lafaurie-Bergeron, Anne [1 ,2 ,3 ,8 ]
Robin, Marie [1 ,2 ,3 ,7 ]
Xhaard, Alienor [1 ,2 ,3 ,7 ]
Toubert, Antoine [1 ,2 ,3 ,4 ,9 ]
Charron, Dominique [1 ,2 ,3 ,4 ,10 ]
Guigue, Nicolas [1 ,2 ,3 ,11 ]
Socie, Gerard [1 ,2 ,3 ,6 ]
Bengoufa, Djaouida [1 ,2 ,3 ,4 ]
机构
[1] Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
[2] AP HP, Paris, France
[3] Hop St Louis, F-75010 Paris, France
[4] Hop St Louis, Lab Immunol & Histocompatibilite, F-75010 Paris, France
[5] Hop St Louis, Serv Dermatol, F-75010 Paris, France
[6] Hop St Louis, INSERM, U976, Lab Immunol Dermatol & Oncol, F-75010 Paris, France
[7] Hop St Louis, Serv Hematol Greffe, F-75010 Paris, France
[8] Hop St Louis, Serv Pneumol, F-75010 Paris, France
[9] INSERM, U1160, Paris, France
[10] INSERM, UMRS 940, Paris, France
[11] Hop St Louis, Lab Parasitol, F-75010 Paris, France
关键词
Anti-angiotensin type 1 receptor antibodies; Chronic graft-versus-host disease; PDGF RECEPTOR; STIMULATORY AUTOANTIBODIES; ACTIVATING ANTIBODIES; TRANSPLANTATION; MANIFESTATIONS; SEVERITY; ORGAN;
D O I
10.1097/TP.0000000000000182
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Activating anti-angiotensin type 1 receptor antibodies (AT1R-AA) have been described in patients with systemic scleroderma, an auto-immune disorder with clinical fibrotic features. Chronic graft-versus-host disease (cGvHD) after hematopoietic stem cell transplantation may have clinical fibrotic features, whose pathogenesis may be similar with systemic sclerosis. Objective. To evaluate the presence of AT1R-AA and their association with clinical and biological symptoms in cGvHD patients. Material and Methods. Sera from 87 patients including 45 extensive cGvHD and 42 hematopoietic stem cell transplantation patients without cGvHD were retrospectively analyzed for the presence of AT1R-AA using an enzymatic immunoassay. Results. The frequency of AT1R-AA was significantly increased (odds ratio [OR]-3.4, P=0.04) in the cGvHD group (24.4%) compared with the non-cGvHD group (7.1%). In the cGvHD group the positivity of AT1R-AA was significantly associated with: i/ the presence of antinuclear antibodies (OR=5.9, P=0.04) ii/a more severe global and organ-specific cGvHD scoring (PG0.05), iii/ the presence of active skin or mucosal erosions (OR=19.2, P<0.01). There was no difference between the number and the types of organs involved by the cGvHD between the AT1R-AA-positive versus AT1R-AA-negative subgroups. Conclusion. This preliminary study suggests a potential role and prognostic value of AT1R-AA in cGvHD.
引用
收藏
页码:470 / 474
页数:5
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