Anemia after late introduction of sirolimus may correlate with biochemical evidence of a chronic inflammatory state

被引:81
作者
Thaunat, O
Beaumont, C
Chatenoud, L
Lechaton, S
Mamzer-Bruneel, MF
Varet, B
Kreis, H
Morelon, E
机构
[1] Hop Necker Enfants Malad, Serv Transplantat Renale, Dept Renal Transplantat, F-75015 Paris, France
[2] Univ Paris 07, INSERM U409, Paris, France
[3] Hop Necker Enfants Malad, INSERM U480, Paris, France
[4] Hop Necker Enfants Malad, Dept Hematol, Paris, France
[5] Hop Edouard Herriot, Dept Renal Transplantat, Lyon, France
关键词
anemia; sirolimus; inflammation;
D O I
10.1097/01.tp.0000179106.07382.6a
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. The responsibility of sirolimus (SRL) for postrenal transplant anemia has never been proven, because SRL is usually combined with myelotoxic drugs, and because of the high incidence of anemia in the posttransplant period. Methods. We retrospectively analyzed anemia in 46 renal transplant recipients, who had been switched from calcineurin inhibitors to SRL for biopsy-proven chronic allograft nephropathy. Results. The mean decrease in hemoglobin (Hb) after SRL introduction was 2.8 g/dl. The 24 patients, whose Hb fell by 2 g/dl, displayed microcytic aregenerative anemia with low serum iron despite high ferritinemia, consistent with anemia of chronic inflammatory states. Fibrinogen and CRP levels increased in these patients after sirolimus introduction. We subsequently focused our study on eight patients without confounding factors of anemia. Anemia improved in all eight after SRL withdrawal. IL6 and TNF alpha at the nadir of anemia were significantly higher than before SRL introduction and after its withdrawal. Decreases in Hb correlated with increases in proinflammatory cytokine levels in a linear regression model. Unchanged serum IL10 levels measured at the nadir of anemia were discordant with the inflammatory state. Conclusions. Late introduction of SRL may induce anemia and correlates with biochemical evidence of a chronic inflammatory state possibly due to defective IL10-dependent inflammatory autoregulation.
引用
收藏
页码:1212 / 1219
页数:8
相关论文
共 27 条
[1]  
ALVAREZHERNANDEZ X, 1989, LAB INVEST, V61, P319
[2]   Soluble transferrin receptor for the evaluation of erythropoiesis and iron status [J].
Beguin, Y .
CLINICA CHIMICA ACTA, 2003, 329 (1-2) :9-22
[3]   Early experience with sirolimus in lung transplant recipients with chronic allograft rejection [J].
Cahill, BC ;
Somerville, KT ;
Crompton, JA ;
Parker, ST ;
O'Rourke, MK ;
Stringham, JC ;
Karwande, SV .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2003, 22 (02) :169-176
[4]  
Davis D, 1997, BRIT J RHEUMATOL, V36, P950
[5]   Adverse drug reactions: definitions, diagnosis, and management [J].
Edwards, IR ;
Aronson, JK .
LANCET, 2000, 356 (9237) :1255-1259
[6]  
Fijen, 2000, Eur J Intern Med, V11, P89, DOI 10.1016/S0953-6205(00)00068-6
[7]   Cytokine-stimulated T cells induce macrophage IL-10 production dependent on phosphatidylinositol 3-kinase and p70S6K: implications for rheumatoid arthritis [J].
Foey, A ;
Green, P ;
Foxwell, B ;
Feldmann, M ;
Brennan, F .
ARTHRITIS RESEARCH, 2002, 4 (01) :64-70
[8]   Sirolimus-induced thrombocytopenia and leukopenia in renal transplant recipients: Risk factors, incidence, progression, and management [J].
Hong, JC ;
Kahan, BD .
TRANSPLANTATION, 2000, 69 (10) :2085-2090
[9]   Multidimensional assessment of graft vascular disease (GVD) in aortic grafts by serial intravascular ultrasound in rhesus monkeys [J].
Ikonen, TS ;
Briffa, N ;
Gummert, JF ;
Honda, Y ;
Hayase, M ;
Hausen, B ;
Billingham, ME ;
Yock, PG ;
Robbins, RC ;
Morris, RE .
TRANSPLANTATION, 2000, 70 (03) :420-429
[10]   Inhibition of proliferation but not erythroid differentiation of J2E cells by rapamycin [J].
Jaster, R ;
Bittorf, T ;
Klinken, SP ;
Brock, J .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (09) :1181-1185