Proinflammatory cytokines and their role in the development of major transplant-related complications in the early phase after allogeneic bone marrow transplantation

被引:125
|
作者
Schots, R
Kaufman, L
Van Riet, I
Ben Othman, T
De Waele, M
Van Camp, B
Demanet, C
机构
[1] Free Univ Brussels, Akad Ziekenhuis, BMT Unit, B-1090 Brussels, Belgium
[2] Free Univ Brussels, Akad Ziekenhuis, Dept Med Stat, B-1090 Brussels, Belgium
[3] Free Univ Brussels, Akad Ziekenhuis, Hematol Immunol HLA, B-1090 Brussels, Belgium
关键词
interleukin-6; interleukin-8; tumor necrosis factor-alpha; major complications; allogeneic marrow transplantation;
D O I
10.1038/sj.leu.2402946
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Serum levels of interleukin-6 (IL-6), interleukin-8 (IL-8) and tumor necrosis factor (TNF)-alpha were frequently measured during the first 30 days after allogeneic bone marrow transplantation (BMT) in 84 consecutive adult patients. Major transplant-related complications (MTCs) occurred in 33% of cases and included veno-occlusive liver disease, idiopathic pneumonia syndrome, severe endothelial leakage syndrome and >grade II acute graft-versus-host disease. Compared with patients having minor complications, those with MTCs developed higher levels at times of maximal clinical signs ( all cytokines, P<0.001), between days 0 - 5 post-BMT (IL-6 and IL-8, P<0.05) and days 6 - 10 (L-6, P<0.001; IL-8 and TNF, P<0.01) post-BMT. We could not discriminate patterns of cytokine release that were specific for any subtype of MTC. Higher levels of IL-8 during days 0 - 5 were associated ( P = 0.044) with early (<40 days) death. Multivariate analysis including patient and transplant characteristics as well as post-BMT levels of C-reactive protein showed that high average levels of one or more of the cytokines within the first 10 days post-BMT were independently associated with MTC (Odd's ratio: 2.3 [1.2-4.5], P = 0.011). This study shows that systemic release of proinflammatory cytokines contributes to the development of MTC and provides a rationale for pre-emptive anti-inflammatory treatment in selected patients.
引用
收藏
页码:1150 / 1156
页数:7
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