Holler E, Ertl B, Hintermeier-Knabe R, Roncarolo M G, Eissner G, Mayer F, Fraunberger P, Behrends U, Pfannes W, Kolb H J, Wilmanns W
Med. Klinik III, Klinikum Grosshadern, München, Germany.
Leuk Lymphoma. 1997 Apr;25(3-4):217-24. doi: 10.3109/10428199709114161.
Intensity of pretransplant conditioning has been closely correlated with regimen related toxicity in patients receiving allogeneic bone marrow transplantation (BMT). In this review, we summarize evidence for a direct link between inflammatory reactions induced by irradiation and cytotoxic treatment and occurrence of acute graft-versus-host disease (GvHD) as well as endothelial complications: In our studies, de novo release of TNFalpha during conditioning was associated with an increased risk of severe GvHD and mortality following BMT, whereas increased spontaneous production of IL-10, an endogenous TNF-antagonist, prior to conditioning protected from these complications. Immunogenetic differences in cytokine regulation and costimulation by endotoxin proved to be important cofactors determining the extent of inflammatory cytokine release in individual patients. Pathophysiological relevance of these findings seems to be confirmed by experimental as well as first clinical trials using TNF-antibodies and related antagonists during pretransplant conditioning. Preclinical experiments suggest additional, cytokine independent inflammatory reactions induced by irradiation such as expression of ICAM-1 and endothelial cell apoptosis. Although the exact impact of these findings on pathophysiology of BMT related complications needs further clarification by future studies, conditioning related inflammation as a first crucial step in induction of GvHD and complications has to be considered when designing new protocols for preparation of patients for allogeneic BMT.
在接受异基因骨髓移植(BMT)的患者中,移植前预处理的强度与方案相关毒性密切相关。在本综述中,我们总结了辐射和细胞毒性治疗诱导的炎症反应与急性移植物抗宿主病(GvHD)以及内皮并发症发生之间直接联系的证据:在我们的研究中,预处理期间TNFα的从头释放与BMT后严重GvHD和死亡率的风险增加相关,而预处理前内源性TNF拮抗剂IL-10的自发产生增加可预防这些并发症。细胞因子调节和内毒素共刺激的免疫遗传差异被证明是决定个体患者炎症细胞因子释放程度的重要辅助因素。这些发现的病理生理相关性似乎通过在移植前预处理期间使用TNF抗体和相关拮抗剂的实验以及首次临床试验得到了证实。临床前实验表明,辐射可诱导其他与细胞因子无关的炎症反应,如ICAM-1的表达和内皮细胞凋亡。尽管这些发现对BMT相关并发症病理生理学的确切影响需要未来的研究进一步阐明,但在设计异基因BMT患者预处理的新方案时,必须将预处理相关炎症视为诱导GvHD和并发症的第一个关键步骤。