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首页> 外文期刊>Bone marrow transplantation >Gut protection by palifermin during autologous haematopoietic SCT.
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Gut protection by palifermin during autologous haematopoietic SCT.

机译:自体造血SCT期间palifermin对肠的保护作用。

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摘要

Conditioning therapy in connection with haematopoietic SCT (HSCT) induces a disruption of the intestinal barrier function facilitating the permeation of bacteria and endotoxin through the bowel wall with subsequent increased risk of septicaemia and a worsening of GVHD in the allogeneic setting. Palifermin (recombinant human keratinocyte growth factor) reduces the severity of oral mucositis with HSCT. The present trial investigates its effect on intestinal barrier function. Seventeen lymphoma patients undergoing autologous HSCT received palifermin. Intestinal permeability was assessed before the conditioning therapy and on days +4 and +14. Clinical oral and gastrointestinal toxicity was prospectively assessed in parallel. A comparison was made with matched historical study patients (n=21). Patients treated with palifermin had a significantly better preserved intestinal barrier function (P=0.01 on day +4) and were in less need of total parenteral nutrition (P=0.005) as compared with controls. No significant reduction of clinical gastrointestinal or oral toxicity was observed. The intestinal barrier function, normally disrupted by the conditioning therapy, is preserved by palifermin. Whether intestinal barrier preservation protects from invasive infections, and in the allogeneic setting diminishes GVHD severity, remains to be investigated in randomized controlled trials.
机译:与造血SCT(HSCT)相关的条件疗法会引起肠屏障功能的破坏,从而促进细菌和内毒素通过肠壁的渗透,继而在同种异体环境中增加败血病的风险和GVHD的恶化。 Palifermin(重组人角质形成细胞生长因子)可降低HSCT引起的口腔粘膜炎的严重程度。本试验研究了其对肠屏障功能的影响。接受自体HSCT的17名淋巴瘤患者接受了palifermin。在调理治疗之前以及第4天和+14天评估肠道通透性。平行评估了临床口服和胃肠道毒性。与匹配的历史研究患者进行比较(n = 21)。与对照组相比,接受palifermin治疗的患者的肠道屏障功能得到了显着改善(P = 0.01,+ 4天),并且不需要总肠胃外营养(P = 0.005)。没有观察到临床胃肠道或口服毒性的显着降低。正常情况下,调理疗法会破坏肠屏障功能,而palifermin可以保留这种屏障。肠道屏障的保存是否能防止侵袭性感染,以及在同种异体环境下是否能降低GVHD的严重性,尚需在随机对照试验中进行研究。

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