van Sandick Johanna W, Gisbertz Suzanne S, ten Berge Ineke J M, Boermeester Marja A, van der Pouw Kraan Tineke C T M, Out Theo A, Obertop Hugo, van Lanschot J Jan B
Department of Surgery, Academic Medical Center, Amsterdam, The Netherlands.
Ann Surg. 2003 Jan;237(1):35-43. doi: 10.1097/00000658-200301000-00006.
To investigate alterations in immune responses after transhiatal versus transthoracic esophageal resection and to evaluate the role of preoperative immune functions in predicting postoperative infectious complications.
Impaired immune defense is associated with a decreased resistance to infection. Patients undergoing esophageal resection via a transhiatal or transthoracic approach are prone to develop infectious complications. There are no randomized data on immune responses after two major surgical interventions.
The study group consisted of 20 patients who were randomly allocated to a limited transhiatal or extended transthoracic esophagectomy for cancer. Blood samples were taken before the operation and at regular intervals thereafter from day 1 to day 10. Monocyte and T-helper type 1 (Th1) and type 2 (Th2) lymphocyte functions were assessed in stimulated whole blood cultures.
Both surgical groups had severely depressed in vitro production of interleukin (IL)-12, IL-10, interferon-gamma, IL-2, IL-4, and IL-13 on postoperative day 1. Depression of Th2-type cytokine production was more profound after transthoracic than after transhiatal esophagectomy (IL-4, P=.005; IL-13,P=.007). Postoperative reduction in Th1-type cytokine production was similar between the two groups (interferon-gamma, P=.40; IL-2, P=.06). Irrespective of the surgical approach, patients who developed major infectious complications after surgery presented with a diminished T-cell cytokine production before the operation compared to those who had a relatively uneventful recovery (IL-4, P=.045; interferon-gamma, P=.064). In regression analysis, the occurrence of postoperative major infection was best predicted by increased duration of anesthesia ( P<.0001) and low preoperative interferon-gamma production ( P=.006).
Both transhiatal and transthoracic esophagectomy induced severely depressed monocyte and T-lymphocyte cytokine production. The extent of the surgical procedure had a differential immunosuppressive impact on Th2-type but not on Th1-type cell activity, indicating that the two Th pathways were downregulated through distinct mechanisms. Preoperative interferon-gamma determination would be useful to anticipate the occurrence of postoperative major infectious complications.
研究经裂孔与经胸食管切除术后免疫反应的变化,并评估术前免疫功能在预测术后感染性并发症中的作用。
免疫防御受损与抗感染能力下降有关。经裂孔或经胸途径行食管切除术的患者易发生感染性并发症。目前尚无关于这两种主要手术干预后免疫反应的随机数据。
研究组由20例因癌症随机分配接受有限经裂孔或扩大经胸食管切除术的患者组成。术前及术后第1天至第10天定期采集血样。在刺激的全血培养物中评估单核细胞及1型辅助性T细胞(Th1)和2型辅助性T细胞(Th2)淋巴细胞功能。
两个手术组术后第1天白细胞介素(IL)-12、IL-10、γ干扰素、IL-2、IL-4和IL-13的体外产生均严重受抑。经胸食管切除术后Th2型细胞因子产生的抑制比经裂孔食管切除术后更明显(IL-4,P = 0.005;IL-13,P = 0.007)。两组术后Th1型细胞因子产生的减少相似(γ干扰素,P = 0.40;IL-2,P = 0.06)。无论手术方式如何,与恢复相对顺利的患者相比,术后发生严重感染性并发症的患者术前T细胞细胞因子产生减少(IL-4,P = 0.045;γ干扰素,P = 0.064)。回归分析显示,术后严重感染的发生最能通过麻醉时间延长(P < 0.0001)和术前γ干扰素产生量低(P = 0.006)来预测。
经裂孔和经胸食管切除术均导致单核细胞和T淋巴细胞细胞因子产生严重受抑。手术范围对Th2型而非Th1型细胞活性有不同的免疫抑制作用,表明两条Th途径通过不同机制下调。术前测定γ干扰素有助于预测术后严重感染性并发症的发生。