Rixen D, Livingston D H, Loder P, Denny T N
Department of Surgery, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, USA.
Crit Care Med. 1996 Nov;24(11):1787-92. doi: 10.1097/00003246-199611000-00005.
To study the immunomodulatory effect of the histamine receptor antagonist, ranitidine, in patients admitted to the intensive care unit after severe head injury.
Randomized, prospective, double-blind study.
Surgical intensive care unit of a university Level I trauma center.
Twenty patients admitted with a Glasgow Coma Scale score of < 10 who were enrolled as part of a prospective, multicenter trial to assess the impact of multiple risk factors and ranitidine prophylaxis on the development of stress-related upper gastrointestinal bleeding.
Continuous infusion of ranitidine at 6.25 mg/hr (n = 9) or placebo (n = 11) for a maximum of 5 days.
Before the patients were enrolled in the study and on completion of treatment, lymphocyte cell-surface antigen expression was determined by flow cytometry (n = 14 patients); mitogen-stimulated interferon-gamma and interleukin-2 production were measured by enzyme-linked immunosorbent assay (n = 19 patients). Treatment with ranitidine, but not placebo, was associated with a significant increase in CD4+ lymphocytes (33% to 49%; p < .05) and a significant decrease in CD8+ lymphocytes (41% to 27%; p < .05). Also, the mitogen-stimulated interferon-gamma production increased from 121 to 269 pg/mL (p < .05) in patients treated with ranitidine, but not in patients treated with placebo. There were no significant differences in interleukin-2 production or circulating B-cell concentrations between both groups.
This study demonstrates an immunostimulatory effect of the histamine-2-receptor antagonist, ranitidine, both at the cellular and mediator levels in patients after head injury.
研究组胺受体拮抗剂雷尼替丁对重度颅脑损伤后入住重症监护病房患者的免疫调节作用。
随机、前瞻性、双盲研究。
某大学一级创伤中心的外科重症监护病房。
20名格拉斯哥昏迷量表评分<10分的患者,他们作为一项前瞻性多中心试验的一部分入组,该试验旨在评估多种危险因素和雷尼替丁预防对与应激相关的上消化道出血发生的影响。
以6.25毫克/小时的速度持续输注雷尼替丁(n = 9)或安慰剂(n = 11),最长持续5天。
在患者入组研究前及治疗结束时,通过流式细胞术测定淋巴细胞表面抗原表达(n = 14例患者);通过酶联免疫吸附测定法测量丝裂原刺激的γ干扰素和白细胞介素-2产生量(n = 19例患者)。雷尼替丁治疗而非安慰剂治疗与CD4 +淋巴细胞显著增加(从33%增至49%;p <.05)及CD8 +淋巴细胞显著减少(从41%降至27%;p <.05)相关。此外,接受雷尼替丁治疗的患者丝裂原刺激的γ干扰素产生量从121 pg/mL增至269 pg/mL(p <.05),而接受安慰剂治疗的患者未出现此情况。两组间白细胞介素-2产生量或循环B细胞浓度无显著差异。
本研究证明组胺2受体拮抗剂雷尼替丁在颅脑损伤患者的细胞和介质水平均具有免疫刺激作用。