Ohkusa Toshifumi, Nomura Tetsuya, Terai Takeshi, Miwa Hiroto, Kobayashi Osamu, Hojo Mariko, Takei Yoshiyuki, Ogihara Tatsuo, Hirai Shu, Okayasu Isao, Sato Nobuhiro
Department of Gastroenterology, Juntendo University School of Medicine, Tokyo, Japan.
Scand J Gastroenterol. 2005 Nov;40(11):1334-42. doi: 10.1080/00365520510023648.
It is proposed that Fusobacterium varium might be one of the elusive pathogenic factors in ulcerative colitis (UC). Our goal was to assess whether an antibiotic combination therapy against F. varium is effective for induction and maintenance of remission of UC.
Twenty chronic, active UC patients with F. varium infection were enrolled consecutively and were randomly assigned to receive amoxicillin, tetracycline or metronidazole per os for 2 weeks (treatment group; n=10), or no antibiotics (control group; n=10). F. varium was sensitive to the antibiotics. Symptom assessment, endoscopic and histological evaluations were performed blind before enrollment at 3-5 months and 12-14 months after the treatment. Serum immunoglobulins to F. varium were measured using an enzyme-linked immunosorbent assay (ELISA). Immunohistochemical detection of F. varium in biopsy specimens was carried out using the avidin-biotin complex method.
The clinical activity, endoscopic and histological scores in the treatment group decreased significantly at 3-5 and 12-14 months after the end of treatment compared with those in the control group (p=0.001-0.036). The remission rate in the treatment group was higher than that in the control group (p=0.037). In addition, the titers of antibody to F. varium and the F. varium density in the mucosa decreased at both the short- and long-term follow-ups in the treatment group (p=0.0002-0.049). No serious drug-related toxicity was observed during the trial.
The 2-week antibiotic combination therapy against F. varium was effective and safe in patients with chronic, active ulcerative colitis in this long-term follow-up study.
有人提出多变梭杆菌可能是溃疡性结肠炎(UC)中难以捉摸的致病因素之一。我们的目标是评估针对多变梭杆菌的抗生素联合疗法对诱导和维持UC缓解是否有效。
连续纳入20例患有多变梭杆菌感染的慢性活动性UC患者,并随机分配接受口服阿莫西林、四环素或甲硝唑治疗2周(治疗组;n = 10),或不使用抗生素(对照组;n = 10)。多变梭杆菌对这些抗生素敏感。在入组前3 - 5个月以及治疗后12 - 14个月进行盲法症状评估、内镜和组织学评估。使用酶联免疫吸附测定(ELISA)检测血清中针对多变梭杆菌的免疫球蛋白。使用抗生物素蛋白 - 生物素复合物方法对活检标本中的多变梭杆菌进行免疫组织化学检测。
与对照组相比,治疗组在治疗结束后3 - 5个月和12 - 14个月时的临床活动度、内镜和组织学评分显著降低(p = 0.001 - 0.036)。治疗组的缓解率高于对照组(p = 0.037)。此外,在治疗组的短期和长期随访中,针对多变梭杆菌的抗体滴度和黏膜中多变梭杆菌密度均降低(p = 0.0002 - 0.049)。试验期间未观察到严重的药物相关毒性。
在这项长期随访研究中,针对多变梭杆菌的2周抗生素联合疗法对慢性活动性溃疡性结肠炎患者有效且安全。