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卡介苗甲醇提取残渣对人体的影响。

Effects of methanol extraction residue of Bacillus calmette-Guérin in humans.

作者信息

Perloff M, Holland J F, Lumb G J, Bekesi J G

出版信息

Cancer Res. 1977 Apr;37(4):1191-6.

PMID:321117
Abstract

Forty patients with histologically confirmed neoplastic diseases were treated with the methanol extraction residue of Bacillus Calmette-Guérin (MER). Thirty-six received concomitant chemotherapy. MER was initially given intradermally twice a month, 1 week apart, at a dose of 200 mug into each of five sites draining different lymph node-bearing areas on the anterior body surface. Thirty-seven patients developed local ulcerations at least 0.5 cm in diameter at MER injection sites. Typical lesion evolution was characterized by erythema and induration followed by vesicle formation and central necrosis. Either granulation tissue or a thick nonulcerated eschar preceded healing, leaving a linear, flat scar. Systemic toxicity consisted of malaise, fever, and myalgias on the day of MER administration. No hematological or biochemical changes directly attributable to MER were observed. Dose titrations in decreasing 10-fold dilutions in a linear array in a single anatomical region were carried out on 35 occasions. All patients but three developed at least a 5-mm induration to the 1-mug dose within 2 weeks of titration. Dose reductions were necessary in 19 instances. The minimal dose that produced a 1-cm inflammatory lesion with central necrosis was 0.01 mug. Serial biopsies were performed. These indicated a time-related series of changes from a nonspecific inflammatory lesion to an acute inflammatory response with microabscesses, followed by noncaseating granulomata and ultimately fibrosis. MER is a quantifiable nonviable immunostimulant that obeys dose-response relationships in its cutaneous lesions.

摘要

40例经组织学确诊的肿瘤性疾病患者接受了卡介苗甲醇提取残渣(MER)治疗。36例同时接受了化疗。MER最初通过皮内注射给药,每月2次,间隔1周,在前体表不同的含淋巴结区域引流的5个部位,每个部位注射剂量为200μg。37例患者在MER注射部位出现直径至少0.5cm的局部溃疡。典型的病变演变特征为红斑和硬结,随后形成水疱和中央坏死。愈合前要么是肉芽组织要么是厚的未溃疡焦痂,留下线性、扁平瘢痕。全身毒性表现为MER给药当天出现不适、发热和肌痛。未观察到直接归因于MER的血液学或生化变化。在35个病例中,在单一解剖区域以线性排列按10倍递减稀释进行剂量滴定。除3例患者外,所有患者在滴定后2周内对1μg剂量至少出现5mm的硬结。19例需要减少剂量。产生1cm炎性病变伴中央坏死的最小剂量为0.01μg。进行了系列活检。这些活检显示了一系列与时间相关的变化,从非特异性炎性病变到伴有微脓肿的急性炎症反应,随后是非干酪性肉芽肿,最终是纤维化。MER是一种可量化的无活性免疫刺激剂,其皮肤病变遵循剂量反应关系。

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