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硬脂酸红霉素或阿莫西林对慢性支气管炎患者进行化学预防——对细胞免疫和体液免疫功能的影响。

Chemoprophylaxis with erythromycin stearate or amoxycillin in patients with chronic bronchitis--effects on cellular and humoral immune functions.

作者信息

Ras G J, Anderson R, Eftychis H A, Koch U, Theron A, Van Wyk H A, Olivier L R

出版信息

S Afr Med J. 1984;66(25):955-8.

PMID:6515508
Abstract

Twenty-six patients aged between 27 and 71 years with chronic bronchitis were divided into a control group of 6 and two groups of 10 patients each who received either erythromycin stearate or amoxycillin 1500 mg/d for 2 weeks and 1000 mg/d for 12 weeks thereafter. Immunological function tests were performed before starting chemotherapy and thereafter at 2 weeks and 14 weeks. Clinical evaluations and lung function tests showed no significant changes in any of the groups during the study period. In the control group no changes in cellular and humoral immune functions were noted. In the group receiving amoxycillin decreased responses of lymphocytes to the mitogen phytohaemagglutinin were observed after 14 days. In the erythromycin-treated group, increased polymorphonuclear leucocyte (PMNL) motility and mitogen-induced transformation were observed at 14 days but these increases were not statistically significant. In this group the markedly depressed PMNL migration found in 3 individuals before treatment improved considerably. These results indicate that chemotherapy and chemoprophylaxis with either amoxycillin or erythromycin stearate do not compromise the host immunodefences.

摘要

26例年龄在27至71岁之间的慢性支气管炎患者被分为一个6人的对照组和两个各有10名患者的组,后两组患者分别接受硬脂酸红霉素或阿莫西林治疗,治疗方案为:前2周每天1500毫克,之后12周每天1000毫克。在开始化疗前、化疗2周后和14周后进行免疫功能测试。临床评估和肺功能测试显示,在研究期间,任何一组均无显著变化。对照组的细胞免疫和体液免疫功能未见变化。在接受阿莫西林治疗的组中,14天后观察到淋巴细胞对有丝分裂原植物血凝素的反应降低。在红霉素治疗组中,14天时观察到多形核白细胞(PMNL)活力增加和有丝分裂原诱导的转化,但这些增加无统计学意义。在该组中,治疗前3名患者中发现的明显降低的PMNL迁移有了相当大的改善。这些结果表明,用阿莫西林或硬脂酸红霉素进行化疗和化学预防不会损害宿主的免疫防御能力。

相似文献

1
Chemoprophylaxis with erythromycin stearate or amoxycillin in patients with chronic bronchitis--effects on cellular and humoral immune functions.硬脂酸红霉素或阿莫西林对慢性支气管炎患者进行化学预防——对细胞免疫和体液免疫功能的影响。
S Afr Med J. 1984;66(25):955-8.
2
A preliminary comparison of erythromycin, co-trimoxazole and amoxycillin in patients with acute exacerbations of chronic bronchitis admitted to hospital.红霉素、复方新诺明和阿莫西林治疗慢性支气管炎急性加重期住院患者的初步比较
J Int Med Res. 1980;8 Suppl 2:51-8.
3
Effects of two erythromycins, doxycycline and phenoxymethylpenicillin on human leucocyte chemotaxis in vitro.两种红霉素、强力霉素和苯氧甲基青霉素对人白细胞体外趋化性的影响。
J Antimicrob Chemother. 1988 Jun;21 Suppl D:29-32. doi: 10.1093/jac/21.suppl_d.29.
4
A randomised, prospective, single-blind comparison of cefadroxil and amoxycillin in the treatment of acute exacerbations of chronic bronchitis.头孢羟氨苄与阿莫西林治疗慢性支气管炎急性加重的随机、前瞻性、单盲对照研究
Br J Clin Pract. 1989 Jan;43(1):19-23.
5
Enhancement of human polymorphonuclear leucocyte motility by erythromycin in vitro and in vivo.
S Afr Med J. 1984 Aug 4;66(5):173-7.
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Ambroxol plus amoxicillin in the treatment of exacerbations of chronic bronchitis.氨溴索加阿莫西林治疗慢性支气管炎急性加重期
Arzneimittelforschung. 1987 Aug;37(8):969-71.
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Evaluation of efficacy and safety of erdosteine in patients affected by chronic bronchitis during an infective exacerbation phase and receiving amoxycillin as basic treatment (ECOBES, European Chronic Obstructive Bronchitis Erdosteine Study).在感染加重期接受阿莫西林作为基础治疗的慢性支气管炎患者中评价厄多司坦的疗效和安全性(ECOBES,欧洲慢性阻塞性支气管炎厄多司坦研究)
Int J Clin Pharmacol Ther. 1995 Nov;33(11):612-8.
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An in-vitro study of oral therapeutic doses of co-trimoxazole and erythromycin stearate on abnormal polymorphonuclear leucocyte migration.口服治疗剂量的复方新诺明和硬脂酸红霉素对异常多形核白细胞迁移的体外研究。
J Antimicrob Chemother. 1986 Feb;17(2):185-93. doi: 10.1093/jac/17.2.185.
9
Studies on the effects of ingestion of a single 500 mg oral dose of erythromycin stearate on leucocyte motility and transformation and on release in vitro of prostaglandin E2 by stimulated leucocytes.关于单次口服500毫克硬脂酸红霉素对白细胞运动性、转化以及刺激白细胞体外释放前列腺素E2的影响的研究。
J Antimicrob Chemother. 1984 Jul;14(1):41-50. doi: 10.1093/jac/14.1.41.
10
Twice daily dosing of erythromycin acistrate in the treatment of acute bronchitis and pneumonia.
Arzneimittelforschung. 1993 Sep;43(9):1014-7.

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