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使用基于单克隆抗体的酶联免疫吸附测定法在体外监测药物对雄性吉氏盘尾丝虫的疗效。

The use of monoclonal antibody-based ELISAs to monitor the efficacy of drugs against male Onchocerca gibsoni in vitro.

作者信息

More S J, Copeman D B

机构信息

Graduate School of Tropical Veterinary Science and Agriculture, James Cook University of North Queensland, Townsville, Australia.

出版信息

Trop Med Parasitol. 1991 Mar;42(1):21-4.

PMID:2052851
Abstract

Four monoclonal antibodies directed against antigens of Onchocerca gibsoni were used in antigen detection ELISAs to monitor the efficacy of CGP 20309, CGP 20376, CGP 21833, CGP 24589 and CGP 26702 at 5 micrograms/ml against male O. gibsoni in vitro. No significant differences (P less than 0.05) in antigen output between treated and control groups of parasites were recorded. However, consistently higher levels of antigen from treated (CGP 21833) as compared to control parasites were measured with all four assays, with differences being higher in the first 2 to 3 days post treatment than subsequently. The sensitivity of comparisons between groups was reduced by the high variability in output of antigen both between worms and also from the same worm, in part as a result of mechanical damage to worms sustained during collection or manipulation in vitro. This problem was reduced by zero handling once worms were established in vitro and it is recommended that future work should include a 24 to 48 hour period before treatment commences to detect raised antigen levels associated with physically damaged parasites so they can be excluded. It was concluded that this type of assay has no intrinsic technical or logistical advantage over other published methods of assessing drug-related damage in in vitro filarial screens. Nevertheless, further work using antigen detection ELISAs in this context is justified since these assays, unlike all other methods of assessing drug-induced damage in vitro, have direct application for use in identifying chemotherapeutic effects against similar parasites in vivo.

摘要

使用四种针对吉氏盘尾丝虫抗原的单克隆抗体进行抗原检测酶联免疫吸附测定(ELISA),以监测5微克/毫升的CGP 20309、CGP 20376、CGP 21833、CGP 24589和CGP 26702在体外对雄性吉氏盘尾丝虫的疗效。未记录到处理组和对照组寄生虫之间抗原输出的显著差异(P小于0.05)。然而,在所有四种检测中,与对照寄生虫相比,处理组(CGP 21833)的抗原水平始终较高,处理后前2至3天的差异比随后的差异更大。组间比较的敏感性因蠕虫之间以及同一蠕虫的抗原输出高度可变而降低,部分原因是在体外收集或操作过程中蠕虫受到机械损伤。一旦蠕虫在体外稳定,通过零处理减少了这个问题,建议未来的工作应在开始处理前包括24至48小时的时间段,以检测与物理损伤寄生虫相关的抗原水平升高,以便将它们排除。得出的结论是,这种类型的检测在评估体外丝状线虫筛选中与药物相关损伤的其他已发表方法相比,没有内在的技术或后勤优势。然而,在这种情况下使用抗原检测ELISA进行进一步工作是合理的,因为与所有其他评估体外药物诱导损伤的方法不同,这些检测可直接用于识别体内对类似寄生虫的化疗效果。

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