Williams D L, Pretus H A, McNamee R B, Jones E L
Department of Physiology, Tulane University School of Medicine, New Orleans, LA 70112.
Dev Biol Stand. 1992;77:129-36.
A major barrier to the understanding, development and utilization of natural product complex carbohydrate immunomodulators has been the lack of standardization during pre-clinical efficacy and safety testing. In addition, it has been our experience that no single assay system or model is adequate for assessing preclinical efficacy and safety of these agents. To address these important issues, our laboratory group has developed a sequential multi-assay protocol for the preclinical evaluation of natural product complex carbohydrate immunomodulators. This sequential multi-assay screening protocol is divided into four phases: 1) physiochemical characterization of the carbohydrate polymer; 2) evaluation of immune stimulatory activity; 3) assessing in vivo anti-microbial activity and anti-tumor efficacy and 4) preclinical safety evaluation. This sequential protocol provides an effective, reproducible and rational approach to the preclinical assessment of complex carbohydrate immunomodulators that, in our experience, is predictive of clinical safety and efficacy.
天然产物复合碳水化合物免疫调节剂在理解、开发和利用方面的一个主要障碍是临床前疗效和安全性测试期间缺乏标准化。此外,我们的经验是,没有单一的检测系统或模型足以评估这些药物的临床前疗效和安全性。为了解决这些重要问题,我们实验室团队开发了一种用于天然产物复合碳水化合物免疫调节剂临床前评估的顺序多检测方案。这种顺序多检测筛选方案分为四个阶段:1)碳水化合物聚合物的物理化学表征;2)免疫刺激活性评估;3)评估体内抗菌活性和抗肿瘤疗效;4)临床前安全性评估。这种顺序方案为复合碳水化合物免疫调节剂的临床前评估提供了一种有效、可重复且合理的方法,根据我们的经验,该方法可预测临床安全性和疗效。