Hadden J W, Hadden E M, Coffey R G
Infect Immun. 1976 Feb;13(2):382-7. doi: 10.1128/iai.13.2.382-387.1976.
The need for agents designed to modify immune response in the treatment of patients with viral infection, immunodeficiency, or cancer prompted the present study on the mechanisms of action of isoprinosine, a compound developed for antiviral use and whose therapeutic activity may involve the immune system. The effect of isoprinosine on in vitro proliferation of human peripheral blood lymphocytes stimulated by phytohemagglutinin (PHA) and on lymphocyte levels of cyclic adenosine 3',5'-monophosphate and cyclic guanosine 3',5'-monophosphate was analyzed. Over a concentration range from 0.2 to 250 mug/ml, isoprinosine augmented PHA-induced proliferation; maximal stimulation was observed between 25 to 50 mug/ml. Isoprinosine in the absence of PHA had no effect on proliferation. The relative lack of effect of isoprinosine during a 90-min exposure and the lack of effect on lymphocyte cyclic nucleotide levels indicate that isoprinosine potentiates the PHA response by a mechanism different than a number of hormonal agents and such immunopotentiators as levamisole, polyadenylic-acid, and endotoxin. Further evaluation of isoprinosine as an immunopotentiator is indicated.
在治疗病毒感染、免疫缺陷或癌症患者时,需要能够调节免疫反应的药物,这促使了本研究对异嘌呤醇的作用机制进行探讨。异嘌呤醇是一种开发用于抗病毒的化合物,其治疗活性可能涉及免疫系统。分析了异嘌呤醇对植物血凝素(PHA)刺激的人外周血淋巴细胞体外增殖以及淋巴细胞中环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)水平的影响。在0.2至250μg/ml的浓度范围内,异嘌呤醇增强了PHA诱导的增殖;在25至50μg/ml之间观察到最大刺激作用。在无PHA的情况下,异嘌呤醇对增殖无影响。异嘌呤醇在90分钟暴露期间相对缺乏作用以及对淋巴细胞环核苷酸水平无影响,表明异嘌呤醇增强PHA反应的机制不同于许多激素药物以及诸如左旋咪唑、聚腺苷酸和内毒素等免疫增强剂。提示需要对异嘌呤醇作为免疫增强剂进行进一步评估。