Morahan P S, Munson A E, Regelson W, Commerford S L, Hamilton L D
Proc Natl Acad Sci U S A. 1972 Apr;69(4):842-6. doi: 10.1073/pnas.69.4.842.
The decrease of the molecular size of poly(I.C) to less than 10(6) decreases its ability to induce interferon, protect mice against virus, or enhance the immune response. Immune adjuvant activity appeared more sensitive to molecular weight than the other protective activities. The composition of the complex-the molecular size of the individual homopolymers when one was large and the other small-did not affect antiviral activity; the activity of a complex made from large poly(I) and small poly(C) was similar to one made from small poly(I) and large poly(C). Molecular size of the complex did not profoundly alter the side effects of poly(I.C). At 2 mg/kg, none of the complexes markedly altered phagocytic function. Only the largest complex sensitized the mouse to endotoxin. However, all of the complexes studied profoundly inhibited drug metabolism by the liver microsomal enzymes between 24 and 72 hr after their inoculation. Decreasing the molecular weight did not alter this inhibition.
聚肌胞苷酸(poly(I.C))分子大小降至10⁶以下会降低其诱导干扰素的能力、保护小鼠抵御病毒的能力或增强免疫反应的能力。免疫佐剂活性似乎比其他保护活性对分子量更为敏感。复合物的组成——当一种均聚物大而另一种均聚物小时,各均聚物的分子大小——并不影响抗病毒活性;由大的聚肌苷酸(poly(I))和小的聚胞苷酸(poly(C))制成的复合物的活性与由小的poly(I)和大的poly(C)制成的复合物相似。复合物的分子大小并未深刻改变poly(I.C)的副作用。在2毫克/千克时,没有一种复合物能显著改变吞噬功能。只有最大的复合物会使小鼠对内毒素敏感。然而,所有研究的复合物在接种后24至72小时之间都会深刻抑制肝脏微粒体酶的药物代谢。降低分子量并不会改变这种抑制作用。