Schindler L, Brücher J, Kirchner H
Immunobiology. 1984 Jan;166(1):62-71. doi: 10.1016/S0171-2985(84)80144-8.
Injection of silica did not brake the resistance against MHV3 conferred to C57BL/6 mice by injection of C. parvum. However, silica itself had a marked protective effect against MHV3 infection that was maximal when injecting 1 mg 2 hrs before virus infection. The protective effect of silica was observed in a number of inbred mouse strains that differ in their relative resistance to MHV3 infection. No viral titers were observed in the spleen and liver of mice which had received MHV3 plus silica, whereas high titers were observed in the virus-infected controls. Injection of silica caused a marked decrease in the number of esterase-positive macrophages in the peritoneal wash-out population, that may be compatible with the possibility that the cause of the protection is the depletion of target cells for the viral infection. This latter effect, however, was short-lived and 24-48 hrs after injection of silica, high numbers of esterase-positive cells were again observed. This may explain why only little protection was observed when silica was administered 2 days before virus infection.
注射二氧化硅并未打破由注射微小隐孢子虫赋予C57BL/6小鼠的对MHV3的抵抗力。然而,二氧化硅本身对MHV3感染具有显著的保护作用,在病毒感染前2小时注射1毫克时保护作用最大。在对MHV3感染的相对抵抗力不同的多个近交系小鼠品系中都观察到了二氧化硅的保护作用。接受MHV3加二氧化硅的小鼠的脾脏和肝脏中未观察到病毒滴度,而在病毒感染的对照组中观察到高滴度。注射二氧化硅导致腹膜冲洗液中酯酶阳性巨噬细胞数量显著减少,这可能与保护作用的原因是病毒感染靶细胞的耗竭这一可能性相符。然而,后一种效应是短暂的,在注射二氧化硅后24 - 48小时,再次观察到大量酯酶阳性细胞。这可能解释了为什么在病毒感染前2天给予二氧化硅时仅观察到很少的保护作用。