Stevenson M M, Ghadirian E
Centre for the Study of Host Resistance, McGill University, Montreal, Quebec, Canada.
Infect Immun. 1989 Dec;57(12):3936-9. doi: 10.1128/iai.57.12.3936-3939.1989.
The effect of intravenous treatment with human recombinant tumor necrosis factor alpha (rTNF-alpha) on infection of susceptible A/J and resistant C57BL/6 mice with Plasmodium chabaudi AS was examined. Treatment of A/J mice with 10(3) or 10(5) U of rTNF-alpha on days 0, 3, 5, 7, and 9 after intraperitoneal infection with 10(6) parasitized erythrocytes resulted in 80% survival and a significant decrease in the peak parasitemia level. Treatment of susceptible A/J hosts with 10(5) but not 10(3) U of rTNF-alpha resulted in increased survival but did not alter the peak parasitemia level following infection with 10(7) parasitized erythrocytes. Moreover, all surviving A/J mice completely eliminated the parasite by approximately 4 weeks and were fully protected against a secondary infection. Except at a dose of 5 x 10(5) U of rTNF-alpha, which resulted in 100% mortality of infected animals, rTNF-alpha did not alter the course or outcome of infection with P. chabaudi AS in resistant C57BL/6 mice.
研究了用人重组肿瘤坏死因子α(rTNF-α)静脉注射治疗对易感性A/J小鼠和抗性C57BL/6小鼠感染查巴迪疟原虫AS的影响。在腹腔注射10⁶个寄生红细胞后第0、3、5、7和9天,用10³或10⁵单位的rTNF-α治疗A/J小鼠,导致80%的存活率,并使寄生虫血症峰值水平显著降低。用10⁵单位而非10³单位的rTNF-α治疗易感性A/J宿主,可提高存活率,但在感染10⁷个寄生红细胞后并未改变寄生虫血症峰值水平。此外,所有存活的A/J小鼠在约4周时完全清除了寄生虫,并对再次感染具有完全的抵抗力。除了5×10⁵单位的rTNF-α剂量导致感染动物100%死亡外,rTNF-α并未改变抗性C57BL/6小鼠感染查巴迪疟原虫AS的病程或结果。