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短小棒状杆菌对同种异体小鼠白血病L1210的免疫增强作用。

Immunological enhancement of leukemia L1210 by Corynebacterium parvum in allogeneic mice.

作者信息

Berd D A, Mitchell M S

出版信息

Cancer Res. 1976 Nov;36(11 Pt 1):4119-24.

PMID:975053
Abstract

The effect of Corynebacterium parvum on the immune response of C57BL/6 mice (H-2b) to the allogeneic leukemia L1210 (H-2d) was investigated. Mice were either left untreated or given C. parvum i.v. or i.p. in various dosages. Seven days later they were challenged with 2.5 to 10 X 10(6) live L1210 cells i.p. Control animals almost always rejected the challenge. In contrast, most mice pretreated with either 1.0, 0.5, or 0.25 mg of C. parvum i.v. and 1.0 or 0.5 mg i.p. exhibited enhanced growth of leukemia L1210 as indicated by gross ascites and significantly greater weight gain. This sometimes progressed to the death of the animal, but more often regressed after several days. Spleen cell-mediated cytotoxicity to alloantigens, evaluated in vitro by release of 51Cr from P815Y (H-2d) target cells, was significantly decreased in the mice pretreated with either 1.0 or 0.5 mg of C. parvum i.v. or 0.5 mg of C. parvum i.p. This suppression could not be reversed by reduction of the concentration of macrophages in the spleen cell suspensions. Complement-dependent cytotoxic antibody, measured by release of 51Cr from L1210 cells, was profoundly suppressed in mice pretreated with C. parvum i.v. in dosages ranging from 1.0 to 0.1 mg. These data suggest an immunological basis for the enhanced growth of leukemia L1210 caused by C. parvum at these schedules.

摘要

研究了短小棒状杆菌对C57BL/6小鼠(H-2b)针对同种异体白血病L1210(H-2d)的免疫反应的影响。小鼠要么不进行处理,要么静脉内或腹腔内给予不同剂量的短小棒状杆菌。7天后,它们腹腔内接种2.5至10×10⁶个活的L1210细胞进行攻击。对照动物几乎总是能抵御这种攻击。相反,大多数静脉内给予1.0、0.5或0.25mg短小棒状杆菌以及腹腔内给予1.0或0.5mg短小棒状杆菌预处理的小鼠,白血病L1210的生长增强,表现为明显的腹水和显著更大的体重增加。这有时会发展到动物死亡,但更常见的是几天后病情会缓解。通过P815Y(H-2d)靶细胞释放⁵¹Cr在体外评估的脾细胞介导的对同种异体抗原的细胞毒性,在静脉内给予1.0或0.5mg短小棒状杆菌或腹腔内给予0.5mg短小棒状杆菌预处理的小鼠中显著降低。这种抑制不能通过降低脾细胞悬液中巨噬细胞的浓度来逆转。通过L1210细胞释放⁵¹Cr测量的补体依赖性细胞毒性抗体,在静脉内给予剂量范围为1.0至0.1mg短小棒状杆菌预处理的小鼠中受到严重抑制。这些数据表明在这些给药方案下,短小棒状杆菌导致白血病L1210生长增强存在免疫学基础。

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