Rossi B C, Dean R T, Terry R J
Department of Applied Biology, Brunel University, Uxbridge, UK.
Parasite Immunol. 1987 Nov;9(6):697-704. doi: 10.1111/j.1365-3024.1987.tb00539.x.
We have previously shown that peritoneal macrophages from Trypanosoma brucei infected mice, but not from uninfected mice, expressed high levels of procoagulant activity that could not be produced in vitro by incubation of unstimulated macrophages with bloodstream forms of trypanosomes. In the present study we demonstrate that trypanosome-induced macrophage activation can be achieved in vitro by providing either sensitized (day 7 of infection) lymphocytes and trypanosomes or the supernatant fluid from this interaction. The ability of lymphocytes to secrete macrophage-activating lymphokines is enhanced up to day 12 of infection but was absent in the later stages. Although enhancement of the procoagulant activity occurred in infected nude mice, it seems that macrophage function in African trypanosomiasis, as regards the expression of procoagulant activity, is regulated by T-lymphocytes.
我们之前已经表明,来自感染布氏锥虫小鼠的腹腔巨噬细胞,而非未感染小鼠的腹腔巨噬细胞,表达高水平的促凝血活性,而未受刺激的巨噬细胞与锥虫血流形式在体外孵育无法产生这种活性。在本研究中,我们证明通过提供致敏(感染第7天)淋巴细胞和锥虫或这种相互作用的上清液,可在体外实现锥虫诱导的巨噬细胞活化。淋巴细胞分泌巨噬细胞活化淋巴因子的能力在感染第12天前增强,但在后期阶段则不存在。虽然感染的裸鼠中促凝血活性增强,但就促凝血活性的表达而言,非洲锥虫病中巨噬细胞的功能似乎受T淋巴细胞调节。