Thorne K J, Blackwell J M
Adv Parasitol. 1983;22:43-151. doi: 10.1016/s0065-308x(08)60461-3.
Cell-mediated immunity represents an important host defence mechanism against protozoal infections. The effector cells directly involved are neutrophils, macrophages and, ultimately, activated macrophages. Within this simple scheme there are, however, considerable variations in activity. Effector cells from different animal species, and even from different strains of the same species, may be more or less effective in controlling a certain protozoal infection. Different protozoa differ in their susceptibility to cell-mediated killing according to genus, species, strain and morphological form. The most susceptible morphological form is that which occurs in the insect vector, and which has not yet adapted to protect itself from the vertebrate host. Epimastigotes of Trypanosoma and promastigotes of Leishmania are readily killed by phagocytic cells, while the corresponding trypomastigote and amastigote forms are considerably more resistant. Protozoa which live in macrophages, such as amastigotes of Leishmania, endozoites (tachyzoites) of Toxoplasma and amastigotes of reticulotropic strains of T. cruzi, have developed a remarkable resistance to the microbicidal activity of the host cell. Conversely, amastigotes of myotropic strains of T. cruzi, which live in muscle cells, have not developed this resistance to cell-mediated killing by macrophages. Readily accessible protozoa, such as T. brucei trypomastigotes and Plasmodium merozoites in the bloodstream, while they lack the marked resistance developed by reticulotropic protozoa, have a partial protection since they are attacked by phagocytic cells only when specific antibody is present. Granulocyte-mediated killing can be largely attributed to neutrophils. Eosinophils appear to play only a minor role and compete ineffectually when neutrophils are also present. The only group of protozoal species which may be significantly controlled by eosinophils are the stercorarian species of Trypanosoma. In vitro experiments show that antibody-coated trypomastigotes of T. cruzi can be killed by eosinophils, although there is little evidence that this occurs in vivo. Interestingly, this is the only species that has been reported to be susceptible to the major basic protein of eosinophils, a toxic component of the lysosomal granules which is very active against helminths. Neutrophils are not very active against endozoites of Toxoplasma gondii, Trypanosoma, trypomastigotes of salivarian Trypanosoma, free merozoites of Plasmodium, and promastigotes and amastigotes of Leishmania.(ABSTRACT TRUNCATED AT 400 WORDS)
细胞介导的免疫是宿主抵御原生动物感染的重要防御机制。直接参与的效应细胞是中性粒细胞、巨噬细胞,最终是活化的巨噬细胞。然而,在这个简单的机制中,活性存在相当大的差异。来自不同动物物种,甚至同一物种不同品系的效应细胞,在控制某种原生动物感染方面可能或多或少有效。不同的原生动物根据属、种、品系和形态形式,对细胞介导的杀伤敏感性不同。最敏感的形态形式是存在于昆虫媒介中且尚未适应保护自身免受脊椎动物宿主攻击的形式。锥虫的上鞭毛体和利什曼原虫的前鞭毛体很容易被吞噬细胞杀死,而相应的锥鞭毛体和无鞭毛体形式则具有更强的抗性。生活在巨噬细胞内的原生动物,如利什曼原虫的无鞭毛体、弓形虫的内殖子(速殖子)和克氏锥虫网状嗜性菌株的无鞭毛体,对宿主细胞的杀菌活性已产生显著抗性。相反,生活在肌肉细胞中的克氏锥虫亲肌性菌株的无鞭毛体,对巨噬细胞介导的杀伤尚未产生这种抗性。易于接触的原生动物,如血液中的布氏锥虫锥鞭毛体和疟原虫裂殖子,虽然缺乏网状嗜性原生动物所具有的显著抗性,但由于只有在存在特异性抗体时才会受到吞噬细胞攻击,所以具有部分保护作用。粒细胞介导的杀伤主要归因于中性粒细胞。嗜酸性粒细胞似乎只起次要作用,当中性粒细胞也存在时,其竞争效果不佳。唯一可能被嗜酸性粒细胞显著控制的原生动物种类是粪源性锥虫。体外实验表明,克氏锥虫的抗体包被锥鞭毛体可被嗜酸性粒细胞杀死,尽管几乎没有证据表明这在体内发生。有趣的是,这是唯一被报道对嗜酸性粒细胞主要碱性蛋白敏感的物种,该蛋白是溶酶体颗粒的一种有毒成分,对蠕虫非常有活性。中性粒细胞对刚地弓形虫的内殖子、锥虫、涎源性锥虫的锥鞭毛体、疟原虫的游离裂殖子以及利什曼原虫的前鞭毛体和无鞭毛体活性不强。(摘要截选至400字)