Preston P M, Brown C G, Richardson W
Division of Biological Sciences, Ashworth Laboratories, University of Edinburgh, Scotland, UK.
Parasite Immunol. 1992 Mar;14(2):125-41. doi: 10.1111/j.1365-3024.1992.tb00456.x.
The following bovine (Bo) and human (Hu) cytokines--Bo rTNF-a, Bo rIFN-g, Hu IFN-a, Hu rIL-1, Hu rIL-2--significantly inhibited the in vitro development of trophozoite-infected cells of three stocks of Theileria annulata and of Theileria parva (Muguga). However, none of these cytokines inhibited the proliferation of established T. annulata or T. parva macroschizont-infected cell lines. Indeed, Bo rTNF-a and Hu rIL-2 consistently enhanced the proliferation of macroschizont-infected cell lines of both species and the blastogenesis of uninfected lymphocytes in trophozoite-infected cultures. These results suggest that cytokines could help in resistance to challenge infections by preventing the further development of trophozoite-infected cells but provide no evidence that any of the above cytokines directly help to resolve primary infections by inhibiting the growth of macroschizont-infected cells. These findings also suggest that both TNF-a and IL-2 could play a role in the pathogenesis of Theileria infections by promoting the proliferation of macroschizont-infected cells and the associated lymphoid hyperplasia.
以下牛(Bo)和人(Hu)细胞因子——牛重组肿瘤坏死因子-α(Bo rTNF-a)、牛重组干扰素-γ(Bo rIFN-g)、人干扰素-α(Hu IFN-a)、人重组白细胞介素-1(Hu rIL-1)、人重组白细胞介素-2(Hu rIL-2)——显著抑制了环形泰勒虫(Theileria annulata)三个虫株以及小泰勒虫(Theileria parva,穆古加株)滋养体感染细胞的体外发育。然而,这些细胞因子均未抑制已建立的环形泰勒虫或小泰勒虫大裂殖体感染细胞系的增殖。实际上,牛重组肿瘤坏死因子-α和人重组白细胞介素-2持续增强了这两种虫种大裂殖体感染细胞系的增殖以及滋养体感染培养物中未感染淋巴细胞的母细胞化。这些结果表明,细胞因子可通过阻止滋养体感染细胞的进一步发育来帮助抵抗感染攻击,但没有证据表明上述任何一种细胞因子通过抑制大裂殖体感染细胞的生长直接有助于解决原发性感染。这些发现还表明,肿瘤坏死因子-α和白细胞介素-2都可能通过促进大裂殖体感染细胞的增殖和相关的淋巴样增生在泰勒虫感染发病机制中发挥作用。