Taylor M J, Van Es R P, Townson S, Bianco A E
Wellcome Research Centre for Parasitic Infections, Department of Biology, Imperial College of Science, Technology, London.
Parasitology. 1992 Dec;105 ( Pt 3):445-51. doi: 10.1017/s003118200007462x.
The survival, growth and development of Onchocerca lienalis 3rd-stage (L3) larvae implanted into mice within micropore chambers has been studied with a view to developing a vaccination model for studies of protective immunity in onchocerciasis. The influence of host genetics on worm recoveries and development (growth and moulting rate) was analysed in a panel of inbred mice (CBA, BALB/c, DBA/2, SJL, 129J, C57BL/10 (B10), C3H/He and NIH), together with mice of BALB and B10 backgrounds with different major histocompatibility complex (H-2) genes (BALB/c, BALB.K, BALB.B and B10, B10.D2/n, B10.BR, B10.S). Parasite recoveries and development were similar in all mouse genotypes tested. They were unaffected by procedures designed to block or modulate phagocytic cell function with carbon or carrageenan, or to suppress inflammation by treatment with hydrocortisone acetate. A comparison of chambers sealed with membranes designed to admit (5.0 microns pore size) or exclude (0.2 microns pore size) host cells demonstrated no effect on the percentage recovery of living larvae, although dead larvae were more frequently retrieved when cells were excluded. Recoveries and rates of development of larvae implanted into immunodeficient scid mice and athymic Hooded rats were similar to those recorded in immunocompetent controls. We conclude that host genetic factors and immunocompetence are not significant determinants of survival, growth or development of O. lienalis larvae implanted within micropore chambers into naive mice. Despite its limitations, the use of this system merits further investigation as an approach to the study of protective immunity against developing larvae in onchocerciasis.
为了开发一种用于盘尾丝虫病保护性免疫研究的疫苗接种模型,研究人员对植入微孔室的小鼠体内的链尾盘尾丝虫第三期(L3)幼虫的存活、生长和发育情况进行了研究。在一组近交系小鼠(CBA、BALB/c、DBA/2、SJL、129J、C57BL/10(B10)、C3H/He和NIH)以及具有不同主要组织相容性复合体(H-2)基因的BALB和B10背景的小鼠(BALB/c、BALB.K、BALB.B和B10、B10.D2/n、B10.BR、B10.S)中,分析了宿主遗传学对蠕虫回收率和发育(生长和蜕皮率)的影响。在所测试的所有小鼠基因型中,寄生虫的回收率和发育情况相似。它们不受旨在用碳或角叉菜胶阻断或调节吞噬细胞功能,或用醋酸氢化可的松治疗抑制炎症的程序的影响。对用设计为允许(孔径5.0微米)或排除(孔径0.2微米)宿主细胞的膜密封的室进行比较,结果表明对活幼虫的回收率百分比没有影响,尽管在排除细胞时更频繁地回收死幼虫。植入免疫缺陷的scid小鼠和无胸腺带帽大鼠体内的幼虫的回收率和发育率与免疫 competent 对照组中记录的相似。我们得出结论,宿主遗传因素和免疫能力不是植入微孔室的幼稚小鼠体内的链尾盘尾丝虫幼虫存活、生长或发育的重要决定因素。尽管有其局限性,但作为研究盘尾丝虫病中发育幼虫的保护性免疫的一种方法,该系统的使用值得进一步研究。