Wright M D, Rogers M V, Davern K M, Mitchell G F
Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Infect Immun. 1988 Nov;56(11):2948-52. doi: 10.1128/iai.56.11.2948-2952.1988.
Mice of the strain WEHI 129/J are genetically resistant to chronic Schistosoma mansoni infection. Resistance is expressed in at least 50% of mice, with the remaining mice showing normal susceptibility to infection. The serum antibody specificities in the resistant proportion of WEHI 129/J were analyzed at various times after exposure to cercariae by using both Western blotting and immunoprecipitation. Comparisons with the susceptible proportion of WEHI 129/J and other permissive mouse strains revealed four antigens that were differentially recognized by resistant mice at various times of infection: Sm25, an Mr 25,000 integral membrane protein of adult worms that was better recognized by resistant mice 40 to 50 days after exposure; Sm67, an Mr 67,000 water-soluble antigen of adult worms that was better recognized by resistant mice at days 30 to 40; Sm120, an Mr 120,000 antigen expressed by cercariae and adult worms that was differentially recognized, although inconsistently, at days 20 to 40 postexposure; and Sm26, an Mr 26,000 glutathione S-transferase that was uniquely recognized by resistant mice at day 20 in two of three experiments. Analysis of antibody specificities in (BALB/c x WEHI 129/J)F1 x WEHI 129/J backcross mice indicated that high responsiveness to Sm25 at days 40 to 50 correlated with resistance. The candidacy of these four molecules as vaccines for schistosomiasis mansoni is discussed.
WEHI 129/J品系小鼠对曼氏血吸虫慢性感染具有遗传抗性。至少50%的小鼠表现出抗性,其余小鼠对感染表现出正常易感性。通过蛋白质印迹法和免疫沉淀法,分析了WEHI 129/J抗性小鼠在接触尾蚴后不同时间的血清抗体特异性。与WEHI 129/J易感小鼠及其他易感小鼠品系的比较显示,有四种抗原在感染的不同时间被抗性小鼠差异识别:Sm25,一种成虫的分子量为25000的整合膜蛋白,在接触后40至50天被抗性小鼠更好地识别;Sm67,一种成虫的分子量为67000的水溶性抗原,在第30至40天被抗性小鼠更好地识别;Sm120,一种由尾蚴和成虫表达的分子量为120000的抗原,在接触后20至40天被差异识别,尽管并不一致;以及Sm26,一种分子量为26000的谷胱甘肽S-转移酶,在三个实验中的两个实验中,抗性小鼠在第20天独特地识别了该抗原。对(BALB/c×WEHI 129/J)F1×WEHI 129/J回交小鼠抗体特异性的分析表明,在第40至50天对Sm25的高反应性与抗性相关。讨论了这四种分子作为曼氏血吸虫病疫苗的候选可能性。