Heyworth M F, Pappo J
Cell Biology Section, VA Medical Center, San Francisco, CA 94121.
Immunology. 1990 Aug;70(4):535-9.
The principal aims of this work were (i) to identify the molecular weight (MW) of Giardia muris trophozoite antigens that are recognized by IgA in small intestinal secretions from G. muris-infected mice, and (ii) to determine whether mouse intestinal Giardia-specific IgA is directed against trophozoite surfaces. BALB/c mice were infected with G. muris cysts, and intestinal secretions were harvested from these mice at various times after the start of Giardia infection, and from uninfected mice. Flow cytometry showed that intestinal IgA from G. muris-infected mice, but not from uninfected mice, became bound to trophozoite surfaces in vitro. Western blotting of trophozoite proteins with mouse intestinal secretions showed that IgA from Giardia-infected mice reacted specifically with a broad protein band of approximately 30,000 MW. This finding suggests that one or more trophozoite proteins of approximately 30,000 MW are targets for intestinal antibody in mice infected with G. muris.
(i)确定感染鼠贾第虫的小鼠小肠分泌物中被IgA识别的鼠贾第虫滋养体抗原的分子量(MW),以及(ii)确定小鼠肠道贾第虫特异性IgA是否针对滋养体表面。将BALB/c小鼠感染鼠贾第虫囊肿,在贾第虫感染开始后的不同时间从这些小鼠以及未感染的小鼠中收集肠道分泌物。流式细胞术显示,感染鼠贾第虫的小鼠而非未感染的小鼠的肠道IgA在体外与滋养体表面结合。用小鼠肠道分泌物对滋养体蛋白进行蛋白质印迹分析表明,来自感染贾第虫小鼠的IgA与一条约30,000 MW的宽蛋白带发生特异性反应。这一发现表明,在感染鼠贾第虫的小鼠中,一种或多种约30,000 MW的滋养体蛋白是肠道抗体的靶标。