华中师范大学学报(自然科学版)
華中師範大學學報(自然科學版)
화중사범대학학보(자연과학판)
JOURNAL OF CENTRAL CHINA NORMAL UNIVERSITY(NATURAL SCIENCES)
2003年
3期
388-394
,共7页
陈思礼%陈强%周雨丝%李玲%陈思义%吴风娇%陈思祗%丁书茂%SPITHILL Terry
陳思禮%陳彊%週雨絲%李玲%陳思義%吳風嬌%陳思祗%丁書茂%SPITHILL Terry
진사례%진강%주우사%리령%진사의%오풍교%진사지%정서무%SPITHILL Terry
巨片形吸虫%感染%同型抗体%ADCC%体外杀虫实验
巨片形吸蟲%感染%同型抗體%ADCC%體外殺蟲實驗
거편형흡충%감염%동형항체%ADCC%체외살충실험
infection with F. gigantica%role of immunological protection%ADCC%in vitro killing assay
以印尼短尾羊(ITT)和美利奴细毛羊( Merino )两种品系的绵羊为实验动物,研究动物感染巨片形吸虫后所产生的抗体依赖性细胞介导的细胞毒反应的免疫应答.结果显示:对巨片形吸虫感染具有抗性的印尼短尾羊不产生特异性的IgG2, 而易感品系的美利奴细毛羊感染巨片形吸虫后体内产生高滴度特异性IgG2抗体.特异性IgG2抗体在免疫应答中起着封闭抗体的作用,抑制巨噬细胞抗体依赖性细胞介导的细胞毒反应.由于印尼短尾羊不产生特异性IgG2抗体,对巨噬细胞抗体依赖性细胞介导的细胞毒反应不产生抑制作用,因此印尼短尾羊对巨片形吸虫的感染具有一定的抵抗力.使用纯化的IgG1 和和IgG2进行体外杀虫试验,结果IgG1有很强的促进体外杀虫效果,而自感染巨片形吸虫的美利奴细毛羊血清标本纯化的IgG2没有体外杀虫作用.体外实验还显示嗜酸性粒细胞在免疫血清、补体和IL-5的共同参与下具有较强的杀虫作用.
以印尼短尾羊(ITT)和美利奴細毛羊( Merino )兩種品繫的綿羊為實驗動物,研究動物感染巨片形吸蟲後所產生的抗體依賴性細胞介導的細胞毒反應的免疫應答.結果顯示:對巨片形吸蟲感染具有抗性的印尼短尾羊不產生特異性的IgG2, 而易感品繫的美利奴細毛羊感染巨片形吸蟲後體內產生高滴度特異性IgG2抗體.特異性IgG2抗體在免疫應答中起著封閉抗體的作用,抑製巨噬細胞抗體依賴性細胞介導的細胞毒反應.由于印尼短尾羊不產生特異性IgG2抗體,對巨噬細胞抗體依賴性細胞介導的細胞毒反應不產生抑製作用,因此印尼短尾羊對巨片形吸蟲的感染具有一定的牴抗力.使用純化的IgG1 和和IgG2進行體外殺蟲試驗,結果IgG1有很彊的促進體外殺蟲效果,而自感染巨片形吸蟲的美利奴細毛羊血清標本純化的IgG2沒有體外殺蟲作用.體外實驗還顯示嗜痠性粒細胞在免疫血清、補體和IL-5的共同參與下具有較彊的殺蟲作用.
이인니단미양(ITT)화미리노세모양( Merino )량충품계적면양위실험동물,연구동물감염거편형흡충후소산생적항체의뢰성세포개도적세포독반응적면역응답.결과현시:대거편형흡충감염구유항성적인니단미양불산생특이성적IgG2, 이역감품계적미리노세모양감염거편형흡충후체내산생고적도특이성IgG2항체.특이성IgG2항체재면역응답중기착봉폐항체적작용,억제거서세포항체의뢰성세포개도적세포독반응.유우인니단미양불산생특이성IgG2항체,대거서세포항체의뢰성세포개도적세포독반응불산생억제작용,인차인니단미양대거편형흡충적감염구유일정적저항력.사용순화적IgG1 화화IgG2진행체외살충시험,결과IgG1유흔강적촉진체외살충효과,이자감염거편형흡충적미리노세모양혈청표본순화적IgG2몰유체외살충작용.체외실험환현시기산성립세포재면역혈청、보체화IL-5적공동삼여하구유교강적살충작용.
The study was carried out in two breeds of sheep, Indonesia Thin Tail (ITT) and Merino, both infected with F. gigantica. Kinetic analysis of Fasciola gigantica specific antibody responses revealed that resistant ITT do not produce a parasite specific IgG2 response; whereas susceptible Merino sheep produce a high parasite specific IgG2 response. The IgG2 produced in Merino sheep might act as a blocking antibody for antibody dependant cell mediated cytotoxicity by macrophages. Whereas, ITT appeared to down regulate IgG2 response, which might enable these sheep to possess an enhanced capacity of killing F. gigantica. The purified IgG1 and IgG2 were used in in vitro killing assays. IgG1 promotes the highest amount of killing compared to immune sera and IgG2 using purified Merino sera antibodies for in vitro killing assays. F. gigantica cultured in increasing amount of IgG1 had a trend of increasing the death rate. Parasites cultured in 10 ug/ml of IgG1 showed the highest amount of death. F. gigantica cultured in eosinophils with immune ITT sera (Day35) was 55% death after 24 hours. It should be that using purified eosinophils with immune ITT serum resulted in a strong trend of killing occurring in those wells which contained a combination of immune sera complement, IL-5 and eosinophils.