Lee S G, Shin H J, Im K I
Kisaengchunghak Chapchi. 1989 Sep;27(3):177-86. doi: 10.3347/kjp.1989.27.3.177.
Observations were made on the differences in cell-mediated immune responses in the mice infected with strongly pathogenic Naegleria fowleri ITMAP 359, weakly pathogenic Naegleria jadini 0400, or non-pathogenic Naegleria gruberi EGB, respectively. Variations in cell-mediated responses and changes in antibody titers according to the duration after infection were noted. Infections were done by dropping 5 microliters saline suspension containing 10 x 10(4) trophozoites cultured axenically in the CGVS medium into the right nasal cavity of ICR mice aging about 6-7 weeks, under the anesthesia by intraperitoneal injection of secobarbital. Following infection, delayed type hypersensitivity(DTH) responses in the footpad and blastogenic responses of the mouse spleen cells using [3H]-thymidine were observed on the day 1, 4, 7, 10 and 14 after infection. For the preparation of amoeba lysates, each of cultured trophozoites were homogenized with an ultrasonicator, and centrifugated at 20,000 g. The supernatants of amoeba lysates were used as the mitogen and antigen for ELISA. Concanavalin A(Con. A) and lipopolysaccharide(LPS) were also used as mitogens in the blastogenic response. 1. The mice infected with N. fowleri showed the mortality rate of 75.7%. The rate was 6.2% for the N. jadini infected group, while no dead mouse was observed for N. gruberi infections. 2. In regard to DTH responses in the N. fowleri infected mice, the level increased in comparison to the control group but declined after 7 days. An increase was also noted for the N. jadini group after 1 day, but gradual decreases were observed through the infection period. In addition, no difference was noted between the N. gruberi infected and control groups. 3. Concerning the blastogenic response of the splenocytes, it increased after 10 days in the experimental group of N. fowleri infection, but the differences were not statistically significant compared with control group. It was evident that N. jadini group was not different from control group either, while there was a tendency of decrease in N. gruberi infected group. In regard to the blastogenic response of the splenocytes by LPS, it was found that the N. fowleri, N. jadini and N. gruberi infected groups had no differences from the control group. 4. The serum antibody titer of N. fowleri and N. jadini infected mice increased from the day 7 and 14 after infection respectively, while the N. gruberi infected mice showed no increase.(ABSTRACT TRUNCATED AT 400 WORDS)
分别对感染强致病性福氏耐格里阿米巴ITMAP 359、弱致病性贾氏耐格里阿米巴0400或非致病性格氏耐格里阿米巴EGB的小鼠的细胞介导免疫反应差异进行了观察。记录了感染后不同时间细胞介导反应的变化以及抗体滴度的变化。通过在腹腔注射司可巴比妥麻醉下,将5微升含有在CGVS培养基中无菌培养的10×10⁴个滋养体的盐水悬液滴入约6 - 7周龄的ICR小鼠的右鼻腔进行感染。感染后,在感染后第1、4、7、10和14天观察足垫中的迟发型超敏反应(DTH)以及使用[³H] - 胸腺嘧啶核苷检测小鼠脾细胞的增殖反应。为制备阿米巴裂解物,将每种培养的滋养体用超声破碎仪匀浆,并以20,000 g离心。阿米巴裂解物的上清液用作ELISA的促有丝分裂原和抗原。刀豆球蛋白A(Con. A)和脂多糖(LPS)也用作增殖反应中的促有丝分裂原。1. 感染福氏耐格里阿米巴的小鼠死亡率为75.7%。感染贾氏耐格里阿米巴组的死亡率为6.2%,而感染格氏耐格里阿米巴组未观察到死亡小鼠。2. 关于感染福氏耐格里阿米巴小鼠的DTH反应,与对照组相比水平升高,但7天后下降。感染贾氏耐格里阿米巴组在1天后也有升高,但在整个感染期逐渐下降。此外,感染格氏耐格里阿米巴组与对照组之间未观察到差异。3. 关于脾细胞的增殖反应,感染福氏耐格里阿米巴的实验组在10天后升高,但与对照组相比差异无统计学意义。显然,感染贾氏耐格里阿米巴组与对照组也无差异,而感染格氏耐格里阿米巴组有下降趋势。关于LPS刺激脾细胞的增殖反应,发现感染福氏耐格里阿米巴、贾氏耐格里阿米巴和格氏耐格里阿米巴组与对照组无差异。4. 感染福氏耐格里阿米巴和贾氏耐格里阿米巴的小鼠血清抗体滴度分别在感染后第7天和第14天升高,而感染格氏耐格里阿米巴的小鼠未升高。(摘要截断于400字)