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从溶组织内阿米巴无菌培养物中制备标准化阿米巴抗原并进行评估。

Preparation and evaluation of standardized amoeba antigen from axenic cultures of Entamoeba histolytica.

作者信息

Thompson P E, Graedel S K, Schneider C R, Stucki W B, Gordon R M

出版信息

Bull World Health Organ. 1968;39(3):349-65.

Abstract

The successful mass cultivation of Entamoeba histolytica strains in pure culture has made it possible to produce pure amoeba antigens, which should improve the prospects for immunodiagnostic research and simplify the interpretation of the results obtained in tests for amoeba antibodies.The authors have mass-produced immunodiagnostic antigens for amoebiasis serology from 2 axenic strains of E. histolytica and standardized them as dry powders, which upon reconstitution contained approximately 1.8 mg N/ml, or roughly the equivalent of 10 x 10(6) amoebae per ml.The antigens were evaluated with 121 sera from subjects in Costa Rica, South Africa, Taiwan, Thailand and the USA, 49 of the sera being from cases of amoebic liver abscess, 41 from symptomatic intestinal amoebiasis, 19 from asymptomatic intestinal amoebiasis, and 12 from subjects presumed not to have amoebiasis.Positive results with the indirect haemagglutination test were obtained with 100% of amoebic liver abscess sera, 90.2% of those from symptomatic intestinal amoebiasis, 57.9% of those from asymptomatic intestinal amoebiasis, and 16.7% of the normal sera. Positive complement-fixation tests for the respective groups were obtained in 83.8%, 63.3%, 10.5% and 0%, and positive agar-gel diffusion in 79.6%, 53.7%, 0% and 0%.These results compare favourably with earlier reports of similar studies in which non-axenic cultures were used and agree well with those of investigators in different parts of the world to whom samples of the axenic antigens were sent.The authors conclude that the axenic antigens from either strain used, or from the 2 strains pooled, are of broad usefulness in the detection of amoebic antibodies, but point out that the limitations of the tests now used in amoeba serology are not yet clearly understood and that the pattern of antibody persistence after infection requires further study.

摘要

溶组织内阿米巴菌株在纯培养中的成功大规模培养,使得生产纯阿米巴抗原成为可能,这有望改善免疫诊断研究的前景,并简化阿米巴抗体检测结果的解读。作者从两株无菌培养的溶组织内阿米巴大规模生产了用于阿米巴病血清学检测的免疫诊断抗原,并将其制成干粉进行标准化,复溶后每毫升含约1.8毫克氮,大致相当于每毫升10×10⁶个阿米巴。用来自哥斯达黎加、南非、台湾、泰国和美国受试者的121份血清对这些抗原进行了评估,其中49份血清来自阿米巴肝脓肿病例,41份来自有症状的肠道阿米巴病患者,19份来自无症状的肠道阿米巴病患者,12份来自推测未患阿米巴病的受试者。间接血凝试验中,100%的阿米巴肝脓肿血清、90.2%的有症状肠道阿米巴病血清、57.9%的无症状肠道阿米巴病血清以及16.7%的正常血清呈阳性结果。相应组别的补体结合试验阳性率分别为83.8%、63.3%、10.5%和0%,琼脂凝胶扩散试验阳性率分别为79.6%、53.7%、0%和0%。这些结果与早期使用非无菌培养物的类似研究报告相比更具优势,并且与世界各地收到无菌抗原样本的研究人员的结果非常吻合。作者得出结论,所用任一菌株或两株混合菌株的无菌抗原在检测阿米巴抗体方面具有广泛用途,但指出目前阿米巴血清学检测的局限性尚未完全明确理解,感染后抗体持续存在的模式需要进一步研究。

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