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作 者:曾益新[1] 李济忠[1] 简少文[1] 李端[1] 李满枝[1] 宋立兵[1] 张玲[1] 汪慧民[1]
机构地区:[1]中山医科大学肿瘤研究所病因研究室,广东广州510060
出 处:《癌症》2001年第3期235-238,共4页Chinese Journal of Cancer
基 金:国家"九五"科技攻关基金项目 (96-906-01-03);广东省重点实验室基金项目 (998077035)
摘 要:目的:建立在唾液标本中检出 EB病毒 IgA抗体的方法,以快速、特异诊断鼻咽癌。方法:人工合成 EBV-DNA酶及 EA-D多肽片段,分别作为捕捉抗原,采用 ELISA法检测鼻咽癌患者和健康人血清及唾液中 IgA/ EBV-DNA酶和 EA-D抗体。结果:通过检出 O.D值,经统计学处理,选出鼻咽癌诊断阈值为:血清 O.D值≥ 0.3,唾液 O.D值≥ 0.45( DNA酶与 EA-D两者阈值一致)。鼻咽癌与健康者两组间 DNA酶与 EA-D的 IgA滴度均为 P< 0.0001,有非常显著性差异,与病理确诊相比,阳性符合率为 72.6%~ 77.3%。结论:证实 EBV合成肽链作为捕捉抗原,唾液为标本,用 ELISA法是可行的,方法简便,重复性好,价廉,但诊断符合率需进一步提高。Objective: This study was designed to establish a salivary EBV-EA IgA and DNase IgA test technique, and seek a fast and specific diagnostic technique for nasopharyngeal carcinoma (NPC). Methods: Polypeptides of EBV-DNase(ED) and EA-D was synthesized as catching antigens. With ELISA technique, IgA/ED and IgA/EA-D were evaluated respectively in saliva and serum from NPC patients and healthy volunteers. Results: After statistic analysis of the optical density(OD) values of samples, the diagnostic criteria of NPC in the examination of either IgA/ED or IgA/EA-D was defined as following: OD≥ 0.3 for serum and OD≥ 0.45 for saliva. Significantly statistical difference existed between the values of either IgA/ED or IgA/EA-D titer in patients with NPC and the values in healthy volunteers,P< 0.0001. The coincidence rates between the diagnosis of above IgA/ED or IgA/EA-D titer testes and corresponding histological diagnosis were 72.6%- 77.3% . Conclusion: The Elisa test to detect salivary IgA/ED and IgA/EA-D with synthesized polypeptides is a simple, repeatable, and cheap technique with stability and sensitivity. However its coincidence rate with histology should be improved.
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