首页|HBsAg ELISA+/HBV DNA NAT-献血者血清学与分子生物学特征分析

HBsAg ELISA+/HBV DNA NAT-献血者血清学与分子生物学特征分析

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目的 了解西安地区无偿献血人群HBsAg ELISA检测结果与HBV DNA检测结果不一致的标本相关血清学标志物的分布情况。方法 收集 2022 年 11 月 1 日—2023 年 4 月 30 日陕西省血液中心HBsAg ELISA+/HBV DNA NAT-(ELISA+/NAT-)标本共计 71 份,对其采用电化学发光法检测乙肝血清学标志物,同时复检巢式PCR扩增HBV S区和C区基因片段。结果 双ELISA+/NAT-标本(n=30)巢式PCR检测阳性率远高于单ELISA+/NAT-标本(n=41)(60%vs 24。40%,P<0。05)。前者献血者 100%为初次献血者,血清抗-HBc阳性率 100%,血清学模式以1、4、5 此 3 项阳性(80%)为主;后者献血者中 31。7%为重复献血者,血清抗-HBc阳性率仅为 19。51%,血清学模式以单 2 项阳性(43。90%)和全阴(36。58%)为主。结论 单ELISA+结果存在较多假阳性,导致不必要的血液报废;而NAT-标本可能存在低水平的HBV DNA,产生漏检风险。建议针对单HBsAg ELISA+/NAT-献血者,采用多套系统多种方法追溯检测,提高献血者HBV筛查的准确度,减少不必要的血液浪费。
Serological characteristics of HBsAg positive/HBV DNA non-reactive blood donors
Objective To explore the distribution of serological markers related to samples whose serological test results were inconsistent with HBV DNA test results among voluntary blood donors in Xi'an.Methods A total of 71 HBsAg ELISA positive and NAT non-reactive(ELISA+/NAT-)blood samples were collected from Shaanxi Blood Center from November 1,2022 to April 30,2023.The serological markers of hepatitis B were detected by electrochemiluminescence method,and the HBV S region and C region gene fragments were amplified by nested-PCR.Results The positive rate of nested-PCR in double ELISA+/NAT-group(n=30)was statistically higher than that of ELISA+/NAT-group(n=41)(60%vs 24.4%,P<0.05).Donors in double ELISA+/NAT-group were all first-time blood donors,with the positive rate of anti-HBc in serum of100%,and the serological pattern was mainly positive for items 1,4 and 5 items(80%).Among the ELISA+/NAT-group,31.7%were repeat blood donors,with the positive rate of anti-HBc in serum of only 19.51%,and the serological patterns were mainly single anti-HBs positive(43.90%)and all negative(36.58%).Conclusion There are false positives in the test results of ELISA+/NAT-group,which leads to unnecessary blood discarding.Meanwhile,the samples with nega-tive NAT may have low levels of HBV DNA,which may lead to missed detection.It is suggested that multiple systems and methods should be applied to trace the blood donors who are HBsAg positive and NAT non-reactive,so as to improve the ac-curacy of HBV screening of blood donors and reduce blood waste.

HBsAgvoluntary blood donorsnested-PCRHBV DNA

景媛媛、范云、郭燕、张文娟、段勇、冯娜

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陕西省血液中心,陕西 西安 710061

乙型肝炎表面抗原 无偿献血者 巢式PCR HBV DNA

西安市卫生健康委一般研究项目

2020yb48

2024

中国输血杂志
中国输血协会 中国医学科学院输血研究所

中国输血杂志

CSTPCD
影响因子:1.279
ISSN:1004-549X
年,卷(期):2024.37(4)
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