• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

JOURNAL OF CLINICAL TRANSFUSION AND LABORATORY MEDICINE ›› 2025, Vol. 27 ›› Issue (5): 681-688.DOI: 10.3969/j.issn.1671-2587.2025.05.015

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Advances in Ultra-sensitive HBV Detection Technologies and Their Transfusion Applications

YI Meng1, ZHONG Xiaolong2, WANG Yang1, DU Xiaolin1, FAN Bin1, DUAN Xiaoqiong1   

  1. 1Institute of Blood Transfusion, Chinese Academy of Medical Sciences & Peking Union Medical College, Chengdu 610052;
    2The Third Hospital of Mianyang, Sichuan Mental Health Center, Mianyang 621000
  • Received:2025-09-01 Revised:2025-09-08 Online:2025-10-20 Published:2025-10-11

Abstract: Occult hepatitis B virus infection (OBI), characterized by extremely low viral loads and the persistent latency of intrahepatic cccDNA, poses a profound challenge to global public health security. Its prevention and control have long been constrained by the sensitivity limitations of conventional diagnostic methods, highlighting the urgent need for technological breakthroughs. Emerging detection technologies are driving progress from multiple perspectives: droplet digital PCR enables ultra-sensitive quantification through micro-compartmentalized amplification; CRISPR-Cas systems coupled with isothermal amplification are advancing the development of point-of-care diagnostics; third-generation sequencing technologies open new dimensions for viral genome analysis; and nanomaterial-mediated signal amplification mechanisms are reshaping screening models at the primary-care level. This review summarizes recent advances in OBI diagnostic technologies, provides a comprehensive analysis of their advantages, limitations, and transfusion-related applications, and offers recommendations to support improved OBI risk control in blood transfusion and the development of novel diagnostic strategies tailored to China's national context.

Key words: Occult hepatitis B virus infection (OBI), Transfusion safety, Blood screening, Ultra-sensitive detection, Droplet digital PCR (ddPCR), CRISPR-Cas

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