Division of Gastroenterology and Hepatology and Shanghai Institute of Digestive Disease, Renji Hospital, Shanghai Jiao Tong University, Shanghai, China; Hepatology, Department of Clinical Research, University of Bern, Bern, Switzerland.
NIHR Biomedical Research Centre, Translational Gastroenterology Unit, University of Oxford, Oxford, UK; Peter Medarwar Building for Pathogen Research, University of Oxford, Oxford, UK.
Lancet Gastroenterol Hepatol. 2017 Feb;2(2):123-134. doi: 10.1016/S2468-1253(16)30076-0. Epub 2017 Jan 12.
Serum samples identified as positive for total anti-HBc, but negative for both HBsAg and anti-HBs, are referred to as anti-HBc alone. This serological response is compatible with acute, resolved, and chronic hepatitis B virus (HBV)infection but might also signify occult HBV infection. Once the anti-HBc alone pattern is detected, false-positive reactivity should be ruled out and further analyses can resolve the clinical status of the donor. The identification of anti-HBc positivity in the absence of HBsAg in organ transplant donors and in candidate patients for chemotherapy and immunosuppressive therapy requires further investigation because of the risk of HBV reactivation. False-positive detection, acute infection during the window phase, and resolved or chronic HBV infection are all possible and only distinguishable if the additional assays are done and measures of liver damage are taken into account. Measurement of serum anti-HBs responses after the administration of HBV vaccination can be useful to distinguish this serological profile. In view of the low risk of HBV reactivation in anti-HBc alone patients who are candidates for immunosuppressive treatment, such patients might not require pre-emptive antiviral therapy, but should be followed up on a monthly basis for alanine aminotransferase followed by quantitative HBV DNA testing in those with alanine aminotransferase increase. According to specific guidelines, nucleoside analogue prophylaxis is recommended in anti-HBc-positive liver allograft recipients and anti-HBc alone individuals who receive chemotherapy or biological therapy and should be continued for 6-12 months after discontinuation of such immunosuppressive therapies to protect against HBV reactivation.
血清样本如果总抗-HBc 阳性而 HBsAg 和抗-HBs 均阴性,则被称为单纯抗-HBc。这种血清学反应与急性、已恢复和慢性乙型肝炎病毒(HBV)感染相兼容,但也可能表示隐匿性 HBV 感染。一旦检测到单纯抗-HBc 模式,应排除假阳性反应,并进一步分析以确定供体的临床状况。在器官移植供体和接受化疗和免疫抑制治疗的候选患者中,在缺乏 HBsAg 的情况下发现抗-HBc 阳性,由于 HBV 再激活的风险,需要进一步调查。假阳性检测、窗口期急性感染、已恢复或慢性 HBV 感染均有可能,只有在进行额外检测并考虑肝脏损伤措施的情况下才能区分。在接种 HBV 疫苗后测量血清抗-HBs 反应有助于区分这种血清学特征。鉴于单纯抗-HBc 患者接受免疫抑制治疗的 HBV 再激活风险较低,此类患者可能不需要预防性抗病毒治疗,但应每月监测丙氨酸氨基转移酶,随后在丙氨酸氨基转移酶升高的患者中进行定量 HBV DNA 检测。根据具体指南,建议对接受化疗或生物治疗的抗-HBc 阳性肝移植受者和单纯抗-HBc 个体进行核苷类似物预防,并在停止此类免疫抑制治疗后继续预防 6-12 个月,以防止 HBV 再激活。