Infectious Disease Section, Department of Transfusion Medicine, National Institute for Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Transfusion. 2012 Sep;52(9):1940-8. doi: 10.1111/j.1537-2995.2011.03524.x. Epub 2012 Feb 5.
Recombinant immunoblot assay (RIBA) is used to determine the specificity of antibody to hepatitis C virus (anti-HCV). The RIBA result is recorded as positive, negative, or indeterminate. The interpretation and significance of RIBA-indeterminate reactions are unclear. We addressed the clinical relevance of these reactions in the context of the natural history of HCV infection in a prospectively followed cohort of anti-HCV-positive blood donors.
Donor demographics, exposure history, and humoral and cell-mediated immunity (CMI) were compared in 15 RIBA-indeterminate subjects, nine chronic HCV carriers, and eight spontaneously recovered subjects. Serum samples were tested for anti-HCV by a quantitative, liquid luciferase immunoprecipitation system (LIPS). CMI was assessed by interferon-γ enzyme-linked immunosorbent spot assay.
In the LIPS assay, the sum of antibody responses to six HCV antigens showed significant (p < 0.001) stepwise diminution progressing from chronic carriers to spontaneously recovered to RIBA-indeterminate subjects. CMI responses in RIBA-indeterminate subjects were similar to spontaneously recovered subjects and greater than chronic carriers and controls (p < 0.008). A parenteral risk factor was identified in only 13% of RIBA-indeterminate subjects compared to 89% of chronic carriers and 87% of spontaneously recovered subjects. RIBA-indeterminate donors were older than the other groups.
The CMI and LIPS results suggest that persistent RIBA-indeterminate reactions represent waning anti-HCV responses in persons who have recovered from a remote HCV infection. In such cases, detectable antibody may ultimately disappear leaving no residual serologic evidence of prior HCV infection, as reported in a minority of long-term HCV-recovered subjects.
重组免疫印迹分析(RIBA)用于确定针对丙型肝炎病毒(抗-HCV)的抗体的特异性。RIBA 结果记录为阳性、阴性或不确定。RIBA 不确定反应的解释和意义尚不清楚。我们在一个前瞻性随访的抗-HCV 阳性献血者队列中,根据 HCV 感染的自然史,探讨了这些反应的临床相关性。
在 15 例 RIBA 不确定受试者、9 例慢性 HCV 携带者和 8 例自发恢复受试者中,比较了供体人口统计学、暴露史以及体液和细胞介导免疫(CMI)。通过定量液体荧光素酶免疫沉淀系统(LIPS)检测血清样本中的抗-HCV。通过干扰素-γ酶联免疫斑点测定法评估 CMI。
在 LIPS 检测中,对六个 HCV 抗原的抗体反应总和显示出显著(p<0.001)的逐步减少,从慢性携带者进展到自发恢复再到 RIBA 不确定受试者。RIBA 不确定受试者的 CMI 反应与自发恢复受试者相似,且大于慢性携带者和对照组(p<0.008)。与 89%的慢性携带者和 87%的自发恢复受试者相比,仅在 13%的 RIBA 不确定受试者中确定了一个与注射有关的危险因素。RIBA 不确定供体比其他组年龄更大。
CMI 和 LIPS 结果表明,在从 HCV 感染中恢复的个体中,持续的 RIBA 不确定反应代表抗-HCV 反应的减弱。在这种情况下,最终可能会消失可检测的抗体,从而在少数长期 HCV 恢复的受试者中报告的先前 HCV 感染的残留血清学证据。