LeFor W M, Shires D L, McGonigle A F, Shires D L
Transplantation Immunology Laboratory, LifeLink Foundation, Inc., Tampa, Florida, USA.
Clin Transplant. 1995 Aug;9(4):297-300.
Concern about false negative serology tests for infectious diseases in hemodiluted cadaver donors resulted in issuance of new regulations and guidelines from the FDA and CDC. Bone or tissue from donors receiving > or = 4 units of blood, blood products, colloids or crystalloids within 48 h of sampling must be quarantined unless: (a) a pretransfusion serum is available; or (b) an adequate algorithm is employed to ensure hemodilution is insufficient to alter test results, i.e. cause false negatives. Left undefined in these regulations is, what is an adequate algorithm and what amount of hemodilution would cause false negatives. A pretransfusion sample was not available for about 20% of our donors and many had incomplete infusion histories. We used the unambiguous quantitation of serum albumin and total protein to define hemodilution and, if present, hemoconcentration of sera by ultrafiltration to normal protein levels prior to serology testing. Control experiments showed excellent correlation between serum dilution and protein concentration (r > 0.99) and a quantitative recovery of 96.9 +/- 1.4% upon hemoconcentration. Known positive sera (CMV-Ab; HTLV-1Ab; HIV-1,2Ab; HBsAb; HCV-Ab; HBsAg) were spiked into normal sera and diluted up to 1:2000, well beyond detectable levels. A qualitative recovery of 100% and a quantitative recovery of 97.6 +/- 7.5% of antibody or antigen reactivity was achieved upon hemoconcentration and retesting. In two studies, 14% (30/210) and 43% (23/54) of cadaver donors had serum proteins below normal limits and their sera was hemoconcentrated.(ABSTRACT TRUNCATED AT 250 WORDS)
对血液稀释的尸体供体中传染病血清学检测假阴性的担忧,促使美国食品药品监督管理局(FDA)和疾病控制与预防中心(CDC)发布了新的法规和指南。在采样后48小时内接受≥4单位血液、血液制品、胶体或晶体液的供体的骨或组织必须进行隔离,除非:(a)有输血前血清;或(b)采用适当算法确保血液稀释不足以改变检测结果,即导致假阴性。这些法规未明确规定什么是适当算法以及何种程度的血液稀释会导致假阴性。我们约20%的供体没有输血前样本,且许多供体的输液史不完整。我们使用血清白蛋白和总蛋白的明确定量来定义血液稀释情况,若存在血液稀释,则在血清学检测前通过超滤将血清浓缩至正常蛋白水平。对照实验表明血清稀释与蛋白浓度之间具有极佳的相关性(r>0.99),浓缩后定量回收率为96.9±1.4%。将已知阳性血清(巨细胞病毒抗体;人类嗜T淋巴细胞病毒1型抗体;人类免疫缺陷病毒1、2型抗体;乙肝表面抗体;丙肝抗体;乙肝表面抗原)加入正常血清中,稀释至1:2000,远超可检测水平。浓缩并重新检测后,抗体或抗原反应性的定性回收率为100%,定量回收率为97.6±7.5%。在两项研究中,14%(30/210)和43%(23/54)的尸体供体血清蛋白低于正常水平,其血清被浓缩。(摘要截短于250字)