血友病和地中海贫血患者丙型肝炎病毒(HCV)感染的血清学特征评估

Romanian journal of virology Pub Date : 1996-01-01
C Antipa, S Ruţă, C Cernescu
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引用次数: 0

摘要

多次输血患者是丙型肝炎(HCV)获得的主要危险群体。用病毒污染的血液或血液衍生物治疗的血友病患者和地中海贫血患者经常表现出抗hcv抗体和慢性肝炎的迹象。对13例血友病患者、18例地中海贫血患者和14例受其他疾病影响的多次输血患者进行了丙型肝炎病毒感染的血清学分析。采用ORTHO HCV 3.0 ELISA试剂盒检测抗HCV抗体的存在,并用Western-blot Murex证实。血清分型使用了模拟NS4区域免疫优势表位的合成肽,这是ELISA阻断反应(Murex)中六种HCV基因型的特征。血清1型流行(51.1%),血清2型在13.3%的患者中检测到,在地中海贫血病例中频率更高。其余样品为多反应性,未检测到单独的血清3型。血清1型和血清2型单反应样品的Western-blot条带图谱不同。通过对年轻患者(地中海贫血患者,平均年龄15.17 +/- 6.5岁)和老年患者(血友病患者,平均年龄32.64 +/- 13.5岁)的多反应性样本的分析,我们提出了不同的再感染获得顺序。感染其中一种亚型并不会对其他亚型的再感染产生保护作用。然而,在再次感染的情况下,症状明显减弱,表明存在有助于保护的交叉抗原反应。这种保护在2型原发性感染的情况下更为明显,部分原因是由NS4基因组片段编码的抗原。
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Serological profile assessment of the infection with hepatitis C virus (HCV) in haemophiliacs and thalassemic patients.

Polytransfused patients represent a major risk group for hepatitis C (HCV) acquirement. Haemophiliacs and thalassemic patients treated with virus contaminated blood or blood derivatives frequently exhibit anti-HCV antibodies and signs of chronic hepatitis. The serological profile for the HCV infection was investigated in 13 haemophiliacs, 18 cases of thalassemia and in 14 polytransfused patients affected by other diseases. The presence of anti-HCV antibodies was detected by means of the ORTHO HCV 3.0 ELISA kit and confirmed by Western-blot Murex. The serotyping used synthetic peptides mimicking the immunodominant epitopes in the NS4 region, characteristic of each of the six HCV genotypes in an ELISA blocking reaction (Murex). Serotype 1 was prevalent (51.1%), while serotype 2 was detected in 13.3% of patients, with a higher frequency in thalassemia cases. The remaining samples were multireactive, and serotype 3 alone was not detected. The profile of Western-blot bands was distinct for the monoreactive samples belonging to serotype 1 or 2. The analysis of the multireactive samples in young (thalassemic, age mean 15.17 +/- 6.5) and aged patients (haemophiliacs, age mean 32.64 +/- 13.5) allows us to suggest a different succession of reinfection acquirements. The infection with one of the subtypes does not confer protection against the reinfection with others. However, a certain attenuation of the symptomatology is obvious in the case of reinfections, indicating the existence of crossantigenic reactivities which contribute to protection. This protection is more evident in the case of primary infection with type 2 and is partially due to antigens coded by the NS4 genomic segment.

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