Modrow Susanne, Dorsch Simone
Institut für Medizinische Mikrobiologie, Unversität Regensburg, Franz-Josef-Strauss-Allee 11, 93053 Regensburg, Germany.
Pathol Biol (Paris). 2002 Jun;50(5):326-31. doi: 10.1016/s0369-8114(02)00302-4.
Parvovirus B19 is the causative agent of erythema infectiosum. In addition, the infection may be associated with other disease manifestations: anemia and aplastic crisis, thrombo- or granulocytopenies; spontaneous abortion or hydrops fetalis in pregnant women; acute and chronic arthritis in adults and children, myocarditis and hepatitis. Both acute and persistent courses of B19-infections have been reported. All patients develop IgG against the capsid proteins VP1 and VP2, the majority of virus neutralizing antibodies that offer life-long protection against reinfections are directed against the VP1-unique region. IgM is mainly directed against VP2-specific epitopes. These antibodies may be present for only a rather short period of two to ten weeks after acute infection. IgG-antibodies against the nonstructural protein NS1 are preferentially found in patients which are unable to eliminate the virus and develop persisting viremia or virus persistence in distinct organs, e.g. synovial fluid, liver, bone marrow.
细小病毒B19是传染性红斑的病原体。此外,该感染可能与其他疾病表现相关:贫血和再生障碍危象、血小板减少或粒细胞减少;孕妇的自然流产或胎儿水肿;成人和儿童的急性和慢性关节炎、心肌炎和肝炎。已有关于B19感染急性病程和持续病程的报道。所有患者都会产生针对衣壳蛋白VP1和VP2的IgG,大多数具有病毒中和作用且能提供终身抗再感染保护的抗体是针对VP1独特区域的。IgM主要针对VP2特异性表位。这些抗体在急性感染后可能仅在相当短的两到十周内出现。针对非结构蛋白NS1的IgG抗体优先在无法清除病毒并出现持续病毒血症或病毒在不同器官(如滑液、肝脏、骨髓)持续存在的患者中发现。