Consequences of genetic diversity of human erythrovirus on infectious security of labile blood products and drugs derived from blood

被引:0
|
作者
Servant-Delmas, A. [1 ]
Mercier, M. [1 ]
Lefrere, J. -J. [1 ]
Laperche, S. [1 ]
机构
[1] Inst Natl Transfus Sanguine, Dept Agents Transmissibles Sang, F-75015 Paris, France
关键词
B19; parvovirus; genetic diversity; genotypes; safety; plasma derivatives;
D O I
10.1684/vir.2008.0211
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sequence analysis of human erythroviruses shows an organization into three genotypes; genotype 1 with B19 Parvovirus (B19V) and 2 new genotypes with a genetic diversity markedly distinct from that of B19V. The frequency of each genotype depends on geographic origin and population. Human erythroviruses infection can be transmitted by transfusion. In immunocompetent recipients, B19V exposure is generally inconsequential, since a large proportion is immunized. However, such a contamination may have severe clinical outcome in not immunized patients with shortened red cell survival, in seronegative pregnant women and in immunocompromised patients. No prevention of blood transmission is currently performed, but a preventive strategy could be discussed for at-risk recipients. In plasma derivatives, B19V-DNA screening is done with a threshold of 10(4) IU/mL. With recent data of a new classification on the human erythroviruses genotypes, DNA testing assays would be validated in accordance with genetic variability, in order to guarantee optimal safety.
引用
收藏
页码:419 / 427
页数:9
相关论文
共 50 条
  • [1] Drugs derived from blood 2/2
    Faure, Sebastien
    ACTUALITES PHARMACEUTIQUES, 2014, 53 (536): : 55 - 58
  • [2] Genetic diversity of human erythroviruses. Consequences on infectious safety of plasma derivatives
    Servant-Delmas, A.
    Mercier, M.
    Laperche, S.
    Lefrere, J. -J.
    TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2009, 16 (5-6) : 482 - 488
  • [3] Drugs derived from blood 1/2
    Faure, Sebastien
    ACTUALITES PHARMACEUTIQUES, 2014, 53 (535): : 51 - 53
  • [4] Evaluation of actual traceability of labile blood products from patients' records
    Ingrand, P
    Salmi, LR
    Benz-Lemoine, E
    Dupuis, M
    TRANSFUSION CLINIQUE ET BIOLOGIQUE, 1998, 5 (06) : 397 - 407
  • [5] Virus safety of human blood, plasma, and derived products
    Guertler, LG
    THROMBOSIS RESEARCH, 2002, 107 : S39 - S45
  • [7] Cell-Derived Microparticles in Blood Products from Thalassemic Blood Donors
    Noulsri, Egarit
    Lerdwana, Surada
    Palasuwan, Duangdao
    Palasuwan, Attakorn
    LABORATORY MEDICINE, 2021, 52 (02) : 150 - 157
  • [8] The genetic diversity of viruses:: consequences for blood screening and prevention of viral infection.
    Barin, F
    Laperche, S
    Couroucé, AM
    TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2000, 7 (05) : 472 - 478
  • [9] NEW ADDITIONAL RELEASE CRITERIA FOR BLOOD PRODUCTS DERIVED FROM POOLED HUMAN PLASMA
    HAMMERLE, T
    HIMMELSPACH, M
    FALKNER, FG
    ZERLAUTH, G
    IGEL, H
    BARRETT, N
    DORNER, F
    THROMBOSIS AND HAEMOSTASIS, 1995, 73 (06) : 1023 - 1023
  • [10] Activation of human polymorphonuclear leukocytes by products derived from the peroxidation of human red blood cell membranes
    Hall, LM
    Murphy, RC
    CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (09) : 1024 - 1031