Ebola virus convalescent blood products: Where we are now and where we may need to go

被引:47
作者
Burnouf, Thierry [1 ]
Seghatchian, Jerard [2 ]
机构
[1] Taipei Med Univ, Coll Oral Med, Grad Inst Biomed Mat & Tissue Engn, Taipei, Taiwan
[2] Int Consultancy Blood Components Qual Safety Impr, London, England
关键词
Ebola; Blood; Plasma; Convalescent plasma; Transfusion; Immunoglobulins; Mini-pool; Viral inactivation; Emerging pathogens; Virus; ANTIBODY-DEPENDENT ENHANCEMENT; ACUTE RESPIRATORY SYNDROME; FRESH-FROZEN PLASMA; PASSIVE IMMUNOTHERAPY; PATHOGEN INACTIVATION; SERONEGATIVE PLASMA; INFLUENZA PNEUMONIA; HEMORRHAGIC-FEVER; SARS PATIENTS; INFECTION;
D O I
10.1016/j.transci.2014.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The world is regularly exposed to emerging infections with the potential to burst into a pandemic. One possible way to treat patients, when no other treatment is yet developed, is passive immunization performed by transfusing blood, plasma or plasma immunoglobulin fractions obtained from convalescent donors who have recovered from the disease and have developed protective antibodies. The most recent on-going epidemic is caused by the Ebola virus, a filovirus responsible for Ebola virus disease, a severe, often lethal, hemorrhagic fever. Recently, the use of convalescent blood products was proposed by the WHO as one early option for treating patients with Ebola virus disease. This publication provides an overview of the various convalescent blood products and technological options that could theoretically be considered when there is a need to rely on this therapeutic approach. In countries without access to advanced blood-processing technologies, the choice may initially be restricted to convalescent whole blood or plasma. In technologically advanced countries, additional options for convalescent blood products are available, including virally inactivated plasma and fractionated immunoglobulins. The preparation of minipool immunoglobulins is also a realistic option to consider. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:120 / 125
页数:6
相关论文
共 67 条
  • [1] [Anonymous], 2014, POSITION PAPER COLLE
  • [2] Measles-virus-neutralizing antibodies in intravenous immunoglobulins
    Audet, Susette
    Virata-Theimer, Maria Luisa
    Beeler, Judy A.
    Scott, Dorothy E.
    Frazier, Douglas J.
    Mikolajczyk, Malgorzata G.
    Eller, Nancy
    Chen, Feng-ming
    Yu, Mei-ying W.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2006, 194 (06) : 781 - 789
  • [3] AVENARD G, 1979, NOUV PRESSE MED, V8, P673
  • [4] Characterization of plasma protein activity in riboflavin and UV light-treated fresh frozen plasma during 2 years of storage at-30°C
    Bihm, D. J.
    Ettinger, A.
    Buytaert-Hoefen, K. A.
    Hendrix, B. K.
    Maldonado-Codina, G.
    Rock, G.
    Giclas, P. C.
    Goodrich, R. P.
    [J]. VOX SANGUINIS, 2010, 98 (02) : 108 - 115
  • [5] Protecting the blood supply from emerging pathogens: The role of pathogen inactivation
    Blajchman, M. A.
    [J]. TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2009, 16 (02) : 70 - 74
  • [6] Interhuman transmissibility of Middle East respiratory syndrome coronavirus: estimation of pandemic risk
    Breban, Romulus
    Riou, Julien
    Fontanet, Arnaud
    [J]. LANCET, 2013, 382 (9893) : 694 - 699
  • [7] BRN WBRN, 2014, POT US CONV PLASM MA
  • [8] Nanofiltration of single plasma donations: feasibility study
    Burnouf, T
    Radosevich, M
    El-Ekiaby, M
    Satoh, S
    Sato, T
    Amin, SN
    Savidge, GF
    Goubran, HA
    [J]. VOX SANGUINIS, 2003, 84 (02) : 111 - 119
  • [9] Burnouf T, 2007, World Health Organ Tech Rep S, V941, P189
  • [10] Modern plasma fractionation
    Burnouf, Thierry
    [J]. TRANSFUSION MEDICINE REVIEWS, 2007, 21 (02) : 101 - 117