Prevalence of Serum IgG and Neutralizing Factors Against Adeno-Associated Virus (AAV) Types 1, 2, 5, 6, 8, and 9 in the Healthy Population: Implications for Gene Therapy Using AAV Vectors

被引:741
作者
Boutin, Sylvie
Monteilhet, Virginie
Veron, Philippe
Leborgne, Christian
Benveniste, Olivier [2 ]
Montus, Marie Francoise
Masurier, Carole [1 ]
机构
[1] Genethon, Serv Immunol, R&D, Immunol Lab, F-91002 Evry, France
[2] Hop La Pitie Salpetriere, AP HP, Fac Med Pierre & Marie Curie, F-75013 Paris, France
关键词
HERPES-SIMPLEX VIRUS; T-CELL RESPONSES; SKELETAL-MUSCLE; IMMUNE-RESPONSES; HEMOPHILIA-B; FACTOR-IX; SUBCLASS RESPONSES; SEROTYPE-9; LEADS; CYSTIC-FIBROSIS; ANTI-HBS;
D O I
10.1089/hum.2009.182
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Adeno-associated viruses (AAVs) are small, nonenveloped single-stranded DNA viruses that require helper viruses to facilitate efficient replication. Despite the presence of humoral responses to the wild-type AAV in humans, AAV remains one of the most promising candidates for therapeutic gene transfer to treat many genetic and acquired diseases. Characterization of the IgG subclass responses to AAV and study of the prevalence of both IgG and neutralizing factors to AAV types 1, 2, 5, 6, 8, and 9 in the human population are of importance for the development of new strategies to overcome these immune responses. Natural exposure to AAV types 1, 2, 5, 6, 8, and 9 can result in the production of antibodies from all four IgG subclasses, with a predominant IgG1 response and low IgG2, IgG3, and IgG4 responses. Prevalences of anti-AAV1 and -AAV2 total IgG determined by enzyme-linked immunosorbent assay were higher (67 and 72%) than those of anti-AAV5 (40%), anti-AAV6 (46%), anti-AAV8 (38%), and anti-AAV9 (47%). Furthermore, data showed that cross-reactions are important. The two highest neutralizing factor seroprevalences were observed for AAV2 (59%) and AAV1 (50.5%) and the lowest were observed for AAV8 (19%) and AAV5 (3.2%). Vectors based on AAV5, AAV8, and AAV9 may have an advantage for gene therapy in humans. Furthermore, among individuals seropositive for AAV5, AAV8, and AAV9, about 70-100% present low titers. Better characterization of the preexisting humoral responses to the AAV capsid and cross-reactivity will allow development of new strategies to circumvent AAV acquired immune responses.
引用
收藏
页码:704 / 712
页数:9
相关论文
共 62 条
  • [1] AALBERSE RC, 1983, J IMMUNOL, V130, P722
  • [2] BIRD P, 1990, IMMUNOLOGY, V69, P355
  • [3] Three aspects of super-recursive algorithms and hypercomputation or finding black swans
    Burgin, M
    Klinger, A
    [J]. THEORETICAL COMPUTER SCIENCE, 2004, 317 (1-3) : 1 - 11
  • [4] Worldwide Epidemiology of Neutralizing Antibodies to Adeno-Associated Viruses
    Calcedo, Roberto
    Vandenberghe, Luk H.
    Gao, Guangping
    Lin, Jianping
    Wilson, James M.
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2009, 199 (03) : 381 - 390
  • [5] Cloning and characterization of adeno-associated virus type 5
    Chiorini, JA
    Kim, F
    Yang, L
    Kotin, RM
    [J]. JOURNAL OF VIROLOGY, 1999, 73 (02) : 1309 - 1319
  • [6] Immune responses to adenovirus and adeno-associated virus in humans
    Chirmule, N
    Propert, KJ
    Magosin, SA
    Qian, Y
    Qian, R
    Wilson, JM
    [J]. GENE THERAPY, 1999, 6 (09) : 1574 - 1583
  • [7] Recombinant adeno-associated virus type 2, 4, and 5 vectors: Transduction of variant cell types and regions in the mammalian central nervous system
    Davidson, BL
    Stein, CS
    Heth, JA
    Martins, I
    Kotin, RM
    Derksen, TA
    Zabner, J
    Ghodsi, A
    Chiorini, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) : 3428 - 3432
  • [8] HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ACTIVATES THE CLASSICAL PATHWAY OF COMPLEMENT BY DIRECT C1-BINDING THROUGH SPECIFIC SITES IN THE TRANSMEMBRANE GLYCOPROTEIN-GP41
    EBENBICHLER, CF
    THIELENS, NM
    VORNHAGEN, R
    MARSCHANG, P
    ARLAUD, GJ
    DIERICH, MP
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (06) : 1417 - 1424
  • [9] Erles K, 1999, J MED VIROL, V59, P406, DOI 10.1002/(SICI)1096-9071(199911)59:3<406::AID-JMV22>3.0.CO
  • [10] 2-N