Immune responses to adenovirus and adeno-associated virus in humans

被引:567
作者
Chirmule, N
Propert, KJ
Magosin, SA
Qian, Y
Qian, R
Wilson, JM
机构
[1] Univ Penn, Inst Human Gene Therapy, Stellar Chance Labs 304, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Mol & Cellular Engn, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[5] Wistar Inst, Philadelphia, PA 19104 USA
关键词
adenovirus; AAV; neutralizing antibodies; lymphoproliferation; cytokines; humans;
D O I
10.1038/sj.gt.3300994
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vectors based on human adenovirus (Ad) and adenoassociated Virus (AAV) are being evaluated for human gene therapy. The response of the host to the vector, in terms of antigen-specific immunity, will play a substantial role in clinical outcome. We have surveyed cohorts of normal subjects and cystic fibrosis patients for pre-existing immunity to these viruses, caused by naturally acquired infections. A number of humoral and cellular assays to adenovirus serotype 5 (Ad5) and adeno-associated virus serotype 2 (AAV2) were performed from serum and peripheral blood mononuclear cells. Virtually all subjects had Ig to Ad5 although only 55% of these antibodies neutralized virus (NAB). Approximately two of three patients demonstrated CD4(+) T cells that proliferated to Ad antigens of which most were of the TH, subset, based on cytokine secretion. A substantially different pattern of immune responses was observed to AAV2. Although virtually all patients had Ig to AAV2, most of these antibodies were not neutralizing (32% NAB) and only 5% of patients had peripheral blood lymphocytes that proliferated in response to AAV2 antigens. These studies demonstrate marked heterogeneity in pre-existing immunity to Ad5 and AAV2 in human populations. The impact of these findings on outcome following gene therapy will require further study.
引用
收藏
页码:1574 / 1583
页数:10
相关论文
共 30 条
  • [1] Functional diversity of helper T lymphocytes
    Abbas, AK
    Murphy, KM
    Sher, A
    [J]. NATURE, 1996, 383 (6603) : 787 - 793
  • [2] ADENOVIRUS-ASSOCIATED DEFECTIVE VIRUS PARTICLES
    ATCHISON, RW
    CASTO, BC
    HAMMON, WM
    [J]. SCIENCE, 1965, 149 (3685) : 754 - &
  • [3] Interactions between the immune system and gene therapy vectors: Bidirectional regulation of response and expression
    Bromberg, JS
    Debruyne, LA
    Qin, LH
    [J]. ADVANCES IN IMMUNOLOGY, VOL 69, 1998, 69 : 353 - 409
  • [4] ADMINISTRATION OF AN ADENOVIRUS CONTAINING THE HUMAN CFTR CDNA TO THE RESPIRATORY-TRACT OF INDIVIDUALS WITH CYSTIC-FIBROSIS
    CRYSTAL, RG
    MCELVANEY, NG
    ROSENFELD, MA
    CHU, CS
    MASTRANGELI, A
    HAY, JG
    BRODY, SL
    JAFFE, HA
    EISSA, NT
    DANEL, C
    [J]. NATURE GENETICS, 1994, 8 (01) : 42 - 51
  • [5] TRANSFER OF GENES TO HUMANS - EARLY LESSONS AND OBSTACLES TO SUCCESS
    CRYSTAL, RG
    [J]. SCIENCE, 1995, 270 (5235) : 404 - 410
  • [6] Recombinant adeno-associated virus for muscle directed gene therapy
    Fisher, KJ
    Jooss, K
    Alston, J
    Yang, YP
    Haecker, SE
    High, K
    Pathak, R
    Raper, SE
    Wilson, JM
    [J]. NATURE MEDICINE, 1997, 3 (03) : 306 - 312
  • [7] CHARACTERIZATION OF HUMAN PROLIFERATIVE T-CELL RESPONSES TO ADENOVIRUS
    FLOMENBERG, P
    PIASKOWSKI, V
    TRUITT, RL
    CASPER, JT
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (05) : 1090 - 1096
  • [8] FLOTTE TR, 1995, GENE THER, V2, P357
  • [9] Induction of circulating myelin basic protein and proteolipid protein-specific transforming growth factor-beta 1-secreting Th3 T cells by oral administration of myelin in multiple sclerosis patients
    Fukaura, H
    Kent, SC
    Pietrusewicz, MJ
    Khoury, SJ
    Weiner, HL
    Hafler, DA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (01) : 70 - 77
  • [10] Phase I trial of recombinant adenovirus gene transfer in lung cancer - Longitudinal study of the immune responses to transgene and viral products
    GaherySegard, H
    MolinierFrenkel, V
    LeBoulaire, C
    Saulnier, P
    Opolon, P
    Lengagne, R
    Gautier, E
    LeCesne, A
    Zitvogel, L
    Venet, A
    Schatz, C
    Courtney, M
    LeChevalier, T
    Tursz, T
    Guillet, JG
    Farace, F
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (09) : 2218 - 2226