Cardiac gene therapy in large animals: bridge from bench to bedside

被引:0
|
作者
K Ishikawa
L Tilemann
D Ladage
J Aguero
L Leonardson
K Fish
Y Kawase
机构
[1] Cardiovascular Research Center,Department of Cardiology
[2] Mount Sinai School of Medicine,undefined
[3] Gifu Heart Center,undefined
来源
Gene Therapy | 2012年 / 19卷
关键词
model; heart failure; vector; delivery;
D O I
暂无
中图分类号
学科分类号
摘要
Several clinical trials are evaluating gene transfer as a therapeutic approach to treat cardiac diseases. Although it has just started on the path to clinical application, recent advances in gene delivery technologies with increasing knowledge of underlying mechanisms raise great expectations for the cardiac gene therapy. Although in vivo experiments using small animals provide the therapeutic potential of gene transfer, there exist many fundamental differences between the small animal and the human hearts. Before applying the therapy to clinical patients, large animal studies are a prerequisite to validate the efficacy in an animal model more relevant to the human heart. Several key factors including vector type, injected dose, delivery method and targeted cardiac disease are all important factors that determine the therapeutic efficacy. Selecting the most optimal combination of these factors is essential for successful gene therapy. In addition to the efficacy, safety profiles need to be addressed as well. In this regard, large animal studies are best suited for comprehensive evaluation at the preclinical stages of therapeutic development to ensure safe and effective gene transfer. As the cardiac gene therapy expands its potential, large animal studies will become more important to bridge the bench side knowledge to the clinical arena.
引用
收藏
页码:670 / 677
页数:7
相关论文
共 50 条
  • [21] Gene therapy targeting hematopoietic stem cells: From the bench to the bedside
    Cavazzana-Calvo, M.
    Hacein-Bey-Abina, S.
    Garrigue, A.
    Wang, G.
    Bushman, F.
    Fischer, A.
    BLOOD CELLS MOLECULES AND DISEASES, 2008, 40 (02) : 259 - 259
  • [22] Gene therapy as an adjuvant treatment for malignant gliomas: from bench to bedside
    Germano, Isabelle M.
    Binello, Emanuela
    JOURNAL OF NEURO-ONCOLOGY, 2009, 93 (01) : 79 - 87
  • [23] Progress in clinical gene therapy; from the bench to the bedside and vice versa
    Gerritsen, WR
    Grill, J
    Dirven, C
    Kruyt, F
    van Beusechem, VW
    CANCER GENE THERAPY, 2001, 8 (09) : 686 - 686
  • [24] GENE THERAPY FOR BETA-THALASSEMIA: FROM THE BENCH TO THE BEDSIDE AND BACK
    Ferrari, Giuliana
    EXPERIMENTAL HEMATOLOGY, 2022, 111 : S26 - S26
  • [25] Gene therapy as an adjuvant treatment for malignant gliomas: from bench to bedside
    Isabelle M. Germano
    Emanuela Binello
    Journal of Neuro-Oncology, 2009, 93 : 79 - 87
  • [26] Autologous gene therapy for hemoglobinopathies: From bench to patient's bedside
    Locatelli, Franco
    Cavazzana, Marina
    Frangoul, Haydar
    de la Fuente, Josu
    Algeri, Mattia
    Meisel, Roland
    MOLECULAR THERAPY, 2024, 32 (05) : 1202 - 1218
  • [27] Myoblast therapy: From bench to bedside
    Liu, Zhongmin
    Wu, Yanling
    Chen, Bing-Guan
    CELL TRANSPLANTATION, 2006, 15 (06) : 455 - 462
  • [28] Cancer Therapy from Bench to Bedside
    Oh, William K.
    Burakoff, Steven J.
    MOUNT SINAI JOURNAL OF MEDICINE, 2010, 77 (06): : 571 - 572
  • [29] Bioinspired hydrogels build a bridge from bench to bedside
    Seidi, Khaled
    Ayoubi-Joshaghani, Mohammad Hosein
    Azizi, Mehdi
    Javaheri, Tahereh
    Jaymand, Mehdi
    Alizadeh, Effat
    Webster, Thomas J.
    Yazdi, Amirhossein Ahmadieh
    Niazi, Mostafa
    Hamblin, Michael R.
    Amoozgar, Zohreh
    Jahanban-Esfahlan, Rana
    NANO TODAY, 2021, 39
  • [30] Cardiac alternans: From bedside to bench and back
    Chiamvimonvat, Nipavan
    HEART RHYTHM, 2023, 20 (03)