Csaky K, Nussenblatt R
National Eye Institute, Bethesda, MD 20892, USA.
Springer Semin Immunopathol. 1999;21(2):191-7. doi: 10.1007/BF00810250.
Gene therapy may become a powerful therapeutic modality in the treatment of both ocular inflammatory disease and as a means of preventing rejection following tissue transplantation. By directly introducing into ocular cells genes that encode proteins capable of down-regulating the immune response, gene therapy has potential for both therapy and as a method for studying mechanisms of disease. While marked and rapid advances in the study of gene therapy have been realized, technical questions regarding the appropriate vector or the choice of efficacious immunomodulatory protein still remain.
基因治疗可能会成为治疗眼部炎症性疾病以及预防组织移植后排斥反应的一种强有力的治疗方式。通过将编码能够下调免疫反应的蛋白质的基因直接导入眼细胞,基因治疗在治疗和研究疾病机制方面都具有潜力。虽然基因治疗研究已取得显著且快速的进展,但关于合适的载体或有效免疫调节蛋白的选择等技术问题仍然存在。