Chiang B L
Graduate Institute of Immunology, Taipei, Taiwan.
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1998 Sep-Oct;39(5):293-6.
Increasing prevalence of atopic diseases has become a major problem in most developing and developed countries. In the past several years, most of our studies have focused on the regulatory mechanisms of immunotherapy and exploration of novel treatment for childhood asthma, including the regulation of type 1 (TH1) and type 2 (TH2) cells, the change of cytokines and chemokines during immunotherapy and also possible novel approaches to immunotherapy in childhood atopic diseases. With further characterization of mechanisms involved in the pathogenesis of atopic diseases and immunological changes during immunotherapy, it may shed light on designing the novel treatments for atopic diseases. The data further suggested advanced immunotherapy with combined allergen and certain stimulators enhancing TH1 activity or allergen gene immunization might contribute to more efficient immunotherapy in the future.
在大多数发展中国家和发达国家,过敏性疾病患病率的上升已成为一个主要问题。在过去几年中,我们的大多数研究都集中在免疫疗法的调节机制以及儿童哮喘新疗法的探索上,包括1型(TH1)和2型(TH2)细胞的调节、免疫疗法期间细胞因子和趋化因子的变化,以及儿童过敏性疾病免疫疗法可能的新方法。随着对过敏性疾病发病机制和免疫疗法期间免疫变化所涉及机制的进一步深入研究,可能会为设计过敏性疾病的新疗法提供思路。数据进一步表明,联合变应原和某些增强TH1活性的刺激剂的先进免疫疗法或变应原基因免疫接种可能有助于未来更有效的免疫疗法。