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New strategies in the treatment and prevention of allergic diseases.

机译:治疗和预防过敏性疾病的新策略。

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Allergic diseases (AD) are more prevalent today than 30 years ago but over the same period, few novel efficacious drugs have been discovered to treat, control or even cure these disorders. Topical or systemic glucocorticosteroids combined with symptom-relieving medications, such as beta 2 -adrenoceptor agonists, leukotriene inhibitors or antihistamines, are still the mainstay of antiallergic treatment. Modified glucocorticosteroids with less adverse effects, better bronchodilators and new selective mediator inhibitors may improve symptom control in the future. Only specific immunotherapy has shown potential for long-lasting disease-modifying effects. Immunomodulation is a therapeutic goal, aiming to modify the dominant helper T cell Type 2 inflammation to a helper T cell Type 1 response using modified allergens, mycobacteria or CpG oligodeoxynucleotides. Humanised monoclonal anti-IgE antibodies are an exciting new immunomodulatory medication that are expected to reach the clinical practice and have recently been licensed in Australia and the US. Advances in molecular, cellular and genetic research of the immunopathophysiology of AD have led to the development of new antagonists for cytokines, chemokines, receptors, second messengers and transcription factors that may become available for clinical use in the next 10 years. Specific diets supplemented with antioxidants or probiotics need further study but offer promise as safe and cheap preventative medicine. The strong genetic component of AD and the Human Genome Project have opened a new field of research, and modification or replacement of target genes has a curative potential with exciting new therapeutic developments in the years ahead.
机译:与30年前相比,今天的过敏性疾病(AD)更为普遍,但在同一时期,很少发现能治疗,控制甚至治愈这些疾病的新型有效药物。局部或全身性糖皮质激素联合缓解症状的药物(如β2-肾上腺素受体激动剂,白三烯抑制剂或抗组胺药)仍然是抗过敏治疗的主要手段。修饰后的糖皮质激素类药物副作用较小,更好的支气管扩张药和新型选择性介导抑制剂可能在将来改善症状控制。仅特定的免疫疗法已显示出持久的改善疾病作用的潜力。免疫调节是一个治疗目标,旨在使用修饰的变应原,分枝杆菌或CpG寡脱氧核苷酸将2型主要辅助T细胞炎症改变为1型辅助T细胞反应。人源化单克隆抗IgE抗体是一种令人兴奋的新型免疫调节药物,有望达到临床实践,最近已在澳大利亚和美国获得许可。 AD的免疫病理生理学的分子,细胞和遗传学研究的进展,导致了针对细胞因子,趋化因子,受体,第二信使和转录因子的新型拮抗剂的开发,这些拮抗剂可能在未来十年内用于临床。补充抗氧化剂或益生菌的特殊饮食需要进一步研究,但有望作为安全和廉价的预防药物。 AD的强大遗传成分和人类基因组计划开辟了一个新的研究领域,并且靶基因的修饰或替换在未来几年中将具有令人兴奋的新疗法发展的治疗潜力。

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