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抗IgE及其他基于免疫调节的过敏性哮喘新疗法。

Anti-IgE and other new immunomodulation-based therapies for allergic asthma.

作者信息

Jonkers R E, van der Zee J S

机构信息

Department of Pulmonology, Academic Medical Centre, Amsterdam, The Netherlands.

出版信息

Neth J Med. 2005 Apr;63(4):121-8.

Abstract

Understanding of the cellular and molecular mechanisms in asthma has lead to the recognition of a number of potential therapeutic targets, a few of which have been evaluated in clinical studies. Parenteral administrations of both anti-IL-5 and IL-12 inhibit eosinophil recruitment to the airways, but display a lack of clinical efficacy. Interrupting the IL-4 pathway thus far has also shown disappointing results in clinical studies. Omalizumab is the first anti-IgE monoclonal antibody developed for the treatment of moderate to severe asthmatics to receive FDA approval. In a number of clinical trials treatment with omalizumab was associated with moderate improvements in a number of relevant endpoints, including the rate of occurrence of disease exacerbations. Newer DNA-based therapeutic strategies including DNA vaccination and the antisense oligonucleotides show promise but thus far have only been tested in animal models.

摘要

对哮喘细胞和分子机制的理解已促使人们认识到一些潜在的治疗靶点,其中少数已在临床研究中得到评估。抗IL-5和IL-12的肠胃外给药可抑制嗜酸性粒细胞向气道募集,但临床疗效欠佳。迄今为止,阻断IL-4通路在临床研究中也显示出令人失望的结果。奥马珠单抗是首个获批用于治疗中重度哮喘患者的抗IgE单克隆抗体。在多项临床试验中,奥马珠单抗治疗与一些相关终点指标的适度改善相关,包括疾病加重的发生率。包括DNA疫苗接种和反义寡核苷酸在内的更新的基于DNA的治疗策略显示出前景,但迄今为止仅在动物模型中进行了测试。

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