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原发性干燥综合征中新兴的生物疗法。

Emerging biological therapies in primary Sjogren's syndrome.

作者信息

Ramos-Casals M, Brito-Zerón P

机构信息

Department of Autoimmune Diseases, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Hospital Clinic, Barcelona, Spain.

出版信息

Rheumatology (Oxford). 2007 Sep;46(9):1389-96. doi: 10.1093/rheumatology/kem078. Epub 2007 Jun 22.

DOI:10.1093/rheumatology/kem078
PMID:17586555
Abstract

Sjögren's syndrome (SS) is a systemic autoimmune disease that mainly affects the exocrine glands and usually presents as persistent dryness of the mouth and eyes. SS primarily affects white perimenopausal women, with an incidence of 4-5 cases per 100 000. Recent studies have analysed new therapeutic approaches, focusing mainly on the use of biological agents. B-cell targeted therapies seem to be the most promising agents in primary SS, especially rituximab, which has been used in more than 50 reported cases. Other promising B-cell targeted therapies include epratuzumab and belimumab, while T-cell targeted agents (efalizumab, abatacept, alefacept) should currently be considered as possible future options. In the near future, biological agents will play key roles in the treatment of severe involvement, broadening the therapeutic options in primary SS and offering a more optimistic point of view of the treatment of this disease, which, at present, is often considered to lack adequate specific therapy. However, the possible risks and benefits of using these agents should be carefully balanced, and a reasonable assessment of the risk of serious adverse events versus the benefits of treatment should be made. The use of biological agents targeting molecules and receptors involved in the aetiopathogenesis of primary SS opens a new era in the therapeutic management of patients with primary SS.

摘要

干燥综合征(SS)是一种全身性自身免疫性疾病,主要影响外分泌腺,通常表现为口腔和眼睛持续干燥。SS主要影响围绝经期女性,发病率为每10万人中有4 - 5例。最近的研究分析了新的治疗方法,主要集中在生物制剂的使用上。B细胞靶向疗法似乎是原发性SS中最有前景的药物,尤其是利妥昔单抗,已有50多例报道使用过。其他有前景的B细胞靶向疗法包括依帕珠单抗和贝利木单抗,而T细胞靶向药物(依法利珠单抗、阿巴西普、阿来西普)目前应被视为未来可能的选择。在不久的将来,生物制剂将在严重受累的治疗中发挥关键作用,拓宽原发性SS的治疗选择,并为这种目前常被认为缺乏足够特异性治疗的疾病的治疗提供更乐观的前景。然而,使用这些药物可能的风险和益处应仔细权衡,并且应对严重不良事件的风险与治疗益处进行合理评估。针对原发性SS发病机制中涉及的分子和受体使用生物制剂,开启了原发性SS患者治疗管理的新时代。

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