Feist E, Dörner T
Med. Klinik mit Schwerpunkt Rheumatologie und Klinische Immunologie, Charite Universitätsmedizin Berlin, CC12, Charitéplatz 1, 10098, Berlin.
Z Rheumatol. 2013 Feb;72(1):49-58. doi: 10.1007/s00393-011-0885-4.
Nowadays B and T-cell directed biologics in addition to TNF inhibitors are established as effective and safe treatment options for rheumatoid arthritis. As shown by the approval of rituximab for the treatment of systemic vasculitis, these drugs can also be useful for the treatment of other systemic autoimmune diseases; however, to optimize therapeutic strategies, predictive factors for treatment response as well as a good characterized safety profile are essential. So far implementation of real personalized medicine is not feasible in the field of rheumatology, but first biomarkers have already been identified and provide promising results. In this context, it has been shown that a B-cell directed therapy with rituximab is more effective in seropositive patients with rheumatoid arthritis. In addition, characterization of the cytokine milieu as well as of circulating and tissue infiltrating B and T-cell subsets might be useful for prediction of treatment response in the near future.
如今,除肿瘤坏死因子抑制剂外,B细胞和T细胞定向生物制剂已被确立为类风湿性关节炎有效且安全的治疗选择。如利妥昔单抗获批用于治疗系统性血管炎所示,这些药物也可用于治疗其他系统性自身免疫性疾病;然而,为优化治疗策略,治疗反应的预测因素以及良好的安全性特征至关重要。到目前为止,在风湿病领域实施真正的个性化医疗尚不可行,但已经鉴定出首批生物标志物并取得了有前景的结果。在这种情况下,已表明利妥昔单抗的B细胞定向疗法对类风湿性关节炎血清阳性患者更有效。此外,细胞因子环境以及循环和组织浸润的B细胞和T细胞亚群的特征在不久的将来可能有助于预测治疗反应。