医学
肉芽肿伴多发性血管炎
显微镜下多血管炎
美罗华
抗中性粒细胞胞浆抗体
环磷酰胺
发病机制
临床试验
血管炎
耐火材料(行星科学)
免疫学
内科学
病理
抗体
疾病
化疗
天体生物学
物理
作者
Alvise Berti,Divi Cornec,Anisha B. Dua
标识
DOI:10.1016/j.rdc.2023.03.004
摘要
We have made significant headway in our ability to induce and maintain remission in patients with granulomatosis with polyangiitis and microscopic polyangiitis. With increased understanding of the pathogenesis of antineutrophilic cytoplasmic antibody-associated vasculitides (AAV), therapeutic targets have been identified and studied in clinical trials. From initial induction strategies including glucocorticoids and cyclophosphamide, we have discovered effective induction regimens with rituximab and complement inhibition that can significantly decrease the glucocorticoid cumulative doses in patients with AAV. There are many trials underway evaluating management strategies for refractory patients and exploring new and old therapies that may help to continuously improve outcomes for patients with AAV.
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