Jennette J C, Falk R J
University of North Carolina School of Medicine, Chapel Hill.
Curr Opin Rheumatol. 1992 Feb;4(1):9-15.
Antineutrophil cytoplasmic autoantibodies are a useful diagnostic serologic marker for a variety of well-known vasculitic syndromes, including Wegener's granulomatosis, polyarteritis nodosa (especially microscopic polyarteritis nodosa), Churg-Strauss syndrome, and pulmonary-renal syndrome with alveolar capillaritis. Although most patients with antineutrophil cytoplasmic autoantibody-associated disease have systemic disease, disease limited to one organ does occur, eg, isolated necrotizing glomerulonephritis, isolated respiratory tract disease, or isolated orbital disease. Antineutrophil cytoplasmic autoantibody titers may be useful in modulating treatment regimens. There is in vitro evidence that antineutrophil cytoplasmic autoantibodies are directly involved in the pathogenesis of antineutrophil cytoplasmic autoantibody-associated vasculitides.
抗中性粒细胞胞浆自身抗体是多种知名血管炎综合征的有用诊断血清学标志物,包括韦格纳肉芽肿、结节性多动脉炎(尤其是显微镜下多动脉炎)、变应性肉芽肿性血管炎和伴有肺泡毛细血管炎的肺肾综合征。虽然大多数抗中性粒细胞胞浆自身抗体相关疾病患者患有全身性疾病,但局限于一个器官的疾病确实会发生,例如孤立性坏死性肾小球肾炎、孤立性呼吸道疾病或孤立性眼眶疾病。抗中性粒细胞胞浆自身抗体滴度可能有助于调整治疗方案。有体外证据表明,抗中性粒细胞胞浆自身抗体直接参与抗中性粒细胞胞浆自身抗体相关血管炎的发病机制。