Wallis W J, Loughran T P, Kadin M E, Clark E A, Starkebaum G A
Ann Intern Med. 1985 Sep;103(3):357-62. doi: 10.7326/0003-4819-103-3-357.
Five patients with polyarthritis and neutropenia had numerous circulating large granular lymphocytes with a phenotype attributed to immature natural killer cells. All five had splenomegaly and recurrent infections. Arthritis was most prominent at the wrists and hands, and all patients were considered to have atypical cases of Felty's syndrome. Antinuclear antibodies, rheumatoid factor, antineutrophil antibodies, and immune complexes were detected in most patients. Bone marrow biopsies revealed a maturation arrest at the myelocyte stage and lymphoid infiltrates. Large lymphocytes with azurophilic cytoplasmic granules were found on peripheral blood smears and showed a characteristic reactivity pattern with monoclonal antibodies suggesting a natural killer cell lineage. Peripheral blood mononuclear cells showed less than normal natural killer activity against K562 target cells. Increased numbers of large granular lymphocytes with a phenotype of immature natural killer cells may be important in the pathogenesis of neutropenia, humoral immune disturbances, and synovitis in a subset of patients with Felty's syndrome.
五名患有多关节炎和中性粒细胞减少症的患者循环中存在大量大颗粒淋巴细胞,其表型归因于未成熟的自然杀伤细胞。所有五名患者均有脾肿大和反复感染。关节炎在手腕和手部最为突出,所有患者均被认为患有费尔蒂综合征的非典型病例。大多数患者检测到抗核抗体、类风湿因子、抗中性粒细胞抗体和免疫复合物。骨髓活检显示在髓细胞阶段成熟停滞和淋巴细胞浸润。在外周血涂片上发现了带有嗜天青细胞质颗粒的大淋巴细胞,并且与单克隆抗体显示出特征性反应模式,提示为自然杀伤细胞谱系。外周血单核细胞对K562靶细胞的自然杀伤活性低于正常水平。具有未成熟自然杀伤细胞表型的大颗粒淋巴细胞数量增加可能在一部分费尔蒂综合征患者的中性粒细胞减少症、体液免疫紊乱和滑膜炎的发病机制中起重要作用。