Kelly C A
Queen Elizabeth Hospital, Gateshead, Tyne and Wear, UK.
Baillieres Clin Rheumatol. 1993 Feb;7(1):17-29. doi: 10.1016/s0950-3579(05)80266-3.
In summary, it appears that factors such as smoking and the presence of secondary Sjögren's syndrome might be important in predisposing the rheumatoid patient to the development of lung disease. Genetic factors may moderate or magnify these risks. At a cellular level, specific macrophage colonies within the lung may interact with a subgroup of CD4 T lymphocytes to produce unopposed B-cell activation, leading to local IgM production and the formation of immune complexes. This can damage lung both directly by cytolysis and indirectly by granulocyte recruitment through the release of neutrophil chemotaxins. Early in the evolution of these processes, steroids appear able to reduce lymphocyte numbers and prevent lung damage occurring, presumably by immunological mechanisms, while later they may reduce granulocyte numbers and activity, halting further progression of lung disease in some patients, perhaps by a direct anti-inflammatory effect. Confirmation of these mechanisms and the development of more specific therapeutic tools is probably dependent on studies which examine lung tissue directly by biopsy and may be aided by the application of more sensitive imaging techniques.
总之,吸烟和继发性干燥综合征等因素似乎在使类风湿患者易患肺部疾病方面很重要。遗传因素可能会减轻或放大这些风险。在细胞水平上,肺内特定的巨噬细胞集落可能与CD4 T淋巴细胞亚群相互作用,导致无对抗的B细胞活化,从而导致局部IgM产生和免疫复合物形成。这可通过细胞溶解直接损伤肺,并通过释放中性粒细胞趋化因子募集粒细胞间接损伤肺。在这些过程演变的早期,类固醇似乎能够减少淋巴细胞数量并预防肺损伤的发生,推测是通过免疫机制,而在后期它们可能减少粒细胞数量和活性,在一些患者中阻止肺部疾病的进一步发展,可能是通过直接的抗炎作用。对这些机制的证实以及更具特异性治疗工具的开发可能依赖于通过活检直接检查肺组织的研究,并且可能借助更敏感的成像技术得到辅助。