Pulmonary Manifestations of Primary Sjogren's Syndrome: Underlying Immunological Mechanisms, Clinical Presentation, and Management

被引:52
作者
Gupta, Sarthak [1 ]
Ferrada, Marcela A. [1 ]
Hasni, Sarfaraz A. [1 ]
机构
[1] NIAMSD, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
primary Sjogren's syndrome; interstitial lung disease; ILD; pulmonary manifestations; pSS; lung involvement; INTERSTITIAL LUNG-DISEASE; GLAND EPITHELIAL-CELLS; FOLLOW-UP; SURFACTANT PROTEINS; SYNDROME PREVALENCE; SALIVARY-GLANDS; HIGH EXPRESSION; TH17; CELLS; SP-A; INVOLVEMENT;
D O I
10.3389/fimmu.2019.01327
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pulmonary involvement in primary Sjogren's syndrome (pSS) is an understudied entity with important clinical implications. Its prevalence has been reported in up to 20% of pSS patients. Pulmonary manifestations of pSS are diverse with involvement of airway and/or lung parenchyma. Histopathology of lung lesions suggests a predominance of submucosal mononuclear cell infiltration consisting predominantly of CD4+ T cells. Current understanding of the pathophysiology of lung disease in pSS suggests a similar process driving the pulmonary process as those in the salivary glands, with epithelial cells playing a critical role in the initiation, maintenance, and symptomatology of the disease. Clinical manifestations of lung involvement in pSS are as varied as the underlying pathology and can be vague and non-specific, thus delaying diagnosis. Management options depend on the underlying pathology but are generally limited due to lack of systematic randomized controlled trials. This review helps summarize our current understanding of lung involvement in pSS.
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页数:9
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