Baerlecken Niklas, Pursche Nils, Witte Torsten, Kniesch Katja, Höpfner Marius, Ernst Diana, Moosig Frank, Seeliger Benjamin, Prasse Antje
Private Practice Rheumatology, 50996 Cologne, Germany.
Department of Clinical Immunology and Rheumatology, Hannover Medical School, 30625 Hannover, Germany.
J Clin Med. 2020 Mar 6;9(3):715. doi: 10.3390/jcm9030715.
Sarcoidosis is characterized by multiorgan involvement and granulomatous inflammation. Its origin is unknown and the potential role of autoimmunity has not been sufficiently determined. We investigated the presence of autoantibodies in sarcoidosis using protein array technology. The derivation cohort consisted of patients with sarcoidosis ( = 25) and controls including autoimmune disease and blood donors ( = 246). In addition, we tested a validation cohort including pulmonary sarcoidosis patients ( = 58) and healthy controls ( = 13). Initially, sera of three patients with sarcoidosis were screened using a protein array with 28.000 proteins against controls. Thereby we identified the Negative Elongation Factor E (NELF-E) as an autoantigen. With confirmatory Enzyme-linked Immunosorbent Assay (ELISA)testing, 29/82 patients (35%) with sarcoidosis had antibodies against NELF-E of the Immunoglobulin (Ig) G type, whereas 18/253 (7%) sera of the controls were positive for NELF-E. Clinically, there was an association of the frequency of NELF-E antibody detection with lung parenchymal involvement and corresponding x-ray types. NELF-E autoantibodies are associated with sarcoidosis and should be further investigated.
结节病的特征是多器官受累和肉芽肿性炎症。其病因不明,自身免疫的潜在作用尚未得到充分确定。我们使用蛋白质芯片技术研究结节病中自身抗体的存在情况。衍生队列包括结节病患者(n = 25)和对照组,对照组包括自身免疫性疾病患者和献血者(n = 246)。此外,我们测试了一个验证队列,包括肺部结节病患者(n = 58)和健康对照(n = 13)。最初,使用含有28,000种蛋白质的蛋白质芯片对3例结节病患者的血清与对照进行筛查。由此我们确定负延伸因子E(NELF-E)为自身抗原。通过验证性酶联免疫吸附测定(ELISA)检测,29/82例(35%)结节病患者有免疫球蛋白(Ig)G型抗NELF-E抗体,而18/253例(7%)对照血清NELF-E呈阳性。临床上,NELF-E抗体检测频率与肺实质受累及相应的X线类型有关。NELF-E自身抗体与结节病相关,应进一步研究。