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结节病患者中衍生的循环免疫复合物

-Derived Circulating Immune Complexes in Sarcoidosis Patients.

作者信息

Uchida Keisuke, Furukawa Asuka, Yoneyama Akiko, Furusawa Haruhiko, Kobayashi Daisuke, Ito Takashi, Yamamoto Kurara, Sekine Masaki, Miura Keiko, Akashi Takumi, Eishi Yoshinobu, Ohashi Kenichi

机构信息

Division of Surgical Pathology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan.

Department of Human Pathology, Graduate School and Faculty of Medicine, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.

出版信息

Microorganisms. 2021 Oct 21;9(11):2194. doi: 10.3390/microorganisms9112194.

Abstract

is a potential etiologic agent of sarcoidosis and a dysregulated immune response to the commensal bacterium is suspected to cause granuloma formation. -derived insoluble immune complexes were recently demonstrated in sinus macrophages of sarcoidosis lymph nodes, suggesting local proliferation of the bacterium in affected organs. In the present study, we developed a method for detecting -derived immune complexes in human blood by measuring the concentration of -specific lipoteichoic acid (PLTA) detectable after an antigen retrieval pretreatment of plasma samples. Before pretreatment, anti-PLTA antibody was detected and PLTA could not be detected, in all plasma samples from 51 sarcoidosis patients and 35 healthy volunteers. After pretreatment, however, a significant level of PLTA (>105 ng/mL) was detected in 33 (65%) sarcoidosis patients and 5 (14%) control subjects, with 86% specificity and 65% sensitivity for sarcoidosis. In both groups, plasma anti-PLTA antibody titers did not differ between samples with and without detection of PLTA. PLTA levels were abnormally increased (>202 ng/mL) in 21 (41%) sarcoidosis patients. These findings suggest that -derived circulating immune complexes present in human blood are abnormally increased in many sarcoidosis patients, presumably due to local proliferation of the bacterium in the affected organs.

摘要

是结节病的一种潜在病因,并且怀疑对共生菌的免疫反应失调会导致肉芽肿形成。最近在结节病淋巴结的窦巨噬细胞中发现了源自该菌的不溶性免疫复合物,这表明该菌在受影响器官中局部增殖。在本研究中,我们开发了一种通过测量血浆样本抗原修复预处理后可检测到的特异性脂磷壁酸(PLTA)浓度来检测人血中源自该菌的免疫复合物的方法。预处理前,在51例结节病患者和35名健康志愿者的所有血浆样本中均检测到抗PLTA抗体,但未检测到PLTA。然而,预处理后,33例(65%)结节病患者和5例(14%)对照受试者中检测到显著水平的PLTA(>105 ng/mL),对结节病的特异性为86%,敏感性为65%。在两组中,检测到和未检测到PLTA的样本之间血浆抗PLTA抗体滴度没有差异。21例(41%)结节病患者的PLTA水平异常升高(>202 ng/mL)。这些发现表明,许多结节病患者血液中存在的源自该菌的循环免疫复合物异常增加,推测是由于该菌在受影响器官中局部增殖所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42eb/8625486/0158974eec1e/microorganisms-09-02194-g001.jpg

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