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SBT2171对小鼠胶原诱导性关节炎的预防作用

Preventive Effect of SBT2171 on Collagen-Induced Arthritis in Mice.

作者信息

Yamashita Maya, Matsumoto Kurumi, Endo Tsutomu, Ukibe Ken, Hosoya Tomohiro, Matsubara Yumi, Nakagawa Hisako, Sakai Fumihiko, Miyazaki Tadaaki

机构信息

Milk Science Research Institute, Megmilk Snow Brand Co., Ltd.Saitama, Japan.

Department of Orthopedic Surgery, Graduate School of Medicine, Hokkaido UniversitySapporo, Japan.

出版信息

Front Microbiol. 2017 Jun 21;8:1159. doi: 10.3389/fmicb.2017.01159. eCollection 2017.

Abstract

We recently reported that the intraperitoneal inoculation of SBT2171 inhibited the development of collagen-induced arthritis (CIA), a murine model of rheumatoid arthritis (RA). In the present study, we evaluated the effect of the oral administration of SBT2171 on CIA development and on the regulation of antigen-specific antibody production and inflammatory immune cells, which have been implicated in the development of RA. Both oral administration and intraperitoneal inoculation of SBT2171 reduced joint swelling, body weight loss, and the serum level of bovine type II collagen (CII)-specific antibodies in the CIA mouse model. The intraperitoneal inoculation also decreased the arthritis incidence, joint damage, and serum level of interleukin (IL)-6. In addition, the numbers of total immune cells, total B cells, germinal center B cells, and CD4 T cells in the draining lymph nodes were decreased following intraperitoneal inoculation of SBT2171. These findings demonstrate the ability of SBT2171 to downregulate the abundance of immune cells and the subsequent production of CII-specific antibodies and IL-6, thereby suppressing the CIA symptoms, indicating its potential for use in the prevention of RA.

摘要

我们最近报道,腹腔注射SBT2171可抑制胶原诱导的关节炎(CIA)的发展,CIA是类风湿性关节炎(RA)的一种小鼠模型。在本研究中,我们评估了口服SBT2171对CIA发展以及对与RA发展相关的抗原特异性抗体产生和炎性免疫细胞调节的影响。在CIA小鼠模型中,口服和腹腔注射SBT2171均能减轻关节肿胀、体重减轻以及牛II型胶原(CII)特异性抗体的血清水平。腹腔注射还降低了关节炎发病率、关节损伤以及白细胞介素(IL)-6的血清水平。此外,腹腔注射SBT2171后,引流淋巴结中的总免疫细胞、总B细胞、生发中心B细胞和CD4 T细胞数量减少。这些发现证明了SBT2171下调免疫细胞丰度以及随后产生CII特异性抗体和IL-6的能力,从而抑制CIA症状,表明其在预防RA方面的应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3875/5478730/3b983478cf1e/fmicb-08-01159-g001.jpg

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