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类风湿关节炎患者滑膜组织及软骨-血管翳交界处肿瘤坏死因子α的定位

Localization of tumor necrosis factor alpha in synovial tissues and at the cartilage-pannus junction in patients with rheumatoid arthritis.

作者信息

Chu C Q, Field M, Feldmann M, Maini R N

机构信息

Division of Clinical Immunology, Mathilda and Terence Kennedy Institute of Rheumatology, Hammersmith, London, England.

出版信息

Arthritis Rheum. 1991 Sep;34(9):1125-32. doi: 10.1002/art.1780340908.

Abstract

Using immunoaffinity-purified polyclonal anti-human recombinant tumor necrosis factor alpha (TNF alpha) F(ab')2 fragments and immunohistochemical techniques, the cells that make TNF alpha were localized in the inflamed synovial tissue of patients with rheumatoid arthritis (RA) and osteoarthritis (OA). Anti-TNF alpha antibody-stained cells were demonstrated in 9 of 11 RA and 2 of 4 OA but none of 5 normal synovial membranes examined. In RA, 26-64% of the lining layer cells were positive for TNF alpha. In the interaggregate area, 10-30% of the cells contained TNF alpha, often in a perivascular distribution, and up to 19% of the cells in lymphoid aggregates stained for TNF alpha. Some endothelial cells also stained with these antibodies. In OA tissues, the TNF alpha-containing cells were found predominantly in the deeper layer. Cells containing TNF alpha were also found at the cartilage-pannus junction in all 4 RA specimens examined. Double immunofluorescence analysis demonstrated that most TNF alpha-secreting cells in the RA synovial membrane expressed the monocyte/macrophage marker antigens CD11b and CD14, and a few expressed the T cell marker CD3. Our findings provide histologic evidence that TNF alpha is locally produced in the lining and deeper layers of the synovium by cells of the monocyte/macrophage lineage, supporting its role in inflammation. Further, our findings demonstrate that TNF alpha is produced by cells at the cartilage-pannus junction, which could affect chondrocyte metabolism, leading to the cartilage degradation in RA.

摘要

利用免疫亲和纯化的多克隆抗人重组肿瘤坏死因子α(TNFα)F(ab')2片段和免疫组织化学技术,产生TNFα的细胞定位于类风湿性关节炎(RA)和骨关节炎(OA)患者的炎症滑膜组织中。在11例RA患者中的9例以及4例OA患者中的2例检测到抗TNFα抗体染色的细胞,但在所检查的5例正常滑膜中均未检测到。在RA中,26% - 64%的衬里层细胞TNFα呈阳性。在聚集物间区域,10% - 30%的细胞含有TNFα,常呈血管周围分布,在淋巴样聚集体中高达19%的细胞TNFα染色呈阳性。一些内皮细胞也被这些抗体染色。在OA组织中,含TNFα的细胞主要见于较深层。在所检查的所有4例RA标本的软骨 - 血管翳交界处也发现了含TNFα的细胞。双重免疫荧光分析表明,RA滑膜中大多数分泌TNFα的细胞表达单核细胞/巨噬细胞标志物抗原CD11b和CD14,少数表达T细胞标志物CD3。我们的研究结果提供了组织学证据,表明TNFα由单核细胞/巨噬细胞谱系的细胞在滑膜衬里层和较深层局部产生,支持其在炎症中的作用。此外,我们的研究结果表明,软骨 - 血管翳交界处的细胞产生TNFα,这可能影响软骨细胞代谢,导致RA中的软骨降解。

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