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抗风湿病情改善药物对类风湿滑膜作用的研究:金制剂或青霉胺治疗后T淋巴细胞亚群及HLA - DP和DQ抗原表达的降低

An investigation of the action of disease modifying antirheumatic drugs on the rheumatoid synovial membrane: reduction in T lymphocyte subpopulations and HLA-DP and DQ antigen expression after gold or penicillamine therapy.

作者信息

Walters M T, Smith J L, Moore K, Evans P R, Cawley M I

出版信息

Ann Rheum Dis. 1987 Jan;46(1):7-16. doi: 10.1136/ard.46.1.7.

DOI:10.1136/ard.46.1.7
PMID:3101623
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1002051/
Abstract

Synovial needle biopsy specimens from the knee joints of seven patients with rheumatoid arthritis (RA) were examined immunohistochemically before and after six months' treatment with either gold or penicillamine (disease modifying drugs, DMDs). There were significant reductions in the numbers of infiltrating T lymphocytes and a disproportionate fall in the numbers of lymphocytes of the helper/inducer subset when compared with those of the suppressor/cytotoxic subset. This resulted in a fall in the ratio of helper/inducer to suppressor/cytotoxic cells. The immunohistological changes correlated with improvements in erythrocyte sedimentation rate (ESR), serum immunoglobulins, visual analogue pain assessment, grip strength, and Ritchie articular index. A second group of nine patients with RA, already well established on DMD therapy, did not show similar changes after the six month period. The HLA class II antigens DR, DQ, and DP were widely expressed on lymphocytes, macrophages, and synovial lining cells of a group of patients with RA who had never received disease modifying drug therapy. After treatment there was a significant reduction in the expression of HLA-DP and DQ antigens.

摘要

对7例类风湿性关节炎(RA)患者膝关节的滑膜针吸活检标本在接受金制剂或青霉胺(病情缓解药物,DMDs)治疗6个月前后进行免疫组织化学检查。与抑制/细胞毒性亚群的淋巴细胞数量相比,浸润性T淋巴细胞数量显著减少,辅助/诱导亚群的淋巴细胞数量下降不成比例。这导致辅助/诱导细胞与抑制/细胞毒性细胞的比例下降。免疫组织学变化与红细胞沉降率(ESR)、血清免疫球蛋白、视觉模拟疼痛评估、握力和里奇关节指数的改善相关。另一组9例已接受DMD治疗且病情稳定的RA患者在6个月后未出现类似变化。一组从未接受过病情缓解药物治疗的RA患者的淋巴细胞、巨噬细胞和滑膜衬里细胞广泛表达HLA - II类抗原DR、DQ和DP。治疗后,HLA - DP和DQ抗原的表达显著降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/1834654be071/annrheumd00280-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/776ea174d0ce/annrheumd00280-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/f8a0c69663fe/annrheumd00280-0027-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/4dc326572f51/annrheumd00280-0027-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/1834654be071/annrheumd00280-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/776ea174d0ce/annrheumd00280-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/f8a0c69663fe/annrheumd00280-0027-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/4dc326572f51/annrheumd00280-0027-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d19c/1002051/1834654be071/annrheumd00280-0028-a.jpg

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