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非免疫原性佐剂CP20961诱导的Lewis大鼠关节炎:疾病发展的免疫组织化学分析

Arthritis in Lewis rats induced by the non-immunogenic adjuvant CP20961: an immunohistochemical analysis of the developing disease.

作者信息

Meacock S C, Brandon D R, Billingham M E

机构信息

Lilly Research Centre Limited, Windlesham, Surrey, United Kingdom.

出版信息

Ann Rheum Dis. 1994 Oct;53(10):653-8. doi: 10.1136/ard.53.10.653.

DOI:10.1136/ard.53.10.653
PMID:7979577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1005431/
Abstract

OBJECTIVES

The role of lymphocytes and macrophages in developing adjuvant arthritis induced by an injection of CP20961 in inbred Lewis rats was studied over a 32 day period using a novel biotin-avidin immunoperoxidase histochemical technique.

METHODS

Fresh frozen sections of hind paws and spleens, as well as lymph nodes draining the site of the injected adjuvant were immunostained using a panel of monoclonal antibodies specific for subsets of lymphocytes and macrophages and for MHC Class II antigen.

RESULTS

An increase in the numbers of activated T-lymphocytes was detected early in the draining lymph nodes before hind paw swelling had begun. The presence of these cells in significant numbers was only observed in the vicinity of the joint after joint swelling and damage had begun. Macrophages were among the first cells to invade the swollen paws and later were found with T-lymphocytes and cells bearing the MHC class II antigen at the face of eroding and re-organising bone.

CONCLUSIONS

The activity of T-lymphocytes in initiating arthritis appeared to occur early in lymph nodes. Joint destruction was more closely associated with the arrival of macrophages but later arrival of T-lymphocytes may have contributed to the maintenance of chronic inflammation.

摘要

目的

采用一种新型生物素-抗生物素蛋白免疫过氧化物酶组织化学技术,在32天的时间里研究淋巴细胞和巨噬细胞在近交系Lewis大鼠注射CP20961诱导的佐剂性关节炎发展过程中的作用。

方法

使用一组针对淋巴细胞和巨噬细胞亚群以及MHC II类抗原的单克隆抗体,对后爪、脾脏的新鲜冰冻切片以及注射佐剂部位引流的淋巴结进行免疫染色。

结果

在后爪肿胀开始之前,在引流淋巴结中早期就检测到活化T淋巴细胞数量增加。只有在关节肿胀和损伤开始后,才在关节附近观察到大量这些细胞的存在。巨噬细胞是最早侵入肿胀后爪的细胞之一,后来在侵蚀和重新组织的骨表面发现它们与T淋巴细胞和携带MHC II类抗原的细胞在一起。

结论

T淋巴细胞引发关节炎的活动似乎在淋巴结中早期就发生了。关节破坏与巨噬细胞的到来关系更为密切,但T淋巴细胞较晚到来可能有助于维持慢性炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/1005431/12fd9ef5b5c4/annrheumd00498-0036-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/1005431/749e605a6216/annrheumd00498-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/1005431/393e13faeebf/annrheumd00498-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/1005431/12fd9ef5b5c4/annrheumd00498-0036-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/1005431/749e605a6216/annrheumd00498-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/1005431/393e13faeebf/annrheumd00498-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53b4/1005431/12fd9ef5b5c4/annrheumd00498-0036-b.jpg

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本文引用的文献

1
Studies of arthritis and other lesions induced in rats by the injection of mycobacterial adjuvant. VII. Pathologic details of the arthritis and spondylitis.关于注射分枝杆菌佐剂诱导大鼠产生关节炎及其他病变的研究。VII. 关节炎和脊柱炎的病理细节。
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Cysteine proteinase activity in the development of arthritis in an adjuvant model of the rat.
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Adjuvant polyarthritis. IV. Induction by a synthetic adjuvant: immunologic, histopathologic, and other studies.佐剂性多关节炎。IV. 由一种合成佐剂诱导:免疫学、组织病理学及其他研究。
抗CD2单克隆抗体(mAb)OX34可抑制大鼠佐剂性关节炎的引发和持续发展。
Ann Rheum Dis. 1997 Dec;56(12):716-22. doi: 10.1136/ard.56.12.716.
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Two subsets of rat T lymphocytes defined with monoclonal antibodies.用单克隆抗体定义的大鼠T淋巴细胞的两个亚群。
Eur J Immunol. 1980 Aug;10(8):609-15. doi: 10.1002/eji.1830100807.
5
The roles of host and donor cells in the rejection of skin allografts by T cell-deprived rats injected with syngeneic T cells.宿主细胞和供体细胞在注射同基因T细胞的T细胞缺失大鼠皮肤同种异体移植排斥反应中的作用。
Eur J Immunol. 1982 Jun;12(6):511-8. doi: 10.1002/eji.1830120612.
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The cellular basis of adjuvant arthritis. II. Characterization of the cells mediating passive transfer.佐剂性关节炎的细胞基础。II. 介导被动转移的细胞的特性
Cell Immunol. 1983 Aug;80(1):198-204. doi: 10.1016/0008-8749(83)90106-5.
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The heterogeneity of mononuclear phagocytes in lymphoid organs: distinct macrophage subpopulations in the rat recognized by monoclonal antibodies ED1, ED2 and ED3.淋巴器官中单核吞噬细胞的异质性:单克隆抗体ED1、ED2和ED3识别的大鼠体内不同巨噬细胞亚群。
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