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本文引用的文献

1
Adenoviral transfer of the viral IL-10 gene periarticularly to mouse paws suppresses development of collagen-induced arthritis in both injected and uninjected paws.将病毒白细胞介素-10基因经关节周围注射到小鼠爪部,可抑制注射爪和未注射爪中胶原诱导性关节炎的发展。
J Immunol. 1999 Mar 15;162(6):3625-32.
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Gene therapy for rheumatoid arthritis.
Springer Semin Immunopathol. 1998;20(1-2):197-209. doi: 10.1007/BF00832007.
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Different roles of tumour necrosis factor alpha and interleukin 1 in murine streptococcal cell wall arthritis.肿瘤坏死因子α和白细胞介素1在小鼠链球菌细胞壁关节炎中的不同作用
Cytokine. 1998 Sep;10(9):690-702. doi: 10.1006/cyto.1998.0372.
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Inhibition of collagen-induced arthritis in mice by viral IL-10 gene transfer.病毒白细胞介素-10基因转移对小鼠胶原诱导性关节炎的抑制作用。
J Immunol. 1998 Aug 1;161(3):1516-24.
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Regulatory role of interleukin 10 in joint inflammation and cartilage destruction in murine streptococcal cell wall (SCW) arthritis. More therapeutic benefit with IL-4/IL-10 combination therapy than with IL-10 treatment alone.白细胞介素10在小鼠链球菌细胞壁(SCW)关节炎关节炎症和软骨破坏中的调节作用。白细胞介素4/白细胞介素10联合治疗比单独使用白细胞介素10治疗具有更多的治疗益处。
Cytokine. 1998 May;10(5):361-9. doi: 10.1006/cyto.1997.0298.
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Adenovirus-mediated transfer of viral IL-10 gene inhibits murine collagen-induced arthritis.腺病毒介导的病毒白细胞介素-10基因转移可抑制小鼠胶原诱导的关节炎。
J Immunol. 1998 Jun 1;160(11):5213-20.
7
Direct adenovirus-mediated gene transfer of interleukin 1 and tumor necrosis factor alpha soluble receptors to rabbit knees with experimental arthritis has local and distal anti-arthritic effects.将白细胞介素1和肿瘤坏死因子α可溶性受体通过腺病毒直接介导的基因转移至患实验性关节炎的兔膝关节,具有局部和远端抗关节炎作用。
Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4613-8. doi: 10.1073/pnas.95.8.4613.
8
Dual role of IL-12 in early and late stages of murine collagen type II arthritis.白细胞介素-12在小鼠II型胶原性关节炎早期和晚期的双重作用
J Immunol. 1997 Oct 15;159(8):4094-102.
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Lessons for joint destruction from animal models.
Curr Opin Rheumatol. 1997 May;9(3):221-8. doi: 10.1097/00002281-199705000-00008.
10
Prevention of murine collagen-induced arthritis in the knee and ipsilateral paw by local expression of human interleukin-1 receptor antagonist protein in the knee.通过在膝关节局部表达人白细胞介素-1受体拮抗剂蛋白预防小鼠膝关节和同侧爪胶原诱导的关节炎。
Arthritis Rheum. 1997 May;40(5):893-900. doi: 10.1002/art.1780400517.

关节内白细胞介素-10基因转移可调节膝关节和同侧爪子中胶原诱导性关节炎(CIA)的表达。

Intra-articular IL-10 gene transfer regulates the expression of collagen-induced arthritis (CIA) in the knee and ipsilateral paw.

作者信息

Lubberts E, Joosten L A, Van Den Bersselaar L, Helsen M M, Bakker A C, Xing Z, Richards C D, Van Den Berg W B

机构信息

Rheumatology Research Laboratory, Department of Rheumatology, University Hospital Nijmegen, Nijmegen, The Netherlands.

出版信息

Clin Exp Immunol. 2000 May;120(2):375-83. doi: 10.1046/j.1365-2249.2000.01217.x.

DOI:10.1046/j.1365-2249.2000.01217.x
PMID:10792391
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1905648/
Abstract

We studied the effects of local IL-10 application, introduced by a recombinant human type 5 adenovirus vector, in the mouse knee joint during the early phase of CIA. One intra-articular injection with the IL-10-expressing virus (Ad5E1mIL-10) caused substantial over-expression of IL-10 in the mouse knee joint, using virus dosages which did not induce distracting inflammation. High expression of IL-10 was noted for a few days, being maximal at day 1. One intra-articular injection of Ad5E1mIL-10 in the knee joints of collagen type II (CII)-immunized mice, before onset of CIA was noted, reduced the incidence of collagen arthritis in that knee. Of high interest, the protective effect of local IL-10 expression by Ad5E1mIL-10 was not restricted to the knee joint alone. The arthritis incidence in the ipsilateral paw was highly suppressed. In contrast, local IL-10 over-expression was not effective when treatment was started after onset of CIA. Further analysis in the acute streptococcal cell wall-induced arthritis model revealed that local IL-10 over-expression markedly suppressed the production of tumour necrosis factor-alpha (TNF-alpha) and IL-1alpha, but had no significant effect on IL-1beta and IL-12 production in the inflamed synovium. These data indicate that local over-expression of IL-10 in the knee joint of mice regulates the expression of collagen arthritis, probably through down-regulation of TNF-alpha.

摘要

我们研究了在胶原诱导性关节炎(CIA)早期阶段,通过重组人5型腺病毒载体引入的局部白细胞介素-10(IL-10)在小鼠膝关节中的作用。使用不会引起过度炎症的病毒剂量,向小鼠膝关节内注射一次表达IL-10的病毒(Ad5E1mIL-10)会导致小鼠膝关节中IL-10的大量过表达。IL-10高表达持续了几天,在第1天达到最大值。在观察到CIA发病之前,向免疫了II型胶原(CII)的小鼠膝关节内注射一次Ad5E1mIL-10,可降低该膝关节中胶原性关节炎的发病率。有趣的是,Ad5E1mIL-10介导的局部IL-10表达的保护作用并不局限于膝关节。同侧爪子的关节炎发病率也受到高度抑制。相比之下,在CIA发病后开始治疗时,局部IL-10过表达无效。在急性链球菌细胞壁诱导的关节炎模型中的进一步分析表明,局部IL-10过表达显著抑制了肿瘤坏死因子-α(TNF-α)和IL-1α的产生,但对炎症滑膜中IL-1β和IL-12的产生没有显著影响。这些数据表明,小鼠膝关节中局部IL-10过表达可能通过下调TNF-α来调节胶原性关节炎的表达。