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通过全身给予经基因改造以表达FasL的树突状细胞,有效治疗已形成的小鼠胶原诱导性关节炎。

Effective treatment of established mouse collagen-induced arthritis by systemic administration of dendritic cells genetically modified to express FasL.

作者信息

Kim Seon Hee, Kim Sunyoung, Oligino Thomas J, Robbins Paul D

机构信息

Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.

出版信息

Mol Ther. 2002 Nov;6(5):584-90.

Abstract

Previous reports have demonstrated the ability of antigen-presenting cells (APCs), genetically modified to express Fas ligand (FasL), to inhibit T-cell responses through the induction of apoptosis of antigen-specific T cells. Here we have examined the ability of primary mouse bone marrow-derived dendritic cells (DCs), genetically modified by adenoviral infection to express FasL, to inhibit progression of established collagen-induced arthritis (CIA) in DBA/1 mice. Systemic injection of DC/FasL into mice with established CIA resulted in substantial disease amelioration as determined by analysis of paw swelling, arthritic index, and number of arthritic paws. Moreover, a single injection of DC/FasL resulted in extended suppression of disease. We also demonstrate that treatment of arthritic mice with DC/FasL suppressed interferon-gamma (IFN-gamma) production from spleen-derived lymphocytes and reduced T-cell proliferation following collagen stimulation without affecting the levels of anti-collagen antibody isotypes. These results demonstrate that systemic administration of DC/FasL is able to suppress collagen-reactive T cells, resulting in effective and sustained treatment of established CIA.

摘要

先前的报告已证明,经基因改造以表达Fas配体(FasL)的抗原呈递细胞(APC)能够通过诱导抗原特异性T细胞凋亡来抑制T细胞反应。在此,我们研究了经腺病毒感染基因改造以表达FasL的原代小鼠骨髓来源树突状细胞(DC)抑制DBA/1小鼠已建立的胶原诱导性关节炎(CIA)进展的能力。通过对爪子肿胀、关节炎指数和关节炎爪子数量的分析确定,将DC/FasL全身注射到患有已建立CIA的小鼠体内可显著改善疾病。此外,单次注射DC/FasL可导致疾病的长期抑制。我们还证明,用DC/FasL治疗关节炎小鼠可抑制脾源性淋巴细胞产生干扰素-γ(IFN-γ),并减少胶原刺激后T细胞增殖,而不影响抗胶原抗体亚型的水平。这些结果表明,全身给予DC/FasL能够抑制胶原反应性T细胞,从而有效且持续地治疗已建立的CIA。

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