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Interaction of Antithymocyte Globulins with Dendritic Cell Antigens

机译:抗胸腺球蛋白与树突状细胞抗原的相互作用。

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The polyclonal rabbit antithymocyte globulins (ATGs), Thymoglobulin and ATG-Fresenius S, are widely used for prevention and therapy of allograft rejection and graft versus host disease. Dendritic cells (DC) govern immune responses and thus the interaction of ATGs with these cells could potentially contribute to the clinical effects of ATG therapy. Currently there is little information on the DC-antigens targeted by ATGs. In this study we have used a new methodology to identify DC surface antigens recognized by ATGs. By screening an eukaryotic expression library generated from DC with ATGs we could identify several novel ATG antigens including CD81, CD82, CD98, CD99 and CD147. Furthermore, we engineered cells to express previously described ATG antigens and probed them with Thymoglobulin and ATG-Fresenius S. Our results demonstrated strong binding to some but not all of these molecules. We show that previously described antigens and antigens identified in this study account for around 80% of the DC reactivity of ATGs. Analysis of molecules induced by ATG–DC interaction are more in support for an activation of these cells by ATGs than for a specific induction of a tolerogenic DC phenotype.
机译:多克隆兔抗胸腺细胞球蛋白(ATG),胸腺球蛋白和ATG-费森尤斯S广泛用于预防和治疗同种异体移植排斥以及移植物抗宿主疾病。树突状细胞(DC)控制免疫反应,因此ATG与这些细胞的相互作用可能潜在地有助于ATG治疗的临床效果。目前,关于ATG靶向的DC抗原的信息很少。在这项研究中,我们使用了一种新的方法来鉴定被ATG识别的DC表面抗原。通过用ATG筛选从DC产生的真核表达文库,我们可以鉴定出几种新的ATG抗原,包括CD81,CD82,CD98,CD99和CD147。此外,我们对细胞进行了工程改造以表达先前描述的ATG抗原,并用胸腺球蛋白和ATG-费森尤斯S对其进行了探测。我们的结果证明了与某些但并非全部这些分子的强结合。我们显示先前描述的抗原和在这项研究中鉴定的抗原约占ATG的DC反应性的80%。由ATG-DC相互作用诱导的分子分析更多地支持ATG激活这些细胞,而不是特异性诱导耐受DC表型。

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