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通过血管细胞黏附分子(VCAM)靶向二级淋巴器官的抗原可增强免疫反应。

Antigen targeted to secondary lymphoid organs via vascular cell adhesion molecule (VCAM) enhances an immune response.

作者信息

Dyer Christopher M, Lew Andrew M

机构信息

The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Vic. 3050, Australia.

出版信息

Vaccine. 2003 May 16;21(17-18):2115-21. doi: 10.1016/s0264-410x(02)00742-9.

Abstract

The localisation of antigen within secondary lymphoid organs can significantly increase the immune response. Using the monoclonal antibody M/K 2.7, which recognises murine vascular cell adhesion molecule (VCAM), we have shown antigen accumulation within organs of the secondary lymph such as the draining lymph nodes and spleen. Similar accumulation was not apparent in other, non-lymphatic organs. We then compared the immune response to antigen targeted to secondary lymphoid organs, via VCAM recognition, with untargeted antigen. The model antigen used, rat IgG1, was shown to be a weak murine immunogen, not eliciting any measurable antibody or cellular response. However, the same antigen targeted to VCAM, was shown to elicit an IgG1 antibody response and T cell proliferation, also marked by IFNgamma expression. These results confirm the effectiveness of targeting antigen to secondary lymphoid organs in enhancing an immune response and identify VCAM as a useful target.

摘要

抗原在次级淋巴器官内的定位可显著增强免疫反应。利用识别鼠血管细胞黏附分子(VCAM)的单克隆抗体M/K 2.7,我们已证明抗原在次级淋巴器官如引流淋巴结和脾脏内的积累。在其他非淋巴器官中未观察到类似的积累现象。然后,我们将通过VCAM识别靶向次级淋巴器官的抗原的免疫反应与未靶向抗原的免疫反应进行了比较。所使用的模型抗原大鼠IgG1被证明是一种弱的鼠免疫原,不会引发任何可测量的抗体或细胞反应。然而,靶向VCAM的相同抗原却能引发IgG1抗体反应和T细胞增殖,同时也有IFNγ表达作为标志。这些结果证实了将抗原靶向次级淋巴器官在增强免疫反应方面的有效性,并确定VCAM是一个有用的靶点。

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