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人血液中一种新型树突状细胞群体:通过特异性单克隆抗体(M-DC8)进行一步免疫磁珠分离及体外启动细胞毒性T淋巴细胞

A novel dendritic cell population in human blood: one-step immunomagnetic isolation by a specific mAb (M-DC8) and in vitro priming of cytotoxic T lymphocytes.

作者信息

Schäkel K, Mayer E, Federle C, Schmitz M, Riethmüller G, Rieber E P

机构信息

Institute for Immunology, Medical Faculty, Technical University of Dresden, Germany.

出版信息

Eur J Immunol. 1998 Dec;28(12):4084-93. doi: 10.1002/(SICI)1521-4141(199812)28:12<4084::AID-IMMU4084>3.0.CO;2-4.

Abstract

Originating from a common progenitor cell, dendritic cells (DC) appear to develop along early branched pathways into various yet ill-defined subpopulations residing at various sites throughout the body where they capture and present antigen in the most professional fashion. Here we give evidence for a unique subpopulation of human DC circulating in blood that account for 0.5-1% of blood leukocytes only, their most specific characteristic being the expression of a cell surface protein recognized by a novel monoclonal antibody (M-DC8) which enables their isolation by a one-step immunomagnetic procedure. The isolated cells (> 97% pure) present morphologically as typical dendritic cells. They express the Fc(gamma)RIII (CD16), so far not found on DC, and avidly phagocytose latex beads as well as opsonized erythrocytes. These cells not only present antigens efficiently to naive T cells but also induce purified CD8+ T cells to become alloantigen-specific cytotoxic cells. Furthermore, when loaded with a tyrosinase-derived peptide they stimulate T cells from normal donors and melanoma patients to exhibit MHC-restricted specific cytotoxicity against melanoma cells.

摘要

树突状细胞(DC)起源于共同的祖细胞,似乎沿着早期分支途径发育成各种尚未明确的亚群,这些亚群存在于全身各处,在这些部位它们以最专业的方式捕获和呈递抗原。在这里,我们提供证据表明,人类血液中循环的一种独特的DC亚群仅占血液白细胞的0.5%-1%,其最显著的特征是表达一种可被新型单克隆抗体(M-DC8)识别的细胞表面蛋白,这使得它们能够通过一步免疫磁选程序进行分离。分离出的细胞(纯度>97%)在形态上呈现为典型的树突状细胞。它们表达Fc(γ)RIII(CD16),到目前为止在DC上尚未发现,并且能大量吞噬乳胶珠以及调理过的红细胞。这些细胞不仅能有效地将抗原呈递给初始T细胞,还能诱导纯化的CD8+T细胞成为同种抗原特异性细胞毒性细胞。此外,当加载酪氨酸酶衍生肽时,它们会刺激正常供体和黑色素瘤患者的T细胞对黑色素瘤细胞表现出MHC限制的特异性细胞毒性。

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