RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunotherapy of cancer without induction of autoimmunity - CD6 as a therapeutic target.
Immunotherapy of cancer without induction of autoimmunity - CD6 as a therapeutic target.
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CD6细胞表面糖蛋白几乎表达于所有T细胞、一小部分B细胞以及相当比例的人自然杀伤(NK)细胞。CD6具有多种配体和多个功能性表位。它是免疫突触的组成部分,并能通过与多种激酶和衔接分子的复杂相互作用,对T细胞中的信号转导产生正向或负向影响。抗CD6抗体在实验系统和人类中均能有效治疗自身免疫性疾病。最近发现CD318(CDCP1)——一种在多种癌症中驱动肿瘤发生的分子——是CD6的配体,这促使人们研究CD6作为癌症免疫治疗可能的新靶点。一种抗CD6单克隆抗体能迅速使CD6内化,并改变CD8+ T细胞和NK细胞中的基因表达,从而增强人淋巴细胞对来自多种肿瘤的人癌细胞的细胞毒性。本综述以问答形式描述了抗CD6作为癌症候选免疫治疗的最新研究,以及我们对CD6生物学其他方面认识的相关进展,并探讨了这种方法是否可能避免检查点抑制剂治疗癌症时遇到的自身免疫并发症。
The CD6 cell surface glycoprotein is expressed by almost all T cells, a small subset of B cells and a substantial proportion of human natural killer (NK) cells. CD6 has multiple ligands and multiple functional epitopes. It is a component of the immunological synapse, and can positively or negatively influence signal transduction in T cells through complex interactions with multiple kinases and adapter molecules. Antibodies to CD6 are effective in the treatment of autoimmune diseases in experimental systems and in humans. The recent discovery that CD318 (CDCP1), a driver molecule in many cancers, is a ligand for CD6 has prompted investigation of CD6 as a possible new target for immunotherapy of cancer.
A monoclonal antibody to CD6 rapidly internalizes CD6 and alters gene expression in CD8+ T cells and NK cells to augment the cytotoxicity of human lymphocytes to human cancer cells from a range of neoplasms.
This review, using a question and answer format, describes recent work on anti-CD6 as a candidate immunotherapy for cancer as well as relevant advances in our understanding of other aspects of the biology of CD6, and explores the possibility that this approach could avoid the autoimmune complications that are encountered with checkpoint inhibitor treatment of cancer.
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