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癌症治疗的免疫疗法

英文原题:Immunotherapy for cancer treatment.

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Immunotherapy for cancer treatment.

PubMed 2022/01/01(内容时间) Klin Onkol

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研究思路按摘要原文分段

免疫疗法是通过调节免疫反应来治疗许多与免疫系统紊乱相关疾病的有效方法。它涉及多种操纵免疫系统的方式,这些方式要么抑制免疫反应,要么相反地刺激免疫反应。免疫疗法目前不仅在自身免疫性疾病和免疫缺陷病的治疗中具有极其重要的意义,而且也是治疗癌症的一种有前景的方法。利用机体自身抗肿瘤反应的尝试已促成了癌症替代疗法的发现。

本文旨在对当前癌症免疫治疗的可能性进行文献综述。除化疗和放疗等经典方法外,过继性细胞治疗和免疫检查点阻断等治疗手段正日益得到应用。过继性细胞治疗的最新形式是使用表达嵌合抗原受体的T淋巴细胞。这种治疗适用于血液系统恶性肿瘤。近年来,一种利用单克隆抗体阻断免疫检查点治疗癌症的新方法已经出现。目前,抗肿瘤治疗的重点是阻断抑制性分子——细胞毒性T淋巴细胞抗原4(CTLA-4)和程序性细胞死亡1(PD-1)。给予抗CTLA-4受体特异性单克隆抗体可阻断CTLA-4受体与B7配体之间的结合,从而防止对已活化细胞毒性T细胞的抑制。另一类免疫应答检查点包括表达于T淋巴细胞、B淋巴细胞表面,同时也表达于髓系细胞表面的PD-1分子。阻断PD-1受体和PD-L1配体可防止肿瘤细胞对T淋巴细胞的抑制,从而导致免疫系统识别肿瘤细胞并随后将其摧毁的能力增强。阻断PD-1受体和PD-L1配体可防止肿瘤细胞对T淋巴细胞的抑制,从而导致对肿瘤细胞识别的免疫应答增强及其随后的摧毁。肿瘤治疗的另一种形式是给予肿瘤疫苗和肿瘤特异性单克隆抗体(mAbs)。使用mAbs杀伤肿瘤需要肿瘤细胞表面表达肿瘤特异性抗原。通过这些受体,mAb将细胞毒性细胞、毒素、药物或放射性同位素靶向肿瘤细胞,从而将其破坏。此外,mAb能够阻断血管生成,而血管生成对肿瘤细胞增殖至关重要。

展开英文摘要原文

Immunotherapy is an effective way to treat many diseases associated with disorders of the immune system by modulating immune response. It involves several ways of manipulating the immune system, which either suppress the immune response or, on the contrary, stimulates it. Immunotherapy is currently of immense importance not only in the context of the treatment of autoimmune diseases and immunodeficiencies, but it is also a promising method for treating cancer. Efforts to use the bodys own anti-tumor response have led to the discovery of alternative treatments for cancer.

The aim of this paper is to provide a literature review focused on the current possibilities of cancer immunotherapy. In addition to classical procedures such as chemotherapy and radiotherapy, treatments consisting of adoptive cell therapy and blockade of immune checkpoints are being increasingly indicated. The latest form of adoptive cell therapy is the use of T-lymphocytes expressing chimeric antigen receptors. This type of treatment is indicated for hematological cancers. In recent years, a new approach to the treatment of cancer has emerged using blockade of immune checkpoints by monoclonal antibodies. At present, antitumor therapy focuses on blocking of inhibitory molecules - cytotoxic T-lymfocyte antigen 4 (CTLA-4) and programmed cell death 1 (PD-1). Administration of anti-CTLA-4 receptor specific monoclonal antibodies blocks binding between CTLA-4 receptors and B7 ligands, thereby preventing inhibition of activated cytotoxic T cells. Another type of checkpoints of the immune response include PD-1 molecules expressed on the surface of T-lymphocytes, B-lymphocytes, but also on the surface of myeloid cells. Blockade of PD-1 receptors and PD-L1 ligands prevents the inhibition of T-lymphocytes by tumor cells, leading to an increase in the immune systems ability to recognize tumor cells and subsequently destroy them. Blockade of PD-1 receptors and PD-L1 ligands prevents the inhibition of T-lymphocytes by tumor cells, leading to an increased immune response to the recognition of tumor cells and their subsequent destruction. An alternative form of tumor treatment is the administration of tumor vaccines and tumor-specific monoclonal antibodies (mAbs). The use of mAbs to kill tumors requires the expression of tumor-specific antigens on the surface of tumor cells. Through these receptors, mAb targets cytotoxic cells, toxins, drugs, or radioisotopes to tumor cells and thereby destroys them. Also, mAbs are able to block angiogenesis, which is crucial in tumor cell proliferation.

论文信息

作者
Donátová K、Nováková E、Šupolíková M
文献类型
综述
期刊
Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti2022 Summer
原文标识
PubMed 35989085 · DOI 10.48095/ccko2022284