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免疫治疗迈向临床肿瘤学模式的当前技术与未来展望

英文原题:Current Technologies and Future Perspectives in Immunotherapy towards a Clinical Oncology Approach.

查看英文原题

Current Technologies and Future Perspectives in Immunotherapy towards a Clinical Oncology Approach.

PubMed 2024/01/18(内容时间) Biomedicines Q2 · IF 4.5(JCR 2025)

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中文摘要

免疫疗法现已被确立为一种有效的治疗范式,通过调节免疫系统,或刺激或抑制免疫组分如 CD4+ T 细胞、CD8+ T 细胞、B 细胞、单核细胞、巨噬细胞、树突状细胞和NK 细胞,从而对多种恶性肿瘤和其他疾病产生抗肿瘤免疫应答。通过靶向表达于免疫细胞表面的几种免疫检查点抑制剂或阻断剂(例如 PD-1、PD-L1、PD-L2、CTLA-4、LAG3 和 TIM-3),已开发出多种单克隆抗体和多克隆抗体并已在临床转化。

此外,基于NK 细胞的、基于树突状细胞的和 CAR-T 细胞疗法也已被证明是有前景且有效的免疫治疗策略。特别是,CAR-T 细胞疗法受益于 CRISPR-Cas9 基因组编辑技术的进步,使得能够生成多种具有增强抗肿瘤免疫力的修饰 CAR-T 细胞。

然而,新出现的 SARS-CoV-2 感染可通过释放促炎性白细胞介素和细胞因子如 IL-1、IL-2、IL-6 和 IL-10,以及 IFN- 和 TNF-,分别劫持患者的免疫系统,这可进一步促进中性粒细胞外渗和血管的血管舒张。尽管先进免疫治疗技术取得了重大进展,但在一定治疗期后,由于对免疫治疗产生耐药性,癌症会复发。耐药性可以是原发性的(即肿瘤细胞对治疗无反应),或继发性或获得性免疫耐药(即肿瘤细胞逐渐对 ICIs 治疗产生耐药性)。

在此背景下,本综述旨在探讨现有的抗癌免疫治疗技术及免疫治疗药物的耐药机制,并阐释COVID-19对癌症治疗的影响。此外,我们将讨论这些策略未来如何用于应对癌症耐药性。

最后,我们将强调采取切实步骤,为制定明智的政策奠定基础,以干预和分配资源来照护癌症患者。

展开英文摘要原文

Immunotherapy is now established as a potent therapeutic paradigm engendering antitumor immune response against a wide range of malignancies and other diseases by modulating the immune system either through the stimulation or suppression of immune components such as CD4 + T cells, CD8 + T cells, B cells, monocytes, macrophages, dendritic cells, and natural killer cells.

By targeting several immune checkpoint inhibitors or blockers (e. g. , PD-1, PD-L1, PD-L2, CTLA-4, LAG3, and TIM-3) expressed on the surface of immune cells, several monoclonal antibodies and polyclonal antibodies have been developed and already translated clinically.

In addition, natural killer cell-based, dendritic cell-based, and CAR T cell therapies have been also shown to be promising and effective immunotherapeutic approaches. In particular, CAR T cell therapy has benefited from advancements in CRISPR-Cas9 genome editing technology, allowing the generation of several modified CAR T cells with enhanced antitumor immunity.

However, the emerging SARS-CoV-2 infection could hijack a patient's immune system by releasing pro-inflammatory interleukins and cytokines such as IL-1 , IL-2, IL-6, and IL-10, and IFN- and TNF- , respectively, which can further promote neutrophil extravasation and the vasodilation of blood vessels. Despite the significant development of advanced immunotherapeutic technologies, after a certain period of treatment, cancer relapses due to the development of resistance to immunotherapy.

Resistance may be primary (where tumor cells do not respond to the treatment), or secondary or acquired immune resistance (where tumor cells develop resistance gradually to ICIs therapy). In this context, this review aims to address the existing immunotherapeutic technologies against cancer and the resistance mechanisms against immunotherapeutic drugs, and explain the impact of COVID-19 on cancer treatment.

In addition, we will discuss what will be the future implementation of these strategies against cancer drug resistance.

Finally, we will emphasize the practical steps to lay the groundwork for enlightened policy for intervention and resource allocation to care for cancer patients.

论文信息

作者
Adhikary S、Pathak S、Palani V、Acar A、Banerjee A、Al-Dewik NI、Essa MM、Mohammed SGAA
第一作者单位
Medical Biotechnology, Faculty of Allied Health Sciences, Chettinad Academy of Research and Education (CARE), Chettinad Hospital and Research Institute (CHRI), Chennai 603103, India.India
通讯作者单位
Research & Policy Division, Q3 Research Institute (QRI), Ypsilanti, MI 48917, USA.United States
文献类型
综述
期刊
Biomedicines2024 Jan 18
原文标识
PubMed 38255322 · DOI 10.3390/biomedicines12010217