基因工程T细胞和肿瘤浸润性淋巴细胞治疗。

IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Heinz Läubli, Andreas Holbro
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引用次数: 0

摘要

近年来,血液肿瘤学取得了重大进展,特别是通过创新免疫治疗方法的发展,如CAR - T细胞(嵌合抗原受体T细胞)和肿瘤浸润性淋巴细胞治疗。这两种方法都是利用病人自身的免疫系统来治疗癌症,但方式不同。CAR - T细胞疗法是一种免疫疗法,患者自身的T细胞经过基因修饰。CAR - T细胞疗法已被证明对血液学b细胞肿瘤特别有效,如b细胞急性淋巴细胞白血病(B-ALL)和b细胞淋巴瘤,以及多发性骨髓瘤。另一方面,肿瘤浸润淋巴细胞疗法利用T细胞的自然能力,通过T细胞受体识别肿瘤细胞的肿瘤相关抗原。从患者身上取出肿瘤组织,然后从中分离肿瘤浸润淋巴细胞。这些肿瘤浸润淋巴细胞在体外扩增以增加其数量和活性。本文综述了这些创新疗法的原理。这两种疗法都代表了个性化癌症治疗的重大进步,为癌症患者带来了新的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetically engineered T cell and tumour-infiltrating lymphocyte therapies.

Haemato-oncology has made significant progress in recent years, particularly through the development of innovative immunotherapeutic approaches such as CAR T cell (chimeric antigen receptor T cell) and tumour-infiltrating lymphocyte therapies. Both methods use the patient's own immune system to treat cancer, but in different ways. CAR T cell therapy is a form of immunotherapy in which the patient's own T cells are genetically modified. CAR T cell therapies have proven to be particularly effective in haematological B-cell neoplasms, such as B-cell acute lymphoblastic leukaemia (B-ALL) and B-cell lymphomas, as well as in multiple myeloma. Tumour-infiltrating lymphocyte therapy, on the other hand, exploits the natural ability of T cells to recognise tumour-associated antigens of tumour cells with the T cell receptor. Tumour tissue is taken from the patient then tumour-infiltrating lymphocytes are isolated from it. These tumour-infiltrating lymphocytes are expanded ex vivo to increase their number and activity. This review discusses the principles of these innovative therapies. Both therapies represent significant advances in personalised cancer treatment and offer new hope for our cancer patients.

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来源期刊
Swiss medical weekly
Swiss medical weekly 医学-医学:内科
CiteScore
5.00
自引率
0.00%
发文量
0
审稿时长
3-8 weeks
期刊介绍: The Swiss Medical Weekly accepts for consideration original and review articles from all fields of medicine. The quality of SMW publications is guaranteed by a consistent policy of rigorous single-blind peer review. All editorial decisions are made by research-active academics.
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