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人类胶质瘤免疫治疗的最新进展

Recent advances in immunotherapy for human glioma.

作者信息

Carpentier Antoine F, Meng Yuxia

机构信息

Department of Neurology, Mazarin, Salpêtrière Hospital, Paris, France.

出版信息

Curr Opin Oncol. 2006 Nov;18(6):631-6. doi: 10.1097/01.cco.0000245321.34658.f4.

Abstract

PURPOSE OF REVIEW

The present review focuses on recent progress in tumour immunology and immunotherapeutic trials in malignant gliomas.

RECENT FINDINGS

Major advances have been made in the understanding of antitumour immunity in patients with glioma. Patients with glioblastoma can spontaneously develop antitumour activity with activated CD8+ T cells. Infiltration of myeloid suppressor cells into tumours and increased regulatory T-cell fraction appear to play a critical role in tumour tolerance, however. T-regulatory removal suppresses CD4+ T-cell proliferative defects and can induce tumour rejection in a murine model. Clinical trials using active immunotherapy with dendritic cells loaded with tumour-eluted peptides or tumour lysate have successfully induced antitumour cytotoxicity and some radiologic responses. Other promising approaches targeting the mechanisms of tolerance that could be referred to as 'corrective immunotherapy' are currently on going.

SUMMARY

Improvements in clinical methods and large randomized trials are now needed to prove the usefulness of cancer vaccines. Indeed, comprehensive analysis of tumour immunology and new immunization protocols suggest that immunotherapy can become an efficacious treatment in the near future. Combination with radiotherapy or chemotherapy should be investigated.

摘要

综述目的

本综述聚焦于恶性胶质瘤肿瘤免疫学及免疫治疗试验的最新进展。

最新发现

在对胶质瘤患者抗肿瘤免疫的理解方面取得了重大进展。胶质母细胞瘤患者可通过活化的CD8 + T细胞自发产生抗肿瘤活性。然而,髓系抑制细胞浸润肿瘤以及调节性T细胞比例增加似乎在肿瘤耐受中起关键作用。在小鼠模型中,去除调节性T细胞可抑制CD4 + T细胞增殖缺陷并能诱导肿瘤排斥。使用负载肿瘤洗脱肽或肿瘤裂解物的树突状细胞进行主动免疫治疗的临床试验已成功诱导出抗肿瘤细胞毒性及一些影像学反应。目前正在进行其他针对耐受机制的有前景的方法,可称之为“矫正免疫疗法”。

总结

现在需要改进临床方法并开展大型随机试验以证明癌症疫苗的有效性。事实上,对肿瘤免疫学的全面分析及新的免疫方案表明,免疫疗法在不久的将来可能成为一种有效的治疗方法。应研究其与放疗或化疗的联合应用。

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