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血液系统恶性肿瘤中的抗原发现与治疗靶点

Antigen Discovery and Therapeutic Targeting in Hematologic Malignancies.

作者信息

Braun David A, Wu Catherine J

机构信息

From the *Department of Medical Oncology, Dana-Farber Cancer Institute; †Department of Medicine, Brigham and Women's Hospital, Harvard Medical School; and ‡Massachusetts General Hospital Cancer Center, Boston; and §Broad Institute of MIT and Harvard, Cambridge, MA.

出版信息

Cancer J. 2017 Mar/Apr;23(2):115-124. doi: 10.1097/PPO.0000000000000257.

DOI:10.1097/PPO.0000000000000257
PMID:28410299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5856170/
Abstract

Historically, immune-based therapies have played a leading role in the treatment of hematologic malignancies, with the efficacy of stem cell transplantation largely attributable to donor immunity against malignant cells. As new and more targeted immunotherapies have developed, their role in the treatment of hematologic malignancies is evolving and expanding. Herein, we discuss approaches for antigen discovery and review known and novel tumor antigens in hematologic malignancies. We further explore the role of established and investigational immunotherapies in hematologic malignancies, with a focus on personalization of treatment modalities such as cancer vaccines and adoptive cell therapy. Finally, we identify areas of active investigation and development. Immunotherapy is at an exciting crossroads for the treatment of hematologic malignancies, with further investigation aimed at producing effective, targeted immune therapies that maximize antitumor effects while minimizing toxicity.

摘要

从历史上看,基于免疫的疗法在血液系统恶性肿瘤的治疗中发挥了主导作用,干细胞移植的疗效很大程度上归因于供体对恶性细胞的免疫作用。随着更新、更具针对性的免疫疗法的发展,它们在血液系统恶性肿瘤治疗中的作用正在不断演变和扩大。在此,我们讨论抗原发现的方法,并回顾血液系统恶性肿瘤中已知和新发现的肿瘤抗原。我们进一步探讨既定和正在研究的免疫疗法在血液系统恶性肿瘤中的作用,重点关注癌症疫苗和过继性细胞疗法等治疗方式的个性化。最后,我们确定了积极研究和开发的领域。免疫疗法正处于血液系统恶性肿瘤治疗令人兴奋的十字路口,进一步的研究旨在开发有效的、有针对性的免疫疗法,在将毒性降至最低的同时最大化抗肿瘤效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/99ef086be63b/nihms948941f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/1d7a498f6910/nihms948941f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/56ce0e8f5aa0/nihms948941f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/41b05b0f1db5/nihms948941f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/99ef086be63b/nihms948941f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/1d7a498f6910/nihms948941f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/56ce0e8f5aa0/nihms948941f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/41b05b0f1db5/nihms948941f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e31/5856170/99ef086be63b/nihms948941f4.jpg

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Sci Transl Med. 2016 Dec 7;8(368):368ra171. doi: 10.1126/scitranslmed.aag1298.
3
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NSC-34运动神经元样细胞的转录组分析表明,大麻二酚影响突触通路:与大麻二酚的比较研究。
Life (Basel). 2020 Oct 1;10(10):227. doi: 10.3390/life10100227.
4
Engineered tissues and strategies to overcome challenges in drug development.工程化组织和策略以克服药物开发中的挑战。
Adv Drug Deliv Rev. 2020;158:116-139. doi: 10.1016/j.addr.2020.09.012. Epub 2020 Sep 26.
5
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Int J Mol Sci. 2020 Sep 6;21(18):6514. doi: 10.3390/ijms21186514.
6
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4
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Clin Cancer Res. 2016 Dec 1;22(23):5642-5650. doi: 10.1158/1078-0432.CCR-16-0066. Epub 2016 Oct 3.
5
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N Engl J Med. 2016 Aug 25;375(8):754-66. doi: 10.1056/NEJMoa1606038.
6
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Nat Rev Cancer. 2016 Aug 23;16(9):566-81. doi: 10.1038/nrc.2016.97.
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