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Oncoimmunology. 2017 Mar 28;6(5):e1308618. doi: 10.1080/2162402X.2017.1308618. eCollection 2017.
2
The role of surface molecule CD229 in Multiple Myeloma.表面分子 CD229 在多发性骨髓瘤中的作用。
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SLAM-family receptors come of age as a potential molecular target in cancer immunotherapy.SLAM 家族受体作为癌症免疫治疗的潜在分子靶点崭露头角。
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[SLAM family proteins as therapeutic targets in multiple myeloma].[作为多发性骨髓瘤治疗靶点的信号淋巴细胞激活分子家族蛋白]
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SLAMF receptors: key regulators of tumor progression and emerging targets for cancer immunotherapy.信号淋巴细胞激活分子家族受体:肿瘤进展的关键调节因子及癌症免疫治疗的新兴靶点
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Dysregulated immune proteins in plasma in the UK Biobank predict multiple myeloma 12 years before clinical diagnosis.英国生物银行中血浆免疫蛋白失调可在临床诊断前12年预测多发性骨髓瘤。
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The CC' loop of IgV domains of the immune checkpoint receptors, plays a key role in receptor:ligand affinity modulation.免疫检查点受体的 IgV 结构域的 CC' 环在受体配体亲和力调节中起着关键作用。
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本文引用的文献

1
Elotuzumab in combination with thalidomide and low-dose dexamethasone: a phase 2 single-arm safety study in patients with relapsed/refractory multiple myeloma.埃罗妥珠单抗联合沙利度胺及低剂量地塞米松:一项针对复发/难治性多发性骨髓瘤患者的2期单臂安全性研究。
Br J Haematol. 2016 Nov;175(3):448-456. doi: 10.1111/bjh.14263. Epub 2016 Jul 19.
2
Differential expression of CD150/SLAMF1 in normal and malignant B cells on the different stages of maturation.CD150/SLAMF1在正常和恶性B细胞成熟不同阶段的差异表达。
Exp Oncol. 2016 Jun;38(2):101-7.
3
Randomized phase 2 study: elotuzumab plus bortezomib/dexamethasone vs bortezomib/dexamethasone for relapsed/refractory MM.随机2期研究:埃罗妥珠单抗联合硼替佐米/地塞米松对比硼替佐米/地塞米松用于复发/难治性多发性骨髓瘤
Blood. 2016 Jun 9;127(23):2833-40. doi: 10.1182/blood-2016-01-694604. Epub 2016 Apr 18.
4
Cancer statistics, 2016.癌症统计数据,2016 年。
CA Cancer J Clin. 2016 Jan-Feb;66(1):7-30. doi: 10.3322/caac.21332. Epub 2016 Jan 7.
5
SLAM family receptors in normal immunity and immune pathologies.正常免疫和免疫病理中的信号淋巴细胞激活分子家族受体
Curr Opin Immunol. 2016 Feb;38:45-51. doi: 10.1016/j.coi.2015.11.003. Epub 2015 Dec 2.
6
Targeting of Ly9 (CD229) Disrupts Marginal Zone and B1 B Cell Homeostasis and Antibody Responses.靶向Ly9(CD229)会破坏边缘区和B1 B细胞的稳态及抗体反应。
J Immunol. 2016 Jan 15;196(2):726-37. doi: 10.4049/jimmunol.1501266. Epub 2015 Dec 14.
7
CD229 Expression on Bone Marrow Plasma Cells from Patients with Multiple Myeloma and Monoclonal Gammopathies of Uncertain Significance.多发性骨髓瘤和意义未明的单克隆丙种球蛋白病患者骨髓浆细胞上的CD229表达
Acta Haematol. 2016;135(1):11-4. doi: 10.1159/000380939. Epub 2015 Aug 15.
8
Elotuzumab Therapy for Relapsed or Refractory Multiple Myeloma.依鲁替尼联合来那度胺和地塞米松治疗复发/难治性多发性骨髓瘤的疗效和安全性:一项多中心、开放标签的 II 期研究
N Engl J Med. 2015 Aug 13;373(7):621-31. doi: 10.1056/NEJMoa1505654. Epub 2015 Jun 2.
9
CD229 is expressed on the surface of plasma cells carrying an aberrant phenotype and chemotherapy-resistant precursor cells in multiple myeloma.CD229在携带异常表型的浆细胞以及多发性骨髓瘤中化疗耐药的前体细胞表面表达。
Hum Vaccin Immunother. 2015;11(7):1606-11. doi: 10.1080/21645515.2015.1046658.
10
Migration of myeloid cells during inflammation is differentially regulated by the cell surface receptors Slamf1 and Slamf8.在炎症过程中,髓样细胞的迁移受细胞表面受体Slamf1和Slamf8的差异调节。
PLoS One. 2015 Mar 23;10(3):e0121968. doi: 10.1371/journal.pone.0121968. eCollection 2015.

靶向信号淋巴细胞激活分子(SLAM)受体家族的新型抗骨髓瘤免疫疗法。

Novel anti-myeloma immunotherapies targeting the SLAM family of receptors.

作者信息

Radhakrishnan Sabarinath Venniyil, Bhardwaj Neelam, Luetkens Tim, Atanackovic Djordje

机构信息

Multiple Myeloma Program & Cancer Immunotherapy, Hematology and Hematologic Malignancies, University of Utah/Huntsman Cancer Institute, Salt Lake City, UT, USA.

出版信息

Oncoimmunology. 2017 Mar 28;6(5):e1308618. doi: 10.1080/2162402X.2017.1308618. eCollection 2017.

DOI:10.1080/2162402X.2017.1308618
PMID:28638731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5468000/
Abstract

Treatment for multiple myeloma (MM) has significantly advanced in the last decade with the introduction of proteasome inhibitors and immunomodulatory therapies. Unfortunately, MM continues to cause significant morbidity and most patients eventually succumb to the disease. As in other areas of cancer, immunotherapy in MM has also evolved and holds promise to deliver long-lasting remissions or even cure. The signaling lymphocyte activation molecules (SLAM) family of surface proteins represents a group of potential targets for immunotherapy in MM as some of the family members are expressed consistently on plasma cells and also on myeloma propagating pre-plasma cells. Here, we review the SLAM family members in detail, describe their tissue distribution, biologic pathways, as well as relevant pre-clinical studies and clinical trials in MM. Our review demonstrates the value of SLAM family receptors as potential targets for anti-myeloma immunotherapies and outlines how immunotherapeutic approaches can be developed.

摘要

在过去十年中,随着蛋白酶体抑制剂和免疫调节疗法的引入,多发性骨髓瘤(MM)的治疗取得了显著进展。不幸的是,MM仍然会导致严重的发病率,并且大多数患者最终会死于该疾病。与癌症的其他领域一样,MM的免疫疗法也在不断发展,有望实现长期缓解甚至治愈。信号淋巴细胞激活分子(SLAM)家族的表面蛋白是MM免疫疗法的一组潜在靶点,因为该家族的一些成员在浆细胞以及骨髓瘤增殖前体细胞上持续表达。在这里,我们详细回顾了SLAM家族成员,描述了它们的组织分布、生物学途径,以及MM相关的临床前研究和临床试验。我们的综述证明了SLAM家族受体作为抗骨髓瘤免疫疗法潜在靶点的价值,并概述了如何开发免疫治疗方法。