CAR-NK细胞治疗血液肿瘤的研究进展

刘洪秀, 韩艳秋. CAR-NK细胞治疗血液肿瘤的研究进展[J]. 临床血液学杂志, 2023, 36(1): 76-80. doi: 10.13201/j.issn.1004-2806.2023.01.016
引用本文: 刘洪秀, 韩艳秋. CAR-NK细胞治疗血液肿瘤的研究进展[J]. 临床血液学杂志, 2023, 36(1): 76-80. doi: 10.13201/j.issn.1004-2806.2023.01.016
LIU Hongxiu, HAN Yanqiu. Outlook for CAR-NK immunotherapy in hematological malignancy[J]. J Clin Hematol, 2023, 36(1): 76-80. doi: 10.13201/j.issn.1004-2806.2023.01.016
Citation: LIU Hongxiu, HAN Yanqiu. Outlook for CAR-NK immunotherapy in hematological malignancy[J]. J Clin Hematol, 2023, 36(1): 76-80. doi: 10.13201/j.issn.1004-2806.2023.01.016

CAR-NK细胞治疗血液肿瘤的研究进展

  • 基金项目:
    内蒙古自治区科技计划项目(No:201702117)
详细信息

Outlook for CAR-NK immunotherapy in hematological malignancy

More Information
  • NK细胞作为固有免疫细胞在肿瘤免疫监视中发挥重要作用。相比CAR-T其神经毒性、细胞因子释放综合征等不良反应和移植物抗宿主病鲜有发生,因此有希望成为嵌合抗原受体细胞免疫治疗更好的细胞来源。目前CAR-NK细胞的研究仍多使用根据T细胞激活原理设计的CAR。该文针对NK细胞激活原理设计的CAR结构、可用于免疫治疗的NK细胞来源和CAR-NK细胞在白血病、淋巴瘤、骨髓瘤的临床前景及临床研究进展进行综述。分析得出,“现货型”CAR-NK细胞将是血液肿瘤治疗的新方向,如何增加CAR-NK细胞在体内的存活时间仍是其应用于临床亟须解决的问题。
  • 加载中
  • [1]

    Roma S, Carpen L, Raveane A, et al. The Dual Role of Innate Lymphoid and Natural Killer Cells in Cancer. from Phenotype to Single-Cell Transcriptomics, Functions and Clinical Uses[J]. Cancers(Basel), 2021, 13(20): 5042.

    [2]

    Shimasaki N, Jain A, Campana D. NK cells for cancer immunotherapy[J]. Nat Rev Drug Discov, 2020, 19(3): 200-218. doi: 10.1038/s41573-019-0052-1

    [3]

    赵恺, 徐开林. 嵌合抗原受体T细胞的结构演变及展望[J]. 中华血液学杂志, 2020, 41(11): 964-968. doi: 10.3760/cma.j.issn.0253-2727.2020.11.019

    [4]

    Chang YH, Connolly J, Shimasaki N, et al. A chimeric receptor with NKG2D specificity enhances natural killer cell activation and killing of tumor cells[J]. Cancer Res, 2013, 73(6): 1777-1786. doi: 10.1158/0008-5472.CAN-12-3558

    [5]

    Li Y, Hermanson DL, Moriarity BS, et al. Human iPSC-Derived Natural Killer Cells Engineered with Chimeric Antigen Receptors Enhance Anti-tumor Activity[J]. Cell Stem Cell, 2018, 23(2): 181-192.e5. doi: 10.1016/j.stem.2018.06.002

    [6]

    Leivas A, Valeri A, Córdoba L, et al. NKG2D-CAR-transduced natural killer cells efficiently target multiple myeloma[J]. Blood Cancer J, 2021, 11(8): 146. doi: 10.1038/s41408-021-00537-w

    [7]

    Agresta L, Hoebe K, Janssen EM. The Emerging Role of CD244 Signaling in Immune Cells of the Tumor Microenvironment[J]. Front Immunol, 2018, 9: 2809. doi: 10.3389/fimmu.2018.02809

    [8]

    Altvater B, Landmeier S, Pscherer S, et al. 2B4(CD244) signaling by recombinant antigen-specific chimeric receptors costimulates natural killer cell activation to leukemia and neuroblastoma cells[J]. Clin Cancer Res, 2009, 15(15): 4857-4866. doi: 10.1158/1078-0432.CCR-08-2810

    [9]

    Xu Y, Liu Q, Zhong M, et al. 2B4 costimulatory domain enhancing cytotoxic ability of anti-CD5 chimeric antigen receptor engineered natural killer cells against T cell malignancies[J]. J Hematol Oncol, 2019, 12(1): 49. doi: 10.1186/s13045-019-0732-7

    [10]

    Romee R, Foley B, Lenvik T, et al. NK cell CD16 surface expression and function is regulated by a disintegrin and metalloprotease-17(ADAM17)[J]. Blood, 2013, 121(18): 3599-3608. doi: 10.1182/blood-2012-04-425397

    [11]

    Zhu H, Blum RH, Bjordahl R, et al. Pluripotent stem cell-derived NK cells with high-affinity noncleavable CD16a mediate improved antitumor activity[J]. Blood, 2020, 135(6): 399-410. doi: 10.1182/blood.2019000621

    [12]

    Salman H, Pinz KG, Wada M, et al. Preclinical Targeting of Human Acute Myeloid Leukemia Using CD4- specific Chimeric Antigen Receptor(CAR)T Cells and NK Cells[J]. J Cancer, 2019, 10(18): 4408-4419. doi: 10.7150/jca.28952

    [13]

    Sivori S, Vacca P, Del Zotto G, et al. Human NK cells: surface receptors, inhibitory checkpoints, and translational applications[J]. Cell Mol Immunol, 2019, 16(5): 430-441. doi: 10.1038/s41423-019-0206-4

    [14]

    Miller JS, Soignier Y, Panoskaltsis-Mortari A, et al. Successful adoptive transfer and in vivo expansion of human haploidentical NK cells in patients with cancer[J]. Blood, 2005, 105(8): 3051-3057. doi: 10.1182/blood-2004-07-2974

    [15]

    Scoville SD, Nalin AP, Chen L, et al. Human AML activates the aryl hydrocarbon receptor pathway to impair NK cell development and function[J]. Blood, 2018, 132(17): 1792-1804. doi: 10.1182/blood-2018-03-838474

    [16]

    Uphoff CC, Denkmann SA, Steube KG, et al. Detection of EBV, HBV, HCV, HIV-1, HTLV-Ⅰ and-Ⅱ, and SMRV in human and other primate cell lines[J]. J Biomed Biotechnol, 2010, 2010: 904767.

    [17]

    Luevano M, Daryouzeh M, Alnabhan R, et al. The unique profile of cord blood natural killer cells balances incomplete maturation and effective killing function upon activation[J]. Hum Immunol, 2012, 73(3): 248-257. doi: 10.1016/j.humimm.2011.12.015

    [18]

    Nomura A, Takada H, Jin CH, et al. Functional analyses of cord blood natural killer cells and T cells: a distinctive interleukin-18 response[J]. Exp Hematol, 2001, 29(10): 1169-1176. doi: 10.1016/S0301-472X(01)00689-0

    [19]

    Liu E, Tong Y, Dotti G, et al. Cord blood NK cells engineered to express IL-15 and a CD19-targeted CAR show long-term persistence and potent antitumor activity[J]. Leukemia, 2018, 32(2): 520-531. doi: 10.1038/leu.2017.226

    [20]

    Heipertz EL, Zynda ER, Stav-Noraas TE, et al. Current Perspectives on "Off-The-Shelf" Allogeneic NK and CAR-NK Cell Therapies[J]. Front Immunol, 2021, 12: 732135. doi: 10.3389/fimmu.2021.732135

    [21]

    Woll PS, Grzywacz B, Tian X, et al. Human embryonic stem cells diferentiate into a homogeneous population of natural killer cells with potent in vivo antitumor activity[J]. Blood, 2009, 113(24): 6094-6101. doi: 10.1182/blood-2008-06-165225

    [22]

    杜为, 崔丽娟, 徐迎, 等. 脐带血单个核细胞诱导多能干细胞来源自然杀伤细胞的生物学特性[J]. 中华细胞与干细胞杂志(电子版), 2021, 11(6): 329-336. doi: 10.3877/cma.j.issn.2095-1221.2021.06.002

    [23]

    Tang X, Yang L, Li Z, et al. Erratum: First-in-man clinical trial of CAR NK-92 cells: safety test of CD33-CAR NK-92 cells in patients with relapsed and refractory acute myeloid leukemia[J]. Am J Cancer Res, 2018, 8(9): 1899.

    [24]

    Bachier C, Borthakur G, Hosing C, et al. A Phase 1 study of NKX101, an allogeneic CAR natural killer(NK)cell therapy, in subjects with relapsed/refractory(R/R)acute myeloid leukemia(AML)or higher-risk myelodysplastic syndrome(MDS)[J]. Blood, 2020, 136(Suppl 1): 42-43.

    [25]

    Oelsner S, Waldmann A, Billmeier A, et al. Genetically engineered CAR NK cells display selective cytotoxicity against FLT3-positive B-ALL and inhibit in vivo leukemia growth[J]. Int J Cancer, 2019, 145(7): 1935-1945.

    [26]

    Liu E, Marin D, Banerjee P, et al. Use of CAR-Transduced Natural Killer Cells in CD19-Positive Lymphoid Tumors[J]. N Engl J Med, 2020, 382(6): 545-553. doi: 10.1056/NEJMoa1910607

    [27]

    Strati P, Bachanova V, Goodman A, et al. Preliminary results of a phase Ⅰ trial of FT516, an of the-shelf natural killer(NK)cell therapy derived from a clonal master induced pluripotent stem cell(iPSC)line expressing highafnity, non-cleavable CD16(hnCD16), in patients(pts)with relapsed/refractory(R/R)B-cell lymphoma(BCL)[J]. J Clin Oncol, 2021, 39(15 Suppl): 7541.

    [28]

    Chu J, Deng Y, Benson DM, et al. CS1-specific chimeric antigen receptor(CAR)-engineered natural killer cells enhance in vitro and in vivo antitumor activity against human multiple myeloma[J]. Leukemia, 2014, 28(4): 917-927. doi: 10.1038/leu.2013.279

    [29]

    Hambach J, Riecken K, Cichutek S, et al. Targeting CD38- expressing multiple myeloma and burkitt lymphoma cells in vitro with nanobody based chimeric antigen receptors(Nb-CARs)[J]. Cells, 2020, 9(2): 321. doi: 10.3390/cells9020321

    [30]

    Goodridge JP, Bjordahl R, Mahmood S, et al. FT576 path to frst-of-kind clinical trial: translation of a versatile multi-antigen specifc of-the-shelf NK cell for treatment of multiple myeloma[J]. Cancer Res, 2021, 81(13 Suppl): 1550.

    [31]

    Ryan B, Svetlana G, Karrune W, et al. FT538: Preclinical Development of an Off-the-Shelf Adoptive NK Cell Immunotherapy with Targeted Disruption of CD38 to Prevent Anti-CD38 Antibody-Mediated Fratricide and Enhance ADCC in Multiple Myeloma When Combined with Daratumumab[J]. Blood, 2019, 134(Suppl 1): 133.

    [32]

    Soldierer M, Bister A, Haist C, et al. Genetic Engineering and Enrichment of Human NK Cells for CAR-Enhanced Immunotherapy of Hematological Malignancies[J]. Front Immunol, 2022, 13: 847008. doi: 10.3389/fimmu.2022.847008

    [33]

    Gang M, Marin ND, Wong P, et al. CAR-modified memory-like NK cells exhibit potent responses to NK-resistant lymphomas[J]. Blood, 2020, 136(20): 2308-2318. doi: 10.1182/blood.2020006619

  • 加载中
计量
  • 文章访问数:  1279
  • PDF下载数:  125
  • 施引文献:  0
出版历程
收稿日期:  2022-03-21
刊出日期:  2023-01-01

目录