Targeting CD73 in the tumor microenvironment with MEDI9447

被引:234
|
作者
Hay, Carl M. [1 ]
Sult, Erin [1 ]
Huang, Qihui [1 ]
Mulgrew, Kathy [1 ]
Fuhrmann, Stacy R. [1 ]
McGlinchey, Kelly A. [1 ]
Hammond, Scott A. [1 ]
Rothstein, Raymond [1 ]
Rios-Doria, Jonathan [1 ]
Poon, Edmund [2 ]
Holoweckyj, Nick [1 ]
Durham, Nicholas M. [1 ]
Leow, Ching Ching [3 ]
Diedrich, Gundo [4 ]
Damschroder, Melissa [1 ]
Herbst, Ronald [1 ]
Hollingsworth, Robert E. [1 ]
Sachsenmeier, Kris F. [1 ]
机构
[1] MedImmune LLC, Gaithersburg, MD USA
[2] MedImmune LLC, MedImmune, Cambridge, England
[3] Astrazeneca, Gaithersburg, MD USA
[4] MacroGenics Inc, Macrogen, Rockville, MD USA
来源
ONCOIMMUNOLOGY | 2016年 / 5卷 / 08期
关键词
Adenosine; CD73; MEDI9447; monoclonal antibody; syngeneic tumor model; tumor microenvironment; T-CELL INFILTRATION; CANCER-IMMUNOTHERAPY; ADENOSINE; ANTIBODY; THERAPY; INHIBITION; PROTECTS; MOLECULE; MELANOMA; ADHESION;
D O I
10.1080/2162402X.2016.1208875
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MEDI9447 is a human monoclonal antibody that is specific for the ectoenzyme CD73 and currently undergoing Phase I clinical trials. Here we show that MEDI9447 is a potent inhibitor of CD73 ectonucleotidase activity, with wide ranging immune regulatory consequences. MEDI9447 results in relief from adenosine monophosphate (AMP)-mediated lymphocyte suppression in vitro and inhibition of mouse syngeneic tumor growth in vivo. In contrast with other cancer immunotherapy agents such as checkpoint inhibitors or T-cell agonists, MEDI9447 drives changes in both myeloid and lymphoid infiltrating leukocyte populations within the tumor microenvironment of mouse models. Changes include significant alterations in a number of tumor micro-environmental subpopulations including increases in CD8(+) effector cells and activated macrophages. Furthermore, these changes correlate directly with responder and non-responder subpopulations within animal studies using syngeneic tumors. Combination data showing additive activity between MEDI9447 and anti-PD-1 antibodies using human cells in vitro and mouse tumor models further demonstrate the potential value of relieving adenosine-mediated immunosuppression. Based on these data, a Phase I study to test the safety, tolerability, and clinical activity of MEDI9447 in cancer patients was initiated (NCT02503774).
引用
收藏
页数:10
相关论文
共 50 条
  • [41] CD73 as a therapeutic target for pancreatic neuroendocrine tumor stem cells
    Katsuta, Eriko
    Tanaka, Shinji
    Mogushi, Kaoru
    Shimada, Shu
    Akiyama, Yoshimitsu
    Aihara, Arihiro
    Matsumura, Satoshi
    Mitsunori, Yusuke
    Ban, Daisuke
    Ochiai, Takanori
    Kudo, Atsushi
    Fukamachi, Hiroshi
    Tanaka, Hiroshi
    Nakayama, Koh
    Arii, Shigeki
    Tanabe, Minoru
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2016, 48 (02) : 657 - 669
  • [42] The CD73 immune checkpoint promotes tumor cell metabolic fitness
    Allard, David
    Cousineau, Isabelle
    Ma, Eric H.
    Allard, Bertrand
    Bareche, Yacine
    Fleury, Hubert
    Stagg, John
    ELIFE, 2023, 12
  • [43] CD73: A therapeutic target for pancreatic neuroendocrine tumor stem cells
    Katsuta, Eriko
    Tanaka, Shinji
    Mogushi, Kaoru
    Shimada, Shu
    Akiyama, Yoshimitsu
    Aihara, Arihiro
    Matsumura, Satoshi
    Mitsunori, Yusuke
    Ban, Daisuke
    Ochiai, Takanori
    Kudo, Atsushi
    Fulcamachi, Hiroshi
    Tanaka, Hiroshi
    Nakayama, Koh
    Arii, Shigeki
    Tanabe, Minoru
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2016, 38 : S5 - S5
  • [44] ENGINEERED NATURAL KILLER CELLS REACTIVELY BLOCK TIGIT AND CD73 IN THE GBM MICROENVIRONMENT
    Lupo, Kyle
    Matosevic, Sandro
    JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2021, 9 : A139 - A139
  • [45] Safety, efficacy and pharmacodynamics (PD) of MEDI9447 (oleclumab) alone or in combination with durvalumab in advanced colorectal cancer (CRC) or pancreatic cancer (panc).
    Overman, Michael J.
    LoRusso, Patricia
    Strickler, John H.
    Patel, Sandip Pravin
    Clarke, Stephen John
    Noonan, Anne M.
    Prasanna, Thiru
    Amin, Manik A.
    Nemunaitis, John J.
    Desai, Jayesh
    O'Byrne, Kenneth John
    George, Thomas J.
    Englert, Judson
    She, Dewei
    Cooper, Zachary A.
    Wu, Yuling
    Khan, Anis
    Kumar, Rakesh
    Bendell, Johanna C.
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
  • [46] Targeting Metabolism of Extracellular Nucleotides via Inhibition of Ectonucleotidases CD73 and CD39
    Jeffrey, Jenna L.
    Lawson, Kenneth, V
    Powers, Jay P.
    JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (22) : 13444 - 13465
  • [47] Targeting the Immunomodulatory CD73/Adenosine System to Improve the Therapeutic Gain of Radiotherapy
    de Leve, Simone
    Wirsdoerfer, Florian
    Jendrossek, Verena
    FRONTIERS IN IMMUNOLOGY, 2019, 10
  • [48] A new generation of immunotherapies targeting the CD39 / CD73 / adenosine pathway to promote the anti-tumor immune response
    Gros, Laurent
    Paturel, Carine
    Perrot, Ivan
    Bensussan, Armand
    Eliaou, Jean-Francois
    Bastid, Jeremy
    Bonnefoy, Nathalie
    M S-MEDECINE SCIENCES, 2020, 36 (02): : 112 - +
  • [49] The role of emmprin on the tumor cells and CD73 on the fibroblasts in tumor-stromal interaction
    Aoki, Mikiko
    Koga, Kaori
    Hamasaki, Makoto
    Nabeshima, Kazuki
    CANCER SCIENCE, 2022, 113 : 1108 - 1108
  • [50] AK119, A CD73 TARGETING ANTIBODY WITH DUAL MECHANISM OF ACTION
    Huang, Zhaoliang
    Pang, Xinghua
    Zhong, Tingting
    Jin, Chunshan
    Chen, Na
    He, Xinrong
    Xia, Dennis
    Jin, Xiaoping
    Wang, Zhongmin
    Xia, Xu
    Li, Baiyong
    JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2021, 9 : A783 - A784