Phase Ia Study of FoxP3+ CD4 Treg Depletion by Infusion of a Humanized Anti-CCR4 Antibody, KW-0761, in Cancer Patients

被引:181
作者
Kurose, Koji [1 ]
Ohue, Yoshihiro [1 ]
Wada, Hisashi [2 ]
Iida, Shinsuke [3 ]
Ishida, Takashi [3 ]
Kojima, Takashi [4 ]
Doi, Toshihiko [4 ]
Suzuki, Susumu [5 ]
Isobe, Midori [1 ]
Funakoshi, Takeru [6 ]
Kakimi, Kazuhiro [7 ]
Nishikawa, Hiroyoshi [8 ]
Udono, Heiichiro [9 ]
Oka, Mikio [1 ]
Ueda, Ryuzo [5 ]
Nakayama, Eiichi [10 ]
机构
[1] Kawasaki Med Sch, Dept Resp Med, Kurashiki, Okayama, Japan
[2] Osaka Univ, Dept Clin Res Tumor Immunol, Grad Sch Med, Suita, Osaka, Japan
[3] Nagoya City Univ, Dept Hematol & Oncol, Grad Sch Med Sci, Nagoya, Aichi, Japan
[4] Exploratory Oncol Res & Clin Trial Ctr, Kashiwa, Chiba, Japan
[5] Aichi Med Univ, Dept Tumor Immunol, Nagakute, Aichi 48011, Japan
[6] Keio Univ, Sch Med, Dept Dermatol, Shinjuku Ku, Tokyo, Japan
[7] Tokyo Univ Hosp, Dept Immunotherapeut, Tokyo 113, Japan
[8] Osaka Univ, Immunol Frontier Res Ctr, Expt Immunol, Suita, Osaka, Japan
[9] Okayama Univ, Dept Immunol, Grad Sch Med Dent & Pharmaceut Sci, Kita Ku, Okayama 7008530, Japan
[10] Kawasaki Univ Med Welf, Fac Hlth & Welf, Kurashiki, Okayama 7010193, Japan
关键词
T-CELL LEUKEMIA; LUNG-CANCER; EXPRESSION; TUMORS; CCR4; RESPONSES; MAB; LYMPHOMA; NY-ESO-1; THERAPY;
D O I
10.1158/1078-0432.CCR-15-0357
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: FoxP3(+) Tregs inhibit immune responses against tumors. KW-0761 is a humanized anti-human CCR4 monoclonal antibody (mAb) that has antibody-dependent cellular cytotoxicity activity. Depletion of CCR4-expressing FoxP3(+) CD4 Tregs by KW-0761 infusion was investigated in solid cancer patients. Experimental Design: We conducted a phase Ia clinical trial of KW-0761 infusion in 7 lung and 3 esophageal cancer patients. Toxicity, clinical efficacy, changes in lymphocyte subpopulations, including Tregs, and induction of immune responses were analyzed. Results: The results showed that KW-0761 infusion in a dose range between0.1mg/kg and 1.0mg/kgwas safe andwell tolerated. Nodose-limiting toxicitywas observed. Four of 10 patients showed stable disease during treatment and were long survivors. The monitoring of FoxP3(+) Tregs in the peripheral blood mononuclear cells during treatment indicated efficient depletion of those cells, even at the lowest dose of 0.1 mg/kg used. The reduction in Th 1 CD4 T cells and CD8 T cells was limited, whereas a significant reduction was observed with Th 2 and Th 17 CD4 T cells. Immune responses to cancer/testis (CT) antigens and an autoantibody response to thyroid peroxidase were observed in some patients. Conclusions: The findings showed Tregs depletion and the possible occurrence of an immune response following KW-0761 infusion. Combined use of KW-0761 to deplete FoxP3(+) Tregs with other immunotherapies, such as cancer vaccines or checkpoint inhibitors, is a promising approach to augment immune responses. (C) 2015 AACR.
引用
收藏
页码:4327 / 4336
页数:10
相关论文
共 37 条
  • [1] Orchestrating the orchestrators: chemokines in control of T cell traffic
    Bromley, Shannon K.
    Mempel, Thorsten R.
    Luster, Andrew D.
    [J]. NATURE IMMUNOLOGY, 2008, 9 (09) : 970 - 980
  • [2] OX40 engagement depletes intratumoral Tregs via activating FcγRs, leading to antitumor efficacy
    Bulliard, Yannick
    Jolicoeur, Rose
    Zhang, Jimin
    Dranoff, Glenn
    Wilson, Nicholas S.
    Brogdon, Jennifer L.
    [J]. IMMUNOLOGY AND CELL BIOLOGY, 2014, 92 (06) : 475 - 480
  • [3] A testicular antigen aberrantly expressed in human cancers detected by autologous antibody screening
    Chen, YT
    Scanlan, MJ
    Sahin, U
    Tureci, O
    Gure, AO
    Tsang, SL
    Williamson, B
    Stockert, E
    Pfreundschuh, M
    Old, LJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) : 1914 - 1918
  • [4] New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)
    Eisenhauer, E. A.
    Therasse, P.
    Bogaerts, J.
    Schwartz, L. H.
    Sargent, D.
    Ford, R.
    Dancey, J.
    Arbuck, S.
    Gwyther, S.
    Mooney, M.
    Rubinstein, L.
    Shankar, L.
    Dodd, L.
    Kaplan, R.
    Lacombe, D.
    Verweij, J.
    [J]. EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) : 228 - 247
  • [5] Identification of a new subset of myeloid suppressor cells in peripheral blood of melanoma patients with modulation by a granulocyte-macrophage colony-stimulation factor based antitumor vaccine
    Filipazzi, Paola
    Valenti, Roberta
    Huber, Veronica
    Pilla, Lorenzo
    Canese, Paola
    Iero, Manuela
    Castelli, Chiara
    Mariani, Luigi
    Parmiani, Giorgio
    Rivoltini, Licia
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (18) : 2546 - 2553
  • [6] The immune contexture in human tumours: impact on clinical outcome
    Fridman, Wolf Herman
    Pages, Franck
    Sautes-Fridman, Catherine
    Galon, Jerome
    [J]. NATURE REVIEWS CANCER, 2012, 12 (04) : 298 - 306
  • [7] Funt S.A., 2014, ONCOLOGY WILLISTON P, V11, P28
  • [8] Coordinated regulation of myeloid cells by tumours
    Gabrilovich, Dmitry I.
    Ostrand-Rosenberg, Suzanne
    Bronte, Vincenzo
    [J]. NATURE REVIEWS IMMUNOLOGY, 2012, 12 (04) : 253 - 268
  • [9] Control of regulatory T cell development by the transcription factor Foxp3
    Hori, S
    Nomura, T
    Sakaguchi, S
    [J]. SCIENCE, 2003, 299 (5609) : 1057 - 1061
  • [10] Ishida T, 2003, CLIN CANCER RES, V9, P3625