Antibody therapy for Adult T-cell leukemia-lymphoma

Int J Hematol. 2011 Nov;94(5):443-52. doi: 10.1007/s12185-011-0941-5. Epub 2011 Oct 13.


Adult T-cell leukemia-lymphoma (ATL) has a very poor prognosis. Since there currently are limited treatment options for ATL patients, several novel agents are being developed and tested clinically. Antibody therapy against ATL was initially started with interleukin-2 receptor α-subunit, CD25, as a target molecule in the late 1980s, and is currently ongoing. CC chemokine receptor 4 (CCR4) was postulated as a novel molecular target in ATL antibody therapy, and humanized anti-CCR4 mAb (KW-0761), whose Fc region was defucosylated to enhance antibody-dependent cellular cytotoxicity, was developed. A phase I study of KW-0761 in relapsed ATL and peripheral T-cell lymphoma was started in 2006, and a subsequent phase II study was completed in 2010. KW-0761 showed a clinically meaningful antitumor activity in patients with relapsed ATL, with an acceptable toxicity profile. The prognosis of ATL patients should be improved in the near future with clinical applications of novel treatment strategies, including those involving KW-0761 and other promising antibody therapies targeting CD25 or CD30.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / therapeutic use*
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Antibody-Dependent Cell Cytotoxicity / genetics
  • Antibody-Dependent Cell Cytotoxicity / immunology*
  • Carrier State / drug therapy
  • Clinical Trials as Topic
  • Humans
  • Interleukin-2 Receptor alpha Subunit / immunology*
  • Leukemia-Lymphoma, Adult T-Cell / drug therapy*
  • Leukemia-Lymphoma, Adult T-Cell / immunology*
  • Molecular Targeted Therapy*
  • Receptors, CCR4 / immunology*


  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • CCR4 protein, human
  • Interleukin-2 Receptor alpha Subunit
  • Receptors, CCR4
  • mogamulizumab