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Expression of the ULBP ligands for NKG2D by B‐NHL cells plays an important role in determining their susceptibility to rituximab‐induced ADCC
Author(s) -
Inagaki Atsushi,
Ishida Takashi,
Yano Hiroki,
Ishii Toshihiko,
Kusumoto Shigeru,
Ito Asahi,
Ri Masaki,
Mori Fumiko,
Ding Jianmin,
Komatsu Hirokazu,
Iida Shinsuke,
Ueda Ryuzo
Publication year - 2009
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.24351
Subject(s) - antibody dependent cell mediated cytotoxicity , rituximab , nkg2d , cd20 , monoclonal antibody , lymphoma , cancer research , antibody , immunotherapy , immunology , monoclonal , cytotoxicity , medicine , biology , immune system , in vitro , biochemistry
Antibody‐dependent cellular cytotoxicity (ADCC) is a major antitumor mechanism of action of therapeutic monoclonal antibodies (mAbs). The aim of this study was to identify tumor‐associated factors which determine susceptibility to rituximab‐induced ADCC. Thirty different CD20+ non‐Hodgkin lymphoma cell lines were phenotyped for characteristics such as level of expression of NKG2D ligands, and the influence thereof on susceptibility to rituximab‐induced ADCC was established. The present study demonstrated that tumor cell susceptibility to rituximab‐induced ADCC was determined by 3 major tumor‐associated factors: ( i ) the amount of the target molecule, CD20; ( ii ) the amount of the ligands for inhibitory killer Ig‐like receptors, major histocompatibility complex class I; and ( iii ) the amounts of some of the NKG2D ligands, especially UL16‐binding protein (ULBP) 1–3. The importance of the ULBPs was confirmed using antibody blockade. In conclusion, this is the first report to show the importance for rituximab‐induced ADCC of ULBPs expressed on tumor cells. The ULBPs could be valuable diagnostic biological markers and significant targets for immunotherapy to improve efficacy not only of rituximab but also of other therapeutic mAbs. © 2009 UICC