Antisera induced by infusions of autologous Ad-CD154-leukemia B cells identify ROR1 as an oncofetal,antigen and receptor for Wnt5a

被引:257
作者
Fukuda, Tetsuya [1 ]
Chen, Liguang [1 ,2 ]
Endo, Tomoyuki [1 ]
Tang, Li [1 ,2 ]
Lu, Desheng [1 ]
Castro, Jariuario E. [1 ,2 ]
Widhopf, George F., II [1 ,2 ,3 ]
Rassenti, Laura Z. [1 ,2 ]
Cantwell, Mark J. [1 ]
Prussak, Charles E. [3 ]
Carson, Dennis A. [1 ]
Kipps, Thomas J. [1 ]
机构
[1] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Chron Lymphocyt Leukemia Res Consortium, La Jolla, CA 92093 USA
[3] Memgen, Solana Beach, CA 92075 USA
关键词
chronic lymphocytic leukemia; neoplasia;
D O I
10.1073/pnas.0712148105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We examined the sera of six patients before and after i.v. infusions of autologous chronic lymphocytic leukemia (CLL) cells transduced ex vivo with an adenovirus encoding CD154 (Ad-CD154). Five patients made high-titer antibodies against adenovirus and three made IgG reactive with a leukemia-associated surface antigen, which we identified as ROR1. Anti-ROR1 antibodies were not detected in the sera of untreated patients. We generated anti-ROR1 mAbs and found they reacted specifically with the CLL cells of all patients, but not with nonleukemic leukocytes, a wide variety of normal adult tissues, or blood mononuclear cells, including CD5(+) B cells of healthy adults. ROR1 could bind Wnt5a, which induced activation of NF-kappa B when coexpressed with ROR1 in HEK293 cells and enhanced the survival of CLL cells in vitro, an effect that could be neutralized by posttreatment anti-ROR1 antisera. We conclude that patients with CLL can break immune tolerance to ROR1, which is an oncofetal surface antigen and survival-signaling receptor in this neoplastic disease.
引用
收藏
页码:3047 / 3052
页数:6
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