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Targeting activation-induced cytidine deaminase overcomes tumor evasion of immunotherapy by CTLs.


ABSTRACT: Activation-induced cytidine deaminase (AID) is an enzyme essential for the generation of Ab diversity in B cells and is considered to be a general gene mutator. In addition, AID expression was also implicated in the pathogenesis of human B cell malignancies and associated with poor prognosis. In this study, we report that small interfering RNA silencing of AID in plasmacytoma dramatically increased its susceptibility to immunotherapy by CTLs. AID silencing did not decrease the mutation frequencies of tumor Ag gene P1A. Gene-array analysis showed dramatically altered expression of a number of genes in AID-silenced plasmacytoma cells, and upregulation of CD200 was shown to be in favor of tumor eradication by CTLs. Taken together, we demonstrate a novel function of AID in tumor evasion of CTL therapy and that targeting AID should be beneficial in the immunotherapy of AID-positive tumors.

SUBMITTER: Liu JQ 

PROVIDER: S-EPMC2874093 | biostudies-literature | 2010 May

REPOSITORIES: biostudies-literature

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Targeting activation-induced cytidine deaminase overcomes tumor evasion of immunotherapy by CTLs.

Liu Jin-Qing JQ   Joshi Pramod S PS   Wang Chuansong C   El-Omrani Hani Y HY   Xiao Yi Y   Liu Xiuping X   Hagan John P JP   Liu Chang-Gong CG   Wu Lai-Chu LC   Bai Xue-Feng XF  

Journal of immunology (Baltimore, Md. : 1950) 20100419 10


Activation-induced cytidine deaminase (AID) is an enzyme essential for the generation of Ab diversity in B cells and is considered to be a general gene mutator. In addition, AID expression was also implicated in the pathogenesis of human B cell malignancies and associated with poor prognosis. In this study, we report that small interfering RNA silencing of AID in plasmacytoma dramatically increased its susceptibility to immunotherapy by CTLs. AID silencing did not decrease the mutation frequenci  ...[more]

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