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Regulation of the expression of MHC class I and II by class II transactivator (CIITA) in hematopoietic cells
Author(s) -
Liu Aichun,
Takahashi Masuhiro,
Toba Ken,
Zheng Zhiyin,
Hashimoto Shigeo,
Nikkuni Kohji,
Furukawa Tatsuo,
Koike Tadashi,
Aizawa Yoshifusa
Publication year - 1999
Publication title -
hematological oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 44
eISSN - 1099-1069
pISSN - 0278-0232
DOI - 10.1002/(sici)1099-1069(199912)17:4<149::aid-hon645>3.0.co;2-f
Subject(s) - ciita , biology , mhc class ii , human leukocyte antigen , major histocompatibility complex , mhc class i , transactivation , cancer research , microbiology and biotechnology , antigen , immunology , transcription factor , genetics , gene
In order to develop an effective immunotherapy for hematological malignancies, we investigated the applicability of class II transactivator (CIITA), which had been demonstrated to regulate the expression of MHC class II (MHC‐II) by assembling the transcription factors of MHC‐II molecules, for immunotherapy by potentiating the antigenicity of tumour cells by inducing MHC expression. First, 32 hematopoietic cell lines were analysed for the expression of HLA‐DR, CIITA, RFX5 or HLA‐ABC. Fourteen cell lines were positive and 18 were negative for HLA‐DR. All the 14 HLA‐DR positive cell lines were demonstrated to express CIITA mRNA by RT‐PCR. On the other hand, in all the 18 HLA‐DR negative cell lines, the expression of CIITA was not demonstrated. RFX5, which is one of the transcription factors of MHC‐II, was expressed ubiquitously in all 32 cell lines. Three cell lines out of 23 hematopoietic cell lines examined were negative for HLA‐ABC, and all three of these cell lines were negative for both HLA‐DR and CIITA expression. Furthermore, CIITA cDNA was transfected into K562 cells, which were negative for HLA‐ABC, ‐DR and ‐DQ, but positive for HLA‐DP. The transfection rendered HLA‐DR negative to positive and increased the expression level of HLA‐DP, but HLA‐DQ remained negative. In addition to HLA‐DR, HLA‐ABC was also induced to express by the transfection of CIITA gene. The present study demonstrated that the expression of HLA‐DR in hematopoietic cells is regulated in subordination to CIITA and the expression of HLA‐DR (and HLA‐ABC in K562) is induced by transfection with the CIITA gene. These findings revealed the applicability of CIITA in potentiating anti‐tumour immunity of HLA‐DR negative tumour cells for immunotherapy of hematological malignancies. Copyright © 1999 John Wiley & Sons, Ltd.