Abstract |
Recently, HBZ has been reported to play an important role in the proliferation of adult T-cell leukaemia (ATL) cells and might be a target of novel therapy for ATL. To develop a novel immunotherapy for ATL, we verified the feasibility of cellular immunotherapy targeting HBZ. We established an HBZ-specific and HLA-A*0201-restricted cytotoxic T lymphocyte (CTL) clone. Detailed study using this CTL clone clearly showed that HBZ is certainly an immunogenic protein recognizable by human CTLs; however, HBZ-specific CTLs could not lyse ATL cells. Failure of HBZ-specific CTLs to recognize human T-cell leukemia virus type 1 (HTLV-1)-infected cells might be due to a low level of HBZ protein expression in ATL cells and resistance of HTLV-1-infected cells to CTL-mediated cytotoxicity. Although HBZ plays an important role in the proliferation of HTLV-1-infected cells, it may also provide a novel mechanism that allows them to evade immune recognition.
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Authors | Koichiro Suemori, Hiroshi Fujiwara, Toshiki Ochi, Taiji Ogawa, Masao Matsuoka, Tadashi Matsumoto, Jean-Michel Mesnard, Masaki Yasukawa |
Journal | The Journal of general virology
(J Gen Virol)
Vol. 90
Issue Pt 8
Pg. 1806-1811
(Aug 2009)
ISSN: 0022-1317 [Print] England |
PMID | 19423550
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens, Viral
- Basic-Leucine Zipper Transcription Factors
- HBZ protein, human T-cell leukemia virus type I
- Retroviridae Proteins
- Viral Proteins
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Topics |
- Antigens, Viral
(immunology)
- Basic-Leucine Zipper Transcription Factors
(immunology)
- Cell Line, Tumor
- Cytotoxicity Tests, Immunologic
- Human T-lymphotropic virus 1
(immunology)
- Humans
- Leukemia, T-Cell
(immunology)
- Retroviridae Proteins
- T-Lymphocytes, Cytotoxic
(immunology)
- Viral Proteins
(immunology)
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