Abstract |
It has been shown that allogeneic hematopoietic stem cell transplantation (HSCT) can be one of the therapeutic options for patients with metastatic solid tumors, such as renal cancer. However, the development of relatively severe GVHD seems to be necessary to achieve tumor regression in the current setting. Thus, it is crucial to identify minor histocompatibility antigens (mHags) only expressed in tumor cells but not GVHD target organs. In this study, we examined whether three mHags: ACC-1 and ACC-2 encoded by BCL2A1, and HA-1 encoded by HMHA1, could serve as such targets for melanoma. Real-time PCR and immunohistochemical analysis revealed that the expression of both BCL2A1and HMHA1 in melanoma cell lines and primary melanoma cells was comparable to that of hematopoietic cells. Indeed, melanoma cell lines were efficiently lysed by cytotoxic T lymphocytes specific for ACC-1, ACC-2, and HA-1. Our data suggest that targeting mHags encoded not only by HMHA1, whose aberrant expression in solid tumors has been reported, but also BCL2A1 may bring about beneficial selective graft-versus- tumor effects in a population of melanoma patients for whom these mHags are applicable.
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Authors | Hiroki Torikai, Yoshiki Akatsuka, Yasushi Yatabe, Yasuo Morishima, Yoshihisa Kodera, Kiyotaka Kuzushima, Toshitada Takahashi |
Journal | International journal of hematology
(Int J Hematol)
Vol. 87
Issue 5
Pg. 467-473
(Jun 2008)
ISSN: 0925-5710 [Print] Japan |
PMID | 18414982
(Publication Type: Journal Article)
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Chemical References |
- BCL2-related protein A1
- HA-1 antigen
- Minor Histocompatibility Antigens
- Oligopeptides
- Proto-Oncogene Proteins c-bcl-2
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Topics |
- Cell Line, Transformed
- Gene Expression Regulation, Neoplastic
- Graft vs Host Disease
(immunology, metabolism)
- Graft vs Tumor Effect
(immunology)
- Hematopoietic Stem Cell Transplantation
- Humans
- Immunity, Cellular
- Melanoma
(immunology, metabolism, therapy)
- Minor Histocompatibility Antigens
(biosynthesis, immunology)
- Oligopeptides
(biosynthesis, immunology)
- Proto-Oncogene Proteins c-bcl-2
(biosynthesis, immunology)
- T-Lymphocytes, Cytotoxic
(immunology, metabolism)
- Transplantation, Homologous
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