<Originals>Interferon-γ modulate Ia antigen expression on thymic reticuloepithelial cells in New Zealand mice
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概要
- 論文の詳細を見る
The defect in syngeneic mixed lymphocyte reaction in New Zealand black (NZB) mice, an animal model of human autoimmune diseases, is primarily caused by T cell abnormality in the recognition of self (Ia) antigens. This T cell abnormality is possibly associated with the abnormal activation of T cell in the thymus due to the abnormal expression of Ia antigens on thymic reticuloepithelial cells (TRC) of NZB mice. To correct the T cell abnormality in recognition of Ia antigens, we evaluated the effects of Interferon-γ (IFN-γ) on the Ia antigen expression on TRC : IFN-γwas added to the culture of TRC, and changes in the positive rate and amount of Ia antigens on TRC were studied by flow cytofluorometry. Pretreatment value of the Ia antigens on TRC was lower in NZB mice than in normal mice. However, the addition of IFN-γincreased the value of Ia antigens on TRC in NZB mice to the level similar to that in normal mice. The degree of increase was greater in NZB mice than in normal mice, which suggests that sensitivity to IFN-γis enhanced in the former. These results suggest that the addition of IFN-γmay have corrected the abnormality of T cells during the differentiation process of T cells in the thymus by increasing the Ia antigens on TRC in NZB mice.
- 近畿大学の論文
著者
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Yamazoe Y
Division Of Drug Metabolism And Molecular Toxicology Graduate School Of Pharmaceutical Sciences Toho
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Yamazoe Yasushi
Department Of Pharmacology School Of Medicine Keio University:department Of Analytical Biochemistry
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Ohba Yasuhiro
Department Of Central Clinical Laboratory
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HORIUCHI Atsushi
Third Department of Internal Medicine, Kinki University School of Medicine
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Ohba Yasuhiro
Department Of Clinical Pathology Kinki University School Of Medicine
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Yamazoe Yasushi
Third Department Of Internal Medicine Kinki University School Of Medicine
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Funauchi Masanori
Third Department Of Internal Medicine Kinki University School Of Medicine
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MINODA Masahide
Third Department of Internal Medicine, Kinki University School of Medicine
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HAMADA Kinya
Third Department of Internal Medicine, Kinki University School of Medicine
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HIGASHIKAWA Mitsuhiro
Third Department of Internal Medicine, Kinki University School of Medicine
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SUGISHIMA Hitoshi
Third Department of Internal Medicine, Kinki University School of Medicine
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HIGASHITANI Sumihiko
Third Department of Internal Medicine, Kinki University School of Medicine
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IKEDA Keizo
Third Department of Internal Medicine, Kinki University School of Medicine
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SENDA Shiro
Third Department of Internal Medicine, Kinki University School of Medicine
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AKIYAMA Toshiyuki
Department of Central Laboratory, Kinki University Hospital
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Horiuchi Atsushi
Third Department Of Internal Medicine Kinki University School Of Medicine
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Akiyama Toshiyuki
Department Of Central Clinical Laboratory
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Yamazoe Yasushi
Division Of Drug Metabolism And Molecular Toxicology Graduate School Of Pharmaceutical Sciences Toho
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Ikeda Keizo
Third Department Of Internal Medicine Kinki University School Of Medicine
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Horiuchi Atsushi
Third Department Of Internai Medicine Kinki University Sohool Of Medicine
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Senda Shiro
Third Department Of Internal Medicine Kinki University School Of Medicine
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Hamada Kinya
Third Department Of Internal Medicine Kinki University School Of Medicine
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Minoda M
Third Department Of Internal Medicine Kinki University School Of Medicine
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Sugishima Hitoshi
Third Department Of Internal Medicine Kinki University School Of Medicine
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Higashitani Sumihiko
Third Department Of Internal Medicine Kinki University School Of Medicine
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Higashikawa Mitsuhiro
Third Department Of Internal Medicine Kinki University School Of Medicine
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