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荷瘤小鼠脾脏过度增大的机制 被引量:7

Mechanism of Splenic Excess Augmentation in Tumor-bearing Mice
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摘要 目的研究H22荷瘤小鼠生长过程中脾脏过度增大的机制。方法通对小鼠脾指数与脾脏细胞总数进行相关性分析、检测脾细胞生长周期以及T、B淋巴细胞比例。结果小鼠脾指数与脾脏细胞总数呈显著正相关性(r=1.000,P<0.01);H22荷瘤小鼠与对照组小鼠脾脏细胞的细胞周期无明显差异;H22荷瘤小鼠与对照组小鼠相比脾脏总T淋巴细胞、CD8+T与CD4+T细胞比例增大(P<0.05),B细胞比例基本不变,CD4+/CD8+减小。结论 H22荷瘤小鼠脾脏增大与各类免疫细胞转移至脾脏后滞留有直接的关系,其中CD8+T细胞的积累最显著,脾脏的免疫抑制作用与CD8+T细胞有密切的关系。 Objective To explore the mechanism of splenic excess augmentation in H22-beared mice.Methods Correlation of splenic index and cell count was analyzed.Splenic cell cycle and the variety of lymphocyte were examined by flow cytometry(FCM).Results Significant correlation was observed between splenic index and total cell number(r=1.000,P〈0.01).There was no obvious diversity in splenic cell cycle of mice.The proportion of T cell,CD8+T cell and CD4+T cell increased(P〈0.05).At the same time CD4+/CD8+declined.There was no marked change in the proportion of B cell.Conclusion The excess augmentation in H22 bearing mice was associated with the export of cells which was restrained after the cells entered the spleen,especially the CD8+T cell was detected.CD8+T cell was bound up with immunosuppression of spleen in H22-beared mice.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2012年第8期940-943,共4页 Cancer Research on Prevention and Treatment
基金 国家自然科学基金资助课题(31000755) 科技部科技型中小企业技术创新基金资助课题(10C262112200196)
关键词 脾脏 增大 淋巴细胞 免疫抑制 Spleen Augmentation Lymphocyte Immunosuppression
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  • 1G. Filaci,M. Fravega,D. Fenoglio,M. Rizzi,S. Negrini,R. Viggiani,F. Indiveri.Non-antigen specific CD8+ T suppressor lymphocytes[J].Clinical and Experimental Medicine.2004(2)
  • 2James C. Zimring MD, PhD,Judith A. Kapp.Identification and characterization of CD8+ suppressor T cells[J].Immunologic Research (-).2004(1-3)
  • 3Thomas H. Stanton,Sheila Carbon.Gene(s) affecting the expression of Qa-1[J].Immunogenetics.1982(5)
  • 4Kronenberg M,Steinmetz M,Kobori J,et al.RNA transcripts for I-J polypeptides are apparently not encoded between the I-A and I-E subregions of the murine major histocompatibility complex[].Proceedings of the National Academy of Sciences of the United States of America.1983
  • 5Poussier P,Ning T,Banerjee D,Julius M.A unique subset of self-specific intraintestinal T cells maintains gut integrity[].The Journal of Experimental Medicine.2002
  • 6Okumura K,Herzenberg LA,Murphy DB,McDevitt HO,Herzenberg LA.Selective expression of H-2(i-region)loci controlling determinants on helper and suppressor T lymphocytes[].The Journal of Experimental Medicine.1976
  • 7Anderson LC,Binz H,Wigzell H.Specific unresponsiveness to transplantation antigens induced by auto-immunisation with syngeneic,antigen-specific T lymphoblasts[].Nature.1976
  • 8Askenase PW,Hayden BJ,Gershon RK.Augmentation of delayed-type hypersensitivity by doses of cyclophosphamide which do not affect antibody responses[].The Journal of Experimental Medicine.1975
  • 9Balashov KE,Khoury SJ,Hafler DA,Weiner HL.Inhibition of T cell responses by activated human CD8~+ T cells is mediated by interferon-gamma and is defective in chronic progressive multiple sclerosis[].The Journal of Clinical Investigation.1995
  • 10Fehervari Z,Sakaguchi S.CD4~+ Tregs and immune control[].The Journal of Clinical Investigation.2004

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