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B7-H1阻断对未成熟树突状细胞免疫功能的影响 被引量:7

The immunity effect of B7-H1 blockade on immature dendritic cells
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摘要 目的探讨B7-H1阻断对未成熟树突状细胞(DCs)的免疫刺激活性的影响。方法以细胞因子GM-CSF和IL-4体外诱导人单核细胞来源的树突状细胞,流式细胞仪检测在诱导过程中B7-H1的表达,并以B7-H1单抗阻断处理,分别以流式细胞仪、MTT法、ELISA、ELISPOT法检测B7-H1阻断对DCs的成熟和内吞能力、刺激淋巴细胞增殖、IL-12的分泌、诱导淋巴细胞分化的影响。结果DCs在诱导过程中B7-H1表达逐渐增强,第7d时的阳性表达率为54.12%,以TNF-α诱导成熟后阳性表达率为83.64%;B7-H1阻断对DCs成熟和内吞能力无影响,但可使未成熟DCs刺激淋巴细胞增殖的能力和IL-12的分泌明显增强,并诱导淋巴细胞向分泌IFN-γ的Th1/Tc1的分化。结论B7-H1阻断可增强未成熟DCs的免疫刺激活性,利用B7-H1阻断的DCs瘤苗激发抗肿瘤免疫的方案值得进一步探讨。 AIM: To investigate the immune stimulation capacity of B7-H1 blockade on immature dendritic cells (DCs) in vitro. METHODS: The human monocyte-derived dendritic cells were induced in the presence of cytokine GM-CSF and IL-4. The expression of B7-H1 was detected by FCM. On blockade of B7-H1, the maturation and endocytic activity, T cells stimulatory proliferation capacity, IL-12 production, T cell differentiation effect of DCs were detected by FCM, MTT assay, ELISA and ELISPOT, respectively. RESULTS: The expression of B7-H1 was increased with the induction of DCs. On day 7, the positive expression was 54.12%, and the TNF-α induced mature DCs had the positive expression rate of 83.64%. The blockade of B7-H1 on immature DCs had sharply increased their T cells stimulatory proliferation capacity and IL-12 production, and efficiently induced the development of Th1/Tc1 cells, but had no effect on their maturation and endocytic activity. CONCLUSION: The blockade of B7-H1 on immature DCs increases its immune stimulation activity. It is valuable to investigate the antitumor immune responses of DCs vaccine with B7-H1 blockade.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2005年第5期906-910,共5页 Chinese Journal of Pathophysiology
基金 广州市科技攻关重点项目(No.2003Z2-E4011) 广东省自然科学基金资助项目(No.4009408)
关键词 树突细胞 B7-H1 Dendritic cells B7-H1
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  • 1Dong H, Zhu G, Tamada K, et al. B7-H1, a third member of the B7 family, costimulates T-cell proliferation and secretion of interleukin-10[J]. Nat Med, 1999, 5(12): 1365-1369.
  • 2Dong H, Chen L. B7-H1 pathway and its role in the evasion of tumor immunity[J]. J Mol Med, 2003, 81(5): 281-287.
  • 3Freeman GJ, Long AJ, Iwai Y, et al. Engagement of the PD-1 immunoinhibitory receptor by a novel B7 family member leads to negative regulation of lymphocyte activation[J]. J Exp Med, 2000, 192(7): 1027-1034.
  • 4Selenko-Gebauer N, Majdic O, Szekeres A, et al. B7-H1 (Programmed Death-1 Ligand) on dendritic cells is involved in the induction and maintenance of T cell anergy[J]. J Immunol, 2003, 170(7): 3637-3644.
  • 5Brown JA, Dorfman DM, Ma FR, et al. Blockade of programmed death-1 ligands on dendritic cells enhances T cell activation and cytokine production[J]. J Immunol, 2003, 170(3): 1257-1266.
  • 6John J, Hutchinson J, Dalgleish A, et al. Cryopreservation of immature monocyte-derived dendritic cells results in enhanced cell maturation but reduced endocytic activity and efficiency of adenoviral transduction[J]. J Immunol Methods, 2003, 272(1-2): 35-48.
  • 7Dong H, Strome SE, Salomao DR, et al. Tumor-associated B7-H1 promotes T-cell apoptosis: Apotential mechanism of immune evasion[J]. Nat Med, 2002, 8(8): 793-800.
  • 8Curiel TJ, Wei S, Dong H, et al. Blockade of B7-H1 improves myeloid dendritic cell-mediated antitumor immunity[J]. Nat Med, 2003, 9(5): 562-567.
  • 9Gray CP, Arosio P, Hersey P. Heavy chain ferritin activates regulatory T cells by induction of changes in dendritic cells[J]. Blood, 2002, 99(9): 3326-3334.

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