Analysis of biological response of epidemal components to simple chemicals

表皮成分对简单化学品的生物反应分析

基本信息

  • 批准号:
    10670776
  • 负责人:
  • 金额:
    $ 2.37万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    1998
  • 资助国家:
    日本
  • 起止时间:
    1998 至 1999
  • 项目状态:
    已结题

项目摘要

As is well known in the case of Langerhans cells, dendritic cells (DCs) play a crucial role in the initiation of immunity to simple chemicals such as noted in the contact hypersensitivity. Since DCs are scattered in nonlymphoid organs as immature cells. They must be activated to initiate primary antigen specific immune reactions. Therefore, we hypothesized that some simple chemicals must affect the function of DCs. In this paper, we first demonstrated that human monocyte-derived DCs responded to such simple chemicals as DNCB, TNCB, DNFB, NiClィイD22ィエD2, MnClィイD22ィエD2, CoClィイD22ィエD2, SnClィイD22ィエD2, and CdSOィイD24ィエD2 by augmenting their expression of CD86 or HLA-DR antigen, down-regulating c-Fms expression or increasing their production of TNFα. In addition, the DCs stimulated with the chemicals demonstrated increased allogeneic T cell stimulatory function. Next, we found that, among these chemicals, only NiClィイD22ィエD2 and CoClィイD22ィエD2 induced apoptosis in them. Finally, we examined the effects of these chemicals on CD86 expression by 3 different macrophage subsets and DCs induced from the cultures of human peripheral blood monocytes in the presence of M-CSF, M-CSF + IL-4, GM-CSF, and GM-CSF + IL-4, respectively. Among them, only DCs dramatically augmented their expression of CD86. These observations have revealed unique characteristics of DCs which convert chemical stimuli to augmentation of their antigen presenting function, although their responses to different chemicals were not necessarily uniform in the phenotypic changes cytokine production or in the induction of apoptosis.
众所周知,在朗格汉斯细胞的情况下,树突状细胞(dc)在启动对简单化学物质的免疫方面起着至关重要的作用,例如接触性超敏反应。因为树突状细胞作为未成熟细胞分散在非淋巴器官中。它们必须被激活以启动初级抗原特异性免疫反应。因此,我们假设一些简单的化学物质一定会影响dc的功能。在本文中,我们首先证明了人类monocyte-derived DCs对DNCB等简单的化学物质,TNCB, DNFB, NiClィイD22摊位ィエD2, MnClィイD22摊位ィエD2, CoClィイD22摊位ィエD2, SnClィイD22摊位ィエD2,和CdSOィイD24ィエD2通过增加CD86的表达或HLA-DR抗原,显示c-Fms表达式或增加他们的肿瘤坏死因子α的生产。此外,化学物质刺激的dc表现出增强的同种异体T细胞刺激功能。接下来,我们发现在这些化学物质中,只有NiCl D22 D2和CoCl D22 D2诱导细胞凋亡。最后,我们分别在M-CSF、M-CSF + IL-4、GM-CSF和GM-CSF + IL-4的存在下,检测了这些化学物质对人外周血单核细胞培养的3种不同巨噬细胞亚群和DCs中CD86表达的影响。其中,只有dc显著增强了CD86的表达。这些观察结果揭示了树突状细胞的独特特征,它们将化学刺激转化为增强其抗原呈递功能,尽管它们对不同化学物质的反应在表型变化、细胞因子产生或诱导凋亡方面不一定是一致的。

项目成果

期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Horiuchi N,Aiba S.: "Peripheral blood lymphocytes from psoriatic patients are hyporesponsive to b-streptococcal superantigens." Br J Dematol. 138. 229-235 (1998)
Horiuchi N,Aiba S.:“银屑病患者的外周血淋巴细胞对 b 链球菌超抗原反应低下。”
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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  • 通讯作者:
Matsumura, N., Aiba, S.: "Comparison of immune reactivity profiles against various environmental allergens between adults patients with atopic dermatitis and patients with allergic respiratory diseases"Acta Dermato-Venereologica 1997. 77. 388-391
Matsumura, N., Aiba, S.:“特应性皮炎成人患者与过敏性呼吸道疾病患者针对各种环境过敏原的免疫反应谱的比较”Acta Dermato-Venereologica 1997. 77. 388-391
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    0
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  • 通讯作者:
Manome, H., Aiba, S. and Tagami, H.: "Simple can induce maturation and apoptosis of dendritic cells"Immunology. 98. 481-490 (1999)
Manom​​e, H.、Aiba, S. 和 Tagami, H.:“简单可以诱导树突状细胞的成熟和凋亡”免疫学。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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  • 通讯作者:
Singh, S., Aiba, S., Manome, H., and Tagami, H.: "The effects of dexamethasone, cyclosporine, and vitamin D3 on the activation of dendritic cells stimulated by haptens"Arch Dermatol Res. 281. 548-554 (1999)
Singh, S.、Aiba, S.、Manom​​e, H. 和 Tagami, H.:“地塞米松、环孢菌素和维生素 D3 对半抗原刺激的树突状细胞活化的影响”Arch Dermatol Res。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Kawamura MS.,Aiba S.: "The importance of CD54 and CD86 cotimulato"Arch Dermatol Res. 290. 603-609 (1998)
Kawamura MS.,Aiba S.:“CD54 和 CD86 协同刺激的重要性”Arch Dermatol Res。
  • DOI:
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    0
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AIBA Setsuya其他文献

AIBA Setsuya的其他文献

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{{ truncateString('AIBA Setsuya', 18)}}的其他基金

Analysis of gene expression profiles in inflammatory skin disorders
炎症性皮肤病的基因表达谱分析
  • 批准号:
    23659541
  • 财政年份:
    2011
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
The role of ASK-1 in the pathogenesis of murine contact dermatitis
ASK-1在小鼠接触性皮炎发病机制中的作用
  • 批准号:
    19591295
  • 财政年份:
    2007
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Therapeutic Approach for Allergic or Autoimmune Diseases by Modulation of CD25+CD4+ T Cells
通过调节 CD25 CD4 T 细胞治疗过敏性或自身免疫性疾病
  • 批准号:
    13670863
  • 财政年份:
    2001
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Analysis of altered function of dendritic cells from atopic dermatitis or psoriatic patients
特应性皮炎或银屑病患者树突状细胞功能改变的分析
  • 批准号:
    12670803
  • 财政年份:
    2000
  • 资助金额:
    $ 2.37万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

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使用 CLEM-FIB/SEM 三维构建接触性皮炎诱发阶段的 iSALT
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适合皮肤过敏、湿疹、接触性皮炎或其他皮肤病患者的防过敏内衣
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确定 TRPC3 在过敏性接触性皮炎引起的瘙痒中的功能
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Examination of skin damage after chronic exposure to gaseous volatile organic compounds in relation to contact dermatitis
长期接触气态挥发性有机化合物后与接触性皮炎相关的皮肤损伤检查
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先天免疫系统缺陷小鼠年龄依赖性过敏性接触性皮炎抵抗力丧失的机制
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基于代谢激活引起的特定化学结构可预测过敏性接触性皮炎的发病机制。
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