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本文引用的文献

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Evidence for increased expression of regulatory cytokine receptors interleukin-12R and interleukin-18R in common variable immunodeficiency.普通可变免疫缺陷中调节性细胞因子受体白细胞介素-12受体和白细胞介素-18受体表达增加的证据。
Clin Exp Immunol. 2003 Nov;134(2):321-7. doi: 10.1046/j.1365-2249.2003.02271.x.
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Lipopolysaccharide or whole bacteria block the conversion of inflammatory monocytes into dendritic cells in vivo.脂多糖或完整细菌在体内会阻碍炎性单核细胞向树突状细胞的转化。
J Exp Med. 2003 Oct 20;198(8):1253-63. doi: 10.1084/jem.20030335.
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Novel and detrimental effects of lipopolysaccharide on in vitro generation of immature dendritic cells: involvement of mitogen-activated protein kinase p38.脂多糖对未成熟树突状细胞体外生成的新的有害作用:丝裂原活化蛋白激酶p38的参与
J Immunol. 2003 Nov 1;171(9):4792-800. doi: 10.4049/jimmunol.171.9.4792.
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Fine-scale mapping at IGAD1 and genome-wide genetic linkage analysis implicate HLA-DQ/DR as a major susceptibility locus in selective IgA deficiency and common variable immunodeficiency.IGAD1的精细定位和全基因组遗传连锁分析表明,HLA-DQ/DR是选择性IgA缺乏症和常见可变免疫缺陷的主要易感基因座。
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Interferon-gamma switches monocyte differentiation from dendritic cells to macrophages.γ干扰素可使单核细胞的分化从生成树突状细胞转变为生成巨噬细胞。
Blood. 2003 Jan 1;101(1):143-50. doi: 10.1182/blood-2002-04-1164. Epub 2002 Aug 15.
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Severe deficiency of switched memory B cells (CD27(+)IgM(-)IgD(-)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease.常见变异型免疫缺陷患者亚组中转换记忆B细胞(CD27(+)IgM(-)IgD(-))严重缺乏:一种对异质性疾病进行分类的新方法。
Blood. 2002 Mar 1;99(5):1544-51. doi: 10.1182/blood.v99.5.1544.
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Presentation of antigens by MHC class II molecules: getting the most out of them.MHC II类分子对抗原的呈递:充分利用它们
Mol Immunol. 2001 Sep;38(5):329-46. doi: 10.1016/s0161-5890(01)00069-4.
9
Antibodies to human thymic epithelium form part of the murine autoreactive repertoire.针对人类胸腺上皮的抗体是小鼠自身反应性抗体库的一部分。
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10
Up-regulation of IL-12 in monocytes: a fundamental defect in common variable immunodeficiency.单核细胞中白细胞介素-12的上调:常见可变免疫缺陷的一个基本缺陷。
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常见变异型免疫缺陷中单核细胞衍生树突状细胞的反应

Monocyte derived dendritic cell responses in common variable immunodeficiency.

作者信息

Scott-Taylor T H, Green M R J, Eren E, Webster A D B

机构信息

Department of Immunology, Royal Free Campus, University College London, London, UK.

出版信息

Clin Exp Immunol. 2004 Dec;138(3):484-90. doi: 10.1111/j.1365-2249.2004.02640.x.

DOI:10.1111/j.1365-2249.2004.02640.x
PMID:15544626
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1809244/
Abstract

The phenotype and function of monocyte derived dendritic cells (MdDC) were investigated in 25 patients with common variable immunodeficiency (CVID) to test for abnormalities that might help explain the failure of antibody production. Using MHC class II DR and CD86 as markers of maturation, DCs from the majority of CVID patients were normal. However 5 patients, the majority of whom had affected family members who had previously been shown to have a susceptibility genetic locus in the MHC region, expressed abnormally low levels of DR on repeated testing, in some cases associated with a reduced capacity to support antigen stimulated T cell proliferation; nevertheless costimulatory molecules for production of IL-13, IL-10 and IFN-gamma from T cells were intact. In contrast to DCs from healthy donors, DCs from many CVID patients had high spontaneous production of IL-8 and lipopolysaccharide stimulation often caused a reduction in DR expression. Expression of other cytokines (IL-1a, IL-6 and IL-12), either before or after LPS stimulation, was normal. The data suggests there is a fundamental defect in the maturation of MdDCs in a subset of CVID patients that may compromise antigen presentation and subsequent antibody production.

摘要

对25例普通可变免疫缺陷(CVID)患者的单核细胞衍生树突状细胞(MdDC)的表型和功能进行了研究,以检测可能有助于解释抗体产生失败的异常情况。以MHC II类DR和CD86作为成熟标志物,大多数CVID患者的树突状细胞(DC)是正常的。然而,5例患者(其中大多数患者有受影响的家庭成员,这些家庭成员先前已被证明在MHC区域有易感基因位点)在重复检测中DR表达异常低,在某些情况下与支持抗原刺激的T细胞增殖的能力降低有关;尽管如此,T细胞产生IL-13、IL-10和IFN-γ的共刺激分子是完整的。与健康供体的树突状细胞不同,许多CVID患者的树突状细胞IL-8自发产生水平高,脂多糖刺激常导致DR表达降低。LPS刺激之前或之后,其他细胞因子(IL-1α、IL-6和IL-12)的表达均正常。数据表明,一部分CVID患者的MdDC成熟存在根本缺陷,这可能会损害抗原呈递及随后的抗体产生。