首页> 外文期刊>Human Immunology: Official Journal of the American Society for Histocompatibility and Immunogenetics >Impairment of in vitro generation of monocyte-derived human dendritic cells by inactivated human immunodeficiency virus-1: Involvement of type I interferon produced from plasmacytoid dendritc cells.
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Impairment of in vitro generation of monocyte-derived human dendritic cells by inactivated human immunodeficiency virus-1: Involvement of type I interferon produced from plasmacytoid dendritc cells.

机译:灭活的人类免疫缺陷病毒-1对单核细胞衍生的人树突状细胞体外生成的损害:涉及浆细胞样树突状细胞产生的I型干扰素。

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摘要

In an attempt to simplify the protocol of DC generation in vitro, studies conducted herein show that functional DCs could be generated from bulk peripheral blood mononuclear cells (PBMCs) in media containing GM-CSF and IL-4. Interestingly, when PBMCs, but not purified monocytes, were exposed to either CCR5- or CXCR4-tropic inactivated HIV-1 isolates (iHIV-1) at the initiation of the culture, DC yields were significantly reduced in a dose-dependent manner because of monocyte apoptosis. Similar impairment of DC generation was noted using type I IFNs and poly IC not only in cultures of PBMCs but also using highly enriched monocytes. This effect was reversed by antihuman type I IFN receptor, but not by anti-FasL, anti-TRAIL, anti-TNF, or a mixture of these antibodies. iHIV-1-exposed PBMCs, but not monocytes, produced high levels of IFN-alpha but not IFN-beta. PBMCs depleted of CD123(+) plasmacytoid DCs produced low levels of IFN-alpha and were resistant to iHIV-1-mediated DC impairment. Interestingly, exogenously added TNF reversed the impairment by iHIV-1 in the PBMC cultures. In conclusion, the present results indicate that iHIV-1 impairs the in vitro generation of functional DCs from PBMCs through the induction of IFN-alpha from plasmacytoid DCs in a CD4-dependent fashion in the absence of TNF.
机译:为了简化体外DC产生的方案,本文进行的研究表明可以在含有GM-CSF和IL-4的培养基中从大量外周血单核细胞(PBMC)产生功能性DC。有趣的是,当在培养开始时将PBMC(而非纯化的单核细胞)暴露于CCR5-或CXCR4-tropic灭活的HIV-1分离株(iHIV-1)时,DC产量以剂量依赖性方式显着降低,原因是单核细胞凋亡。不仅在PBMC培养中,而且在高度富集的单核细胞中,使用I型IFN和poly IC都会引起类似的DC生成损伤。抗人I型IFN受体可逆转此作用,但抗FasL,抗TRAIL,抗TNF或这些抗体的混合物不能逆转此作用。暴露于iHIV-1的PBMC(而非单核细胞)产生高水平的IFN-α,但不产生IFN-β。耗尽CD123(+)浆细胞样DC的PBMC产生低水平的IFN-α,并抵抗iHIV-1介导的DC损伤。有趣的是,外源添加的TNF逆转了PBMC培养物中iHIV-1的损伤。总之,目前的结果表明,iHIV-1通过在不存在TNF的情况下以CD4依赖性方式从浆细胞样DC诱导IFN-α来损害PBMC的功能DC的体外产生。

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