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通过酶联免疫斑点分析和定量逆转录聚合酶链反应对人派尔集合淋巴结中干扰素γ、白细胞介素-4、白细胞介素-5和白细胞介素-10产生情况的分析。

An analysis of interferon gamma, IL-4, IL-5 and IL-10 production by ELISPOT and quantitative reverse transcriptase-PCR in human Peyer's patches.

作者信息

Hauer A C, Bajaj-Elliott M, Williams C B, Walker-Smith J A, MacDonald T T

机构信息

Department of Paediatric Gastroenterology, St Bartholomews Hospital, London.

出版信息

Cytokine. 1998 Aug;10(8):627-34. doi: 10.1006/cyto.1997.0337.

Abstract

The cytokine profiles of mononuclear cells freshly isolated from Peyer's patch (PPMC), adjacent ileal lamina propria lymphocytes (LPMC) and peripheral blood (PBMC) in children without histological evidence of gastrointestinal disease has been investigated by single-cell enzyme-linked immunoabsorbent spot forming assay (ELISPOT) and reverse transcriptase (RT)-PCR. In the blood, interferon gamma and IL-4 ELISPOTs were regularly detected albeit at low frequency (< 50/10(5) cells). IL-5 and IL-10 ELISPOTs were not seen in most patients. In Peyer's patches and lamina propria there was a dramatic increase in cytokine secreting cells of all types compared to blood, reaching a very high frequency for interferon gamma in the lamina propria (1000-3000/10(5) cells). IL-4 and IL-5 ELISPOTs were 20-100-fold less common in both PP and LPL. At all sites, cytokine secretion depended on protein synthesis and enrichment for CD4+ cells in PP increased the frequency of all cytokine-secreting cells. Quantification of messenger RNA for cytokines using RT-PCR demonstrated that IL-4 and IL-10 transcripts were significantly greater than interferon gamma transcripts in PP and in lamina propria, IL-4, IL-10 and interferon gamma transcripts were equivalent. IL-5 transcripts were not detected in most samples of PP and lamina propria. These results clearly show that cells secreting interferon gamma predominate in human PP and LPL. However the high mRNA concentrations for IL-4 and IL-10 shows that although these cells are quantitatively few, they are highly transcriptionally active.

摘要

采用单细胞酶联免疫吸附斑点形成试验(ELISPOT)和逆转录酶(RT)-PCR,对无胃肠道疾病组织学证据的儿童的派尔集合淋巴结(PPMC)、相邻回肠固有层淋巴细胞(LPMC)和外周血(PBMC)中新鲜分离的单核细胞的细胞因子谱进行了研究。在血液中,虽然干扰素γ和IL-4 ELISPOT检测频率较低(<50/10⁵细胞),但可定期检测到。大多数患者未检测到IL-5和IL-10 ELISPOT。与血液相比,派尔集合淋巴结和固有层中所有类型的细胞因子分泌细胞显著增加,固有层中干扰素γ的频率非常高(1000 - 3000/10⁵细胞)。IL-4和IL-5 ELISPOT在派尔集合淋巴结和固有层中的出现频率低20 - 100倍。在所有部位,细胞因子分泌依赖于蛋白质合成,派尔集合淋巴结中CD4⁺细胞的富集增加了所有细胞因子分泌细胞的频率。使用RT-PCR对细胞因子信使RNA进行定量分析表明,派尔集合淋巴结和固有层中IL-4和IL-10转录本显著高于干扰素γ转录本,固有层中IL-4、IL-10和干扰素γ转录本相当。大多数派尔集合淋巴结和固有层样本未检测到IL-5转录本。这些结果清楚地表明,分泌干扰素γ的细胞在人派尔集合淋巴结和固有层中占主导地位。然而,IL-4和IL-10的高mRNA浓度表明,尽管这些细胞数量较少,但它们具有高度的转录活性。

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