Suppr超能文献

溃疡性结肠炎患者中高表达 α4 整合素(hi)和 CX3CR1 的促炎单核细胞的吸附耗竭。

Adsorptive depletion of alpha4 integrin(hi)- and CX3CR1hi-expressing proinflammatory monocytes in patients with ulcerative colitis.

机构信息

Department of Clinical Cell Biology, Graduate School of Medicine, Chiba University, Chuo-ku, Chiba-shi, Japan.

出版信息

Dig Dis Sci. 2010 Jul;55(7):1886-95. doi: 10.1007/s10620-009-0974-2. Epub 2009 Nov 12.

Abstract

BACKGROUND

Two main functionally distinct monocytes phenotypes are known: the CD14(hi)CD16(-) "classical" and the CD14(+)CD16(+) "proinflammatory" phenotypes. The latter phenotype is elevated in patients with ulcerative colitis (UC) and is suspected to have a major role in the immunopathogenesis of UC.

AIM

To selectively deplete circulating proinflammatory CD14(+)CD16(+) monocyte phenotype.

METHODS

Seven corticosteroid-naïve patients with UC (clinical activity index = 8.7 +/- 1.3) and seven healthy subjects were included. In patients with UC, granulocyte/monocyte adsorption (GMA) was done with an Adacolumn that selectively adsorbs leucocytes of the myeloid lineage. Blood from all subjects at baseline and from the patients immediately after the first GMA session was processed. Isolated monocytes were subjected to fluorescence-activated cell sorter analyses.

RESULTS

The seven UC patients achieved remission (CAI <or=4) after 5-10 GMA sessions. GMA induced a strong fall in the ratio (%) of CD14(+)CD16(+) to CD14(hi)CD16(-) monocytes, from 10.0 +/- 1.4 to 3.0 +/- 0.9. Further, expressions of alpha4 integrin (374.8 +/- 26.1 mean fluorescence intensity, MFI) and CX(3)CR1 (49.5 +/- 4.6 MFI) were significantly high on CD14(+)CD16(+)monocytes as compared with on CD14(hi)CD16(-) monocytes (169.2 +/- 17.2 and 33.2 +/- 3.6 MFI, respectively). Additionally, GMA significantly increased the ratio of the CD14(hi)CD16(-)CCR2(low) "immature" monocytes from 3.74 +/- 0.62 to 8.11 +/- 0.56 MFI.

CONCLUSIONS

We found high expressions of alpha4 integrin and CX(3)CR1 on monocytes in patients with active UC, known to promote the extravasation of CD14(+)CD16(+) monocytes into the mucosa. GMA effectively depletes CD14(+)CD16(+) monocytes and concomitantly increases CD14(hi)CD16(-)CCR2(low) "immature" monocytes; thus GMA was associated with the emergence of less inflammatory monocyte phenotype in circulation.

摘要

背景

已知两种主要功能不同的单核细胞表型:CD14(hi)CD16(-)“经典”和 CD14(+)CD16(+)“促炎”表型。后一种表型在溃疡性结肠炎(UC)患者中升高,被怀疑在 UC 的免疫发病机制中起主要作用。

目的

选择性耗尽循环中促炎的 CD14(+)CD16(+)单核细胞表型。

方法

纳入 7 例皮质类固醇初治的 UC 患者(临床活动指数=8.7±1.3)和 7 名健康对照者。在 UC 患者中,通过 Adacolumn 进行粒细胞/单核细胞吸附(GMA),该柱选择性吸附髓系白细胞。所有受试者在基线时和患者在第一次 GMA 治疗后立即采血。分离的单核细胞进行荧光激活细胞分选分析。

结果

7 例 UC 患者在 5-10 次 GMA 治疗后达到缓解(CAI≤4)。GMA 诱导 CD14(+)CD16(+)与 CD14(hi)CD16(-)单核细胞的比例(%)明显下降,从 10.0±1.4降至 3.0±0.9。此外,与 CD14(hi)CD16(-)单核细胞相比,CD14(+)CD16(+)单核细胞上的 alpha4 整合素(374.8±26.1 平均荧光强度,MFI)和 CX(3)CR1(49.5±4.6 MFI)的表达明显升高(分别为 169.2±17.2 和 33.2±3.6 MFI)。此外,GMA 显著增加了 CD14(hi)CD16(-)CCR2(低)“幼稚”单核细胞的比例,从 3.74±0.62 升至 8.11±0.56 MFI。

结论

我们发现活动期 UC 患者单核细胞上高表达 alpha4 整合素和 CX(3)CR1,已知这两种物质均能促进 CD14(+)CD16(+)单核细胞渗出到黏膜中。GMA 能有效耗尽 CD14(+)CD16(+)单核细胞,同时增加 CD14(hi)CD16(-)CCR2(低)“幼稚”单核细胞;因此,GMA 与循环中促炎单核细胞表型的出现有关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验