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白细胞介素-4在体外促进特应性皮炎皮肤浸润淋巴细胞的扩增。

Interleukin-4 promotes the expansion of skin-infiltrating lymphocytes from atopic dermatitis in vitro.

作者信息

Reinhold U, Kukel S, Goeden B, Neumann U, Wehrmann W, Kreysel H W

机构信息

Department of Dermatology, University of Bonn, F.R.G.

出版信息

J Invest Dermatol. 1991 Mar;96(3):370-5. doi: 10.1111/1523-1747.ep12466152.

Abstract

Functional studies of lymphocytes in atopic dermatitis (AD) have so far focused on peripheral blood mononuclear cells (PBMC), whereas cells at the involved site, the skin, have not been examined. Accordingly, we have developed methods to generate lymphocyte cultures from biopsies of inflammatory skin areas. Skin-infiltrating lymphocytes (SIL) were isolated from skin biopsies of 6 patients with severe AD and expanded in vitro in the presence of interleukin-2 (IL-2) without additional antigens. After 6-10 d in culture, outgrowth of mononuclear cells from biopsy tissue was observed in all cases. Phenotypic analysis of skin-derived cells revealed the predominance of CD4+ T-helper/inducer phenotype in SIL populations. Parallel cultures of SIL and PBMC showed an increase and expansion of CD8+ T cells in cultured PBMC, whereas the CD4+ phenotype was predominant in SIL cultures. As indicated by their expression of HLA-DR and CD25 antigens, most of the SIL were activated and the cells mainly expressed T-cell receptors (TCR) composed of alpha and beta chains. Different strategies for expansion of SIL in vitro were examined. High levels of IL-4 (1,000 U/ml) in combination with IL-2 (50 U/ml or 1,000 U/ml) preferentially promoted growth of SIL derived from AD and were much more effective than IL-2 alone. No cells expanded in cultures with IL-4 alone. SIL grown with high concentrations of IL-4 contained a significant proportion of double-positive CD4+8+ cells. No other marked differences were observed in the distribution of T cell subsets in cultures propagated under different conditions for 21 d. Our results demonstrate the feasibility of growing infiltrating T lymphocytes from inflammatory skin of AD patients. The use of high concentrations of IL-2 in combination with high levels of IL-4 allows a large expansion of these cells and thus represents a useful strategy to expand cells for further functional and molecular biologic studies.

摘要

迄今为止,对特应性皮炎(AD)中淋巴细胞的功能研究主要集中在外周血单核细胞(PBMC),而病变部位皮肤中的细胞尚未得到研究。因此,我们开发了从炎症性皮肤区域活检组织中生成淋巴细胞培养物的方法。从6例重度AD患者的皮肤活检组织中分离出皮肤浸润淋巴细胞(SIL),并在白细胞介素-2(IL-2)存在下于体外扩增,无需额外抗原。培养6 - 10天后,所有病例均观察到活检组织中有单核细胞生长。对皮肤来源细胞的表型分析显示,SIL群体中CD4 + T辅助/诱导型表型占主导。SIL和PBMC的平行培养显示,培养的PBMC中CD8 + T细胞增加并扩增,而SIL培养物中CD4 +表型占主导。正如它们对HLA - DR和CD25抗原的表达所示,大多数SIL被激活,且细胞主要表达由α和β链组成的T细胞受体(TCR)。研究了体外扩增SIL的不同策略。高浓度IL - 4(1000 U/ml)与IL - 2(50 U/ml或1000 U/ml)联合使用可优先促进源自AD的SIL生长,且比单独使用IL - 2更有效。单独使用IL - 4培养无细胞扩增。用高浓度IL - 4培养的SIL含有显著比例的双阳性CD4 + 8 + 细胞。在不同条件下培养21天的培养物中,T细胞亚群的分布未观察到其他明显差异。我们的结果证明了从AD患者炎症性皮肤中培养浸润性T淋巴细胞的可行性。高浓度IL - 2与高水平IL - 4联合使用可使这些细胞大量扩增,因此是扩增细胞以进行进一步功能和分子生物学研究的有用策略。

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