首页> 美国卫生研究院文献>The American Journal of Pathology >Injection of Pre-Psoriatic Skin with CD4+ T Cells Induces Psoriasis
【2h】

Injection of Pre-Psoriatic Skin with CD4+ T Cells Induces Psoriasis

机译:向牛皮癣前皮肤注射CD4 + T细胞诱导牛皮癣

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Psoriasis is an immunologically mediated skin disease linked to several different class I major histocompatibility complex alleles. However, the phenotype of the pathogenic lymphocyte and nature of the T cell activating event which triggers conversion of symptomless (PN) skin into psoriatic plaques (PP skin) is unknown. This study extends our previous observations in which autologous blood-derived immunocytes were injected into PN skin engrafted onto SCID mice to produce full-fledged PP lesions. The first question addressed is whether injected CD4+ T cells or CD8+ T cells were responsible for phenotypic conversion of PN to PP skin. In five different patients only CD4+ but not CD8+ T cell lines produced psoriatic lesions. Next, immunological events occurring within PN skin following injection of CD4+ T cells in grafts that had sufficient tissue available for detailed analysis was examined. In two patients, intraepidermal resident CD8+ T cells were induced to proliferate during lesion development, expressing acute activation markers CD25 and CD69. In another patient, injection of CD4+ T cells revealed CD69 expression by intraepidermal CD4+ as well as CD8+ T cells. To explore the molecular basis for local T cell activation and proliferation, we discovered that intraepidermal immunocytes, including both CD4 and CD8+ T cells, expressed surface receptors (ie, CD94, CD158a, CD158b) typically confined to natural killer cells (ie, natural killer receptors; NKRs) accumulated immediately before onset of acute lesions. The presence of NKR bearing immunocytes was also observed in 10 of 15 different biopsies of chronic plaques taken directly from patients, whereas PN skin (n = 8) or normal skin from healthy donors (n = 8), did not contain such NKR positive immunocytes. Of particular relevance to psoriasis is that these NKRs recognize various class I alleles including those typically inherited by psoriatic family members such as HLA-C and HLA-B allotypes. We conclude that injection of CD4+ T cells into PN skin triggers a series of local immunologically mediated stimulatory events that produce further T cell activation and appearance of both CD4 and CD8+ T cells that express NKRs.
机译:牛皮癣是一种免疫介导的皮肤疾病,与几种不同的I类主要组织相容性复杂等位基因相关。但是,尚不清楚致病性淋巴细胞的表型和触发无症状(PN)皮肤转化为牛皮癣斑块(PP皮肤)的T细胞活化事件的性质。这项研究扩展了我们以前的观察结果,其中将自体血液来源的免疫细胞注射到植入SCID小鼠的PN皮肤中,以产生完整的PP损伤。解决的第一个问题是注射的CD4 + T细胞或CD8 + T细胞是造成PN向PP皮肤表型转化的原因。在五名不同的患者中,只有CD4 +而不是CD8 + T细胞系产生牛皮癣病灶。接下来,检查了在有足够组织可用于详细分析的移植物中注射CD4 + T细胞后,在PN皮肤内发生的免疫学事件。在两名患者中,表皮内驻留的CD8 + T细胞在病变发展过程中被诱导增殖,表达急性激活标记CD25和CD69。在另一位患者中,CD4 + T细胞的注射显示表皮内CD4 +和CD8 + T细胞表达CD69。为了探索局部T细胞活化和增殖的分子基础,我们发现表皮内免疫细胞(包括CD4和CD8 + T细胞)表达的表面受体(即CD94,CD158a,CD158b)通常局限于自然杀伤细胞(即自然杀伤细胞)。受体; NKRs)在急性病变发作之前立即积累。在直接取自患者的15例慢性斑块活检样本中,有10份中有10份中观察到了带有NKR的免疫细胞,而PN皮肤(n = 8)或健康捐献者的正常皮肤(n = 8)不包含此类NKR阳性免疫细胞。与牛皮癣特别相关的是这些NKR识别各种I类等位基因,包括通常由银屑病家族成员遗传的那些,例如HLA-C和HLA-B等位基因。我们得出的结论是,将CD4 + T细胞注射到PN皮肤中会触发一系列局部免疫介导的刺激事件,这些事件会进一步引起T细胞活化以及表达NKR的CD4和CD8 + T细胞的出现。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号