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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

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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合物 等位基因相关。但是,致病性淋巴细胞的表型 和触发无症状(PN)皮肤转变为牛皮癣斑块(PP皮肤)的T细胞活化事件的性质是 未知。这项研究扩展了我们以前的观察结果,其中将 自体血液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。 第一个要解决的问题是注射的CD4 + T细胞 或CD8 + T细胞是否负责将 PN表皮转化为PP皮肤。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 分析的移植物中注入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CD8 + T细胞在病变发展过程中被诱导增殖,并表达急性激活标记CD25和CD69。在另一位 患者中,注射CD4 + T细胞后发现表皮内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,均表达表面。受体(即CD94, CD158a,CD158b)通常局限于自然杀伤细胞(即 自然杀伤受体; NKR),它们在发作之前即刻积累急性病变。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例中也观察到了带有NKR的免疫细胞,而PN皮肤(n = 8) 或正常皮肤(n = 8),不含 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异型。我们得出结论,将CD4 + T细胞注入 PN皮肤会触发一系列局部免疫介导的刺激性 事件,这些事件会进一步导致T细胞的活化和出现的 表达NKR的CD4和CD8 + T细胞。

著录项

  • 来源
    《American Journal of Pathology》 |1999年第1期|145-158|共14页
  • 作者单位

    From the Department of Pathology and Skin Cancer Research Laboratories, Cardinal Bernardin Cancer Center, Loyola University of Chicago, Maywood, Illinois;

    From the Department of Pathology and Skin Cancer Research Laboratories, Cardinal Bernardin Cancer Center, Loyola University of Chicago, Maywood, Illinois;

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  • 入库时间 2022-08-17 14:17:20

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