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首页> 外文期刊>Clinical and experimental rheumatology >Natural killer cells and gamma/delta T cells in synovial fluid and in peripheral blood of patients with psoriatic arthritis.
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Natural killer cells and gamma/delta T cells in synovial fluid and in peripheral blood of patients with psoriatic arthritis.

机译:银屑病关节炎患者滑液和外周血中的自然杀伤细胞和γ/δT细胞。

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摘要

OBJECTIVE: NK surface markers and gamma/delta TCR antigen are involved in non-MHC-restricted cytotoxicity, which represents a major effector mechanism of the cell-mediated immune response. We evaluated in PsA patients SF and PB lymphocytes expressing these cellular subsets in order to obtain information on the possible role played by them in the disease. METHODS: We studied 29 PsA and 27 RA patients, as well as 27 healthy controls. In 17 PsA and 16 RA patients with knee joint effusion, analysis of SF was performed. SF and PB lymphocyte analysis was performed by direct dual immunofluorescence flow cytomettry using anti-CD3, anti-CD4, anti-CD8, anti-CD19, anti-TCR-gamma/delta-1 and anti-CD16 and anti-CD56 monoclonal antibodies. RESULTS: PsA and RA patients had, with respect to controls, lower values (both as percentages and in absolute numbers) of PB T cells expressing gamma/delta TCR. SF Iymphocytes of PsA and RA patients were characterised, as compared to PB lymphocytes, by lower numbers (both in absolute numbers and in relative terms) of NK and NK-T cells. Considering the absolute numbers of the various lymphocyte subsets, a strong correlation was found in PsA SF between gamma/delta T cells and NK (p < 0.0007) or NK-T cells (p < 0.0003), as well as between NK and NK-T cells (p < 0.0019). There was instead no statistically significant correlation among the different SF or PB lymphocytes and the most relevant clinical or serological parameters. CONCLUSION: This study, analyzing the impairment of different subsets involved in non-MHC-restricted cytotoxicity, suggests that this component of the cell-mediated immune response seems to play a pivotal role in the development of PsA.
机译:目的:NK表面标志物和γ/δTCR抗原参与非MHC限制的细胞毒性作用,这是细胞介导的免疫反应的主要效应机制。我们在PsA患者中评估了表达这些细胞亚群的SF和PB淋巴细胞,以获得有关它们在疾病中可能发挥的作用的信息。方法:我们研究了29位PsA和27位RA患者以及27位健康对照。在17例PsA和16例RA膝关节积液患者中,进行了SF分析。使用抗CD3,抗CD4,抗CD8,抗CD19,抗TCR-γ/δ-1和抗CD16和抗CD56单克隆抗体通过直接双重免疫荧光流式细胞仪进行SF和PB淋巴细胞分析。结果:相对于对照,PsA和RA患者的表达γ/δTCR的PB T细胞的值较低(均以百分比和绝对数表示)。与PB淋巴细胞相比,PsA和RA患者的SF淋巴细胞的特征是NK和NK-T细胞的数量(绝对数和相对数均较低)。考虑到各种淋巴细胞亚群的绝对数量,发现PsA SF与γ/δT细胞和NK(p <0.0007)或NK-T细胞(p <0.0003)以及NK和NK-T细胞之间有很强的相关性。 T细胞(p <0.0019)。相反,不同的SF或PB淋巴细胞与最相关的临床或血清学参数之间无统计学意义的相关性。结论:本研究分析了非MHC限制的细胞毒性涉及的不同亚群的损伤,表明该细胞介导的免疫应答的这一成分似乎在PsA的发展中起着关键作用。

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