Study of pathogenic T-helper cell subsets in Asian Indian patients with Takayasu arteritis.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-01 Epub Date: 2024-02-08 DOI:10.1007/s12026-024-09459-8
P M Punithavathy, Ramesh Babu Telugu, Vinay Murahari Rao, Savit B Prabhu, Jayakanthan Kabeerdoss, Chanduni Syed, George Joseph, Debashish Danda, Meera Thomas, Ruchika Goel
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Abstract

The relapses and refractory disease are a challenge in the management of patients with Takayasu arteritis (TAK). We quantified pathogenic CD4 + memory T helper cells bearing surface markers CD161 and/or p-glycoprotein (MDR1) in patients with TAK. Peripheral blood mononuclear cells of 21 patients with TAK and 16 age-matched controls were stained with anti-CD3, anti-CD4, anti-CD45RA, anti-CD161 and anti-p-glycoprotein antibodies and subjected to flow cytometry by FACS ARIAIII. Eighteen patients underwent follow-up immunophenotyping. Intracellular staining for interleukin-17 and interferon-γ was performed for 18 patients and 11 controls. Surgical arterial biopsies of 6 TAK and 5 non-inflammatory controls were subjected to immunohistochemistry with anti-CD161 and anti-p-glycoprotein. At baseline the frequency of MDR1 + CD4 + and CD161 + MDR1 + CD4 + memory T cells was higher in TAK than controls (p = 0.002 and 0.01, respectively). After stimulation, the frequency of IFN-y + CD161 + cells was higher in TAK than controls (p = 0.028). Modal fluorescence intensity of CD161 + MDR1 + CD45RA - CD4 + cells was higher in active as compared with stable disease (p = 0.041). At 6 months, MDR1 + and CD161 + MDR1 + memory CD4 + T cells decreased significantly only in patients who had complete/partial response to treatment (p = 0.047 and 0.02, respectively). To conclude, MDR1 + and MDR1 + CD161 + CD4 + memory T-helper cells are increased in patients with TAK. These cells decreased only in patients with response to treatment during subsequent follow-up.

Abstract Image

亚裔印度人高安氏动脉炎患者致病性 T 辅助细胞亚群的研究。
复发和难治性疾病是治疗高安动脉炎(TAK)患者的难题。我们对 TAK 患者体内带有表面标记 CD161 和/或 p-糖蛋白(MDR1)的致病性 CD4 + 记忆 T 辅助细胞进行了量化。我们用抗CD3、抗CD4、抗CD45RA、抗CD161和抗p-糖蛋白抗体对21名TAK患者和16名年龄匹配的对照组患者的外周血单核细胞进行了染色,并用FACS ARIAIII进行了流式细胞术检测。18 名患者接受了后续免疫分型。对 18 名患者和 11 名对照组进行了白细胞介素-17 和干扰素-γ 的细胞内染色。对 6 名 TAK 患者和 5 名非炎症对照组患者的手术动脉活检组织进行了抗 CD161 和抗 p-糖蛋白免疫组化。基线时,TAK 中 MDR1 + CD4 + 和 CD161 + MDR1 + CD4 + 记忆 T 细胞的频率高于对照组(p = 0.002 和 0.01)。刺激后,TAK 中 IFN-y + CD161 + 细胞的频率高于对照组(p = 0.028)。活动期与稳定期相比,CD161 + MDR1 + CD45RA - CD4 + 细胞的模态荧光强度更高(p = 0.041)。6 个月时,只有对治疗有完全/部分反应的患者的 MDR1 + 和 CD161 + MDR1 + 记忆 CD4 + T 细胞才会显著减少(p = 0.047 和 0.02)。总之,TAK 患者的 MDR1 + 和 MDR1 + CD161 + CD4 + 记忆 T 辅助细胞增多。在随后的随访中,这些细胞仅在对治疗有反应的患者中减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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