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

IF 3.3 4区 医学 Q3 IMMUNOLOGY Immunologic Research 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.

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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。
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来源期刊
Immunologic Research
Immunologic Research 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
83
审稿时长
6-12 weeks
期刊介绍: IMMUNOLOGIC RESEARCH represents a unique medium for the presentation, interpretation, and clarification of complex scientific data. Information is presented in the form of interpretive synthesis reviews, original research articles, symposia, editorials, and theoretical essays. The scope of coverage extends to cellular immunology, immunogenetics, molecular and structural immunology, immunoregulation and autoimmunity, immunopathology, tumor immunology, host defense and microbial immunity, including viral immunology, immunohematology, mucosal immunity, complement, transplantation immunology, clinical immunology, neuroimmunology, immunoendocrinology, immunotoxicology, translational immunology, and history of immunology.
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