Advanced Eye Center, Post Graduate Institute of Medical Education and Research, Sector 12, Chandigarh, 160012, India.
Department of Internal Medicine, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Eye (Lond). 2019 Jan;33(1):129-135. doi: 10.1038/s41433-018-0157-5. Epub 2018 Sep 5.
To analyze the serum cytokines profile in patients with tubercular multifocal serpiginoid choroiditis (TB MSC) receiving anti-tubercular therapy (ATT) and oral corticosteroids.
In this prospective longitudinal study, patients with active TB MSC were included. Serum levels of interferon (IFN)-γ, interleukin (IL)-10, and tumor necrosis factor (TNF)-α were analyzed using bead-based immunoassay. The levels of transforming growth factor (TGF)-β were measured using cytokine bead array. Serial measurement was performed at baseline, 1, 3, and 6 weeks after initiation of therapy. Patients developing paradoxical worsening (PW) of TB MSC were identified and their serum levels of cytokines were compared with those patients who showed healing of lesions. Comparison of cytokine levels with baseline values was also performed.
Twelve patients (three females) were included in the study. Four patients showed paradoxical worsening of TB MSC at 3.2 ± 1 weeks after initiation of therapy. Compared to patients who showed healing of lesions, patients with PW showed higher baseline IL-10 (not significant; p = 0.28). Among patients developing PW, levels of IFN-γ peaked at 1 week ((p = 0.01) and levels of TNF-α peaked at 3 weeks (p = 0.02) (coinciding with PW) compared to patients who showed healing. There was no significant difference in TGF-β levels at any time point in either group (p > 0.47).
Baseline and serial levels of inflammatory serum cytokines may help in predicting the response to ATT and corticosteroids in TB MSC. Patients with paradoxical worsening may show rise in pro-inflammatory cytokines after initiation of ATT indicating higher bacillary load.
分析接受抗结核治疗(ATT)和口服皮质类固醇治疗的结核性多灶性匐行性脉络膜炎(TBMSC)患者的血清细胞因子谱。
在这项前瞻性纵向研究中,纳入了活动性 TBMSC 患者。使用基于珠的免疫分析检测干扰素(IFN)-γ、白细胞介素(IL)-10 和肿瘤坏死因子(TNF)-α的血清水平。使用细胞因子珠阵列测量转化生长因子(TGF)-β的水平。在治疗开始后的基线、第 1、3 和 6 周进行连续测量。确定发生 TBMSC 反常恶化(PW)的患者,并比较其血清细胞因子水平与病变愈合的患者。还比较了细胞因子水平与基线值的差异。
本研究纳入了 12 名患者(3 名女性)。4 名患者在治疗开始后 3.2±1 周出现 TBMSC 的反常恶化。与病变愈合的患者相比,PW 患者的 IL-10 基线水平更高(无统计学意义;p=0.28)。在发生 PW 的患者中,IFN-γ 水平在第 1 周(p=0.01)和 TNF-α 水平在第 3 周(p=0.02)达到峰值(与 PW 同时),高于病变愈合的患者。在两组中,任何时间点的 TGF-β 水平均无显著差异(p>0.47)。
基线和连续的炎症血清细胞因子水平可能有助于预测 TBMSC 对 ATT 和皮质类固醇的反应。在开始 ATT 后,反常恶化的患者可能会出现促炎细胞因子升高,表明细菌负荷更高。