Rao Vidhya R, Iqbal Sana, Young Bradford A, Mun Christine, Jain Sandeep, Kaja Simon
Department of Ophthalmology, Loyola University Chicago, Maywood, IL, United States.
Research Service, Edward Hines Jr. Veterans Affairs Hospital, Hines, IL, United States.
Front Pharmacol. 2024 Dec 12;15:1465776. doi: 10.3389/fphar.2024.1465776. eCollection 2024.
This study investigated the efficacy of pooled human immune globulins (Flebogamma DIF) to combat the formation of neutrophil extracellular traps (NETs) and NETosis, along with neutrophil adhesion to corneal epithelial cells in response to dry eye disease relevant stimuli.
Human neutrophils were isolated by bead-based immunomagnetic depletion of non-target cells from human whole blood. NETosis was induced using phorbol 12-myristate 13-acetate (PMA) or anti-citrullinated histone 4 R3 antibody (H4R3 ACPA). Extracellular DNA was used as a surrogate biomarker of NETosis, and it was quantified using a 96-well, plate reader-based fluorescent assay and by confocal microscopy in 8-well chambers using the DNA dye, SYTOX Green. Neutrophils were labeled with calcein-AM and adhesion to human corneal epithelial cells was measured. The efficacy of a dose-range of pooled human immune globulin (Flebogamma DIF, 0.01%-5%) was tested in all assays.
Pooled human immune globulins (Flebogamma DIF) dose-dependently inhibited both PMA and H4R3 ACPA induced NETosis, with concentrations ≥2.5% fully preventing release of extracellular DNA over a 2-16 h time period. Similarly, Flebogamma 5% DIF prevented NETosis against PMA (20 nM) and a dose range (0.1-10 μg/mL) of H4R3 ACPA. Both PMA and H4R3 ACPA increased adhesion of neutrophils to corneal epithelial cells by 20% and 5%, respectively. Flebogamma DIF treatment resulted in a dose-dependent reduction of neutrophil adhesion, with Flebogamma 5% DIF reducing adhesion to baseline levels.
These findings show the dose-dependent efficacy of pooled human immune globulins, specifically Flebogamma DIF against experimentally and pathologically induced NETosis and neutrophil adhesion to corneal epithelial cells, . The results from this study support the continued clinical development of Flebogamma 5% DIF as a novel and efficacious treatment for the signs and symptoms of dry eye disease.
本研究调查了人免疫球蛋白混合液(Flebogamma DIF)对抗中性粒细胞胞外诱捕网(NETs)形成和NETosis的效果,以及在干眼症相关刺激下中性粒细胞与角膜上皮细胞的黏附情况。
通过基于磁珠的免疫磁珠法从人全血中去除非靶细胞来分离人中性粒细胞。使用佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)或抗瓜氨酸化组蛋白4 R3抗体(H4R3 ACPA)诱导NETosis。将细胞外DNA用作NETosis的替代生物标志物,并使用基于96孔板读数器的荧光测定法以及在8孔培养室中使用DNA染料SYTOX Green通过共聚焦显微镜对其进行定量。用钙黄绿素-AM标记中性粒细胞并测量其与人类角膜上皮细胞的黏附情况。在所有测定中测试了一系列剂量的人免疫球蛋白混合液(Flebogamma DIF,0.01%-5%)的效果。
人免疫球蛋白混合液(Flebogamma DIF)剂量依赖性地抑制PMA和H4R3 ACPA诱导的NETosis,浓度≥2.5%可在2-16小时内完全阻止细胞外DNA的释放。同样,5%的Flebogamma DIF可防止针对PMA(20 nM)和一系列剂量(0.1-10μg/mL)的H4R3 ACPA诱导的NETosis。PMA和H4R3 ACPA分别使中性粒细胞与角膜上皮细胞的黏附增加了20%和5%。Flebogamma DIF处理导致中性粒细胞黏附呈剂量依赖性降低,5%的Flebogamma DIF将黏附降低至基线水平。
这些发现表明人免疫球蛋白混合液具有剂量依赖性疗效,特别是Flebogamma DIF可对抗实验性和病理性诱导的NETosis以及中性粒细胞与角膜上皮细胞的黏附。本研究结果支持将5%的Flebogamma DIF作为一种治疗干眼症体征和症状的新型有效疗法继续进行临床开发。