Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Department of Biomedical Sciences, Cardiff Metropolitan University, Cardiff, UK.
Immun Inflamm Dis. 2017 Jun;5(2):190-199. doi: 10.1002/iid3.153. Epub 2017 Mar 30.
As manuka honey (MH) exhibits immunoregulatory and anti-staphylococcal activities, we aimed to investigate if it could be effective in the treatment of atopic dermatitis (AD).
Adult volunteers with bilateral AD lesions were asked to apply MH on one site overnight for seven consecutive days and leave the contralateral site untreated as possible. Three Item Severity score was used to evaluate the response. Skin swabs were obtained from both sites before and after treatment to investigate the presence of staphylococci and enterotoxin production. In addition, the ability of MH and its methanolic and hexane extracts to down regulate IL4-induced CCL26 protein release from HaCaT cells was evaluated by enzyme linked immunosorbent assay. Also, the ability of MH to modulate calcium ionophore-induced mast cell degranulation was assessed by enzyme immunoassay.
In 14 patients, AD lesions significantly improved post MH treatment versus pre-treatment as compared to control lesions. No significant changes in the skin staphylococci were observed after day 7, irrespective of honey treatment. Consistent with the clinical observation, MH significantly down regulated IL4-induced CCL26 release from HaCaT cells in a dose-dependent manner. This effect was partially lost, though remained significant, when methanolic and hexane extracts of MH were utilized. In addition, mast cell degranulation was significantly inhibited following treatment with MH.
MH is potentially effective in the treatment of AD lesions based on both clinical and cellular studies through different mechanisms. This needs to be confirmed by randomized and controlled clinical trials.
由于麦卢卡蜂蜜(MH)具有免疫调节和抗葡萄球菌活性,我们旨在研究它是否对特应性皮炎(AD)的治疗有效。
有双侧 AD 病变的成年志愿者被要求在一个部位涂抹 MH,每晚一次,连续七天,而对另一侧部位不做任何处理。采用三项严重程度评分来评估反应。在治疗前后从两个部位获取皮肤拭子,以调查葡萄球菌的存在和肠毒素的产生。此外,通过酶联免疫吸附试验评估 MH 及其甲醇和己烷提取物下调 IL4 诱导的 HaCaT 细胞 CCL26 蛋白释放的能力。还通过酶免疫测定评估 MH 调节钙离子载体诱导的肥大细胞脱颗粒的能力。
在 14 名患者中,与对照病变相比,AD 病变在 MH 治疗后明显改善,与治疗前相比。无论是否使用蜂蜜治疗,第 7 天皮肤葡萄球菌均无明显变化。与临床观察一致,MH 以剂量依赖性方式显著下调了 HaCaT 细胞中 IL4 诱导的 CCL26 释放。当使用 MH 的甲醇和己烷提取物时,这种作用虽然部分丧失,但仍然显著。此外,MH 治疗后肥大细胞脱颗粒明显受到抑制。
基于临床和细胞研究,MH 通过不同机制对 AD 病变具有潜在的治疗效果。这需要通过随机对照临床试验来证实。