TY - JOUR
T1 - Honey is potentially effective in the treatment of atopic dermatitis
T2 - Clinical and mechanistic studies
AU - Alangari, Abdullah A.
AU - Morris, Keith
AU - Lwaleed, Bashir A.
AU - Lau, Laurie
AU - Jones, Ken
AU - Cooper, Rose
AU - Jenkins, Rowena
N1 - Publisher Copyright:
© 2017 The Authors. Immunity, Inflammation and Disease Published by John Wiley & Sons Ltd.
PY - 2017/3/30
Y1 - 2017/3/30
N2 - Introduction: As manuka honey (MH) exhibits immunoregulatory and antistaphylococcal activities, we aimed to investigate if it could be effective in the treatment of atopic dermatitis (AD). Methods: 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 ionophoreinduced mast cell degranulation was assessed by enzyme immunoassay. Results: 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. Conclusions: 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.
AB - Introduction: As manuka honey (MH) exhibits immunoregulatory and antistaphylococcal activities, we aimed to investigate if it could be effective in the treatment of atopic dermatitis (AD). Methods: 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 ionophoreinduced mast cell degranulation was assessed by enzyme immunoassay. Results: 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. Conclusions: 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.
KW - Atopic dermatitis
KW - Honey
KW - Keratinocytes
KW - Manuka
KW - Mast cells
UR - http://www.scopus.com/inward/record.url?scp=85037717499&partnerID=8YFLogxK
U2 - 10.1002/iid3.153
DO - 10.1002/iid3.153
M3 - Article
C2 - 28474502
AN - SCOPUS:85037717499
SN - 2050-4527
VL - 5
SP - 190
EP - 199
JO - Immunity, Inflammation and Disease
JF - Immunity, Inflammation and Disease
IS - 2
ER -