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Petrolatum: Barrier repair and antimicrobial responses underlying this 'inert' moisturizer

Authors :
Joel Correa da Rosa
Riana Dutt
Tali Czarnowicki
Xiuzhong Zheng
Mayte Suárez-Fariñas
Peng Xiangyu
Mary Sullivan-Whalen
James G. Krueger
Nikhil Dhingra
Avner Shemer
Dana Malajian
Robert Finney
Saakshi Khattri
Yeriel Estrada
Hui Xu
Patricia Gilleaudeau
Emma Guttman-Yassky
Source :
Journal of Allergy and Clinical Immunology. 137:1091-1102.e7
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Petrolatum is a common moisturizer often used in the prevention of skin infections after ambulatory surgeries and as a maintenance therapy of atopic dermatitis (AD). However, the molecular responses induced by petrolatum in the skin have never been assessed.We sought to define the cutaneous molecular and structural effects induced by petrolatum.Thirty-six healthy subjects and 13 patients with moderate AD (mean SCORAD score, 39) were studied by using RT-PCR, gene arrays, immunohistochemistry, and immunofluorescence performed on control skin, petrolatum-occluded skin, and skin occluded with a Finn chamber only.Significant upregulations of antimicrobial peptides (S100A8/fold change [FCH], 13.04; S100A9/FCH, 11.28; CCL20/FCH, 8.36; PI3 [elafin]/FCH, 15.40; lipocalin 2/FCH, 6.94, human β-defensin 2 [DEFB4A]/FCH, 4.96; P.001 for all) and innate immune genes (IL6, IL8, and IL1B; P.01) were observed in petrolatum-occluded skin compared with expression in both control and occluded-only skin. Application of petrolatum also induced expression of key barrier differentiation markers (filaggrin and loricrin), increased stratum corneum thickness, and significantly reduced T-cell infiltrates in the setting of "normal-appearing" or nonlesional AD skin, which is known to harbor barrier and immune defects.Petrolatum robustly modulates antimicrobials and epidermal differentiation barrier measures. These data shed light on the beneficial molecular responses of petrolatum in barrier-defective states, such as AD and postoperative wound care.

Details

ISSN :
00916749
Volume :
137
Database :
OpenAIRE
Journal :
Journal of Allergy and Clinical Immunology
Accession number :
edsair.doi.dedup.....2aefbebb0c33f360acc22c119d50f7ca
Full Text :
https://doi.org/10.1016/j.jaci.2015.08.013