Staphylococcal enterotoxins modulate the effector CD4+ T cell response by reshaping the gene expression profile in adults with atopic dermatitis

• Published in: Scientific reports 2019-09, Vol.9 (1), p.13082-8, Article 13082
• Main Authors: Orfali, Raquel Leao, Yoshikawa, Fabio Seiti Yamada, Oliveira, Luanda Mara da Silva, Pereira, Natalli Zanete, de Lima, Josenilson Feitosa, Ramos, Yasmim Álefe Leuzzi, Duarte, Alberto José da Silva, Sato, Maria Notomi, Aoki, Valeria
• Format: Article
• Language: English
• Subjects: 13/21; 13/31; 38/61; 38/77; 692/420/256; 692/420/2780/2152/1566/1618; Adult; Anergy; Atopic dermatitis; CD38 antigen; CD4 antigen; CD4-Positive T-Lymphocytes - drug effects; CD4-Positive T-Lymphocytes - immunology; Cell activation; Dermatitis; Dermatitis, Atopic - genetics; Dermatitis, Atopic - immunology; Eczema; Egr-2 protein; Enterotoxins - pharmacology; Female; Flow cytometry; Gene expression; Humanities and Social Sciences; Humans; Interleukin 1; Interleukin 13; Interleukin 22; Lymphocytes; Lymphocytes T; Male; multidisciplinary; Science; Science (multidisciplinary); Skin; Staphylococcal enterotoxin A; Transcriptome - drug effects; Young Adult; γ-Interferon
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-019-49421-5

Staphylococcus aureus colonizes the skin of atopic dermatitis (AD) individuals, but the impact of its enterotoxins on the chronic activation of CD4 + T cells demands further analysis. We aimed to analyze the CD4 + T cell anergy profile and their phenotypic and functional features through differential expression of cellular activation markers, cytokine production and response to staphylococcal enterotoxin A (SEA). A panel of 84 genes relevant to T cell anergy was assessed by PCR array in FACS-sorted CD4 + T cells, and the most prominent genes were validated by RT-qPCR. We evaluated frequencies of circulating CD4 + T cells secreting single or multiple (polyfunctional) cytokines (IL-17A, IL-22, TNF, IFN-γ, and MIP-1β) and expression of activation marker CD38 in response to SEA stimulation by flow cytometry. Our main findings indicated upregulation of anergy-related genes ( EGR2 and IL13) promoted by SEA in AD patients, associated to a compromised polyfunctional response particularly in CD4 + CD38 + T cells in response to antigen stimulation. The pathogenic role of staphylococcal enterotoxins in adult AD can be explained by their ability to downmodulate the activated effector T cell response, altering gene expression profile such as EGR2 induction, and may contribute to negative regulation of polyfunctional CD4 + T cells in these patients.