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1.
Cytokine ; 180: 156634, 2024 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-38810500

RESUMO

BACKGROUND: Serine protease-like (Spl) proteins produced by Staphylococcus (S.) aureus have been associated with allergic inflammation. However, effects of Spls on the epidermal immune response have not been investigated. OBJECTIVES: To assess the epidermal immune response to SplA, SplD and SplE dependent on differentiation of keratinocytes and a Th2 or Th17 cytokine milieu. METHODS: Human keratinocytes of healthy controls and a STAT3-hyper-IgE syndrome (STAT3-HIES) patient were cultured in different calcium concentrations in the presence of Spls and Th2 or Th17 cytokines. Keratinocyte-specific IL-8 production and concomitant migration of neutrophils were assessed. RESULTS: SplE and more significantly SplA, induced IL-8 in keratinocytes. Suprabasal-like keratinocytes showed a higher Spl-mediated IL-8 production and neutrophil migration compared to basal-like keratinocytes. Th17 cytokines amplified Spl-mediated IL-8 production, which correlated with neutrophil recruitment. Neutrophil recruitment by keratinocytes of the STAT3-HIES patient was similar to healthy control cells. CONCLUSION: S. aureus-specific Spl proteases synergized with IL-17A on human keratinocytes with respect to IL-8 release and neutrophil migration, highlighting the importance of keratinocytes and Th17 immunity in barrier function.


Assuntos
Interleucina-17 , Interleucina-8 , Queratinócitos , Neutrófilos , Staphylococcus aureus , Humanos , Queratinócitos/metabolismo , Queratinócitos/imunologia , Queratinócitos/efeitos dos fármacos , Interleucina-17/metabolismo , Interleucina-8/metabolismo , Staphylococcus aureus/imunologia , Neutrófilos/metabolismo , Neutrófilos/imunologia , Células Th17/imunologia , Células Th17/metabolismo , Proteínas de Bactérias/metabolismo , Fator de Transcrição STAT3/metabolismo , Movimento Celular/efeitos dos fármacos , Serina Proteases/metabolismo , Células Cultivadas
2.
Allergy ; 69(7): 943-53, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24898675

RESUMO

BACKGROUND: Increased serum IgE levels are characteristic but not specific for allergic diseases. Particularly, severe atopic dermatitis (AD) overlaps with hyper-IgE syndromes (HIES) regarding eczema, eosinophilia, and increased serum IgE levels. HIES are primary immunodeficiencies due to monogenetic defects such as in the genes DOCK8 and STAT3. As it is not known to date why allergic manifestations are not present in all HIES entities, we assessed the specificity of serum IgE of AD and HIES patients in the context of clinical and immunological findings. METHODS: Clinical data, skin prick tests, specific IgE to aero- and food allergens, and T helper (Th) subpopulations were compared in AD and molecularly defined HIES patients. RESULTS: Total serum IgE levels were similarly increased in STAT3-HIES, DOCK8-HIES, and AD patients. The ratio of aeroallergen-specific IgE to total IgE was highest in AD, whereas DOCK8-HIES patients showed the highest specific serum IgE against food allergens. Overall, clinical allergy and skin prick test results complied with the specific IgE results. Th2-cell numbers were significantly increased in DOCK8-HIES and AD patients compared to STAT3-HIES patients and controls. AD patients showed significantly higher nTreg-cell counts compared to STAT3-HIES and control individuals. High Th17-cell counts were associated with asthma. Specific IgE values, skin prick test, and T-cell subsets of STAT3-HIES patients were comparable with those of healthy individuals except decreased Th17-cell counts. CONCLUSION: Hyper-IgE syndromes and atopic dermatitis patients showed different sensitization pattern of serum IgE corresponding to the allergic disease manifestations and Th-cell subset data, suggesting a key role of DOCK8 in the development of food allergy.


Assuntos
Dermatite Atópica/imunologia , Fatores de Troca do Nucleotídeo Guanina/imunologia , Imunoglobulina E/imunologia , Síndrome de Job/imunologia , Fator de Transcrição STAT3/imunologia , Adulto , Análise Mutacional de DNA , Dermatite Atópica/sangue , Feminino , Citometria de Fluxo , Fatores de Troca do Nucleotídeo Guanina/genética , Humanos , Imunoglobulina E/sangue , Síndrome de Job/sangue , Síndrome de Job/genética , Masculino , Pessoa de Meia-Idade , Fator de Transcrição STAT3/genética , Testes Cutâneos , Linfócitos T Auxiliares-Indutores/imunologia , Adulto Jovem
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