Functionality of natural killer cells in obese asthma phenotypes

Background Obesity‐associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early‐onset allergic (EoOA) and late‐onset non‐allergic (LoOA) OA are suggested subtypes of this phenotype. Natural Killer (NK) cells are key elements of inna...

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Published inClinical and experimental allergy Vol. 52; no. 12; pp. 1432 - 1439
Main Authors Pur Ozyigit, Leyla, Aktas, Esin Cetin, Gelmez, Yusuf Metin, Ozturk, Ayse Bilge, Gemicioglu, Bilun, Deniz, Gunnur
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.12.2022
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Abstract Background Obesity‐associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early‐onset allergic (EoOA) and late‐onset non‐allergic (LoOA) OA are suggested subtypes of this phenotype. Natural Killer (NK) cells are key elements of innate immunity involved in cytotoxicity and immune regulation, with uncertain role in OA pathogenesis. Methods Early‐onset allergic and LoOA patients together with obese non‐asthmatic (ONA) controls have been enrolled in the study. Peripheral blood samples have been collected for analysis. Percentages of total NK cells, CD3−CD56dim and CD3−CD56bright NK cell subsets, cytotoxic activity, intracellular interferon‐γ, interleukin (IL)‐10, IL‐13, IL‐17 secretion and activatory receptors (NKG2D, NKp46i and NKp44) have been investigated by flow cytometry. The effect of IL‐12 and IL‐23 stimulation on NK cells and intracellular cytokines in different groups have also been analysed and compared with unstimulated conditions. Results Results of ONA (n = 5, age 42 ± 8), EoOA (n = 5, age 42 ± 10) and LoOA (n = 8, age 46 ± 8) patients have analysed. Body Mass Index has been found to be negatively correlated with CD69 (p = .022, r = −0.534). NKG2D receptor has been significantly low in CD56dim cells of asthma population (p = .046). NKp44 receptor expression has increased after IL‐12 stimulation in EoOA and control group (p = .02). Intracellular IL‐10 content has increased in LoOA and control subjects (p = .018, p = .03) but not in the EoOA group. Intracellular IL‐17 level has found be higher in allergic OA group. LoOA patients showed a decreased NK cytotoxicity compared with the early‐onset asthma group (p = .05). Conclusion Our study suggests an impaired NK receptor expression, activation and reduced cytotoxicity in OA patients together with variances between different subtypes of this phenotype. This data would be beneficial for tailoring a more personalized treatment strategy combatting steroid resistance and frequent exacerbations in this group of patients.
AbstractList Background Obesity‐associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early‐onset allergic (EoOA) and late‐onset non‐allergic (LoOA) OA are suggested subtypes of this phenotype. Natural Killer (NK) cells are key elements of innate immunity involved in cytotoxicity and immune regulation, with uncertain role in OA pathogenesis. Methods Early‐onset allergic and LoOA patients together with obese non‐asthmatic (ONA) controls have been enrolled in the study. Peripheral blood samples have been collected for analysis. Percentages of total NK cells, CD3−CD56dim and CD3−CD56bright NK cell subsets, cytotoxic activity, intracellular interferon‐γ, interleukin (IL)‐10, IL‐13, IL‐17 secretion and activatory receptors (NKG2D, NKp46i and NKp44) have been investigated by flow cytometry. The effect of IL‐12 and IL‐23 stimulation on NK cells and intracellular cytokines in different groups have also been analysed and compared with unstimulated conditions. Results Results of ONA (n = 5, age 42 ± 8), EoOA (n = 5, age 42 ± 10) and LoOA (n = 8, age 46 ± 8) patients have analysed. Body Mass Index has been found to be negatively correlated with CD69 (p = .022, r = −0.534). NKG2D receptor has been significantly low in CD56dim cells of asthma population (p = .046). NKp44 receptor expression has increased after IL‐12 stimulation in EoOA and control group (p = .02). Intracellular IL‐10 content has increased in LoOA and control subjects (p = .018, p = .03) but not in the EoOA group. Intracellular IL‐17 level has found be higher in allergic OA group. LoOA patients showed a decreased NK cytotoxicity compared with the early‐onset asthma group (p = .05). Conclusion Our study suggests an impaired NK receptor expression, activation and reduced cytotoxicity in OA patients together with variances between different subtypes of this phenotype. This data would be beneficial for tailoring a more personalized treatment strategy combatting steroid resistance and frequent exacerbations in this group of patients.
BackgroundObesity‐associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early‐onset allergic (EoOA) and late‐onset non‐allergic (LoOA) OA are suggested subtypes of this phenotype. Natural Killer (NK) cells are key elements of innate immunity involved in cytotoxicity and immune regulation, with uncertain role in OA pathogenesis.MethodsEarly‐onset allergic and LoOA patients together with obese non‐asthmatic (ONA) controls have been enrolled in the study. Peripheral blood samples have been collected for analysis. Percentages of total NK cells, CD3−CD56dim and CD3−CD56bright NK cell subsets, cytotoxic activity, intracellular interferon‐γ, interleukin (IL)‐10, IL‐13, IL‐17 secretion and activatory receptors (NKG2D, NKp46i and NKp44) have been investigated by flow cytometry. The effect of IL‐12 and IL‐23 stimulation on NK cells and intracellular cytokines in different groups have also been analysed and compared with unstimulated conditions.ResultsResults of ONA (n = 5, age 42 ± 8), EoOA (n = 5, age 42 ± 10) and LoOA (n = 8, age 46 ± 8) patients have analysed. Body Mass Index has been found to be negatively correlated with CD69 (p = .022, r = −0.534). NKG2D receptor has been significantly low in CD56dim cells of asthma population (p = .046). NKp44 receptor expression has increased after IL‐12 stimulation in EoOA and control group (p = .02). Intracellular IL‐10 content has increased in LoOA and control subjects (p = .018, p = .03) but not in the EoOA group. Intracellular IL‐17 level has found be higher in allergic OA group. LoOA patients showed a decreased NK cytotoxicity compared with the early‐onset asthma group (p = .05).ConclusionOur study suggests an impaired NK receptor expression, activation and reduced cytotoxicity in OA patients together with variances between different subtypes of this phenotype. This data would be beneficial for tailoring a more personalized treatment strategy combatting steroid resistance and frequent exacerbations in this group of patients.
Obesity-associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early-onset allergic (EoOA) and late-onset non-allergic (LoOA) OA are suggested subtypes of this phenotype. Natural Killer (NK) cells are key elements of innate immunity involved in cytotoxicity and immune regulation, with uncertain role in OA pathogenesis.BACKGROUNDObesity-associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early-onset allergic (EoOA) and late-onset non-allergic (LoOA) OA are suggested subtypes of this phenotype. Natural Killer (NK) cells are key elements of innate immunity involved in cytotoxicity and immune regulation, with uncertain role in OA pathogenesis.Early-onset allergic and LoOA patients together with obese non-asthmatic (ONA) controls have been enrolled in the study. Peripheral blood samples have been collected for analysis. Percentages of total NK cells, CD3- CD56dim and CD3- CD56bright NK cell subsets, cytotoxic activity, intracellular interferon-γ, interleukin (IL)-10, IL-13, IL-17 secretion and activatory receptors (NKG2D, NKp46i and NKp44) have been investigated by flow cytometry. The effect of IL-12 and IL-23 stimulation on NK cells and intracellular cytokines in different groups have also been analysed and compared with unstimulated conditions.METHODSEarly-onset allergic and LoOA patients together with obese non-asthmatic (ONA) controls have been enrolled in the study. Peripheral blood samples have been collected for analysis. Percentages of total NK cells, CD3- CD56dim and CD3- CD56bright NK cell subsets, cytotoxic activity, intracellular interferon-γ, interleukin (IL)-10, IL-13, IL-17 secretion and activatory receptors (NKG2D, NKp46i and NKp44) have been investigated by flow cytometry. The effect of IL-12 and IL-23 stimulation on NK cells and intracellular cytokines in different groups have also been analysed and compared with unstimulated conditions.Results of ONA (n = 5, age 42 ± 8), EoOA (n = 5, age 42 ± 10) and LoOA (n = 8, age 46 ± 8) patients have analysed. Body Mass Index has been found to be negatively correlated with CD69 (p = .022, r = -0.534). NKG2D receptor has been significantly low in CD56dim cells of asthma population (p = .046). NKp44 receptor expression has increased after IL-12 stimulation in EoOA and control group (p = .02). Intracellular IL-10 content has increased in LoOA and control subjects (p = .018, p = .03) but not in the EoOA group. Intracellular IL-17 level has found be higher in allergic OA group. LoOA patients showed a decreased NK cytotoxicity compared with the early-onset asthma group (p = .05).RESULTSResults of ONA (n = 5, age 42 ± 8), EoOA (n = 5, age 42 ± 10) and LoOA (n = 8, age 46 ± 8) patients have analysed. Body Mass Index has been found to be negatively correlated with CD69 (p = .022, r = -0.534). NKG2D receptor has been significantly low in CD56dim cells of asthma population (p = .046). NKp44 receptor expression has increased after IL-12 stimulation in EoOA and control group (p = .02). Intracellular IL-10 content has increased in LoOA and control subjects (p = .018, p = .03) but not in the EoOA group. Intracellular IL-17 level has found be higher in allergic OA group. LoOA patients showed a decreased NK cytotoxicity compared with the early-onset asthma group (p = .05).Our study suggests an impaired NK receptor expression, activation and reduced cytotoxicity in OA patients together with variances between different subtypes of this phenotype. This data would be beneficial for tailoring a more personalized treatment strategy combatting steroid resistance and frequent exacerbations in this group of patients.CONCLUSIONOur study suggests an impaired NK receptor expression, activation and reduced cytotoxicity in OA patients together with variances between different subtypes of this phenotype. This data would be beneficial for tailoring a more personalized treatment strategy combatting steroid resistance and frequent exacerbations in this group of patients.
Obesity-associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early-onset allergic (EoOA) and late-onset non-allergic (LoOA) OA are suggested subtypes of this phenotype. Natural Killer (NK) cells are key elements of innate immunity involved in cytotoxicity and immune regulation, with uncertain role in OA pathogenesis. Early-onset allergic and LoOA patients together with obese non-asthmatic (ONA) controls have been enrolled in the study. Peripheral blood samples have been collected for analysis. Percentages of total NK cells, CD3 CD56 and CD3 CD56 NK cell subsets, cytotoxic activity, intracellular interferon-γ, interleukin (IL)-10, IL-13, IL-17 secretion and activatory receptors (NKG2D, NKp46i and NKp44) have been investigated by flow cytometry. The effect of IL-12 and IL-23 stimulation on NK cells and intracellular cytokines in different groups have also been analysed and compared with unstimulated conditions. Results of ONA (n = 5, age 42 ± 8), EoOA (n = 5, age 42 ± 10) and LoOA (n = 8, age 46 ± 8) patients have analysed. Body Mass Index has been found to be negatively correlated with CD69 (p = .022, r = -0.534). NKG2D receptor has been significantly low in CD56 cells of asthma population (p = .046). NKp44 receptor expression has increased after IL-12 stimulation in EoOA and control group (p = .02). Intracellular IL-10 content has increased in LoOA and control subjects (p = .018, p = .03) but not in the EoOA group. Intracellular IL-17 level has found be higher in allergic OA group. LoOA patients showed a decreased NK cytotoxicity compared with the early-onset asthma group (p = .05). Our study suggests an impaired NK receptor expression, activation and reduced cytotoxicity in OA patients together with variances between different subtypes of this phenotype. This data would be beneficial for tailoring a more personalized treatment strategy combatting steroid resistance and frequent exacerbations in this group of patients.
Author Deniz, Gunnur
Pur Ozyigit, Leyla
Aktas, Esin Cetin
Gemicioglu, Bilun
Ozturk, Ayse Bilge
Gelmez, Yusuf Metin
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Keywords phenotype
CD107a
allergy
asthma
CD69
early-onset
NK
cytotoxicity
obesity
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Snippet Background Obesity‐associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early‐onset...
Obesity-associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early-onset allergic (EoOA)...
BackgroundObesity‐associated asthma (OA) is a difficult to treat asthma phenotype due to its severity and poor response to inhaled steroids. Early‐onset...
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crossref
wiley
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StartPage 1432
SubjectTerms Age
allergy
Asthma
Body mass index
CD107a
CD3 antigen
CD69
CD69 antigen
Cytotoxicity
early‐onset
Flow cytometry
Genotype & phenotype
Humans
Immunoregulation
Innate immunity
Interferon
Interferon-gamma
Interleukin-12 - metabolism
Interleukin-12 - pharmacology
Interleukin-17 - metabolism
Intracellular
Killer Cells, Natural - metabolism
Natural killer cells
NKG2 antigen
Obesity
Peripheral blood
phenotype
Phenotypes
Steroid hormones
Title Functionality of natural killer cells in obese asthma phenotypes
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcea.14136
https://www.ncbi.nlm.nih.gov/pubmed/35359028
https://www.proquest.com/docview/2753412718
https://www.proquest.com/docview/2646722711
Volume 52
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