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 in | Clinical and experimental allergy Vol. 52; no. 12; pp. 1432 - 1439 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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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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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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 |
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