Academic Journal

New variants in NLRP3 inflammasome genes increase risk for asthma and Blomia tropicalis-induced allergy in a Brazilian population

التفاصيل البيبلوغرافية
العنوان: New variants in NLRP3 inflammasome genes increase risk for asthma and Blomia tropicalis-induced allergy in a Brazilian population
المؤلفون: Gerson de A. Queiroz, Raimon R. da Silva, Anaque de O. Pires, Ryan dos S. Costa, Neuza M. Alcântara-Neves, Thiago M. da Silva, Mauricio L. Barreto, Sergio C. Oliveira, Camila A. Figueirêdo
المصدر: Cytokine: X, Vol 2, Iss 3, Pp 100032- (2020)
بيانات النشر: Elsevier
سنة النشر: 2020
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: Asthma, Allergy, Inflammasome, Variants, NLRP3, CASP1, Immunologic diseases. Allergy, RC581-607
الوصف: Atopic asthma is a chronic lung disease of lower airways caused mainly due to action of T-helper (Th) 2 type cytokines, eosinophilic inflammation, mucus hypersecretion and airway remodelling. Interleukin (IL)-33 increases type 2 immunity polarization in airway playing critical role in eosinophilic asthma. On the other hand, NLRP3 inflammasome activation results in the release of caspase-1 (Casp-1) which, in its turn, promotes IL-33 inactivation. Recent studies have shown associations between NLRP3 variants and inflammatory diseases. However, no study with genes in NLRP3 inflammassome route has been conducted so far with asthma and atopy in any population to date. Blood samples were collected from 1246 asthmatic and non-asthmatic children. Associations were tested for single nucleotide polymorphism (SNP)s in NLRP3 and CASP1 with asthma and markers of atopy and in cultures stimulated with Blomia tropicalis (Bt) mite crude extract. The T allele of rs4925648 (NLRP3) was associated with increased asthma risk (OR 1.50, P = 0.005). In addition, the T allele of rs12130711 polymorphism, whithin the same gene, acted as a protector factor for asthma (OR 0.78, P = 0.038). On the other hand, the C allele of rs4378247 NLRP3 variant was associated with lower levels of IL-13 production when peripheral blood cells were stimulated with Bt (OR 0.39, P = 4E-04). In addition, the greater the number of risk alleles in IL33/NLRP3/CASP1 route the greater was the risk for asthma. The T allele of rs7925706 CASP1 variant was also associated with increased risk for asthma (OR 1.47, P = 0.008). In addition, this same allele increased the eosinophil counts in blood (mm3) in asthmatic individuals compared with non-asthmatic (P = 0.0004). These results suggest that NLRP3 and CASP1 polymorphisms may be associated with susceptibility for asthma and markers of atopy in our population.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 2590-1532
Relation: http://www.sciencedirect.com/science/article/pii/S2590153220300124; https://doaj.org/toc/2590-1532; https://doaj.org/article/fbd34ccbbe6f4ad09da1ec3c26a1f2fa
DOI: 10.1016/j.cytox.2020.100032
الاتاحة: https://doi.org/10.1016/j.cytox.2020.100032
https://doaj.org/article/fbd34ccbbe6f4ad09da1ec3c26a1f2fa
رقم الانضمام: edsbas.80038232
قاعدة البيانات: BASE
الوصف
تدمد:25901532
DOI:10.1016/j.cytox.2020.100032