Phenotypes of antigen-induced responses in guinea pigs: Beyond the asthma model

IF 3 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular immunology Pub Date : 2025-03-01 Epub Date: 2025-01-31 DOI:10.1016/j.molimm.2025.01.014
Marisol Álvarez-González , Ivonne Pacheco-Alba , Paola Moreno-Álvarez , Lizbeth Rogel-Velasco , Silvia Guerrero-Clorio , Angélica Flores-Flores , Mariana Téllez-Araiza , Juana Arellano-García , Angel Quevedo-Razo , Angélica Flores-Martínez , Blanca Bazán-Perkins
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Abstract

Asthma is a heterogeneous and variable disease. In an allergic asthma model using guinea pigs (GPs), we identified three distinct phenotypes: those always showing an obstructive response (R), those never responding (NR), and those sometimes responding (VR). We aimed to assess and compare the functional and immunological characteristics of these groups. GPs were sensitized and challenged with ovalbumin (OVA) every 10 days in a plethysmographic chamber to measure the maximum obstructive response. The control group was sensitized and challenged with saline. Control and NR GPs never duplicated baseline obstruction values. At least three antigenic challenges were needed to identify each phenotype. None of the groups showed late responses. Analysis of at least six antigenic challenges in 125 GPs revealed that 48 % were R, 20 % NR, 29 % VR, and 8 % died from anaphylactic shock. R GPs did not develop antigenic tolerance. During the third or twelfth challenges, we evaluated antigen-induced airway reactivity to histamine: R GPs consistently showed hyperreactivity, NR showed hyperreactivity only on the third challenge, while VR and control groups never showed hyperreactivity. Serum levels of anti-OVA IgE and IgG1 were elevated in all groups compared to controls. IL-4 levels in the lungs and eosinophils counts in bronchoalveolar lavage fluid (BALF) of R and VR were higher than to controls and NR. The number of mast cells in the airway wall also increased in R and VR compared to controls. IFN-γ levels were similar across all groups on the third challenge but increased significantly in NR on the twelfth challenge compared to the other groups. Neutrophil counts in BALF increased in R and VR, and in NR but only at the twelfth challenge compared to controls. Our findings suggest that R and VR guinea pigs serve as valid models for asthma, with VR representing a distinct phenotype characterized by variability and lack of hyperreactivity. Conversely, NR guinea pigs, despite their high IgE and anti-OVA IgG1 levels and hyperresponsiveness at the third challenge, do not align with typical asthma characteristics.
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豚鼠抗原诱导反应的表型:超越哮喘模型。
哮喘是一种多变性疾病。在使用豚鼠(GPs)的过敏性哮喘模型中,我们确定了三种不同的表型:总是显示阻塞性反应(R),从不反应(NR)和有时反应(VR)。我们的目的是评估和比较这些组的功能和免疫学特征。每10天在容积描记室中对全科医生进行致敏和卵清蛋白(OVA)刺激,以测量最大阻塞反应。对照组致敏,生理盐水攻毒。对照组和NR GPs从未重复基线阻塞值。至少需要三个抗原挑战来确定每种表型。没有任何一组出现延迟反应。对125名全科医生中至少6例抗原挑战的分析显示,48 %为R, 20 %为NR, 29 %为VR, 8 %死于过敏性休克。rgp未产生抗原耐受性。在第三次或第十二次挑战时,我们评估了抗原诱导的气道对组胺的反应性:R gp始终表现出高反应性,NR仅在第三次挑战时表现出高反应性,而VR组和对照组从未表现出高反应性。与对照组相比,各组血清抗ova IgE和IgG1水平均升高。R组和VR组肺组织中IL-4水平和支气管肺泡灌洗液(BALF)中嗜酸性粒细胞计数均高于对照组和NR组,气道壁肥大细胞数量均高于对照组和NR组。IFN-γ水平在第三次挑战时各组之间相似,但在第12次挑战时NR与其他组相比显着增加。与对照组相比,R和VR以及NR中BALF中的中性粒细胞计数仅在第12次挑战时增加。我们的研究结果表明,R和VR豚鼠可以作为哮喘的有效模型,VR代表了一种独特的表型,其特征是变异性和缺乏过度反应性。相反,NR豚鼠尽管具有高IgE和抗ova IgG1水平以及在第三次挑战时的高反应性,但不符合典型的哮喘特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular immunology
Molecular immunology 医学-免疫学
CiteScore
6.90
自引率
2.80%
发文量
324
审稿时长
50 days
期刊介绍: Molecular Immunology publishes original articles, reviews and commentaries on all areas of immunology, with a particular focus on description of cellular, biochemical or genetic mechanisms underlying immunological phenomena. Studies on all model organisms, from invertebrates to humans, are suitable. Examples include, but are not restricted to: Infection, autoimmunity, transplantation, immunodeficiencies, inflammation and tumor immunology Mechanisms of induction, regulation and termination of innate and adaptive immunity Intercellular communication, cooperation and regulation Intracellular mechanisms of immunity (endocytosis, protein trafficking, pathogen recognition, antigen presentation, etc) Mechanisms of action of the cells and molecules of the immune system Structural analysis Development of the immune system Comparative immunology and evolution of the immune system "Omics" studies and bioinformatics Vaccines, biotechnology and therapeutic manipulation of the immune system (therapeutic antibodies, cytokines, cellular therapies, etc) Technical developments.
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