IgG to Galactose-Alpha-1,3-Galactose: Impact of Alpha-Gal IgE Sensitization, Blood Type, and Tick Bites.

IF 3 Q3 IMMUNOLOGY
Antibodies Pub Date : 2025-05-16 DOI:10.3390/antib14020043
Samuel M Ailsworth, Matthew MacCallum, Nathan E Richards, Lisa J Workman, Pamela Schoppee Bortz, Thomas Makin, Thomas A E Platts-Mills, Jeffrey M Wilson
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引用次数: 0

Abstract

Background: Antibodies to galactose-alpha-1,3-galactose (alpha-gal), particularly the IgM and IgG isotypes, are abundant in human sera. These antibodies are known to be an important xenotransplantation barrier, but the full implications of these antibodies to health and disease remain incompletely understood. By contrast, IgE to alpha-gal is uncommon in the population but has been associated with tick bites and causally linked with mammalian meat allergy, often now known as alpha-gal syndrome (AGS). To date, there have been few population-based studies that have investigated alpha-gal IgG levels in relation to demographic factors, diet, tick bites, and mammalian meat allergy. Methods: Adults, predominantly healthcare workers, were recruited for a COVID-19 vaccine study. At least one serum sample was collected, and subjects completed questionnaires to provide demographic, diet, and tick exposure data. Alpha-gal IgG, IgE, and total IgG were measured using the ImmunoCAP platform, and blood group was assessed via reverse typing using stored serum. We also assessed alpha-gal IgG levels among subjects with AGS, recruited from an allergy clinic. Results: The median age of the 267 subjects in the vaccine cohort was 42 years, and median alpha-gal IgG levels were 3.0 μg/mL. Alpha-gal IgG levels were higher among the 43 (16.1%) subjects who had alpha-gal IgE sensitization (≥0.1 IU/mL) and among subjects lacking the B blood group antigen (blood groups A and O). Alpha-gal IgG levels did not differ between the subjects who had asymptomatic alpha-gal IgE sensitization and those who had meat allergy. However, both groups had higher alpha-gal IgG levels than subjects who lacked alpha-gal IgE sensitization. Subjects who reported prior tick or chigger bites had higher alpha-gal IgG levels than those without a bite history, regardless of alpha-gal IgE sensitization status. Conclusions: In a population-based cohort, alpha-gal IgG antibodies were found to be prevalent, and levels were increased in subjects with blood groups A and O, subjects who were alpha-gal IgE sensitized, and those who reported a history of tick bites.

半乳糖- α 1,3-半乳糖IgG: α -半乳糖IgE致敏、血型和蜱叮咬的影响。
背景:半乳糖- α -1,3-半乳糖(α -gal)抗体,特别是IgM和IgG同型抗体,在人类血清中含量丰富。已知这些抗体是重要的异种移植屏障,但这些抗体对健康和疾病的全部含义仍未完全了解。相比之下,α -半乳糖的IgE在人群中并不常见,但与蜱虫叮咬有关,并与哺乳动物肉类过敏有因果关系,现在通常被称为α -半乳糖综合征(AGS)。迄今为止,很少有基于人群的研究调查了α -半乳糖IgG水平与人口因素、饮食、蜱叮咬和哺乳动物肉类过敏的关系。方法:招募成人(主要是医护人员)参与COVID-19疫苗研究。至少收集一份血清样本,受试者完成问卷调查,提供人口统计、饮食和蜱虫暴露数据。使用ImmunoCAP平台检测α -半乳糖IgG、IgE和总IgG,并使用储存的血清反向分型评估血型。我们还评估了从过敏诊所招募的AGS患者的α -半乳糖IgG水平。结果:疫苗队列267例受试者中位年龄为42岁,α -半胱氨酸IgG中位水平为3.0 μg/mL。43例(16.1%)有α -半乳糖IgE致敏(≥0.1 IU/mL)和缺乏B血型抗原(A、O型血)的受试者α -半乳糖IgG水平较高。α -半乳糖IgG水平在无症状α -半乳糖IgE致敏的受试者和有肉类过敏的受试者之间没有差异。然而,两组的α -半乳糖IgG水平都高于缺乏α -半乳糖IgE致敏的受试者。无论α -半乳糖IgE致敏状态如何,报告有蜱虫或恙虫叮咬史的受试者α -半乳糖IgG水平高于无叮咬史的受试者。结论:在以人群为基础的队列中,发现α -半乳糖IgG抗体普遍存在,并且在a型和O型血的受试者、α -半乳糖IgE敏感的受试者以及报告有蜱虫叮咬史的受试者中水平升高。
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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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