Analysis of null deletion polymorphism of glutathione S-transferase theta (GSTT-1), associated with anti-GSTT-1 antibodies development in transplantation

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY International Journal of Immunogenetics Pub Date : 2023-08-23 DOI:10.1111/iji.12635
Manuel Muro-Perez, Gema González-Martínez, Pedro Martínez-García, Isabel Legaz, Pilar Zafrilla, Manuel Muro
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Abstract

Glutathione S‐transferase theta 1 (GSTT1) is an enzyme involved in phase II biotransformation processes and a member of a multigene family of detoxifying and clearing reactive oxygen species. GSTT1 is polymorphic like other biotransforming enzymes, allowing variability in hepatic conjugation processes. Immunological recognition of the GSTT1 alloantigen, as evidenced by donor‐specific antibodies formation, has previously been observed in recipients lacking GSTT1 protein (called GSTT1−, GSTT*0, null phenotype or homozygous for the GSTT1 deletion) who receive liver or kidney transplants from GSTT1+ donors and is a risk factor for the development of de novo hepatitis following liver transplants from a GSTT1 expressing donor. Antibodies against GSTT1 are demonstrated in patients who are GSTT1 null and received a transplant from a GSTT1+ donor. Understanding the local population frequency of the GSTT1 deletion is of value in understanding the potential clinical risk of developing post‐transplant complications, which can be attributed to the nonexpression of GSTT1. A population of 173 healthy donors of the Murcia Region in Southeast Spain was evaluated for a null allele of GSTT1 (n = 173). DNA was extracted, and GSTT‐1 null allele detection was performed by real‐time polymerase chain reaction. The frequency of the null GSTT1 genotype (nonexpression or deletion of the homozygous polymorphism of the GSTT1 protein) was 17.9% (n = 31 null allele GSTT1/173 total individuals). Our data suggest that the frequency of null GSTT1 mutations in our population in Southeast Spain is 17.9%, lower than in other Caucasoid populations. This would convert our recipient population into more susceptible to nonlocal potential organ donors and less susceptible to local donors. All recipients bearing this GSTT1 deletion homozygous would be without the protein and triggering an alloantigen in the case of transplantation with a donor without deletion.

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移植中与抗GSTT-1抗体产生相关的谷胱甘肽s -转移酶(GSTT-1)零缺失多态性分析
谷胱甘肽s -转移酶1 (GSTT1)是一种参与II期生物转化过程的酶,是解毒和清除活性氧的多基因家族的成员。GSTT1像其他生物转化酶一样是多态的,允许肝脏结合过程的可变性。GSTT1异体抗原的免疫识别,如供者特异性抗体的形成,先前在GSTT1+供者的肝脏或肾脏移植中缺乏GSTT1蛋白(称为GSTT1−、GSTT*0、无表型或GSTT1缺失纯合)的受者中观察到,这是GSTT1表达供者的肝脏移植后发生新生肝炎的危险因素。在GSTT1无效且接受GSTT1+供体移植的患者中发现了抗GSTT1抗体。了解GSTT1缺失的本地人群频率对于了解发生移植后并发症的潜在临床风险具有价值,这可能归因于GSTT1的不表达。对西班牙东南部穆尔西亚地区173名健康献血者进行GSTT1空等位基因评估(n = 173)。提取DNA,实时聚合酶链反应检测GSTT-1零等位基因。GSTT1空基因型(GSTT1蛋白纯合多态性缺失或不表达)的发生率为17.9% (n = 31个GSTT1空等位基因/173个个体)。我们的数据表明,西班牙东南部人群中GSTT1无效突变的频率为17.9%,低于其他高加索人群。这将使我们的接受者群体更容易受到非本地潜在器官捐赠者的影响,而对本地捐赠者的影响更小。所有携带GSTT1缺失纯合子的受体都没有这种蛋白,在没有缺失的供体移植的情况下会触发异体抗原。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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