先天性免疫错误患儿的癌症发病率:来自一家机构的报告

IF 7.2 2区 医学 Q1 IMMUNOLOGY Journal of Clinical Immunology Pub Date : 2024-05-28 DOI:10.1007/s10875-024-01736-3
María Raquel Mitchell, Luciano Urdinez, Andrea R Bernasconi, Silvia Danielian, María Martha Katsikas, Elisa O Sajaroff, Georgina Roffé, Nélida M Villa, Laura Galluzzo, Marianela Sanz, Alejandro M Palma, Carolina Bouso, Emma Prieto, Verónica Goris, Judith Yancoski, Sergio D Rosenzweig, Matías Oleastro, Adriana Rosé, Walter Cacciavillano, Guido Felizzia, Myriam Guitter, Cristian Sánchez La Rosa, Mailén Ríos, Pedro Zubizarreta, María Sara Felice, Jorge G Rossi
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摘要

背景:先天性免疫错误(IEI)包括几种影响先天性和适应性反应不同组成部分的遗传异常,容易导致传染病、自身免疫和恶性肿瘤。不同的研究(主要是针对成人的研究)都报告说,IEI 患者的癌症发病率较高。然而,部分由于大多数 IEI 亚型(国际免疫学会联盟原发性免疫缺陷委员会将其分为十类)的罕见性,很难对大量患者的风险进行评估,尤其是在儿童时期:目的:记录来自一家转诊机构的儿科群体的癌症发病率,评估他们的风险以及每个 IEI 亚群中的肿瘤类型:方法:广泛查阅 1989 年至 2022 年期间 16 岁前曾患过癌症的 IEI 患者的临床记录:结果:在 1642 名确诊为 IEI 的患者中,有 34 人在 16 岁前罹患癌症,发病率(2.1%)明显高于一般年龄匹配人群(0.22)。血液肿瘤(主要是淋巴瘤)是最常见的恶性肿瘤:本研究是为数不多的专门针对儿童 IEI 病例的报告之一,不仅描述了与年龄匹配的普通人群相比,儿童罹患恶性肿瘤的风险更高(免疫学家在随访过程中必须考虑到这一事实),而且还描述了不同肿瘤与特定 IEI 亚型之间的关联,从而揭示了其中可能涉及的机制。
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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Cancer Prevalence in Children with Inborn Errors of Immunity: Report from a Single Institution.

Background: Inborn Errors of Immunity (IEI) comprise several genetic anomalies that affect different components of the innate and adaptive responses, predisposing to infectious diseases, autoimmunity and malignancy. Different studies, mostly in adults, have reported a higher prevalence of cancer in IEI patients. However, in part due to the rarity of most of these IEI subtypes (classified in ten categories by the Primary Immunodeficiency Committee of the International Union of Immunological Societies), it is difficult to assess the risk in a large number of patients, especially during childhood.

Objective: To document the cancer prevalence in a pediatric cohort from a single referral institution, assessing their risk, together with the type of neoplasia within each IEI subgroup.

Method: An extensive review of clinical records from 1989 to 2022 of IEI patients who at some point developed cancer before the age of sixteen.

Results: Of a total of 1642 patients with IEI diagnosis, 34 developed cancer before 16 years of age, showing a prevalence (2.1%) significantly higher than that of the general age matched population (0.22). Hematologic neoplasms (mostly lymphomas) were the most frequent malignancies.

Conclusion: This study represents one of the few reports focused exclusively in pediatric IEI cases, describing not only the increased risk of developing malignancy compared with the age matched general population (a fact that must be taken into account by immunologists during follow-up) but also the association of the different neoplasms with particular IEI subtypes, thus disclosing the possible mechanisms involved.

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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
期刊最新文献
Similar Kinetics of Pulmonary SARS-CoV-2 Load in Intensive Care Unit Patients with COVID-19 Pneumonia with or Without Autoantibodies Neutralizing Type I Interferons. Expanding the Spectrum of Immune Abnormalities in VICI Syndrome. Correction to: DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans. Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control. Correction to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye.
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