Delavari Samaneh, Wang Yating, Moeini Shad Tannaz, Pashangzadeh Salar, Nazari Farzad, Salami Fereshte, Abolhassani Hassan
Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Science, 1419733151 Tehran, Iran.
Division of Clinical Immunology, Department of Biosciences and Nutrition, Karolinska Institute, 14183 Stockholm, Sweden.
Cancers (Basel). 2023 Jan 26;15(3):764. doi: 10.3390/cancers15030764.
Inborn errors of immunity (IEI) are a heterogeneous group of inherited disorders, and almost 500 genes associated with these disorders have been identified. Defects in IEI genes lead to diverse clinical manifestations including increased susceptibility to recurrent or prolonged infections, immune dysregulation phenotypes (such as severe atopy, allergy, autoimmunity, and uncontrolled inflammation, lymphoproliferation), as well as predisposition to malignancies. Although the majority of IEI patients present hematologic cancers, the characteristics of other types of cancers are not well described in these groups of patients. By investigating 5384 IEI patients registered in the Iranian national registry the clinical and immunologic phenotypes of patients with non-hematologic cancers were compared with other malignant and non-malignant patients. Solid tumors were reported <20% of malignant IEI patients ( = 27/144 patients) and appeared to be very heterogeneous by type and localization as well as molecular defects (mainly due to DNA repair defect resulted from ATM deficiency). The correlation between the type of malignancy and survival status was remarkable as patients with non-hematologic cancers survive higher than IEI patients with hematologic cancers. Our findings showed that different types of malignancy could be associated with specific entities of IEI. Therefore, the education of physicians about the risk of malignancies in IEI is required for personalized treatment and appropriate management of patients.
遗传性免疫缺陷病(IEI)是一组异质性的遗传性疾病,目前已鉴定出近500个与这些疾病相关的基因。IEI基因缺陷会导致多种临床表现,包括反复或长期感染易感性增加、免疫失调表型(如严重特应性、过敏、自身免疫和不受控制的炎症、淋巴细胞增殖)以及易患恶性肿瘤。虽然大多数IEI患者患有血液系统癌症,但在这些患者群体中,其他类型癌症的特征尚未得到充分描述。通过对伊朗国家登记处登记的5384例IEI患者进行调查,将非血液系统癌症患者的临床和免疫表型与其他恶性和非恶性患者进行了比较。实体瘤在恶性IEI患者中的报告率<20%(144例患者中有27例),并且在类型、定位以及分子缺陷方面似乎非常异质(主要是由于ATM缺陷导致的DNA修复缺陷)。恶性肿瘤类型与生存状态之间的相关性显著,因为非血液系统癌症患者的生存率高于血液系统癌症的IEI患者。我们的研究结果表明,不同类型的恶性肿瘤可能与特定的IEI实体相关。因此,为了对患者进行个性化治疗和适当管理,需要对医生进行关于IEI患者发生恶性肿瘤风险的教育。