Sharma Madhubala, Dhaliwal Manpreet, Tyagi Rahul, Goyal Taru, Sharma Saniya, Rawat Amit
AllergyImmunology Unit, Department of Pediatrics, Advanced Pediatrics Center, Postgraduate Institute of Medical Education and Research, Chandigarh 160012, India.
Pathogens. 2023 Mar 27;12(4):518. doi: 10.3390/pathogens12040518.
Inborn errors of immunity (IEI) can present with infections, autoimmunity, lymphoproliferation, granulomas, and malignancy. IEIs are due to genetic abnormalities that disrupt normal host-immune response or immune regulation. The microbiome appears essential for maintaining host immunity, especially in patients with a defective immune system. Altered gut microbiota in patients with IEI can lead to clinical symptoms. Microbial dysbiosis is the consequence of an increase in pro-inflammatory bacteria or a reduction in anti-inflammatory bacteria. However, functional and compositional differences in microbiota are also involved. Dysbiosis and a reduced alpha-diversity are well documented, particularly in conditions like common variable immunodeficiency. Deranged microbiota is also seen in Wiskott-Aldrich syndrome, severe combined immunodeficiency, chronic granulomatous disease, selective immunoglobulin-A deficiency, Hyper IgE syndrome (HIGES), X-linked lymphoproliferative disease-2, immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome, and defects of IL10 signalling. Distinct gastrointestinal, respiratory, and cutaneous symptoms linked to dysbiosis are seen in several IEIs, emphasizing the importance of microbiome identification. In this study, we discuss the processes that maintain immunological homeostasis between commensals and the host and the disruptions thereof in patients with IEIs. As the connection between microbiota, host immunity, and infectious illnesses is better understood, microbiota manipulation as a treatment strategy or infection prevention method would be more readily employed. Therefore, optimal prebiotics, probiotics, postbiotics, and fecal microbial transplantation can be promising strategies to restore the microbiota and decrease disease pathology in patients with IEIs.
遗传性免疫缺陷(IEI)可表现为感染、自身免疫、淋巴细胞增殖、肉芽肿和恶性肿瘤。IEI是由破坏正常宿主免疫反应或免疫调节的基因异常引起的。微生物群似乎对维持宿主免疫力至关重要,尤其是在免疫系统有缺陷的患者中。IEI患者肠道微生物群的改变可导致临床症状。微生物失调是促炎细菌增加或抗炎细菌减少的结果。然而,微生物群的功能和组成差异也有影响。微生物失调和α多样性降低已得到充分记录,尤其是在常见可变免疫缺陷等病症中。在威斯科特-奥尔德里奇综合征、严重联合免疫缺陷、慢性肉芽肿病、选择性免疫球蛋白A缺乏症、高IgE综合征(HIGES)、X连锁淋巴细胞增殖性疾病-2、免疫失调、多内分泌病、肠病、X连锁综合征以及IL10信号缺陷中也可见微生物群紊乱。在几种IEI中可见与微生物失调相关的独特胃肠道、呼吸道和皮肤症状,这强调了微生物群鉴定的重要性。在本研究中,我们讨论了维持共生菌与宿主之间免疫稳态的过程以及IEI患者中这些过程的破坏情况。随着微生物群、宿主免疫力和传染病之间的联系得到更好的理解,微生物群操纵作为一种治疗策略或感染预防方法将更容易被采用。因此,最佳的益生元、益生菌、后生元和粪便微生物移植可能是恢复微生物群并减轻IEI患者疾病病理的有前景的策略。