Department of Pediatrics, NYU Grossman School of Medicine.
NYU Langone Transplant Institute, New York, New York, USA.
Curr Opin Infect Dis. 2024 Aug 1;37(4):227-231. doi: 10.1097/QCO.0000000000001021. Epub 2024 May 14.
The purpose of this focused review is to discuss unusual presentations of viral infections in the context of specific inborn errors of immunity. We will discuss hyper immunoglobulin E (IgE) syndromes, epidermodysplasia verruciformis, and X-linked agammaglobulinemia as examples of inborn errors of immunity associated with specific presentations of viral infection and disease.
Advances in both genetic and viral diagnostics have broadened our understanding of viral pathogenesis in the setting of immune dysfunction and the variable phenotype of inborn errors of immunity. Dedicator of cytokinesis 8 (DOCK8) deficiency is now recognized as an inborn error of immunity within the hyper IgE syndrome phenotype and is associated with unusually aggressive cutaneous disease caused by herpes simplex and other viruses. Studies of patients with epidermodysplasia verruciformis have proven that rarely detected human papillomavirus subtypes may cause malignancy in the absence of adequate host defenses. Finally, patients with X-linked agammaglobulinemia may remain at risk for severe and chronic viral infections, even as immune globulin supplementation reduces the risk of bacterial infection.
Susceptibility to viral infections in patients with inborn errors of immunity is conferred by specific, molecular defects. Recurrent, severe, or otherwise unusual presentations of viral disease should prompt investigation for an underlying genetic defect.
本次集中综述旨在特定先天性免疫缺陷的背景下,讨论病毒感染的不常见表现。我们将讨论高免疫球蛋白 E(IgE)综合征、疣状表皮发育不良和 X 连锁无丙种球蛋白血症,作为与病毒感染和疾病的特定表现相关的先天性免疫缺陷的例子。
在免疫功能障碍和先天性免疫缺陷的可变表型背景下,遗传和病毒诊断技术的进步拓宽了我们对病毒发病机制的理解。现在已知细胞分裂蛋白 8(DOCK8)缺陷是高 IgE 综合征表型中的一种先天性免疫缺陷,并与单纯疱疹和其他病毒引起的异常侵袭性皮肤疾病有关。对疣状表皮发育不良患者的研究证明,在宿主防御不足的情况下,很少检测到的人乳头瘤病毒亚型也可能导致恶性肿瘤。最后,即使免疫球蛋白补充降低了细菌感染的风险,X 连锁无丙种球蛋白血症患者仍可能存在严重和慢性病毒感染的风险。
先天性免疫缺陷患者对病毒感染的易感性是由特定的分子缺陷决定的。反复发生的、严重的或其他不常见的病毒疾病表现应促使调查潜在的遗传缺陷。