Caba Lavinia, Gug Cristina, Gorduza Eusebiu Vlad
Department of Medical Genetics, 'Grigore T. Popa' University of Medicine and Pharmacy, 700115 Iași, Romania.
Department of Microscopic Morphology, 'Victor Babeş' University of Medicine and Pharmacy, 300041 Timisoara, Romania.
Exp Ther Med. 2021 Jan;21(1):84. doi: 10.3892/etm.2020.9517. Epub 2020 Nov 26.
Primary immunodeficiencies are genetic diseases, mainly monogenic, that affect various components of the immune system and stages of the immune response. The category of combined immunodeficiencies with associated or syndromic features comprises over 70 clinical entities, characterized by heterogeneity of clinical presentation, mode of transmission, molecular, biological, mutational and immunological aspects. The mutational spectrum is wide, ranging from structural chromosomal abnormalities to gene mutations. The impact on the function of the proteins encoded by the genes involved is different; loss of function is most common, but situations with gain of function are also described. Most proteins have multiple functions and are components of several protein interaction networks. The pathophysiological mechanisms mainly involve: Missing enzymes, absent or non-functional proteins, abnormal DNA repair pathways, altered signal transduction, developmental arrest in immune differentiation, impairment of cell-to-cell and intracellular communications. Allelic heterogeneity, reduced penetrance and variable expressivity are genetic phenomena that cause diagnostic difficulties, especially since most are rare/very rare diseases, which is equivalent to delaying proper case management. Most primary immunodeficiencies are Mendelian diseases with X-linked or recessive inheritance, and molecular diagnosis allows the identification of family members at risk and the application of appropriate primary and secondary prevention measures in addition to the specific curative ones. In conclusion, recognizing heterogeneity and its sources is extremely important for current medical practice, but also for the theoretical value of improving biological and biomedical applications.
原发性免疫缺陷是遗传性疾病,主要为单基因疾病,会影响免疫系统的各个组成部分以及免疫反应的各个阶段。伴有相关或综合征特征的联合免疫缺陷类别包含70多种临床实体,其特点是临床表现、传播方式、分子、生物学、突变和免疫学方面存在异质性。突变谱很广,从结构性染色体异常到基因突变。对所涉及基因编码的蛋白质功能的影响各不相同;功能丧失最为常见,但也有功能获得的情况。大多数蛋白质具有多种功能,是多个蛋白质相互作用网络的组成部分。病理生理机制主要涉及:缺失的酶、不存在或无功能的蛋白质、异常的DNA修复途径、改变的信号转导、免疫分化中的发育停滞、细胞间和细胞内通讯受损。等位基因异质性、外显率降低和可变表达是导致诊断困难的遗传现象,尤其是因为大多数是罕见/非常罕见的疾病,这等同于延误了适当的病例管理。大多数原发性免疫缺陷是具有X连锁或隐性遗传的孟德尔疾病,分子诊断不仅可以识别有风险的家庭成员,还可以在采取特定治疗措施的基础上,应用适当的一级和二级预防措施。总之,认识到异质性及其来源对于当前的医学实践极为重要,对于改善生物学和生物医学应用的理论价值也很重要。