Lethal Infectious Diseases as Inborn Errors of Immunity: Toward a Synthesis of the Germ and Genetic Theories

被引:85
作者
Casanova, Jean-Laurent [1 ,2 ,3 ,4 ,5 ]
Abel, Laurent [1 ,3 ,4 ]
机构
[1] Rockefeller Univ, Rockefeller Branch, St Giles Lab Human Genet Infect Dis, New York, NY 10065 USA
[2] Howard Hughes Med Inst, New York, NY 10065 USA
[3] Necker Hosp Sick Children, INSERM U1163, Necker Branch, Lab Human Genet Infect Dis, F-75015 Paris, France
[4] Paris Univ, Imagine Inst, F-75015 Paris, France
[5] Necker Hosp Sick Children, Pediat Hematol Immunol Unit, F-75015 Paris, France
来源
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 16, 2021 | 2021年 / 16卷
基金
美国国家卫生研究院;
关键词
primary immunodeficiency; inborn error of immunity; human genetics of infectious diseases; Mendelian infection; monogenic infection; CHRONIC MUCOCUTANEOUS CANDIDIASIS; ANHIDROTIC ECTODERMAL DYSPLASIA; HEREDITARY ANGIONEUROTIC EDEMA; PYOGENIC BACTERIAL-INFECTIONS; HERPES-SIMPLEX ENCEPHALITIS; INFLAMMATORY-BOWEL-DISEASE; CLINICAL-FEATURES; PRIMARY IMMUNODEFICIENCIES; INTERFERON-GAMMA; KAPOSI-SARCOMA;
D O I
10.1146/annurev-pathol-031920-101429
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
It was first demonstrated in the late nineteenth century that human deaths from fever were typically due to infections. As the germ theory gained ground, it replaced the old, unproven theory that deaths from fever reflected a weak personal or even familial constitution. A new enigma emerged at the turn of the twentieth century, when it became apparent that only a small proportion of infected individuals die from primary infections with almost any given microbe. Classical genetics studies gradually revealed that severe infectious diseases could be driven by human genetic predisposition. This idea gained ground with the support of molecular genetics, in three successive, overlapping steps. First, many rare inborn errors of immunity were shown, from 1985 onward, to underlie multiple, recurrent infections with Mendelian inheritance. Second, a handful of rare and familial infections, also segregating as Mendelian traits but striking humans resistant to other infections, were deciphered molecularly beginning in 1996. Third, from 2007 onward, a growing number of rare or common sporadic infections were shown to result from monogenic, but not Mendelian, inborn errors. A synthesis of the hitherto mutually exclusive germ and genetic theories is now in view.
引用
收藏
页码:23 / 50
页数:28
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