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

IF 28.4 1区 医学 Q1 PATHOLOGY
Jean-Laurent Casanova, Laurent Abel
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引用次数: 0

Abstract

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 sporadicinfections 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.

致命的传染病是先天的免疫错误:迈向细菌和遗传理论的综合。
19世纪晚期首次证明,人类因发烧而死亡的典型原因是感染。随着细菌理论的普及,它取代了旧的、未经证实的理论,即发烧死亡反映了个人甚至家族体质的薄弱。在20世纪之交,一个新的谜团出现了,当时很明显,只有一小部分感染者死于几乎任何给定微生物的原发性感染。经典遗传学研究逐渐揭示,严重的传染病可能是由人类遗传易感性驱动的。在分子遗传学的支持下,这个想法在三个连续的、重叠的步骤中获得了支持。首先,从1985年开始,许多罕见的先天性免疫缺陷被证明是孟德尔遗传的多重复发性感染的基础。其次,从1996年开始,一些罕见的和家族性的感染,也作为孟德尔特征分离出来,但引人注目的是人类对其他感染的抵抗力,被分子地破译了。第三,从2007年开始,越来越多的罕见或常见的零星感染被证明是由单基因而不是孟德尔遗传的先天错误造成的。迄今为止相互排斥的胚芽和遗传理论的综合现在正在考虑之中。
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来源期刊
CiteScore
62.60
自引率
0.00%
发文量
40
期刊介绍: The Annual Review of Pathology: Mechanisms of Disease is a scholarly journal that has been published since 2006. Its primary focus is to provide a comprehensive overview of recent advancements in our knowledge of the causes and development of significant human diseases. The journal places particular emphasis on exploring the current and evolving concepts of disease pathogenesis, as well as the molecular genetic and morphological changes associated with various diseases. Additionally, the journal addresses the clinical significance of these findings. In order to increase accessibility and promote the broad dissemination of research, the current volume of the journal has transitioned from a gated subscription model to an open access format. This change has been made possible through the Annual Reviews' Subscribe to Open program, which allows all articles published in this volume to be freely accessible to readers. As part of this transition, all articles in the journal are published under a Creative Commons Attribution (CC BY) license, which encourages open sharing and use of the research.
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