Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Inserm U1163, Necker Hospital for Sick Children, Paris, France; Paris Cité University, Imagine Institute, Paris, France; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Inserm U1163, Necker Hospital for Sick Children, Paris, France; Paris Cité University, Imagine Institute, Paris, France; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA; Department of Pediatrics, Necker Hospital for Sick Children, Paris, France; Howard Hughes Medical Institute, New York, NY, USA.
Immunity. 2024 Jul 9;57(7):1457-1465. doi: 10.1016/j.immuni.2024.05.020.
Regardless of microbial virulence (i.e., the global infection-fatality ratio), age generally drives the prevalence of death from infection in unvaccinated humans. Four mortality patterns are recognized: the common U- and L-shaped curves of endemic infections and the unique W- and J-shaped curves of pandemic infections. We suggest that these patterns result from different sets of human genetic and immunological determinants. In this model, it is the interplay between (1) monogenic genotypes affecting immunity to primary infection that preferentially manifest early in life and related genotypes or their phenocopies, including auto-antibodies, which manifest later in life and (2) the occurrence and persistence of adaptive, acquired immunity to primary or cross-reactive infections, which shapes the age-dependent pattern of human deaths from infection.
无论微生物的毒力(即全球感染病死率)如何,年龄通常是未接种疫苗人群中感染致死的主要驱动因素。有四种公认的死亡模式:地方性感染的常见 U 形和 L 形曲线,以及大流行感染的独特 W 形和 J 形曲线。我们认为这些模式是由不同的人类遗传和免疫决定因素造成的。在该模型中,主要涉及以下两方面的相互作用:(1)影响初次感染免疫的单基因基因型,这些基因型优先在生命早期表现出来,而与这些基因型相关的基因型或其表型,包括自身抗体,则在生命后期表现出来;(2)对初次或交叉反应性感染产生的适应性、获得性免疫的发生和持续存在,这些因素决定了人类感染致死的年龄依赖性模式。