Graham Jessica B, Swarts Jessica L, Leist Sarah R, Schäfer Alexandra, Bell Timothy A, Hock Pablo, Farrington Joe, Shaw Ginger D, Ferris Martin T, Pardo-Manuel de Villena Fernando, Baric Ralph S, Lund Jennifer M
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
iScience. 2024 Feb 2;27(3):109103. doi: 10.1016/j.isci.2024.109103. eCollection 2024 Mar 15.
The response to infection is generally heterogeneous and diverse, with some individuals remaining asymptomatic while others present with severe disease or a diverse range of symptoms. Here, we address the role of host genetics on immune phenotypes and clinical outcomes following viral infection by studying genetically diverse mice from the Collaborative Cross (CC), allowing for use of a small animal model with controlled genetic diversity while maintaining genetic replicates. We demonstrate variation by deeply profiling a broad range of innate and adaptive immune cell phenotypes at steady-state in 63 genetically distinct CC mouse strains and link baseline immune signatures with virologic and clinical disease outcomes following infection of mice with herpes simplex virus 2 (HSV-2) or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This work serves as a resource for CC strain selection based on steady-state immune phenotypes or disease presentation upon viral infection, and further, points to possible pre-infection immune correlates of survival and early viral clearance upon infection.
对感染的反应通常是异质性和多样化的,一些个体保持无症状,而另一些个体则出现严重疾病或各种症状。在这里,我们通过研究协作杂交(CC)中基因多样化的小鼠,探讨宿主遗传学在病毒感染后免疫表型和临床结果中的作用,从而能够使用具有可控遗传多样性的小动物模型,同时保持基因复制品。我们通过对63种基因不同的CC小鼠品系在稳态下的广泛先天性和适应性免疫细胞表型进行深度分析来证明差异,并将基线免疫特征与单纯疱疹病毒2(HSV-2)或严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染小鼠后的病毒学和临床疾病结果联系起来。这项工作为基于稳态免疫表型或病毒感染后的疾病表现选择CC品系提供了资源,并且进一步指出了感染前可能与生存和早期病毒清除相关的免疫因素。