Hartmann Carina R, Khan Robin, Schöning Jennifer, Richter Maximilian, Willers Maike, Pirr Sabine, Heckmann Julia, Dirks Johannes, Morbach Henner, Konrad Monika, Fries Elena, Winkler Magdalene, Büchel Johanna, Seidenspinner Silvia, Fischer Jonas, Vollmuth Claudia, Meinhardt Martin, Marissen Janina, Schmolke Mirco, Haid Sibylle, Pietschmann Thomas, Backes Simone, Dölken Lars, Löber Ulrike, Keil Thomas, Heuschmann Peter U, Wöckel Achim, Ulas Thomas, Forslund-Startceva Sofia K, Härtel Christoph, Viemann Dorothee
Department of Pediatrics, University Hospital Würzburg, Würzburg, Germany.
Department of Pediatric Pneumology, Allergology and Neonatology, Hannover Medical School, Hannover, Germany.
Front Immunol. 2024 Sep 17;15:1443665. doi: 10.3389/fimmu.2024.1443665. eCollection 2024.
Respiratory viral infections (RVIs) are a major global contributor to morbidity and mortality. The susceptibility and outcome of RVIs are strongly age-dependent and show considerable inter-population differences, pointing to genetically and/or environmentally driven developmental variability. The factors determining the age-dependency and shaping the age-related changes of human anti-RVI immunity after birth are still elusive.
We are conducting a prospective birth cohort study aiming at identifying endogenous and environmental factors associated with the susceptibility to RVIs and their impact on cellular and humoral immune responses against the influenza A virus (IAV), respiratory syncytial virus (RSV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The MIAI birth cohort enrolls healthy, full-term neonates born at the University Hospital Würzburg, Germany, with follow-up at four defined time-points during the first year of life. At each study visit, clinical metadata including diet, lifestyle, sociodemographic information, and physical examinations, are collected along with extensive biomaterial sampling. Biomaterials are used to generate comprehensive, integrated multi-omics datasets including transcriptomic, epigenomic, proteomic, metabolomic and microbiomic methods.
The results are expected to capture a holistic picture of the variability of immune trajectories with a focus on cellular and humoral key players involved in the defense of RVIs and the impact of host and environmental factors thereon. Thereby, MIAI aims at providing insights that allow unraveling molecular mechanisms that can be targeted to promote the development of competent anti-RVI immunity in early life and prevent severe RVIs.
https://drks.de/search/de/trial/, identifier DRKS00034278.
呼吸道病毒感染(RVI)是全球发病和死亡的主要原因。RVI的易感性和结果强烈依赖于年龄,并表现出相当大的人群间差异,这表明存在遗传和/或环境驱动的发育变异性。出生后决定人类抗RVI免疫年龄依赖性并塑造与年龄相关变化的因素仍然难以捉摸。
我们正在进行一项前瞻性出生队列研究,旨在确定与RVI易感性相关的内源性和环境因素及其对针对甲型流感病毒(IAV)、呼吸道合胞病毒(RSV)和严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的细胞免疫和体液免疫反应的影响。MIAI出生队列招募在德国维尔茨堡大学医院出生的健康足月新生儿,并在生命的第一年的四个特定时间点进行随访。在每次研究访问时,收集包括饮食、生活方式、社会人口统计学信息和体格检查在内的临床元数据以及大量生物材料样本。生物材料用于生成包括转录组学、表观基因组学、蛋白质组学、代谢组学和微生物组学方法的全面、综合的多组学数据集。
预计结果将全面呈现免疫轨迹的变异性,重点关注参与抵御RVI的细胞和体液关键参与者以及宿主和环境因素对其的影响。因此,MIAI旨在提供见解,以揭示可作为靶点促进生命早期有效抗RVI免疫发展并预防严重RVI的分子机制。