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The SARS-COV-2 virus has had a major impact on morbidity and mortality worldwide, as well as having devastating global economic and societal impact. The overall impact cannot be quantified, some of which is due to the worldwide public health response and not the virus itself. Knowledge of the antibody levels present in a population could offer great insights into current and future response efforts. We need far more information to fully understand what impact immunity will have on the spread and severity of this and future pandemic viruses. This knowledge could change how we handle the next stages of this pandemic, the post pandemic period, and prepare for future pandemics. Therefore, we completed a nationwide serosurvey to enroll a 10,000 person representative sample of the US population to determine how many individuals have been exposed/infected with SARS-CoV-2 during the initial stages of the pandemic. The first portion of this study was published offering insight into the early portion of the pandemic and the epidemiology and immune response early on. We then followed these individuals longitudinally and retested them at 6 months and 12 months to look for seroconversion and history of documented infection. This allows us to assess correlates of protection and the trajectory of antibody titers over time. The data yielded from this study, in conjunction with other similar studies can better guide the decisions that are made as this pandemic continues. We hope to publish these data in the coming year offering even further insight into this pandemic. In addition to our nationwide serosurvey we initiated a project to study individuals with rare diseases. This study in collaboration with the NCATS RDCRN evaluated how the COVID19 pandemic has affected individuals living with over 500 different rare diseases. The RDCRN has initiated an online survey and we initiated biological sampling to allow us to better identify the level of exposure and immunity in this niche community. The manuscript describing the results of this study are currently under review and the data from this study will allow us to better understand how we can better address the pandemic needs of this community that is often overlooked. We have initiated work in collaboration with Jeff Taubenberger's VPES to develop a broadly protective, universal beta-coronavirus vaccine. We are playing a lead role in the design and manufacture of these vaccines. The work on these vaccines continues. We also have collaborated with the VPES to investigate various aspects of SARS-COV2 pathogenesis including a large scale pathology study of those with severe disease, gene expression analysis, and in vitro studies of viral variants. Lastly, we are working on developing challenge models for beta-coronaviruses that may be used to study pathogenesis as well as testing vaccines. We have successfully GMP manufactured an ODC43 virus and are in discussions with University of Maryland and DMID about collaborating to perform a challenge study with that virus. We have also begun production of a 229e coronavirus.
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DOI: 10.1093/infdis/jiaa743
发表时间: 2021-03-03
期刊: The Journal of infectious diseases
影响因子: --
作者: [Klumpp-Thomas C, Kalish H, Hicks J, Mehalko J, Drew M, Memoli MJ, Hall MD, Esposito D, Sadtler K]
通讯作者: Sadtler K
DOI: 10.1007/s10875-021-00997-6
发表时间: 2021-07
期刊: Journal of clinical immunology
影响因子: 9.1
作者: [Hicks J, Klumpp-Thomas C, Kalish H, Shunmugavel A, Mehalko J, Denson JP, Snead KR, Drew M, Corbett KS, Graham BS, Hall MD, Memoli MJ, Esposito D, Sadtler K]
通讯作者: Sadtler K
SARS-CoV-2 Seroprevalence and Drug Use in Trauma Patients from Six Sites in the United States.
美国六个地点的创伤患者中 SARS-CoV-2 血清阳性率和药物使用情况。
DOI: 10.1101/2021.08.10.21261849
发表时间: 2021
期刊: medRxiv : the preprint server for health sciences
影响因子: --
作者: [Ngo,TranB, Karkanitsa,Maria, Adusei,KennethM, Graham,LindseyA, Ricotta,EmilyE, Darrah,JennaR, Blomberg,RichardD, Spathies,Jacquelyn, Pauly,KyleJ, Klumpp-Thomas,Carleen, Travers,Jameson, Mehalko,Jennifer, Drew,Matthew, Hall,MatthewD, ]
通讯作者:
DOI: 10.1038/s41467-020-20383-x
发表时间: 2021-01-04
期刊: Nature communications
影响因子: 16.6
作者: [Klumpp-Thomas C, Kalish H, Drew M, Hunsberger S, Snead K, Fay MP, Mehalko J, Shunmugavel A, Wall V, Frank P, Denson JP, Hong M, Gulten G, Messing S, Hicks J, Michael S, Gillette W, Hall MD, Memoli MJ, Esposito D, Sadtler K]
通讯作者: Sadtler K
Pandemic Influenza Translational Research and novel universal countermeasure development
Coronavirus Pathogenesis and Broadly Protective Vaccine Development
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