J
Jay Rappaport
Researcher at Tulane University
Publications - 32
Citations - 1123
Jay Rappaport is an academic researcher from Tulane University. The author has contributed to research in topics: Coronavirus & Immune system. The author has an hindex of 10, co-authored 32 publications receiving 404 citations.
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Journal ArticleDOI
Adjuvanting a subunit COVID-19 vaccine to induce protective immunity.
Prabhu S. Arunachalam,Alexandra C. Walls,Nadia A. Golden,Caroline Atyeo,Stephanie Fischinger,Chunfeng Li,Pyone P. Aye,Mary Jane Navarro,Lilin Lai,Venkata Viswanadh Edara,Katharina Röltgen,Kenneth A. Rogers,Lisa Shirreff,Douglas E. Ferrell,Samuel Wrenn,Deleah Pettie,John C. Kraft,Marcos C. Miranda,Elizabeth Kepl,Claire Sydeman,Natalie Brunette,Michael E. P. Murphy,Brooke Fiala,Lauren Carter,Alexander G. White,Meera Trisal,Ching-Lin Hsieh,Kasi E. Russell-Lodrigue,Christopher Monjure,Jason Dufour,Skye Spencer,Lara A. Doyle-Meyers,Rudolph Bohm,Nicholas J. Maness,Chad J. Roy,Jessica A. Plante,Kenneth S. Plante,Alex Lee Zhu,Matthew J. Gorman,Sally Shin,Xiaoying Shen,Jane Fontenot,Shakti Gupta,Derek T. O'Hagan,Robbert van der Most,Rino Rappuoli,Robert L. Coffman,David Novack,Jason S. McLellan,Shankar Subramaniam,David C. Montefiori,Scott D. Boyd,JoAnne L. Flynn,Galit Alter,Francois Villinger,Harry Kleanthous,Jay Rappaport,Mehul S. Suthar,Neil P. King,Neil P. King,David Veesler,Bali Pulendran +61 more
TL;DR: In this article, the authors demonstrate the capacity of a subunit vaccine, comprising the SARS-CoV-2 spike protein receptor-binding domain displayed on an I53-50 protein nanoparticle scaffold (hereafter designated RBD-NP), to stimulate robust and durable neutralizing-antibody responses.
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SARS-CoV-2 pandemic and research gaps: Understanding SARS-CoV-2 interaction with the ACE2 receptor and implications for therapy.
TL;DR: Interestingly, SARS-CoV-2 infection downregulates ACE2 expression, which may also play a critical pathogenic role in COVID-19, and targeting ACE2/Ang 1-7 axis and blocking ACE2 interaction with the S protein of Sars-Cov-2 to curtail SARV- CoV- 2 infection are becoming very attractive therapeutics potential for treatment and prevention of CO VID-19.
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A smartphone-read ultrasensitive and quantitative saliva test for COVID-19.
Bo Ning,Tao Yu,Shengwei Zhang,Zhen Huang,Zhen Huang,Di Tian,Zhen Lin,Alex Niu,Nadia A. Golden,Krystle Hensley,Breanna Threeton,Christopher J. Lyon,Xiao-Ming Yin,Chad J. Roy,Nakhle S. Saba,Jay Rappaport,Qingshan Wei,Tony Y. Hu +17 more
TL;DR: An isolation-free smartphone-based saliva assay that can diagnose COVID-19 cases and quantify viral load within 15 min and exhibited a limit of detection below that of the RT-PCR reference assay is described.
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Acute Respiratory Distress in Aged, SARS-CoV-2-Infected African Green Monkeys but Not Rhesus Macaques.
Robert V Blair,Monica Vaccari,Lara A. Doyle-Meyers,Chad J. Roy,Kasi E. Russell-Lodrigue,Marissa Fahlberg,Chris J. Monjure,Brandon J. Beddingfield,Kenneth S. Plante,Jessica A. Plante,Scott C. Weaver,Xuebin Qin,Cecily C. Midkiff,Gabrielle Lehmicke,Nadia A. Golden,Breanna Threeton,Toni Penney,Carolina Allers,Mary B. Barnes,Melissa Pattison,Prasun K. Datta,Nicholas J. Maness,Angela Birnbaum,Tracy Fischer,Rudolf P. Bohm,Jay Rappaport +25 more
TL;DR: This work reports ARDS in two aged African green monkeys infected with SARS-CoV-2 that demonstrated pathological lesions and disease similar to severe COVID-19 in humans and suggests that aged AGMs may be useful for modeling severe disease manifestations including ARDS.
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SARS-CoV-2 Infects Endothelial Cells In Vivo and In Vitro .
Fengming Liu,Kun Han,Robert V Blair,Kornelia Kenst,Zhongnan Qin,Berin Upcin,Philipp Wörsdörfer,Cecily C. Midkiff,Joseph Mudd,Elizaveta Belyaeva,Nicholas S Milligan,Tyler D Rorison,Nicole Wagner,Jochen Bodem,Lars Dölken,Bertal H. Aktas,Richard S. Vander Heide,Xiao-Ming Yin,Jay K. Kolls,Chad J. Roy,Jay Rappaport,Süleyman Ergün,Xuebin Qin +22 more
TL;DR: In this article, the authors showed that SARS-CoV-2 infection can cause fatal inflammatory lung pathology, including thrombosis and increased pulmonary vascular permeability leading to edema and hemorrhage.