The many faces of the anti-COVID immune response
The novel 2019 strain of coronavirus is a source of profound morbidity and mortality worldwide. Compared with recent viral outbreaks, COVID-19 infection has a relatively high mortality rate, the reasons for which are not entirely clear. Furthermore, treatment options for COVID-19 infection are curre...
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Published in | The Journal of experimental medicine Vol. 217; no. 6 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
Rockefeller University Press
01.06.2020
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Subjects | |
Online Access | Get full text |
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Abstract | The novel 2019 strain of coronavirus is a source of profound morbidity and mortality worldwide. Compared with recent viral outbreaks, COVID-19 infection has a relatively high mortality rate, the reasons for which are not entirely clear. Furthermore, treatment options for COVID-19 infection are currently limited. In this Perspective, we explore the contributions of the innate and adaptive immune systems to both viral control as well as toxicity during COVID-19 infections and offer suggestions to both understand and therapeutically modulate anti-COVID immunity. |
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AbstractList | The novel 2019 strain of coronavirus is a source of profound morbidity and mortality worldwide. Compared with recent viral outbreaks, COVID-19 infection has a relatively high mortality rate, the reasons for which are not entirely clear. Furthermore, treatment options for COVID-19 infection are currently limited. In this Perspective, we explore the contributions of the innate and adaptive immune systems to both viral control as well as toxicity during COVID-19 infections and offer suggestions to both understand and therapeutically modulate anti-COVID immunity. This Perspective explores the contributions of the innate and adaptive immune systems to both viral control as well as toxicity during COVID-19 infections and offers suggestions to both understand and therapeutically modulate anti-COVID immunity. The novel 2019 strain of coronavirus is a source of profound morbidity and mortality worldwide. Compared with recent viral outbreaks, COVID-19 infection has a relatively high mortality rate, the reasons for which are not entirely clear. Furthermore, treatment options for COVID-19 infection are currently limited. In this Perspective, we explore the contributions of the innate and adaptive immune systems to both viral control as well as toxicity during COVID-19 infections and offer suggestions to both understand and therapeutically modulate anti-COVID immunity. The novel 2019 strain of coronavirus is a source of profound morbidity and mortality worldwide. Compared with recent viral outbreaks, COVID-19 infection has a relatively high mortality rate, the reasons for which are not entirely clear. Furthermore, treatment options for COVID-19 infection are currently limited. In this Perspective, we explore the contributions of the innate and adaptive immune systems to both viral control as well as toxicity during COVID-19 infections and offer suggestions to both understand and therapeutically modulate anti-COVID immunity.The novel 2019 strain of coronavirus is a source of profound morbidity and mortality worldwide. Compared with recent viral outbreaks, COVID-19 infection has a relatively high mortality rate, the reasons for which are not entirely clear. Furthermore, treatment options for COVID-19 infection are currently limited. In this Perspective, we explore the contributions of the innate and adaptive immune systems to both viral control as well as toxicity during COVID-19 infections and offer suggestions to both understand and therapeutically modulate anti-COVID immunity. |
Author | Vardhana, Santosha A. Wolchok, Jedd D. |
AuthorAffiliation | 3 Parker Institute for Cancer Immunotherapy, San Francisco, CA 4 Human Oncology Pathogenesis Program, Department of Medicine and Ludwig Center, Memorial Sloan Kettering Cancer Center, New York, NY 2 Center for Epigenetics Research, Memorial Sloan Kettering Cancer Center, New York, NY 5 Weill Cornell Medicine and Graduate School of Biomedical Sciences, New York, NY 1 Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY |
AuthorAffiliation_xml | – name: 1 Cancer Biology and Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY – name: 5 Weill Cornell Medicine and Graduate School of Biomedical Sciences, New York, NY – name: 2 Center for Epigenetics Research, Memorial Sloan Kettering Cancer Center, New York, NY – name: 3 Parker Institute for Cancer Immunotherapy, San Francisco, CA – name: 4 Human Oncology Pathogenesis Program, Department of Medicine and Ludwig Center, Memorial Sloan Kettering Cancer Center, New York, NY |
Author_xml | – sequence: 1 givenname: Santosha A. orcidid: 0000-0002-3100-1298 surname: Vardhana fullname: Vardhana, Santosha A. – sequence: 2 givenname: Jedd D. orcidid: 0000-0001-6718-2222 surname: Wolchok fullname: Wolchok, Jedd D. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32353870$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Disclosures: S.A. Vardhana reported personal fees from Immunai and personal fees from ADC Therapeutics outside the submitted work; in addition, S.A. Vardhana had a patent to PCT/US19/27610 pending. J.D. Wolchok reported personal fees from Tizona Pharmaceuticals, Adaptive Biotechnologies, Imvaq, Beigene, and Linneaus; and grants from AstraZeneca, Bristol Myers Squibb, and Sephora outside the submitted work. In addition, J.D. Wolchok had a patent to alphavirus replicon particles expressing TRP2 issued, a patent to Newcastle disease viruses for cancer therapy issued, a patent to xenogeneic DNA vaccines with royalties paid "Merial," a patent to myeloid-derived suppressor cell (MDSC) assay with royalties paid "Serametrix," a patent to anti-PD1 antibody licensed "Agenus," a patent to anti-CTLA4 antibodies licensed "Agenus," a patent to anti-GITR antibodies and methods of use thereof licensed "Agenus/Incyte," a patent to genomic signature to identify responders to ipilimumab in melanoma pending, a patent to engineered vaccinia viruses for cancer immunotherapy pending, a patent to anti-CD40 agonist mAb fused to monophosphoryl lipid A (MPL) for cancer therapy pending, a patent to CAR+ T cells targeting differentiation antigens as means to treat cancer pending, a patent to identifying and treating subjects at risk for checkpoint blockade therapy associated colitis pending, a patent to immunosuppressive follicular helper-like T cells modulated by immune checkpoint blockade pending, and a patent to phosphatidylserine targeting agents and uses thereof for adoptive T-cell therapies pending. J.D. Wolchok is a paid consultant for: Adaptive Biotech, Amgen, Apricity, Ascentage Pharma, Astellas, AstraZeneca, Bayer, Beigene, Bristol Myers Squibb, Celgene, Chugai, Eli Lilly, Elucida, F Star, Imvaq, Janssen, Kyowa Hakko Kirin, Linneaus, Merck, Neon Therapuetics, Novaritis, Polynoma, Psioxus, Recepta, Takara Bio, Trieza, Truvax, Serametrix, Surface Oncology, Syndax, and Syntalogic. |
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Snippet | The novel 2019 strain of coronavirus is a source of profound morbidity and mortality worldwide. Compared with recent viral outbreaks, COVID-19 infection has a... This Perspective explores the contributions of the innate and adaptive immune systems to both viral control as well as toxicity during COVID-19 infections and... |
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SubjectTerms | Adaptive Immunity - drug effects Adaptive Immunity - immunology Betacoronavirus - drug effects Betacoronavirus - immunology Betacoronavirus - pathogenicity Coronavirus Infections - immunology Coronavirus Infections - pathology Coronavirus Infections - therapy COVID-19 Cytokine Release Syndrome - immunology Cytokine Release Syndrome - pathology Cytokine Release Syndrome - therapy Humans Hypoxia - pathology Hypoxia - therapy Immunity, Innate - drug effects Immunity, Innate - immunology Infectious Disease and Host Defense Inflammation - immunology Inflammation - pathology Inflammation - therapy Innate Immunity and Inflammation Interleukin-6 - antagonists & inhibitors Interleukin-6 - immunology Lymphopenia - immunology Lymphopenia - pathology Lymphopenia - therapy Macrophages - immunology Macrophages - pathology Middle East Respiratory Syndrome Coronavirus - immunology Middle East Respiratory Syndrome Coronavirus - pathogenicity Pandemics Pneumonia, Viral - immunology Pneumonia, Viral - pathology Pneumonia, Viral - therapy Respiration, Artificial Respiratory Distress Syndrome - pathology Respiratory Distress Syndrome - therapy SARS-CoV-2 Severe acute respiratory syndrome-related coronavirus - immunology Severe acute respiratory syndrome-related coronavirus - pathogenicity |
Title | The many faces of the anti-COVID immune response |
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