Please use this identifier to cite or link to this item:
https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4909
Title: | Understanding the complexities of SARS-CoV2 infection and its immunology: A road to immune-based therapeutics | Authors: | Kumar, V. | Issue Date: | 2020 | Source: | 88 , 2020 | Journal: | International Immunopharmacology | Abstract: | Emerging infectious diseases always pose a threat to humans along with plant and animal life. SARS-CoV2 is the recently emerged viral infection that originated from Wuhan city of the Republic of China in December 2019. Now, it has become a pandemic. Currently, SARS-CoV2 has infected more than 27.74 million people worldwide, and taken 901,928 human lives. It was named first ‘WH 1 Human CoV’ and later changed to 2019 novel CoV (2019-nCoV). Scientists have established it as a zoonotic viral disease emerged from Chinese horseshoe bats, which do not develop a severe infection. For example, Rhinolophus Chinese horseshoe bats harboring severe acute respiratory syndrome-related coronavirus (SARSr-CoV) or SARSr-Rh-BatCoV appear healthy and clear the virus within 2–4 months period. The article introduces first the concept of EIDs and some past EIDs, which have affected human life. Next section discusses mysteries regarding SARS-CoV2 origin, its evolution, and human transfer. Third section describes COVID-19 clinical symptoms and factors affecting susceptibility or resistance. The fourth section introduces the SARS-CoV2 entry in the host cell, its replication, and the establishment of productive infection. Section five describes the host's immune response associated with asymptomatic, symptomatic, mild to moderate, and severe COVID-19. The subsequent seventh and eighth sections mention the immune status in COVID-19 convalescent patients and re-emergence of COVID-19 in them. Thereafter, the eighth section describes viral strategies to hijack the host antiviral immune response and generate the “cytokine storm”. The ninth section describes about transgenic humane ACE2 (hACE2) receptor expressing mice to study immunity, drugs, and vaccines. The article ends with the development of different immunomodulatory and immunotherapeutics strategies, including vaccines waiting for their approval in humans as prophylaxis or treatment measures.L20078198342020-09-25 | DOI: | 10.1016/j.intimp.2020.106980 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L2007819834&from=exporthttp://dx.doi.org/10.1016/j.intimp.2020.106980 | | Keywords: | gsk 2586881;hydroxychloroquine;immunomodulating agent;interferon;lopinavir plus ritonavir;mavrilimumab;mdr 504;nanobody;neutralizing antibody;polyclonal antibody;remdesivir;ribavirin;ruxolitinib;SARS-CoV-2 vaccine;unclassified drug;unindexed drug;viral protein;antiviral activity;antiviral therapy;asymptomatic infection;cells by body anatomy;coronavirus disease 2019;cytokine storm;disease severity;experimental mouse;host cell;human;immune response;immune status;immunization;immunology;immunomodulation;immunotherapy;nonhuman;pregnancy outcome;pregnant woman;priority journal;prophylaxis;review;Rhinolophus sinicus;Severe acute respiratory syndrome coronavirus 2;virus assembly;virus cell interaction;virus entry;virus pathogenesis;amy 101;gs 5734;virus replication;adenovirus vectoralpha2b interferon;antivirus agent;azithromycin;baricitinib;n4 hydroxycytidine;convalescent plasma;cytidine derivative;cytokine;dextro tyrosylisoleucylcysteinylvalyl 1 methyltryptophylglutaminylaspartyltryptophyl n methylglycylalanylhistidylarginylcysteinyl n methylisoleucinamide 3,13 cyclic sulfide;diltiazem;drug metabolite;eculizumab;gs 704277 | Type: | Article |
Appears in Sites: | Children's Health Queensland Publications |
Show full item record
Items in DORA are protected by copyright, with all rights reserved, unless otherwise indicated.