Limited extent and consequences of pancreatic SARS-CoV-2 infection.
COVID-19
SARS-CoV-2
human coronaviruses
human islets
pancreas
type 1 diabetes
type 2 diabetes
viral infection
Journal
Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691
Informations de publication
Date de publication:
15 03 2022
15 03 2022
Historique:
received:
12
10
2021
revised:
17
12
2021
accepted:
16
02
2022
pubmed:
6
3
2022
medline:
29
3
2022
entrez:
5
3
2022
Statut:
ppublish
Résumé
Concerns that infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the etiological agent of coronavirus disease 2019 (COVID-19), may cause new-onset diabetes persist in an evolving research landscape, and precise risk assessment is hampered by, at times, conflicting evidence. Here, leveraging comprehensive single-cell analyses of in vitro SARS-CoV-2-infected human pancreatic islets, we demonstrate that productive infection is strictly dependent on the SARS-CoV-2 entry receptor ACE2 and targets practically all pancreatic cell types. Importantly, the infection remains highly circumscribed and largely non-cytopathic and, despite a high viral burden in infected subsets, promotes only modest cellular perturbations and inflammatory responses. Similar experimental outcomes are also observed after islet infection with endemic coronaviruses. Thus, the limits of pancreatic SARS-CoV-2 infection, even under in vitro conditions of enhanced virus exposure, challenge the proposition that in vivo targeting of β cells by SARS-CoV-2 precipitates new-onset diabetes. Whether restricted pancreatic damage and immunological alterations accrued by COVID-19 increase cumulative diabetes risk, however, remains to be evaluated.
Identifiants
pubmed: 35247306
pii: S2211-1247(22)00244-3
doi: 10.1016/j.celrep.2022.110508
pmc: PMC8858708
pii:
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
110508Subventions
Organisme : NIAID NIH HHS
ID : P01 AI042288
Pays : United States
Organisme : NIAID NIH HHS
ID : U54 AI142766
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI150748
Pays : United States
Organisme : NIDDK NIH HHS
ID : UC4 DK116284
Pays : United States
Organisme : NIH HHS
ID : S10 OD026880
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI134971
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK130425
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK020541
Pays : United States
Organisme : NIH HHS
ID : S10 OD030463
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI135972
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI151029
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK104162
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK123716
Pays : United States
Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests The A.G.-S. laboratory has received research support from Pfizer, Senhwa Biosciences, Kenall Manufacturing, Avimex, Johnson & Johnson, Dynavax, 7Hills Pharma, Pharmamar, ImmunityBio, Accurius, Nanocomposix, Hexamer, N-fold LLC, Model Medicines, and Merck outside of the reported work. A.G.-S. has consulting agreements outside of the reported work for the following companies, involving cash and/or stock: Vivaldi Biosciences, Contrafect, 7Hills Pharma, Avimex, Vaxalto, Pagoda, Accurius, Esperovax, Farmak, Applied Biological Laboratories, and Pfizer. A.G.-S. is an inventor on patents and patent applications on the use of antivirals and vaccines for the treatment and prevention of virus infections and cancer, owned by the Icahn School of Medicine at Mount Sinai, New York, outside of the reported work.
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