Spatiotemporally organized immunomodulatory response to SARS-CoV-2 virus in primary human broncho-alveolar epithelia.

Immunology Microbiology biological sciences molecular biology

Journal

iScience
ISSN: 2589-0042
Titre abrégé: iScience
Pays: United States
ID NLM: 101724038

Informations de publication

Date de publication:
18 Aug 2023
Historique:
received: 08 03 2023
revised: 04 06 2023
accepted: 08 07 2023
medline: 31 7 2023
pubmed: 31 7 2023
entrez: 31 7 2023
Statut: epublish

Résumé

The COVID-19 pandemic continues to be a health crisis with major unmet medical needs. The early responses from airway epithelial cells, the first target of the virus regulating the progression toward severe disease, are not fully understood. Primary human air-liquid interface cultures representing the broncho-alveolar epithelia were used to study the kinetics and dynamics of SARS-CoV-2 variants infection. The infection measured by nucleoprotein expression, was a late event appearing between day 4-6 post infection for Wuhan-like virus. Other variants demonstrated increasingly accelerated timelines of infection. All variants triggered similar transcriptional signatures, an "early" inflammatory/immune signature preceding a "late" type I/III IFN, but differences in the quality and kinetics were found, consistent with the timing of nucleoprotein expression. Response to virus was spatially organized: CSF3 expression in basal cells and CCL20 in apical cells. Thus, SARS-CoV-2 virus triggers specific responses modulated over time to engage different arms of immune response.

Identifiants

pubmed: 37520727
doi: 10.1016/j.isci.2023.107374
pii: S2589-0042(23)01451-7
pmc: PMC10374611
doi:

Types de publication

Journal Article

Langues

eng

Pagination

107374

Subventions

Organisme : NCI NIH HHS
ID : U54 CA260560
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI142733
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA034196
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK130425
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI141609
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI160706
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI135972
Pays : United States
Organisme : NIAID NIH HHS
ID : 75N93021C00014
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The A.G.-S. laboratory has received research support from GSK, Pfizer, Senhwa Biosciences, Kenall Manufacturing, Blade Therapeutics, Avimex, Johnson & Johnson, Dynavax, 7Hills Pharma, Pharmamar, ImmunityBio, Accurius, Nanocomposix, Hexamer, N-fold LLC, Model Medicines, Atea Pharma, Applied Biological Laboratories and Merck, outside of the reported work. A.G.-S. has consulting agreements for the following companies involving cash and/or stock: Castlevax, Amovir, Vivaldi Biosciences, Contrafect, 7Hills Pharma, Avimex, Pagoda, Accurius, Esperovax, Farmak, Applied Biological Laboratories, Pharmamar, CureLab Oncology, CureLab Veterinary, Synairgen, Paratus and Pfizer, outside of the reported work. A.G.-S. has been an invited speaker in meeting events organized by Seqirus, Janssen, Abbott, and Astrazeneca. A.G.-S. is 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. The M.S. laboratory has received unrelated funding support in sponsored research agreements from Phio Pharmaceuticals, 7Hills Pharma, ArgenX, and Moderna. S.E.C. declares being an employee and stockholder at NanoString Technologies. K.P. is a stockholder in Cue Biopharma and Guardian Bio, scientific advisor to Cue Biopharma and Guardian Bio and co-founder of Guardian Bio. K.P. declares unrelated funding support from Guardian Bio (current) and MERCK (past). All additional authors declare no competing interests.

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Auteurs

Diana Cadena Castaneda (DC)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Sonia Jangra (S)

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Marina Yurieva (M)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Jan Martinek (J)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Megan Callender (M)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Matthew Coxe (M)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Angela Choi (A)

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Juan García-Bernalt Diego (J)

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Jianan Lin (J)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Te-Chia Wu (TC)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Florentina Marches (F)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Damien Chaussabel (D)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Peter Yu (P)

Hartford HealthCare Cancer Institute, Hartford, CT 06102, USA.

Andrew Salner (A)

Hartford HealthCare Cancer Institute, Hartford, CT 06102, USA.

Gabrielle Aucello (G)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Jonathan Koff (J)

Adult Cystic Fibrosis Program, Yale University, New Haven, CT 06519, USA.

Briana Hudson (B)

Nanostring Technologies, Translational Sciences, Seattle, WA 98109, USA.

Sarah E Church (SE)

Nanostring Technologies, Translational Sciences, Seattle, WA 98109, USA.

Kara Gorman (K)

Nanostring Technologies, Translational Sciences, Seattle, WA 98109, USA.

Esperanza Anguiano (E)

Nanostring Technologies, Translational Sciences, Seattle, WA 98109, USA.

Adolfo García-Sastre (A)

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Department of Medicine, Division of Infectious Diseases, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Adam Williams (A)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Michael Schotsaert (M)

Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Karolina Palucka (K)

The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.

Classifications MeSH