Evidence map›Paper›PMID 41949496›Full record

ArticleCurrent protocols2026

Co-Culture Systems to Study Epithelial-Immune Interactions During SARS-CoV-2 Infection.

Scott H Randell, Katherine C Barnett

Abstract read
In one paragraph

Article in Current protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Scott H RandellMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Katherine C BarnettDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID https://orcid.org/0000-0001-9552-5325

Funding

Vector CoreP30DK065988 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Scott H Randell · 2004 to 2026
$26.5M
Regulation of Pathologic Inflammasome Responses to SARS-CoV-2R00AI175479 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Katherine Camille Barnett · 2025 to 2026
$493k
Cystic Fibrosis Foundation ESTHER24R0Michigan Medicine, University of MichiganNIAID NIH HHS R00 AI175479NIDDK NIH HHS P30 DK065988NIH HHS AI175479NIH HHS DK065988
6 · The paper itself

Abstract

Robust inflammatory responses to viral infection are mediated by immune cell populations, including monocytes and dendritic cells. However, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) does not replicate efficiently in these cell types and instead preferentially infects epithelial cell subsets in the airway. Because of this, stimulation of inflammatory cytokine responses from immune cell populations during SARS-CoV-2 infection depends not only on interactions with viral particles but also interactions with infected epithelial cells. In this article, we describe two co-culture systems to study inflammatory cytokine responses generated by epithelial-immune interaction during SARS-CoV-2 infection in vitro. Basic Protocol 1 describes how to set up a partially primary co-culture system consisting of SARS-CoV-2-infected Vero-E6 cells and primary human peripheral blood mononuclear cells (PBMCs) to observe release of the inflammasome-regulated cytokine interleukin-1β (IL-1β). Basic Protocol 2 details a primary, human co-culture system that consists of SARS-CoV-2-infected primary human airway epithelia (HAE) grown at an air-liquid interface (ALI) and primary human PBMCs, and how to observe IL-1β and IL-6 crosstalk between these cell populations during infection. In these Basic Protocols, we include a description of the use of inhibitors in these systems to perturb cytokine responses. We also provide Support Protocols for the culture of HAE and Vero-E6 and for the isolation, storage, and preparation of PBMCs prior to use in these systems. © 2026 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: SARS-CoV-2 infection in a Vero-E6+PBMC co-culture system Support Protocol 1: Vero-E6 culture and passaging Support Protocol 2: Isolation and cryopreservation of PBMCs for use in co-culture Basic Protocol 2: SARS-CoV-2 infection in a primary HAE+PBMC co-culture system Support Protocol 3: Establishment and maturation of HAE grown at an ALI.

Indexed as

COVID-19Epithelial CellsSARS-CoV-2AnimalsChlorocebus aethiopsCoculture TechniquesCytokinesHumansInterleukin-1betaInterleukin-6Leukocytes, MononuclearVero CellsCytokinesInterleukin-1betaInterleukin-6human airway epitheliuminflammasomeinterleukin‐1βinterleukin‐6peripheral blood mononuclear cellsSARS‐CoV‐2

Identifiers

PMID41949496
PMCPMC13060367

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.