Evidence map›Paper›PMID 36137009›Full record

ArticleScience translational medicine2022

SARS-CoV-2 infection drives an inflammatory response in human adipose tissue through infection of adipocytes and macrophages.

Giovanny J Martínez-Colón, Kalani Ratnasiri, Heping Chen, Sizun Jiang, Elizabeth Zanley, Arjun Rustagi, Renu Verma, Han Chen, Jason R Andrews, Kirsten D Mertz and 8 more

Open access · greenAbstract read
In one paragraph

Article in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% of its field
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

82 citing papers in PubMed, 1 synthesis or guideline pooled it, 116 citations in OpenAlex.

  1. Single-cell RNA sequencing offers novel perspectives in viral infection research.Frontiers in cellular and infection microbiology · 2026
    Pooled it
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  18. A survey of SARS-CoV-2 tropism.Infectious diseases & immunity · 2025
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22 more citing papers are in PubMed but not listed here.

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

18 authors at 5 institutions in 3 countries.

Giovanny J Martínez-ColónDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-6792-8004
Kalani RatnasiriProgram in Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-5953-0004
Heping ChenDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0003-0661-2705
Sizun JiangDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-6149-3142
Elizabeth ZanleyDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-1807-5399
Arjun RustagiDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-6921-1012
Renu VermaDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0003-1277-8824
Han ChenDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-1722-8736
Jason R AndrewsDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-5967-251X
Kirsten D MertzInstitute of Pathology, Cantonal Hospital Baselland, 4410 Liestal, Switzerland.ORCID 0000-0002-3074-6925
Alexandar TzankovInstitute of Medical Genetics and Pathology, University Hospital of Basel, University of Basel, 4056 Basel, Switzerland.ORCID 0000-0002-1100-3819
Dan AzaguryDepartment of Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-3992-8792
Jack BoydDepartment of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-3020-5280
Garry P NolanDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-8862-9043
Christian M SchürchDepartment of Pathology and Neuropathology, University Hospital and Comprehensive Cancer Center Tübingen, 72070 Tübingen, Germany.ORCID 0000-0002-1792-1768
Matthias S MatterInstitute of Medical Genetics and Pathology, University Hospital of Basel, University of Basel, 4056 Basel, Switzerland.ORCID 0000-0002-2005-5266
Catherine A BlishDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0001-6946-7627
Tracey L McLaughlinDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0002-4829-8649
Stanford University · USUniversity Hospital of Basel · CHBeth Israel Deaconess Medical Center · USChan Zuckerberg Initiative (United States) · USUniversity Children's Hospital Tübingen · DE

Funding

Diabetes, Endocrinology and Metabolism Training GrantT32DK007217 · NIDDK · STANFORD UNIVERSITY · PI Justin Pierce Annes, David Matthew Maahs · 1987 to 2026
$7.2M
EMERGING INFECTIOUS DISEASEST32AI007502 · NIAID · STANFORD UNIVERSITY · PI Prasanna Jagannathan, DAVID A. RELMAN · 1995 to 2026
$6.8M
Spatial-Temporal Dissection of Stratified Host Tissue Responses to Severe acute respiratory syndrome-related coronaviruses in situ to Understand Intra-host PathogenesisDP2AI171139 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Sizun Jiang · 2022 to 2026
$2.3M
Obesity and COVID-19: Role of Adipose TissueR21AI159024 · NIAID · STANFORD UNIVERSITY · PI MCLAUGHLIN, TRACEY · 2021 to 2022
$433k
NIAID NIH HHS DP2 AI171139NIAID NIH HHS R21 AI159024NIAID NIH HHS T32 AI007502NIDDK NIH HHS T32 DK007217
6 · The paper itself

Abstract

Obesity, characterized by chronic low-grade inflammation of the adipose tissue, is associated with adverse coronavirus disease 2019 (COVID-19) outcomes, yet the underlying mechanism is unknown. To explore whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection of adipose tissue contributes to pathogenesis, we evaluated COVID-19 autopsy cases and deeply profiled the response of adipose tissue to SARS-CoV-2 infection in vitro. In COVID-19 autopsy cases, we identified SARS-CoV-2 RNA in adipocytes with an associated inflammatory infiltrate. We identified two distinct cellular targets of infection: adipocytes and a subset of inflammatory adipose tissue-resident macrophages. Mature adipocytes were permissive to SARS-CoV-2 infection; although macrophages were abortively infected, SARS-CoV-2 initiated inflammatory responses within both the infected macrophages and bystander preadipocytes. These data suggest that SARS-CoV-2 infection of adipose tissue could contribute to COVID-19 severity through replication of virus within adipocytes and through induction of local and systemic inflammation driven by infection of adipose tissue-resident macrophages.

Indexed as

COVID-19RNA, ViralAdipose TissueAutopsyHumansSARS-CoV-2RNA, Viral

Identifiers

PMID36137009
PMCPMC9529056
OpenAlexW4296807072

What OpenQuestion holds

Textmetadata
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.