Evidence map›Paper›PMID 35440562›Full record

ArticleNature communications2022

Differential effects of macrophage subtypes on SARS-CoV-2 infection in a human pluripotent stem cell-derived model.

Qizhou Lian, Kui Zhang, Zhao Zhang, Fuyu Duan, Liyan Guo, Weiren Luo, Bobo Wing-Yee Mok, Abhimanyu Thakur, Xiaoshan Ke, Pedram Motallebnejad and 22 more

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Single-Cell Insights Into Macrophage Subtypes in Pulmonary Infections.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Macrophages and Pulmonary Fibrosis.Current molecular medicine · 2025
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

32 authors.

Qizhou Lian *Cord Blood Bank Center, Cord Blood Bank, Guangzhou Institute of Eugenics and Perinatology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China. qzlian@hku.hk.ORCID 0000-0001-8189-7160
Kui Zhang *The Pritzker School of Molecular Engineering, the University of Chicago, Chicago, IL, 60637, USA.
Zhao Zhang *HKUMed Laboratory of Cellular Therapeutics, and Department of Medicine, the University of Hong Kong, Hong Kong SAR, China.
Fuyu Duan *Cord Blood Bank Center, Cord Blood Bank, Guangzhou Institute of Eugenics and Perinatology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Liyan Guo *Cord Blood Bank Center, Cord Blood Bank, Guangzhou Institute of Eugenics and Perinatology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Weiren LuoDepartment of Pathology, The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen Third People's Hospital, National Clinical Research Centre for Infectious Diseases, Shenzhen, China.ORCID 0000-0002-2762-6332
Bobo Wing-Yee MokDepartment of Microbiology and State Key Laboratory for Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Abhimanyu ThakurThe Pritzker School of Molecular Engineering, the University of Chicago, Chicago, IL, 60637, USA.
Xiaoshan KeThe Pritzker School of Molecular Engineering, the University of Chicago, Chicago, IL, 60637, USA.
Pedram MotallebnejadThe Pritzker School of Molecular Engineering, the University of Chicago, Chicago, IL, 60637, USA.
Vlad NicolaescuMicrobiology, Biosciences Division, the University of Chicago, Chicago, IL, 60637, USA.
Jonathan ChenMcCormick School of Engineering, Northwestern University, Chicago, IL, USA.
Chui Yan MaCord Blood Bank Center, Cord Blood Bank, Guangzhou Institute of Eugenics and Perinatology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Xiaoya ZhouHKUMed Laboratory of Cellular Therapeutics, and Department of Medicine, the University of Hong Kong, Hong Kong SAR, China.
Shuo HanSchool of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Teng HanDepartment of Medicine, Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, NY, 10021, USA.
Wei ZhangGenomic Resource Core Facility, Weill Cornell Medicine, New York, NY, 10065, USA.
Adrian Y TanGenomic Resource Core Facility, Weill Cornell Medicine, New York, NY, 10065, USA.
Tuo ZhangGenomic Resource Core Facility, Weill Cornell Medicine, New York, NY, 10065, USA.ORCID 0000-0001-5396-918X
Xing WangGenomic Resource Core Facility, Weill Cornell Medicine, New York, NY, 10065, USA.
Dong XuGenomic Resource Core Facility, Weill Cornell Medicine, New York, NY, 10065, USA.
Jenny XiangGenomic Resource Core Facility, Weill Cornell Medicine, New York, NY, 10065, USA.
Aimin XuState Key Laboratory of Pharmaceutical Biotechnology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.ORCID 0000-0002-0668-033X
Can LiaoCord Blood Bank Center, Cord Blood Bank, Guangzhou Institute of Eugenics and Perinatology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Fang-Ping HuangInstitute for Advanced Study (IAS), Shenzhen University, Shenzhen, China.
Ya-Wen ChenDepartment of Otolaryngology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Jie NaSchool of Medicine, Tsinghua University, Beijing, China.ORCID 0000-0003-1820-0548
Glenn RandallMicrobiology, Biosciences Division, the University of Chicago, Chicago, IL, 60637, USA.
Hung-Fat TseHKUMed Laboratory of Cellular Therapeutics, and Department of Medicine, the University of Hong Kong, Hong Kong SAR, China.
Zhiwei ChenAIDS Institute and Department of Microbiology, State Key Laboratory of Emergent Infectious Disease, The University of Hong Kong, Hong Kong, China.ORCID 0000-0002-4511-2888
Yin ChenDepartment of Pharmacology and Toxicology, School of Pharmacy, University of Arizona, Tucson, AZ, USA.
Huanhuan Joyce ChenThe Pritzker School of Molecular Engineering, the University of Chicago, Chicago, IL, 60637, USA. joycechen@uchicago.edu.ORCID 0000-0002-1446-7184

Funding

Investigation of sub-lineages in pulmonary neuroendocrine cells and identification of the cells of origin of small cell lung cancerR00CA226353 · NCI · UNIVERSITY OF CHICAGO · PI CHEN, JOYCE HUANHUAN · 2020 to 2022
$747k
Investigation of sub-lineages in pulmonary neuroendocrine cells and identification of the cells of origin of small cell lung cancerK99CA226353 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CHEN, JOYCE HUANHUAN · 2019 to 2019
$84k
NCI NIH HHS K99 CA226353NCI NIH HHS R00 CA226353
6 · The paper itself

Abstract

Dysfunctional immune responses contribute critically to the progression of Coronavirus Disease-2019 (COVID-19), with macrophages as one of the main cell types involved. It is urgent to understand the interactions among permissive cells, macrophages, and the SARS-CoV-2 virus, thereby offering important insights into effective therapeutic strategies. Here, we establish a lung and macrophage co-culture system derived from human pluripotent stem cells (hPSCs), modeling the host-pathogen interaction in SARS-CoV-2 infection. We find that both classically polarized macrophages (M1) and alternatively polarized macrophages (M2) have inhibitory effects on SARS-CoV-2 infection. However, M1 and non-activated (M0) macrophages, but not M2 macrophages, significantly up-regulate inflammatory factors upon viral infection. Moreover, M1 macrophages suppress the growth and enhance apoptosis of lung cells. Inhibition of viral entry using an ACE2 blocking antibody substantially enhances the activity of M2 macrophages. Our studies indicate differential immune response patterns in distinct macrophage phenotypes, which could lead to a range of COVID-19 disease severity.

Indexed as

COVID-19Pluripotent Stem CellsHumansLungMacrophagesSARS-CoV-2

Identifiers

PMID35440562
PMCPMC9018716

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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.