Evidence map›Paper›PMID 34160239›Full record

ArticlemSphere2021

Replication Kinetics, Cell Tropism, and Associated Immune Responses in SARS-CoV-2- and H5N1 Virus-Infected Human Induced Pluripotent Stem Cell-Derived Neural Models.

Lisa Bauer, Bas Lendemeijer, Lonneke Leijten, Carmen W E Embregts, Barry Rockx, Steven A Kushner, Femke M S de Vrij, Debby van Riel

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. iPSC-derived human cortical organoids display profound alterations of cellular homeostasis following SARS-CoV-2 infection and Spike protein exposure.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  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

8 authors at 1 institution in 1 country.

Lisa Bauer *Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Bas Lendemeijer *Department of Psychiatry, Erasmus Medical Center, Rotterdam, The Netherlands.
Lonneke LeijtenDepartment of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Carmen W E EmbregtsDepartment of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Barry RockxDepartment of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Steven A KushnerDepartment of Psychiatry, Erasmus Medical Center, Rotterdam, The Netherlands.
Femke M S de Vrij *Department of Psychiatry, Erasmus Medical Center, Rotterdam, The Netherlands.
Debby van Riel *Department of Viroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
Erasmus MC · NL

Funding

Erasmus MC HUman Disease Model AwardEUR FellowshipNederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO) 024.003.001Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO) 91718308
6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is associated with a wide variety of neurological complications. Even though SARS-CoV-2 is rarely detected in the central nervous system (CNS) or cerebrospinal fluid, evidence is accumulating that SARS-CoV-2 might enter the CNS via the olfactory nerve. However, what happens after SARS-CoV-2 enters the CNS is poorly understood. Therefore, we investigated the replication kinetics, cell tropism, and associated immune responses of SARS-CoV-2 infection in different types of neural cultures derived from human induced pluripotent stem cells (hiPSCs). SARS-CoV-2 was compared to the neurotropic and highly pathogenic H5N1 influenza A virus. SARS-CoV-2 infected a minority of individual mature neurons, without subsequent virus replication and spread, despite angiotensin-converting enzyme 2 (ACE2), transmembrane protease serine 2 (TMPRSS2), and neuropilin-1 (NPR1) expression in all cultures. However, this sparse infection did result in the production of type III interferons and interleukin-8 (IL-8). In contrast, H5N1 virus replicated and spread very efficiently in all cell types in all cultures. Taken together, our findings support the hypothesis that neurological complications might result from local immune responses triggered by virus invasion, rather than abundant SARS-CoV-2 replication in the CNS.

Indexed as

Viral TropismVirus ReplicationAnimalsBrain DiseasesChlorocebus aethiopsCOVID-19DogsHumansInduced Pluripotent Stem CellsInfluenza A Virus, H5N1 SubtypeKineticsMadin Darby Canine Kidney CellsNeuronsSARS-CoV-2Vero CellscoronavirusCOVID-19H5N1 virushiPSC neuronsIL-8influenza A virusinfluenza virusinterferonneurotropismSARS-CoV-2

Identifiers

PMID34160239
PMCPMC8265642
OpenAlexW3175303672

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.