Evidence map›Paper›PMID 32614086›Full record

ArticleHistopathology2020

Insights into pathogenesis of fatal COVID-19 pneumonia from histopathology with immunohistochemical and viral RNA studies.

Jennifer L Sauter, Marina K Baine, Kelly J Butnor, Darren J Buonocore, Jason C Chang, Achim A Jungbluth, Matthias J Szabolcs, Sejal Morjaria, Sharon L Mount, Natasha Rekhtman and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Histopathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 5 pooled it
2.7field-weighted citation impact, top 6% 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

59 citing papers in PubMed, 5 syntheses or guidelines pooled it, 114 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Histopathological findings and clinicopathologic correlation in COVID-19: a systematic review.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
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  13. Alterations in platelet proteome signature and impaired platelet integrin αJournal of thrombosis and haemostasis : JTH · 2023
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  19. Anti-PF4 antibodies associated with disease severity in COVID-19.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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 1 country.

Jennifer L SauterDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID https://orcid.org/0000-0001-6987-2294
Marina K BaineDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Kelly J ButnorDepartment of Laboratory Medicine and Pathology, University of Vermont Medical Center, Burlington, VT, USA.
Darren J BuonocoreDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Jason C ChangDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Achim A JungbluthDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Matthias J SzabolcsDepartment of Pathology and Cell Biology, Columbia University, New York, NY, USA.
Sejal MorjariaInfectious Disease, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Sharon L MountDepartment of Laboratory Medicine and Pathology, University of Vermont Medical Center, Burlington, VT, USA.
Natasha RekhtmanDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Elena SelbsDepartment of Pathology, New York University Long Island School of Medicine, Mineola, NY, USA.
Zong-Mei ShengViral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Yongli XiaoViral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
David E KleinerCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.ORCID https://orcid.org/0000-0003-3442-4453
Stefania PittalugaCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.ORCID https://orcid.org/0000-0001-7688-1439
Jeffery K TaubenbergerViral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Amy V RapkiewiczDepartment of Pathology, New York University Long Island School of Medicine, Mineola, NY, USA.
William D TravisDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID https://orcid.org/0000-0003-3160-6729
Memorial Sloan Kettering Cancer Center · USNational Institutes of Health · USLong Island University · USUniversity of Vermont Medical Center · USColumbia University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Postmortem PathologyZICBC010685 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLEINER, DAVID ERWIN · 2009 to 2025
$14.3M
SARS-CoV-2 PathogenesisZIAAI001271 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI TAUBENBERGER, JEFFERY · 2020 to 2025
$3.1M
Intramural Research Program of the National Institutes of Health and National Institute of Allergy and Infectious Diseases (J.K.T.)NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

introductionWe describe post-mortem pulmonary histopathologic findings of COVID-19 pneumonia in patients with a spectrum of disease course, from rapid demise to prolonged hospitalisation. METHODS AND

resultsHistopathologic findings in post-mortem lung tissue from eight patients who died from COVID-19 pneumonia were reviewed. Immunohistochemistry (IHC) and next-generation sequencing (NGS) were performed to detect virus. Diffuse alveolar damage (DAD) was seen in all cases with a spectrum of acute phase and/or organising phase. IHC with monoclonal antibodies against SARS-CoV-2 viral nucleoprotein and spike protein detected virus in areas of acute but not organising DAD, with intracellular viral antigen and RNA expression seen predominantly in patients with duration of illness less than 10 days. Major vascular findings included thrombi in medium- and large-calibre vessels, platelet microthrombi detected by CD61 IHC and fibrin microthrombi.

conclusionsPresence of SARS-CoV-2 viral RNA by NGS early in the disease course and expression of viral antigen by IHC exclusively in the acute, but not in the organising phase of DAD, suggests that the virus may play a major role in initiating the acute lung injury of DAD, but when DAD progresses to the organising phase the virus may have been cleared from the lung by the patient's immune response. These findings suggest the possibility of a major change during the disease course of COVID-19 pneumonia that may have therapeutic implications. Frequent thrombi and microthrombi may also present potential targets for therapeutic intervention.

Indexed as

AdultAgedAutopsyBetacoronavirusCoronavirus InfectionsCOVID-19FemaleHumansImmunohistochemistryMaleMiddle AgedPandemicsPneumonia, ViralRNA, ViralSARS-CoV-2RNA, ViralCOVID-19diffuse alveolar damageimmunohistochemistrylung histopathologynext-generation sequencingSARS-CoV-2thrombiviral pneumonia

Identifiers

PMID32614086
PMCPMC7361244
OpenAlexW3039084627

What OpenQuestion holds

Textmetadata
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.