Evidence map›Paper›PMID 35969740›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Angiotensin II enhances bacterial clearance via myeloid signaling in a murine sepsis model.

Daniel E Leisman, Jamie R Privratsky, Jake R Lehman, Mabel N Abraham, Omar Y Yaipan, Mariana R Brewer, Ana Nedeljkovic-Kurepa, Christine C Capone, Tiago D Fernandes, Robert Griffiths and 6 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Neonatal critical illness is associated with pancytopenia development in childhood.medRxiv : the preprint server for health sciences · 2026
    Article
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  7. Vasoactive Agents in Burn Patients: Perspectives on Angiotensin-II.Journal of burn care & research : official publication of the American Burn Association · 2025
    Review
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  16. Angiotensin II-Real-Life Use and Literature Review.Medicina (Kaunas, Lithuania) · 2024
    Review
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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

16 authors at 3 institutions in 2 countries.

Daniel E LeismanDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital, Boston, MA 02114.ORCID 0000-0001-9670-9425
Jamie R PrivratskyDivision of Critical Care Medicine, Department of Anesthesiology, Duke University, Durham, NC 27708.
Jake R LehmanInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.ORCID 0000-0001-7965-5402
Mabel N AbrahamInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Omar Y YaipanInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Mariana R BrewerInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Ana Nedeljkovic-KurepaInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Christine C CaponeInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Tiago D FernandesInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Robert GriffithsDepartment of Medicine, Duke University and Durham VA Medical Centers, Durham, NC 27705.
William J SteinInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Marcia B GoldbergCenter for Bacterial Pathogenesis, Division of Infectious Disease, Massachusetts General Hospital, Boston, MA 02114.ORCID 0000-0003-4266-9733
Steven D CrowleyDepartment of Medicine, Duke University and Durham VA Medical Centers, Durham, NC 27705.
Rinaldo BellomoBroad Institute of MIT and Harvard, Cambridge, MA 02142.
Clifford S DeutschmanInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Matthew D TaylorInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, Hofstra-Northwell School of Medicine, Manhasset, NY 11030.
Feinstein Institute for Medical Research · USDuke University · USBroad Institute · US

Funding

Single-cell genomic profiling to identify immune signatures of bacterial sepsis in humansR01AI153142 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI FILBIN, MICHAEL, GOLDBERG, MARCIA B · 2021 to 2025
$5.0M
The interleukin-1 receptor regulates crosstalk between myeloid and renal tubular cells in hypertensionR01DK118019 · NIDDK · DUKE UNIVERSITY · PI CROWLEY, STEVEN D · 2019 to 2022
$1.7M
Orexinergic Modulation of Experimental SepsisR01GM121102 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DEUTSCHMAN, CLIFFORD SCOTT, PAVLOV, VALENTIN ATANASSOV · 2017 to 2020
$1.6M
The Role of the IL-1 Receptor in the AKI to CKD transitionK08GM132689 · NIGMS · DUKE UNIVERSITY · PI PRIVRATSKY, JAMIE R · 2019 to 2023
$900k
Effects of Memory T Cells on the Response to Cecal Ligation and PunctureK08GM132794 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI TAYLOR, MATTHEW DAVID · 2019 to 2022
$782k
The role of the M1 macrophage response in the progression of chronic kidney diseaseI01BX000893 · VA · DURHAM VA MEDICAL CENTER · PI Steven D Crowley · 2012 to 2026
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BLRD VA I01 BX000893NIAID NIH HHS R01 AI153142NIDDK NIH HHS R01 DK118019NIGMS NIH HHS K08 GM132689NIGMS NIH HHS K08 GM132794NIGMS NIH HHS R01 GM121102
6 · The paper itself

Abstract

Sepsis, defined as organ dysfunction caused by a dysregulated host-response to infection, is characterized by immunosuppression. The vasopressor norepinephrine is widely used to treat low blood pressure in sepsis but exacerbates immunosuppression. An alternative vasopressor is angiotensin-II, a peptide hormone of the renin-angiotensin system (RAS), which displays complex immunomodulatory properties that remain unexplored in severe infection. In a murine cecal ligation and puncture (CLP) model of sepsis, we found alterations in the surface levels of RAS proteins on innate leukocytes in peritoneum and spleen. Angiotensin-II treatment induced biphasic, angiotensin-II type 1 receptor (AT1R)-dependent modulation of the systemic inflammatory response and decreased bacterial counts in both the blood and peritoneal compartments, which did not occur with norepinephrine treatment. The effect of angiotensin-II was preserved when treatment was delivered remote from the primary site of infection. At an independent laboratory, angiotensin-II treatment was compared in LysM-Cre AT1aR

Indexed as

Angiotensin IIAnimalsBacteremiaDisease Models, AnimalMiceMice, Inbred C57BLMyeloid CellsNorepinephrineReceptor, Angiotensin, Type 1SepsisSignal TransductionAngiotensin IINorepinephrineReceptor, Angiotensin, Type 1angiotensin IIimmunityinnaterenin-angiotensin systemsepsisvasoconstrictor agents

Identifiers

PMID35969740
PMCPMC9407661
OpenAlexW4291804474

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.