Evidence map›Paper›PMID 38824851›Full record

ArticleThe Journal of surgical research2024

invariant Natural Killer T Cells Modulate the Peritoneal Macrophage Response to Polymicrobial Sepsis.

Daithi S Heffernan, Tristen T Chun, Sean F Monaghan, Chun-Shiang Chung, Alfred Ayala

Abstract read
In one paragraph

Article in The Journal of surgical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

5 authors.

Daithi S HeffernanDivision of Surgical Research, Department of Surgery, Brown University, Rhode Island Hospital, Providence, Rhode Island. Electronic address: DHeffernan@Brown.edu.
Tristen T ChunDivision of Surgical Research, Department of Surgery, Brown University, Rhode Island Hospital, Providence, Rhode Island.
Sean F MonaghanDivision of Surgical Research, Department of Surgery, Brown University, Rhode Island Hospital, Providence, Rhode Island.
Chun-Shiang ChungDivision of Surgical Research, Department of Surgery, Brown University, Rhode Island Hospital, Providence, Rhode Island.
Alfred AyalaDivision of Surgical Research, Department of Surgery, Brown University, Rhode Island Hospital, Providence, Rhode Island.

Funding

Mechanisms of Immune Dysfunction and Morbid Outcome in Response to Shock/SepsisR35GM118097 · NIGMS · RHODE ISLAND HOSPITAL · PI AYALA, ALFRED · 2016 to 2025
$6.3M
DIFFERENTIAL EFFECTS OF SEPSIS ON MACROPHAGE FUNCTIONR01GM046354 · NIGMS · RHODE ISLAND HOSPITAL (PROVIDENCE, RI) · PI AYALA, ALFRED · 1999 to 2016
$4.5M
Improving Sepsis Care with Deep RNA Sequencing DataR35GM142638 · NIGMS · RHODE ISLAND HOSPITAL · PI Sean Farrell Monaghan · 2021 to 2026
$2.6M
Sepsis Induced Changes in iNKT-Cells and their Effect on Phagocyte FunctionK08GM110495 · NIGMS · RHODE ISLAND HOSPITAL · PI HEFFERNAN, DAVID · 2015 to 2018
$786k
NIGMS NIH HHS K08 GM110495NIGMS NIH HHS R01 GM046354NIGMS NIH HHS R35 GM118097NIGMS NIH HHS R35 GM142638
6 · The paper itself

Abstract

introductionA dysregulated immune system is a major driver of the mortality and long-term morbidity from sepsis. With respect to macrophages, it has been shown that phenotypic changes are critical to effector function in response to acute infections, including intra-abdominal sepsis. Invariant natural killer T cells (iNKT cells) have emerged as potential central regulators of the immune response to a variety of infectious insults. Specifically, various iNKT cell:macrophage interactions have been noted across a spectrum of diseases, including acute events such as sepsis. However, the potential for iNKT cells to affect peritoneal macrophages during an abdominal septic event is as yet unknown.

methodsCecal ligation and puncture (CLP) was performed in both wild type (WT) and invariant natural killer T cell knockout (iNKT-/-) mice. 24 h following CLP or sham operation, peritoneal macrophages were collected for analysis. Analysis of macrophage phenotype and function was undertaken to include analysis of bactericidal activity and cytokine or superoxide production.

resultsWithin iNKT

conclusionsThe observations indicate that iNKT cells affect specific phenotypic and functional aspects of peritoneal macrophages during polymicrobial sepsis. Given that pharmacologic agents that affect iNKT cell functioning are currently in clinical trial, these findings may have the potential for translation to critically ill surgical patients with abdominal sepsis.

Indexed as

Macrophages, PeritonealMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsSepsisAnimalsCytokinesDisease Models, AnimalMaleMiceSuperoxidesCytokinesSuperoxidesIntra-abdominal sepsisInvariant natural killer T cellsPeritoneal macrophagesSepsis

Identifiers

PMID38824851
PMCPMC11246799

What OpenQuestion holds

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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.