Evidence map›Paper›PMID 31189573›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Sepsis-Induced State of Immunoparalysis Is Defined by Diminished CD8 T Cell-Mediated Antitumor Immunity.

Derek B Danahy, Samarchith P Kurup, Christina S Winborn, Isaac J Jensen, John T Harty, Thomas S Griffith, Vladimir P Badovinac

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
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  9. Review
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  13. Observational
  14. Article
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  16. Article
  17. NK Cell-Derived IL-10 Supports Host Survival during Sepsis.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  18. Observational
  19. Club Cell Protein 16 Attenuates CD16Journal of immunology research · 2021
    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

7 authors at 2 institutions in 1 country.

Derek B DanahyDepartment of Pathology, University of Iowa, Iowa City, IA 52242.ORCID 0000-0002-3481-8797
Samarchith P KurupDepartment of Microbiology and Immunology, University of Iowa, Iowa City, IA 52242; and.
Christina S WinbornDepartment of Pathology, University of Iowa, Iowa City, IA 52242.
Isaac J JensenDepartment of Pathology, University of Iowa, Iowa City, IA 52242.ORCID 0000-0002-3107-3961
John T HartyDepartment of Pathology, University of Iowa, Iowa City, IA 52242.ORCID 0000-0001-7266-2802
Thomas S GriffithDepartment of Urology, University of Minnesota, Minneapolis, MN 55414.ORCID 0000-0002-7205-9859
Vladimir P BadovinacDepartment of Pathology, University of Iowa, Iowa City, IA 52242; vladimir-badovinac@uiowa.edu.ORCID 0000-0003-3180-2439
University of Iowa · USUniversity of Minnesota · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
TRAINING IN MECHANISMS OF PARASITISMT32AI007511 · NIAID · UNIVERSITY OF IOWA · PI BUTLER, NOAH SULLIVAN, WEBER, MARY · 1996 to 2025
$8.1M
PREDOCTORAL TRAINING PROGRAM IN IMMUNOLOGYT32AI007485 · NIAID · UNIVERSITY OF IOWA · PI Kevin L Legge · 1995 to 2026
$5.4M
Memory CD8 T cell localization and protection from influenzaR01AI114543 · NIAID · UNIVERSITY OF IOWA · PI BADOVINAC, VLADIMIR P, HARTY, JOHN T · 2015 to 2024
$4.4M
Alterations in CD4 T cells during sepsisR01GM115462 · NIGMS · UNIVERSITY OF MINNESOTA · PI GRIFFITH, THOMAS S · 2016 to 2019
$1.2M
Impairment and recovery of CD8 T cell responses after sepsisR01GM113961 · NIGMS · UNIVERSITY OF IOWA · PI BADOVINAC, VLADIMIR P · 2015 to 2018
$1.2M
Using microbially-experienced mice to study the innate immune response in sepsisI01BX001324 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI GRIFFITH, THOMAS S · 2013 to 2025
–
BLRD VA I01 BX001324NCI NIH HHS P30 CA086862NIAID NIH HHS R01 AI114543NIAID NIH HHS T32 AI007485NIAID NIH HHS T32 AI007511NIGMS NIH HHS R01 GM113961NIGMS NIH HHS R01 GM115462
6 · The paper itself

Abstract

Patients who survive sepsis experience long-term immunoparalysis characterized by numerical and/or functional lesions in innate and adaptive immunity that increase the host's susceptibility to secondary complications. The extent to which tumor development/growth is affected in sepsis survivors remains unknown. In this study, we show cecal ligation and puncture (CLP) surgery renders mice permissive to increased B16 melanoma growth weeks/months after sepsis induction. CD8 T cells provide partial protection in this model, and tumors from sepsis survivors had a reduced frequency of CD8 tumor-infiltrating lymphocytes (TILs) concomitant with an increased tumor burden. Interestingly, the postseptic environment reduced the number of CD8 TILs with high expression of activating/inhibitory receptors PD-1 and LAG-3 (denoted PD-1

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CDCD8-Positive T-LymphocytesCecumCell Line, TumorCell ProliferationDisease Models, AnimalFemaleLymphocyte Activation Gene 3 ProteinLymphocyte CountLymphocytes, Tumor-InfiltratingMaleMelanoma, ExperimentalMiceMice, Inbred C57BLAntibodies, MonoclonalAntigens, CDLag3 protein, mouseLymphocyte Activation Gene 3 ProteinPdcd1 protein, mouseProgrammed Cell Death 1 Receptor

Identifiers

PMID31189573
PMCPMC6650357
OpenAlexW2949694356

What OpenQuestion holds

Textmetadata
LicenceTDM
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.