Evidence map›Paper›PMID 31358659›Full record

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

Immune Response Resetting in Ongoing Sepsis.

Alexandre E Nowill, Márcia C Fornazin, Maria C Spago, Vicente Dorgan Neto, Vitória R P Pinheiro, Simônia S S Alexandre, Edgar O Moraes, Gustavo H M F Souza, Marcos N Eberlin, Lygia A Marques and 3 more

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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

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  11. Prolonged Transcriptional Consequences in Survivors of Sepsis.International journal of molecular sciences · 2021
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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

13 authors at 5 institutions in 2 countries.

Alexandre E NowillIntegrated Center for Pediatric OncoHaematological Research, State University of Campinas, Campinas 13083-888, Brazil; aen@nowill.com.br.ORCID 0000-0003-0648-6913
Márcia C FornazinIntegrated Center for Pediatric OncoHaematological Research, State University of Campinas, Campinas 13083-888, Brazil.
Maria C SpagoIntegrated Center for Pediatric OncoHaematological Research, State University of Campinas, Campinas 13083-888, Brazil.
Vicente Dorgan NetoSurgery Department, Santa Casa School of Medical Sciences, São Paulo 01221-020, Brazil.ORCID 0000-0003-1393-1915
Vitória R P PinheiroIntegrated Center for Pediatric OncoHaematological Research, State University of Campinas, Campinas 13083-888, Brazil.
Simônia S S AlexandreIntegrated Center for Pediatric OncoHaematological Research, State University of Campinas, Campinas 13083-888, Brazil; aen@nowill.com.br.
Edgar O MoraesSchool of Engineering, Mackenzie Presbyterian University, São Paulo 01302-907, Brazil.
Gustavo H M F SouzaMass Spectrometry Research and Development Laboratory, Health Sciences Department, Waters Corporation, Barueri 06455-020, Brazil.ORCID 0000-0002-9410-8578
Marcos N EberlinSchool of Engineering, Mackenzie Presbyterian University, São Paulo 01302-907, Brazil.
Lygia A MarquesThomson Mass Spectrometry Laboratory, Institute of Chemistry, State University of Campinas, Campinas 13083-859, Brazil; and.
Eduardo C MeurerThomson Mass Spectrometry Laboratory, Institute of Chemistry, State University of Campinas, Campinas 13083-859, Brazil; and.ORCID 0000-0003-4835-7773
Gilberto C FranchiIntegrated Center for Pediatric OncoHaematological Research, State University of Campinas, Campinas 13083-888, Brazil.ORCID 0000-0002-8138-7088
Pedro O de Campos-LimaBoldrini Children's Center, Campinas 13083-210, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade Presbiteriana Mackenzie · BRCentro Infantil Boldrini · BRFaculdade de Ciências Médicas da Santa Casa de São Paulo · BRWaters (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cure of severe infections, sepsis, and septic shock with antimicrobial drugs is a challenge because morbidity and mortality in these conditions are essentially caused by improper immune response. We have tested the hypothesis that repeated reactivation of established memory to pathogens may reset unfavorable immune responses. We have chosen for this purpose a highly stringent mouse model of polymicrobial sepsis by cecum ligation and puncture. Five weeks after priming with a diverse Ag pool, high-grade sepsis was induced in C57BL/6j mice that was lethal in 24 h if left untreated. Antimicrobial drug (imipenem) alone rescued 9.7% of the animals from death, but >5-fold higher cure rate could be achieved by combining imipenem and two rechallenges with the Ag pool (

Indexed as

AnimalsApoptosisCD3 ComplexCD8-Positive T-LymphocytesCecumCytokinesDisease Models, AnimalFemaleImmunologic MemoryInflammationLipidomicsLysophosphatidylcholinesMiceMice, Inbred C57BLPhosphatidylcholinesProteomicsCD3 ComplexCytokinesLysophosphatidylcholinesPhosphatidylcholines

Identifiers

PMID31358659
PMCPMC6697741
OpenAlexW2965819126

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.