Evidence map›Paper›PMID 24365860›Full record

ArticleCritical care medicine2014

Immunological characterization of compensatory anti-inflammatory response syndrome in patients with severe sepsis: a longitudinal study*.

Henry G Gomez, Sandra M Gonzalez, Jessica M Londoño, Natalia A Hoyos, Cesar D Niño, Alba L Leon, Paula A Velilla, Maria T Rugeles, Fabián A Jaimes

Abstract read
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In one paragraph

Article in Critical care medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Temporal Transitions of the Hyperinflammatory and Hypoinflammatory Phenotypes in Critical Illness.American journal of respiratory and critical care medicine · 2025
    Observational
  3. Observational
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  10. The unleashing of the immune system in COVID-19 and sepsis: the calm before the storm?Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2020
    Article
  11. Review
  12. Article
  13. Review
  14. Immune therapy in sepsis: Are we ready to try again?Journal of the Intensive Care Society · 2018
    Review
  15. Article
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Henry G Gomez1Grupo Inmunovirologia, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia. 2Grupo Académico de Epidemiologia Clínica, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia. 3Departamento de Ciencias Básicas, Facultad Nacional de Salud Pública, Universidad de Antioquia, Medellín, Colombia. 4Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia. 5Departamento de Medicina Interna, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia. 6Unidad de Investigaciones, Hospital Pablo Tobón Uribe, Medellín, Colombia.
Sandra M Gonzalez
Jessica M Londoño
Natalia A Hoyos
Cesar D Niño
Alba L Leon
Paula A Velilla
Maria T Rugeles
Fabián A Jaimes
Universidad de Antioquia · COHospital Pablo Tobon Uribe · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo perform a complete immunological characterization of compensatory anti-inflammatory response syndrome in patients with sepsis and to explore the relationship between these changes and clinical outcomes of 28-day mortality and secondary infections.

designProspective single-center study conducted between April 2011 and December 2012.

settingICUs from Hospital Universitario San Vicente Fundación at Medellin, Colombia. PATIENTS: One hundred forty-eight patients with severe sepsis.

interventionsNone. MEASUREMENTS AND MAIN

resultsAt days 0, 1, 3, 5, 10, and 28, we determined the expression of HLA-DR in monocytes and the apoptosis and the proliferation index in T lymphocytes, as well as the levels of tumor necrosis factor-α, interleukin-6, interleukin-1β, interleukin-10, and transforming growth factor-β in both plasma and cell culture supernatants of peripheral blood mononuclear cells. The mean percentage of HLA-DR was 60.7 at enrollment and increased by 0.9% (95% CI, 0.7-1.2%) per day. The mean percentage of CD4 T cells and CD8 T cells AV+/7-AAD- at enrollment was 37.2% and 20.4%, respectively, but it diminished at a rate of -0.5% (95% CI, -0.7% to -0.3%) and -0.3% (95% CI, -0.4% to -0.2%) per day, respectively. Plasma levels of interleukin-6 and interleukin-10 were 290 and 166 pg/mL and decreased at a rate of -7.8 pg/mL (95% CI, -9.5 to -6.1 pg/mL) and -4 pg/mL (95% CI, -5.1 to -2.8 pg/mL) per day, respectively. After controlling for confounders, only sustained plasma levels of interleukin-6 increase the risk of death (hazard ratio 1.003; 95% CI, 1.001-1.006).

conclusionsWe found no evidence to support a two-phase model of sepsis pathophysiology. However, immunological variables did behave in a mixed and time-dependent manner. Further studies should evaluate changes over time of interleukin-6 plasma levels as a prognostic biomarker for critically ill patients.

Indexed as

AgedAPACHEApoptosisCell ProliferationComorbidityFemaleHLA-DR AntigensHumansInflammation MediatorsIntensive Care UnitsLeukocytes, MononuclearLongitudinal StudiesMaleMiddle AgedOrgan Dysfunction ScoresProspective StudiesHLA-DR AntigensInflammation Mediators

Identifiers

PMID24365860
OpenAlexW2076127324

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.