Evidence map›Paper›PMID 24765217›Full record

ArticleThe open inflammation journal2011

Pediatric Sepsis - Part V: Extracellular Heat Shock Proteins: Alarmins for the Host Immune System.

John S Giuliano, Patrick M Lahni, Hector R Wong, Derek S Wheeler

Open access · bronzeAbstract read
In one paragraph

Article in The open inflammation journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

30 citing papers in PubMed, 64 citations in OpenAlex.

  1. Trial
  2. Article
  3. Role of biomarkers in pediatric sepsis: What evidence says?World journal of clinical pediatrics · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Animal nutrition (Zhongguo xu mu shou yi xue hui) · 2023
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Plasma proteomics of green turtles (Conservation physiology · 2021
    Article
  17. Article
  18. The intersection between immunotherapy and laser interstitial thermal therapy: a multipronged future of neuro-oncology.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2020
    Review
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

John S GiulianoDivision of Critical Care Medicine, Yale-New Haven Children's Hospital; Department of Pediatrics, Yale University School of Medicine; New Haven, CT.
Patrick M LahniDivision of Critical Care Medicine, Cincinnati Children's Hospital, University of Cincinnati; Cincinnati, OH.
Hector R WongDivision of Critical Care Medicine, Cincinnati Children's Hospital, University of Cincinnati; Cincinnati, OH ; Department of Pediatrics, University of Cincinnati; Cincinnati, OH.
Derek S WheelerDivision of Critical Care Medicine, Cincinnati Children's Hospital, University of Cincinnati; Cincinnati, OH ; Department of Pediatrics, University of Cincinnati; Cincinnati, OH.
Cincinnati Children's Hospital Medical Center · US

Funding

The immunomodulatory effects of extracellular Hsp70K08GM077432 · NIGMS · CINCINNATI CHILDRENS HOSP MED CTR · PI WHEELER, DEREK S · 2006 to 2010
$605k
The Host Response to Calfactant for Direct Acute Lung Injury in Critically Ill ChR03HD058246 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI WHEELER, DEREK S · 2008 to 2009
$150k
NICHD NIH HHS R03 HD058246NIGMS NIH HHS K08 GM077432
6 · The paper itself

Abstract

Heat shock proteins (HSPs) are molecular chaperones that facilitate the proper folding and assembly of nascent polypeptides and assist in the refolding and stabilization of damaged polypeptides. Through these largely intracellular functions, the HSPs maintain homeostasis and assure cell survival. However, a growing body of literature suggests that HSPs have important effects in the extracellular environment as well. Extracellular HSPs are released from damaged or stressed cells and appear to act as local "danger signals" that activate stress response programs in surrounding cells. Importantly, extracellular HSPs have been shown to activate the host innate and adaptive immune response. With this in mind, extracellular HSPs are commonly included in a growing list of a family of proteins known as danger-associated molecular patterns (DAMPs) or alarmins, which trigger an immune response to tissue injury, such as may occur with trauma, ischemia-reperfusion injury, oxidative stress, etc. Extracellular HSPs, including Hsp72 (HSPA), Hsp27 (HSPB1), Hsp90 (HSPC), Hsp60 (HSPD), and Chaperonin/Hsp10 (HSPE) are especially attractrive candidates for DAMPs or alarmins which may be particularly relevant in the pathophysiology of the sepsis syndrome.

Identifiers

PMID24765217
PMCPMC3995031
OpenAlexW1968123001

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.