Evidence map›Paper›PMID 27183578›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Hemocyanins Stimulate Innate Immunity by Inducing Different Temporal Patterns of Proinflammatory Cytokine Expression in Macrophages.

Ta-Ying Zhong, Sergio Arancibia, Raimundo Born, Ricardo Tampe, Javiera Villar, Miguel Del Campo, Augusto Manubens, María Inés Becker

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Modified Hemocyanins fromMarine drugs · 2024
    Article
  6. Article
  7. Frontiers in immunology · 2024
    Article
  8. Assessment of theBiomedicines · 2023
    Article
  9. Antitumor Activity of Bioactive Compounds fromPharmaceuticals (Basel, Switzerland) · 2023
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Hemocyanins fromBiomedicines · 2020
    Article
  17. Article
  18. Article
  19. The Journal of biological chemistry · 2019
    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

8 authors at 2 institutions in 2 countries.

Ta-Ying ZhongFundación Ciencia y Tecnología para el Desarrollo, Santiago 7750269, Chile; and.ORCID 0000-0001-6442-8004
Sergio ArancibiaFundación Ciencia y Tecnología para el Desarrollo, Santiago 7750269, Chile; and.ORCID 0000-0002-3421-2920
Raimundo BornFundación Ciencia y Tecnología para el Desarrollo, Santiago 7750269, Chile; and.
Ricardo TampeFundación Ciencia y Tecnología para el Desarrollo, Santiago 7750269, Chile; and.
Javiera VillarFundación Ciencia y Tecnología para el Desarrollo, Santiago 7750269, Chile; and.ORCID 0000-0002-8581-4155
Miguel Del CampoFundación Ciencia y Tecnología para el Desarrollo, Santiago 7750269, Chile; and.ORCID 0000-0003-3300-9784
Augusto ManubensBiosonda Corporation, Santiago 7750269, Chile.ORCID 0000-0002-7931-4314
María Inés BeckerFundación Ciencia y Tecnología para el Desarrollo, Santiago 7750269, Chile; and Biosonda Corporation, Santiago 7750269, Chile mariaines.becker@fucited.cl.ORCID 0000-0002-9711-2222
Fundación para el Desarrollo de la Ecología · BOProduction Development Corporation · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemocyanins induce a potent Th1-dominant immune response with beneficial clinical outcomes when used as a carrier/adjuvant in vaccines and nonspecific immunostimulant in cancer. However, the mechanisms by which hemocyanins trigger innate immune responses, leading to beneficial adaptive immune responses, are unknown. This response is triggered by a proinflammatory signal from various components, of which macrophages are an essential part. To understand how these proteins influence macrophage response, we investigated the effects of mollusks hemocyanins with varying structural and immunological properties, including hemocyanins from Concholepas concholepas, Fissurella latimarginata, and Megathura crenulata (keyhole limpet hemocyanin), on cultures of peritoneal macrophages. Hemocyanins were phagocytosed and slowly processed. Analysis of this process showed differential gene expression along with protein levels of proinflammatory markers, including IL-1β, IL-6, IL-12p40, and TNF-α. An extended expression analysis of 84 cytokines during a 24-h period showed a robust proinflammatory response for F. latimarginata hemocyanin in comparison with keyhole limpet hemocyanin and C. concholepas hemocyanin, which was characterized by an increase in the transcript levels of M1 cytokines involved in leukocyte recruitment. These cytokine genes included chemokines (Cxcl1, Cxcl3, Cxcl5, Ccl2, and Ccl3), ILs (Il1b and Ifng), growth factors (Csf2 and Csf3), and TNF family members (Cd40lg). The protein levels of certain cytokines were increased. However, every hemocyanin maintains downregulated key M2 cytokine genes, including Il4 and Il5 Collectively, our data demonstrate that hemocyanins are able to trigger the release of proinflammatory factors with different patterns of cytokine expression, suggesting differential signaling pathways and transcriptional network mechanisms that lead to the activation of M1-polarized macrophages.

Indexed as

AnimalsCytokinesDown-RegulationGene Expression RegulationHemocyaninsImmunity, InnateMacrophagesMiceMice, Inbred C57BLTime FactorsTranscriptomeCytokinesHemocyanins

Identifiers

PMID27183578
PMCPMC4873724
OpenAlexW2337138803

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.