Evidence map›Paper›PMID 30072995›Full record

ArticleFrontiers in immunology2018

TLR-3 Stimulation Skews M2 Macrophages to M1 Through IFN-αβ Signaling and Restricts Tumor Progression.

Aurobind Vidyarthi, Nargis Khan, Tapan Agnihotri, Shikha Negi, Deepjyoti K Das, Mohammad Aqdas, Deepyan Chatterjee, Oscar R Colegio, Manoj K Tewari, Javed N Agrewala

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 2 pooled it
5.1field-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

97 citing papers in PubMed, 2 syntheses or guidelines pooled it, 152 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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  5. Macrophages in oncoviral infections: from immune regulators to therapeutic targets.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  6. Article
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  10. TIM-3+ Macrophages: Insights into Their Role in Cancer and Inflammation.International journal of molecular sciences · 2026
    Review
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  14. Article
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37 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 2 countries.

Aurobind VidyarthiImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Nargis KhanImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Tapan AgnihotriImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Shikha NegiImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Deepjyoti K DasImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Mohammad AqdasImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Deepyan ChatterjeeImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Oscar R ColegioDepartment of Dermatology, Yale University School of Medicine, New Haven, CT, United States.
Manoj K TewariDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Javed N AgrewalaImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Institute of Microbial Technology · INPost Graduate Institute of Medical Education and Research · INYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During tumor progression, macrophages shift their protective M1-phenotype to pro-tumorigenic M2-subtype. Therefore, conversion of M2 to M1 phenotype may be a potential therapeutic intervention. TLRs are important pathogen recognition receptors expressed by cells of the immune system. Recently, a crucial role of TLR-3 has been suggested in cancer. Consequently, in the current study, we defined the role of TLR-3 in the reversion of M2-macrophages to M1. We analyzed the role of TLR-3 stimulation for skewing M2-macrophages to M1 at mRNA and protein level through qRT-PCR, flow cytometry, western blotting, and ELISA. The effectiveness of TLR-3L stimulation to revert M2-macrophages to M1 was evaluated in the murine tumor model. To determine the role of IFN-αβ signaling

Indexed as

CD206IFN-αβTim-3TLR-3tumor-associated macrophagestumor microenvironment

Identifiers

PMID30072995
PMCPMC6060442
OpenAlexW2834234275

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.