Evidence map›Paper›PMID 26451326›Full record

ArticleOncoimmunology2015

Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages.

Aya Kakizaki, Taku Fujimura, Sadanori Furudate, Yumi Kambayashi, Takeshi Yamauchi, Hideo Yagita, Setsuya Aiba

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2015. 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
3.6field-weighted citation impact, top 6% 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, 74 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Aya KakizakiDepartment of Dermatology; Tohoku University Graduate School of Medicine ; Sendai, Japan.
Taku FujimuraDepartment of Dermatology; Tohoku University Graduate School of Medicine ; Sendai, Japan.
Sadanori FurudateDepartment of Dermatology; Tohoku University Graduate School of Medicine ; Sendai, Japan.
Yumi KambayashiDepartment of Dermatology; Tohoku University Graduate School of Medicine ; Sendai, Japan.
Takeshi YamauchiDepartment of Dermatology; Tohoku University Graduate School of Medicine ; Sendai, Japan.
Hideo YagitaDepartment of Immunology; Juntendo University School of Medicine ; Tokyo, Japan.
Setsuya AibaDepartment of Dermatology; Tohoku University Graduate School of Medicine ; Sendai, Japan.
Tohoku University · JPJuntendo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An imbalance of immunosuppressive cells and cytotoxic cells plays an important role in the tumor-bearing host. Together with regulatory T cells (Tregs), tumor-associated macrophages (TAMs) play roles in maintaining the tumor microenvironment. Since interferon beta (IFN-β) has been clinically used for the treatment of malignant melanoma, we investigated the immunomodulatory effect of IFN-β during melanoma growth to elucidate the effects of IFN-β on the tumor microenvironment by using the B16F10 melanoma model. Peritumorally administered IFN-β significantly decreased the mRNA expression and production of Th2-related chemokines, which suppressed the recruitment of Tregs in B16F10 melanoma. Since the administration of IFN-β augments the expression of PD-1 on TILs, the co-administration of anti-PD-1 Ab augmented the therapeutic effect of IFN-β for the treatment of B16F10 melanoma. Moreover, in parallel with the mouse model, in the human system, IFN-β decreased the production of Th2-related chemokines and augmented the production of Th1-related chemokines from monocyte-derived M2 macrophages. Since these immunomodulatory effects of IFN-β on macrophages were also observed in the lesional skin of human in-transit melanoma, our present data suggest one of the possible immunomodulatory effects of IFN-β and support the possibility of IFN-β in combination with anti-PD-1 Ab for the treatment of melanoma.

Indexed as

IFN-βin-transit melanomaPD-1regulatory T cellstumor-associated macrophages

Identifiers

PMID26451326
PMCPMC4589056
OpenAlexW2414978187

What OpenQuestion holds

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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.