Evidence map›Paper›PMID 40635602›Full record

ReviewInternational journal of cancer2025

CD86, the double agent: Significance of CD86 expression in B-cell malignancies.

Gábor Barna, Gábor Szalóki, Ágnes Márk, Anna Hunyadi, Csilla Kriston

Abstract readReview
In one paragraph

Review in International journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

5 authors.

Gábor BarnaDepartment of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-8895-3062
Gábor SzalókiDepartment of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Ágnes MárkDepartment of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Anna HunyadiDepartment of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Csilla KristonDepartment of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bypassing the anti-tumor functions of the immune system is one of the keys to tumor survival. Tumors, especially hematological tumors, produce or express factors that retune T and B cells to inhibit the immune response. Coreceptors CD28 and CTLA-4, and their ligands, CD80 and CD86, are involved in the immunological synapse and play an important role in immune processes. CD86 is widely expressed in hematological tumors, mainly of B-cell origin, and only a few studies are available about its role in the pathogenesis. This study discusses the importance of CD86 expression in hematological malignancies. Does its presence help or hinder the development and survival of tumor cells? The answer to this question will facilitate a more profound comprehension of the biology of hematological malignancies and the development of new therapeutic options.

Indexed as

B7-2 AntigenB-LymphocytesHematologic NeoplasmsLymphoma, B-CellAnimalsHumansB7-2 AntigenCD86 protein, humanB‐ALLCD86CLLdrug resistanceMM

Identifiers

PMID40635602
PMCPMC12407040

What OpenQuestion holds

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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.