Evidence map›Paper›PMID 33923463›Full record

ReviewCancers2021

Anti-PD-1/PD-L1 Based Combination Immunotherapy to Boost Antigen-Specific CD8

Julia Peña-Asensio, Henar Calvo, Miguel Torralba, Joaquín Miquel, Eduardo Sanz-de-Villalobos, Juan-Ramón Larrubia

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
3.2field-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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Pooled it
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  6. Globulol fromFrontiers in pharmacology · 2026
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  20. Targeting T regulatory (TCancer drug resistance (Alhambra, Calif.) · 2024
    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

6 authors at 2 institutions in 1 country.

Julia Peña-AsensioTranslational Hepatology Unit, Guadalajara University Hospital, 19002 Gudalajara, Spain.ORCID 0000-0002-4220-1287
Henar CalvoTranslational Hepatology Unit, Guadalajara University Hospital, 19002 Gudalajara, Spain.
Miguel TorralbaTranslational Hepatology Unit, Guadalajara University Hospital, 19002 Gudalajara, Spain.
Joaquín MiquelTranslational Hepatology Unit, Guadalajara University Hospital, 19002 Gudalajara, Spain.
Eduardo Sanz-de-VillalobosTranslational Hepatology Unit, Guadalajara University Hospital, 19002 Gudalajara, Spain.
Juan-Ramón LarrubiaTranslational Hepatology Unit, Guadalajara University Hospital, 19002 Gudalajara, Spain.ORCID 0000-0002-6383-848X
Hospital Universitario de Guadalajara · ESUniversidad de Alcalá · ES

Funding

Gilead Sciences GLD14/00217Gilead Sciences GLD16/00014Instituto de Salud Carlos III PI19/00206
6 · The paper itself

Abstract

Thirty to fifty percent of hepatocellular carcinomas (HCC) display an immune class genetic signature. In this type of tumor, HCC-specific CD8 T cells carry out a key role in HCC control. Those potential reactive HCC-specific CD8 T cells recognize either HCC immunogenic neoantigens or aberrantly expressed host's antigens, but they become progressively exhausted or deleted. These cells express the negative immunoregulatory checkpoint programmed cell death protein 1 (PD-1) which impairs T cell receptor signaling by blocking the CD28 positive co-stimulatory signal. The pool of CD8 cells sensitive to anti-PD-1/PD-L1 treatment is the PD-1dim memory-like precursor pool that gives rise to the effector subset involved in HCC control. Due to the epigenetic imprints that are transmitted to the next generation, the effect of PD-1 blockade is transient, and repeated treatments lead to tumor resistance. During long-lasting disease, besides the TCR signaling impairment, T cells develop other failures that should be also set-up to increase T cell reactivity. Therefore, several PD-1 blockade-based combinatory therapies are currently under investigation such as adding antiangiogenics, anti-TGFβ1, blockade of other negative immune checkpoints, or increasing HCC antigen presentation. The effect of these combinations on CD8

Indexed as

CD8 T cell responsecombination therapyhepatocellular carcinomaimmune check-point inhibitorimmunotherapyPD-1PD-L1

Identifiers

PMID33923463
PMCPMC8073815
OpenAlexW3156424361

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.