Evidence map›Paper›PMID 39244214›Full record

ArticleJournal for immunotherapy of cancer2024

MHC class I and II-deficient humanized mice are suitable tools to test the long-term antitumor efficacy of immune checkpoint inhibitors and T-cell engagers.

Iñaki Eguren-Santamaria, Eva Fernández de Piérola, Gracián Camps, Paula Martín-Muñoz, María Campos, Doina Cuculescu, Inmaculada Aguilera-Buenosvinos, Inmaculada Rodríguez López, Rafael Salido-Vallejo, Raluca Alexandru and 5 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

15 authors.

Iñaki Eguren-SantamariaImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain.ORCID http://orcid.org/0000-0003-1581-3728
Eva Fernández de PiérolaImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain.
Gracián CampsImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain.
Paula Martín-MuñozImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain.
María CamposCIC energiGUNE, Alava, Spain.
Doina CuculescuClinical Trial Unit, Clínica Universidad de Navarra, Pamplona, Spain.
Inmaculada Aguilera-BuenosvinosDepartment of Preventive Medicine and Public Health, Universidad de Navarra, Pamplona, Spain.
Inmaculada Rodríguez LópezImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain.
Rafael Salido-VallejoDepartment of Dermatology, Clínica Universidad de Navarra, Pamplona, Spain.
Raluca AlexandruInstituto de Investigación Sanitaria de Navarra, Paplona, Spain.
Carlos E De AndreaInstituto de Investigación Sanitaria de Navarra, Paplona, Spain.
Laura Álvarez-GigliDepartment of Pathology, Clinica Universidad de Navarra, Pamplona, Spain.
Pedro BerraondoImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain.ORCID http://orcid.org/0000-0001-7410-1865
Ignacio MeleroImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain.ORCID http://orcid.org/0000-0002-1360-348X
Miguel F SanmamedImmunology and Immunotherapy, Centro de Investigación Médica Aplicada, Pamplona, Spain msanmamed@unav.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunodeficient mice engrafted with peripheral blood mononuclear cells (PBMCs) are models to study new cancer immunotherapy agents. However, this approach is associated with xenograft-versus-host disease (xGVHD), which starts early after PBMC transfer and limits the duration and interpretation of experiments. Here, we explore different approaches to overcome xGVHD and better support the development of cancer immunotherapies.

methodsImmunodeficient NOD-scid IL2Rg

resultsCD4

conclusionHumanized MHC-dKO immunodeficient mice allow and refine the preclinical testing of immunotherapy agents for which experimentation is precluded in conventional immunodeficient mice due to severe xGVHD.

Indexed as

Immune Checkpoint InhibitorsAnimalsGraft vs Host DiseaseHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHumansMiceMice, Inbred NODMice, SCIDT-LymphocytesXenograft Model Antitumor AssaysHistocompatibility Antigens Class IHistocompatibility Antigens Class IIImmune Checkpoint InhibitorsAntibodies, BispecificDrug Evaluation, PreclinicalImmune Checkpoint InhibitorsImmune ReconstitutionImmunologic Memory

Identifiers

PMID39244214
PMCPMC11381650

What OpenQuestion holds

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LicenceCC BY-NC
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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.