Evidence map›Paper›PMID 36762286›Full record

ArticleMediators of inflammation2023

Improved Antitumor Effect of NK Cells Activated by Neutrophils in a Bone Marrow Transplant Model.

Daisuke Nakato, Shotaro Iwamoto, Keishiro Amano, Takahiro Ito, Hidemi Toyoda, Ryo Hanaki, Mari Morimoto, Kaori Niwa, Isao Tawara, Kyoko Imanaka-Yoshida and 2 more

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 42% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 2 institutions in 1 country.

Daisuke NakatoDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0003-0458-4931
Shotaro IwamotoDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-7710-2449
Keishiro AmanoDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-1715-1601
Takahiro ItoDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0003-1008-647X
Hidemi ToyodaDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-4727-6050
Ryo HanakiDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0003-0010-112X
Mari MorimotoDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0001-5027-9781
Kaori NiwaDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-3217-3892
Isao TawaraDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-5426-9422
Kyoko Imanaka-YoshidaDepartment of Pathology and Matrix Biology, Mie University Graduate school of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-9147-4169
Masahiro OgawaDepartment of Pediatrics, National Hospital Organization Mie-Chuo Medical Center, 2158-5, Hisaimyojincho Hisai, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-5194-4576
Masahiro HirayamaDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Mie, Japan.ORCID https://orcid.org/0000-0002-6850-2782
Mie University · JPMie Chuo Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The licensing process mediated by inhibitory receptors of the Ly49 C-type lectin superfamily that recognizes self-major histocompatibility complex (MHC) class I in mice is essential for the proper antitumor function of natural killer (NK) cells. Several models for NK cell licensing can be exploited for adoptive immunotherapy for cancer. However, the appropriate adoptive transfer setting to induce efficient graft versus tumor/leukemia effects remains elusive, especially after hematopoietic stem cell transplantation (HSCT). In our previous experiment, we showed that intraperitoneal neutrophil administration with their corresponding NK receptor ligand-activated NK cells using congenic mice without HSCT. In this experiment, we demonstrate enhanced antitumor effects of licensed NK cells induced by weekly intraperitoneal injections of irradiated neutrophil-enriched peripheral blood mononuclear cells (PBMNCs) in recipient mice bearing lymphoma. Bone marrow transplantation was performed using BALB/c mice (H-2

Indexed as

Bone Marrow TransplantationLeukocytes, MononuclearLymphomaNeutrophilsAnimalsHistocompatibility Antigens Class IImmunotherapy, AdoptiveKiller Cells, NaturalLigandsMiceMice, Inbred BALB CTransplantation, HomologousHistocompatibility Antigens Class ILigands

Identifiers

PMID36762286
PMCPMC9904906
OpenAlexW4318695218

What OpenQuestion holds

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LicenceCC BY
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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.