Evidence map›Paper›PMID 33239416›Full record

ArticleJournal for immunotherapy of cancer2020

Preclinical platform for long-term evaluation of immuno-oncology drugs using hCD34+ humanized mouse model.

Nahee Park, Kamal Pandey, Sei Kyung Chang, Ah-Young Kwon, Young Bin Cho, Jin Hur, Nar Bahadur Katwal, Seung Ki Kim, Seung Ah Lee, Gun Woo Son and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Humanized mouse models for immuno-oncology research.Nature reviews. Clinical oncology · 2023
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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

13 authors at 1 institution in 1 country.

Nahee ParkHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea.ORCID 0000-0003-2146-6996
Kamal PandeyHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea.ORCID 0000-0003-2144-0577
Sei Kyung ChangDepartment of Radiation Oncology, CHA Bundang Medical Center, Seongnam, South Korea.
Ah-Young KwonDepartment of Pathology, CHA Bundang Medical Center, Seongnam, South Korea.
Young Bin ChoHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea.
Jin HurHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea.
Nar Bahadur KatwalHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea.
Seung Ki KimDepartment of Surgery, CHA Bundang Medical Center, Seongnam, South Korea.
Seung Ah LeeDepartment of Surgery, CHA Bundang Medical Center, Seongnam, South Korea.
Gun Woo SonHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea.
Jong Min JoHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea.
Hee Jung AhnDepartment of Pathology, CHA Bundang Medical Center, Seongnam, South Korea.
Yong Wha MoonHematology and Oncology, Department of Internal Medicine, CHA Bundang Medical Center, Seongnam, South Korea ymoon@cha.ac.kr.ORCID 0000-0002-7943-974X
CHA University Bundang Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWell-characterized preclinical models are essential for immune-oncology research. We investigated the feasibility of our humanized mouse model for evaluating the long-term efficacy of immunotherapy and biomarkers.

methodsHumanized mice were generated by injecting human fetal cord blood-derived CD34+ hematopoietic stem cells to NOD-scid IL2rγnull (NSG) mice myeloablated with irradiation or busulfan. The humanization success was defined as a 25% or higher ratio of human CD45+ cells to mice peripheral blood mononuclear cells.

resultsBusulfan was ultimately selected as the appropriate myeloablative method because it provided a higher success rate of humanization (approximately 80%) and longer survival time (45 weeks). We proved the development of functional T cells by demonstrating the anticancer effect of the programmed cell death-1 (PD-1) inhibitor in our humanized mice but not in non-humanized NSG mice. After confirming the long-lasting humanization state (45 weeks), we further investigated the response durability of the PD-1 inhibitor and biomarkers in our humanized mice. Early increase in serum tumor necrosis factor α levels, late increase in serum interleukin 6 levels and increase in tumor-infiltrating CD8+ T lymphocytes correlated more with a durable response over 60 days than with a non-durable response.

conclusionsOur CD34+ humanized mouse model is the first in vivo platform for testing the long-term efficacy of anticancer immunotherapies and biomarkers, given that none of the preclinical models has ever been evaluated for such a long duration.

Indexed as

AnimalsAntigens, CD34Disease Models, AnimalHumansImmunotherapyMiceAntigens, CD34immunotherapy

Identifiers

PMID33239416
PMCPMC7689593
OpenAlexW3107482518

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.