Evidence map›Paper›PMID 37895424›Full record

ArticleLife (Basel, Switzerland)2023

Anti-CD20 Antibody and Calcineurin Inhibitor Combination Therapy Effectively Suppresses Antibody-Mediated Rejection in Murine Orthotopic Lung Transplantation.

Hiroki Matsumoto, Hidemi Suzuki, Takahiro Yamanaka, Taisuke Kaiho, Atsushi Hata, Terunaga Inage, Takamasa Ito, Toshiko Kamata, Kazuhisa Tanaka, Yuichi Sakairi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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 3 institutions in 1 country.

Hiroki MatsumotoDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Hidemi SuzukiDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.ORCID 0000-0002-8983-433X
Takahiro YamanakaDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Taisuke KaihoDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Atsushi HataDepartment of General Thoracic Surgery, Chiba Cancer Center, Chiba 260-8717, Japan.
Terunaga InageDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Takamasa ItoDepartment of General Thoracic Surgery, Chiba Cancer Center, Chiba 260-8717, Japan.
Toshiko KamataDepartment of Thoracic Surgery, International University of Health and Welfare Atami Hospital, Shizuoka 413-0012, Japan.
Kazuhisa TanakaDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Yuichi SakairiDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.ORCID 0000-0003-0222-0253
Shinichiro MotohashiDepartment of Medical Immunology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Ichiro YoshinoDepartment of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Chiba University · JPChiba Cancer Center · JPInternational University Of Health And Welfare Atami Hospital · JP

Funding

Kaken Pharmaceutical (Japan) JP20K17739
6 · The paper itself

Abstract

Antibody-mediated rejection (AMR) is a risk factor for chronic lung allograft dysfunction, which impedes long-term survival after lung transplantation. There are no reports evaluating the efficacy of the single use of anti-CD20 antibodies (aCD20s) in addition to calcineurin inhibitors in preventing AMR. Thus, this study aimed to evaluate the efficacy of aCD20 treatment in a murine orthotopic lung transplantation model. Murine left lung transplantation was performed using a major alloantigen strain mismatch model (BALBc (H-2d) → C57BL/6 (BL/6) (H-2b)). There were four groups: isograft (BL/6→BL/6) (Iso control), no-medication (Allo control), cyclosporine A (CyA) treated, and CyA plus murine aCD20 (CyA+aCD20) treated groups. Severe neutrophil capillaritis, arteritis, and positive lung C4d staining were observed in the allograft model and CyA-only-treated groups. These findings were significantly improved in the CyA+aCD20 group compared with those in the Allo control and CyA groups. The B cell population in the spleen, lymph node, and graft lung as well as the levels of serum donor-specific IgM and interferon γ were significantly lower in the CyA+aCD20 group than in the CyA group. Calcineurin inhibitor-mediated immunosuppression combined with aCD20 therapy effectively suppressed AMR in lung transplantation by reducing donor-specific antibodies and complement activation.

Indexed as

antibody-mediated rejectionanti-CD20 antibodiescalcineurin inhibitorsdonor specific antibodieslung transplantation

Identifiers

PMID37895424
PMCPMC10608275
OpenAlexW4387572994

What OpenQuestion holds

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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.