Evidence map›Paper›PMID 42681422›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Modeling the Application of Chimeric Antigen Receptor T Cell Therapy to Eliminate Alloantibodies in Mice.

Caroline A Markmann, Vijay G Bhoj

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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
–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

0 citing papers in PubMed.

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

2 authors.

Caroline A MarkmannDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Vijay G BhojDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. vbhoj@pennmedicine.upenn.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cell therapy has begun to show clinical promise as a strategy for immune-modulation in non-malignant conditions. In a murine model, we have demonstrated the utility of CAR T cells targeting B cells and plasma cells for the elimination of alloantibodies that cause allograft rejection. We describe a method for producing murine CAR T cells, their functional assessment in vitro, as well as their application in an in vivo transplant model. Our methods include a CAR production phase that involves retrovirus production, T cell isolation, activation, transduction and passage, and assessment of CAR expression by flow cytometry. Then, we describe methods for studying CAR T function in vitro using a cytotoxicity assay and in vivo using an islet transplant model.

Indexed as

Immunotherapy, AdoptiveIsoantibodiesReceptors, Antigen, T-CellReceptors, Chimeric AntigenT-LymphocytesAnimalsB-LymphocytesFlow CytometryGraft RejectionHumansIslets of Langerhans TransplantationLymphocyte ActivationMiceRetroviridaeTransduction, GeneticIsoantibodiesReceptors, Antigen, T-CellReceptors, Chimeric AntigenAlloantibodyB cellsCAR T cellImmunotherapyPlasma cellsRetrovirusTransplant

Identifiers

PMID42681422

What OpenQuestion holds

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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.