Evidence map›Paper›PMID 42108348›Full record

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

Measurement of T Cell Migration by T Cell-Dependent Bispecific Antibody in Cancer Cells and T Cell Cross-Linking.

Rikuto Nakamura, Ryo Tsumura, Takahiro Anzai, Ryutaro Asano, Masahiro Yasunaga

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

5 authors.

Rikuto NakamuraDivision of Developmental Therapeutics, EPOC, National Cancer Center, Kashiwa, Chiba, 277-8577, Japan.
Ryo TsumuraDivision of Developmental Therapeutics, EPOC, National Cancer Center, Kashiwa, Chiba, 277-8577, Japan.
Takahiro AnzaiDivision of Developmental Therapeutics, EPOC, National Cancer Center, Kashiwa, Chiba, 277-8577, Japan.
Ryutaro AsanoDepartment of Biotechnology and Life Science, Graduate School of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo, 184-8588, Japan.
Masahiro YasunagaDivision of Developmental Therapeutics, EPOC, National Cancer Center, Kashiwa, Chiba, 277-8577, Japan. mayasuna@east.ncc.go.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cell-dependent bispecific antibodies (TDBs) have revolutionized the treatment of innovative cancer therapies with their potent anti-tumor effects, especially against hematologic malignancies. T cell responses to TDBs induce T cell migration, which is believed to play an important role in drug efficacy. Effective migration of T cells within the tumor microenvironment increases their contact with tumor cells and enhances T cell activation and cytotoxic activity against tumor cells. In this protocol, we present a method using TDB co-culture supernatants and a trans-well to evaluate T cell migration. This will provide a reliable approach to analyze in detail the mechanism of T cell migration in TDB-mediated immunotherapy and contribute to improving its drug efficacy.

Indexed as

Antibodies, BispecificAntineoplastic Agents, ImmunologicalCell Migration Assays, LeukocyteT-LymphocytesCell MovementCoculture TechniquesHumansImmunotherapyLymphocyte ActivationNeoplasmsTumor MicroenvironmentAntibodies, BispecificAntineoplastic Agents, ImmunologicalBispecific antibodyT cell invasionT cell migrationTrans-well

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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.