Evidence map›Paper›PMID 42356506›Full record

ReviewPharmaceuticals (Basel, Switzerland)2026

Engineering a Second Interchain Disulfide Bond in the αβ T-Cell Receptor Constant Domain: A Powerful Strategy to Enhance Stability, Pairing Fidelity, and Therapeutic Efficacy in TCR-T Cell Therapy.

Nguyen Trung Quan, Xiangliang Lin, Duong Thi Nhu Xuan, Bui Thi Van Anh

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 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

4 authors.

Nguyen Trung QuanDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong 999077, China.
Xiangliang LinEsco Aster Pte. Ltd., Singapore 139950, Singapore.ORCID 0009-0008-0250-6693
Duong Thi Nhu XuanCollege of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan.
Bui Thi Van AnhEsco Aster Pte. Ltd., Singapore 139950, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adoptive TCR-T cell therapy holds great promise for personalised cancer treatment, yet it is limited by poor surface expression, chain mispairing, and suboptimal stability of introduced TCRs. One effective structure-guided approach is to introduce a second interchain disulfide bond between the α and β constant domains. This review summarises the structural and mechanistic basis of this strategy, its impact on TCR folding, CD3 assembly, mechanotransduction, and anti-tumour function, as well as current engineering approaches, persistent challenges, and future perspectives. Preclinical studies demonstrate improved heterodimer stability, reduced mispairing, higher surface expression, and enhanced signalling, positioning the second disulfide bond as a valuable complementary tool in next-generation TCR engineering.

Indexed as

constant domaindisulfide bondimmunotherapyTCR-T

Identifiers

PMID42356506
PMCPMC13306150

What OpenQuestion holds

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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.