Evidence map›Paper›PMID 41401431›Full record

ArticleBioconjugate chemistry2026

A Tetrameric Biotin-Avidin Scaffold Using Anti-CD19 (FMC63) Traptavidin Fusion Enables High-Avidity CAR-T Cells for Leukemia Therapy.

Hae Li Ko, Young-Youb Kim, Deuk-Ki Lee, Youngheon Park, Younghyeon Kim, Soyi Chae, Dongbum Kim, Yongbin Bang, Sang Hoon Jung, Jeong-Im Sin and 1 more

Abstract read
In one paragraph

Article in Bioconjugate chemistry, 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

11 authors.

Hae Li KoEmerging Infectious Diseases Division, Scripps Korea Antibody Institute (SKAI), 199-10, Dugaebisan-ro, Hongcheon, Gangwon-do 25114, Republic of Korea.
Young-Youb KimResearch and Development Department, Helixmith Co., Ltd., Seoul 07794, Korea.
Deuk-Ki LeeEmerging Infectious Diseases Division, Scripps Korea Antibody Institute (SKAI), 199-10, Dugaebisan-ro, Hongcheon, Gangwon-do 25114, Republic of Korea.ORCID 0000-0003-1978-6229
Youngheon ParkEmerging Infectious Diseases Division, Scripps Korea Antibody Institute (SKAI), 199-10, Dugaebisan-ro, Hongcheon, Gangwon-do 25114, Republic of Korea.
Younghyeon KimEmerging Infectious Diseases Division, Scripps Korea Antibody Institute (SKAI), 199-10, Dugaebisan-ro, Hongcheon, Gangwon-do 25114, Republic of Korea.
Soyi ChaeEmerging Infectious Diseases Division, Scripps Korea Antibody Institute (SKAI), 199-10, Dugaebisan-ro, Hongcheon, Gangwon-do 25114, Republic of Korea.
Dongbum KimEmerging Infectious Diseases Division, Scripps Korea Antibody Institute (SKAI), 199-10, Dugaebisan-ro, Hongcheon, Gangwon-do 25114, Republic of Korea.
Yongbin BangAdvanced Institute of Convergence Technology, Seoul National University, Suwon-si, Gyeonggi-do 16229, Republic of Korea.
Sang Hoon JungNatural Product Drug Development Division, Korea Institute of Science and Technology (KIST), Gangneung 25451, Republic of Korea.
Jeong-Im SinDepartment of Microbiology, College of Medicine, Kangwon National University, Chuncheon, Gangwon-do 24341, Republic of Korea.
Sungjin LeeEmerging Infectious Diseases Division, Scripps Korea Antibody Institute (SKAI), 199-10, Dugaebisan-ro, Hongcheon, Gangwon-do 25114, Republic of Korea.ORCID 0009-0008-6615-392X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor-T cell (CAR-T) therapy shows promise for treating hematologic malignancies but faces limitations including insufficient CAR-T cell activation. We developed a novel tetramer CAR-T (tCAR-T) system targeting CD19, which is overexpressed in hematologic malignancies. We created a tetrameric antibody scaffold by linking anti-CD19 scFv to traptavidin, then engineered T cells expressing CD8 hinge, CD8 transmembrane, costimulatory domains (4-1BB, CD3ζ), and YFP, followed by biotinylation using biotin ligase. The tCAR-T system was assembled via biotin-avidin interaction. This tetrameric arrangement significantly enhanced antibody avidity, promoting stronger antigen engagement and demonstrating potent cytotoxicity against CD19

Indexed as

Antigens, CD19AvidinBiotinImmunotherapy, AdoptiveLeukemiaReceptors, Chimeric AntigenT-LymphocytesAnimalsCell Line, TumorHumansMiceAntigens, CD19AvidinBiotinReceptors, Chimeric Antigen

Identifiers

PMID41401431
PMCPMC12828715

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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.