Evidence map›Paper›PMID 35291652›Full record

ReviewImmune network2022

Development of Bispecific Antibody for Cancer Immunotherapy: Focus on T Cell Engaging Antibody.

Dain Moon, Nara Tae, Yunji Park, Seung-Woo Lee, Dae Hee Kim

Open access · diamondAbstract readReview
In one paragraph

Review in Immune network, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Dain MoonDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.ORCID https://orcid.org/0000-0001-5244-3215
Nara TaeGlobal/Gangwon Innovative Biologics Regional Leading Research Center (GIB-RLRC), Kangwon National University, Chuncheon 24341, Korea.ORCID https://orcid.org/0000-0002-9406-0367
Yunji ParkPohang University of Science and Technology (POSTECH) Biotech Center, POSTECH, Pohang 37673, Korea.ORCID https://orcid.org/0000-0003-0042-202X
Seung-Woo LeeDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea.ORCID https://orcid.org/0000-0002-6714-2463
Dae Hee KimCollege of Pharmacy, Kangwon National University, Chuncheon 24341, Korea.ORCID https://orcid.org/0000-0002-3845-0870
Pohang University of Science and Technology · KRKangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the era of immunotherapeutic control of cancers, many advances in biotechnology, especially in Ab engineering, have provided multiple new candidates as therapeutic immuno-oncology modalities. Bispecific Abs (BsAbs) that recognize 2 different antigens in one molecule are promising drug candidates and have inspired an upsurge in research in both academia and the pharmaceutical industry. Among several BsAbs, T cell engaging BsAb (TCEB), a new class of therapeutic agents designed to simultaneously bind to T cells and tumor cells via tumor cell specific antigens in immunotherapy, is the most promising BsAb. Herein, we are providing an overview of the current status of the development of TCEBs. The diverse formats and characteristics of TCEBs, in addition to the functional mechanisms of BsAbs are discussed. Several aspects of a new TCEB-Blinatumomab-are reviewed, including the current clinical data, challenges of patient treatment, drawbacks regarding toxicities, and resistance of TCEB therapy. Development of the next generation of TCEBs is also discussed in addition to the comparison of TCEB with current chimeric antigen receptor-T therapy.

Indexed as

Adverse effectsBispecific antibodiesBlinatumomabCancer immunotherapyChimeric antigen receptor T cell therapyT cell engager

Identifiers

PMID35291652
PMCPMC8901699
OpenAlexW4214828366

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.