Evidence map›Paper›PMID 39588259›Full record

ArticleInternational journal of nanomedicine2024

Fusing a Novel Anti-CTLA-4 Nanobody to the IgG1 Fc Region Strengthens Its Ability to Induce CD8

Ting-Ting Li, Jin-Hua Yang, Meng-Jie Jiang, Hao-Peng Cui, Xiao-Mei Yang, Xiao-Ling Lu, Ai-Qun Liu

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Ting-Ting LiDepartment of Gastroenterology and Respiratory Medicine & Endoscopy Center, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, 530021, People's Republic of China.
Jin-Hua YangDepartment of Gastroenterology and Respiratory Medicine & Endoscopy Center, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, 530021, People's Republic of China.
Meng-Jie JiangDepartment of Gastroenterology and Respiratory Medicine & Endoscopy Center, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, 530021, People's Republic of China.
Hao-Peng CuiDepartment of Gastroenterology and Respiratory Medicine & Endoscopy Center, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, 530021, People's Republic of China.
Xiao-Mei YangGuangxi Key Laboratory of Nanobody Research, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Xiao-Ling LuGuangxi Key Laboratory of Nanobody Research, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Ai-Qun LiuDepartment of Gastroenterology and Respiratory Medicine & Endoscopy Center, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, 530021, People's Republic of China.ORCID 0000-0001-9608-0794

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Our previously described a nanobody precisely targeting CTLA-4 and demonstrated that it can promote the antitumor response of adoptive T cells. Here we examined whether fusing it to the IgG1 Fc region would induce stronger, longer-lasting T-cell immune responses after exposure to the dendritic-tumor cell fusions. Methods: The fusion of nanobody to Fc region was overexpressed in Results: Proliferation, activation and cytotoxicity of CD8 Conclusion: Fusing our anti-CTLA-4 nanobody to the IgG1 Fc region potentiates its ability to induce strong, persistent CD8

Indexed as

CD8-Positive T-LymphocytesCTLA-4 AntigenImmunoglobulin Fc FragmentsImmunoglobulin GMice, NudeSingle-Domain AntibodiesAnimalsCell Line, TumorCell ProliferationDendritic CellsFemaleHumansLymphocyte ActivationMiceNeoplasmsRecombinant Fusion ProteinsCTLA-4 AntigenImmunoglobulin Fc FragmentsImmunoglobulin GRecombinant Fusion ProteinsSingle-Domain Antibodiesadoptive immunotherapycell fusionCTLA-4nanobodytherapeutic antibody derivative

Identifiers

PMID39588259
PMCPMC11587810

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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.