Evidence map›Paper›PMID 40396376›Full record

ArticleNucleic acids research2025

hAb-Convergent: an antibody rearrangement analysis system for therapeutic antibody engineering based on convergent evolution.

Jinfeng Wang, Xiaomeng Ge, Qinglan Sun, Minlong Chen, Shijie Qin, Dongmei Liu, Tao Deng, Juncai Ma, Songnian Hu, Ronghua Jin and 2 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. 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

12 authors.

Jinfeng WangCAS Key Laboratory of Pathogen Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Xiaomeng GeMicrobial Resource and Big Data Center, Institute of Microbiology of the Chinese Academy of Sciences, Beijing 100101, China.
Qinglan SunMicrobial Resource and Big Data Center, Institute of Microbiology of the Chinese Academy of Sciences, Beijing 100101, China.
Minlong ChenCAS Key Laboratory of Pathogen Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Shijie QinInnovative Vaccine and Immunotherapy Research Center, The Second Affiliated Hospital Zhejiang University School of Medicine, Hangzhou 310009, China.
Dongmei LiuMicrobial Resource and Big Data Center, Institute of Microbiology of the Chinese Academy of Sciences, Beijing 100101, China.
Tao DengCAS Key Laboratory of Pathogen Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.ORCID 0000-0002-8303-0891
Juncai MaMicrobial Resource and Big Data Center, Institute of Microbiology of the Chinese Academy of Sciences, Beijing 100101, China.
Songnian HuState Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.ORCID 0000-0003-3966-3111
Ronghua JinNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing 100015, China.
Zhou TongCAS Key Laboratory of Pathogen Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.ORCID 0000-0002-9867-2838
Linhuan WuMicrobial Resource and Big Data Center, Institute of Microbiology of the Chinese Academy of Sciences, Beijing 100101, China.ORCID 0000-0002-5255-1846

Funding

Chinese Academy of Sciences KFZD-SW-219Chinese Academy of Sciences XDB0830000National Key Research Program of China 2022YFF1203201National Key Research Program of China 2023YFC2308800
6 · The paper itself

Abstract

In therapeutic antibody engineering, utilizing naturally occurring mutations in the human body as a reference for modification is an emerging trend. The theory of convergent evolution presents a viable solution. Nevertheless, the nonuniformity of the antibody rearrangement analysis system and the difficulty in identifying the heavy-chain D-region are significant challenges to research and application. To address these limitations, we developed hAb (human antibody)-Convergent, a novel tool designed to assist users in quickly identifying candidate mutation hotspots of input antibody sequences in real human immune responses for subsequent antibody engineering. It uses antibody rearrangement features-based (V, D, J genes and CDR-H3 length) rather than traditional sequence-based strategies while ensuring the security of the original sequence. Combining more inclusive D-region identification and analysis methods, it can recognize and analyze the convergence of antibodies across various individuals. Additionally, given the limitations of obtaining antibody nucleotide sequences from academic literature, it provides an optimized approach for direct analysis and rapid comparison using amino acid sequences. hAb-Convergent bridges gaps in antibody engineering by linking natural evolution patterns to in vitro design, with implications for universal vaccine development. The tool can be freely accessed at https://nmdc.cn/zoe/.

Indexed as

AntibodiesEvolution, MolecularProtein EngineeringSoftwareComplementarity Determining RegionsGene RearrangementHumansImmunoglobulin Heavy ChainsMutationAntibodiesComplementarity Determining RegionsImmunoglobulin Heavy Chains

Identifiers

PMID40396376
PMCPMC12230731

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.