Evidence map›Paper›PMID 41383500›Full record

ArticleFrontiers in oncology2025

A CD47 antibody with minimized erythrocyte and thrombocyte toxicities.

Min Pei, Xiao-Dong Dai, Xiao-Fan Jiang, Cai-Yi Yuan, Jie Tan, Kai-Feng He, Guo-Jian Liu, Jin-Di Zhu, Huan-Huan Li, Ai-Ling Pan and 4 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

14 authors.

Min PeiInstitute of Biomedicine & Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Xiao-Dong DaiBiotherapeutics Discovery Research Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Xiao-Fan JiangSchool of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Cai-Yi YuanSchool of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Jie TanDepartment of Antibody Discovery, Shanghai Mabstone Biotechnology Ltd., Shanghai, China.
Kai-Feng HeSchool of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Guo-Jian LiuDepartment of Research and Development Center, Dartsbio Pharmaceuticals Ltd., Zhongshan, Guangdong, China.
Jin-Di ZhuBiotherapeutics Discovery Research Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Huan-Huan LiDepartment of Antibody Discovery, Shanghai Mabstone Biotechnology Ltd., Shanghai, China.
Ai-Ling PanSchool of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Ya-Ru WangSchool of Life Science of Technology, ShanghaiTech University, Shanghai, China.
Yi-Li ChenDepartment of Antibody Discovery, Shanghai Mabstone Biotechnology Ltd., Shanghai, China.
Xiao-Jia ChenInstitute of Biomedicine & Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou, China.
Chunhe WangDepartment of Antibody Discovery, Shanghai Mabstone Biotechnology Ltd., Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Blockade of the CD47/SIRPa axis has emerged as a promising approach to enhance macrophage-mediated anti-tumor activities in cancer immunotherapy. However, the clinical application of early CD47 antibodies has been associated with significant hematotoxicities, including hemagglutination, anemia, and thrombopenia. Although several CD47 antibodies have generally avoided hemagglutination, anemia, and thrombopenia remain, potentially mediated by enhanced phagocytosis of erythrocytes and thrombocytes. Methods: 1B2-10 is a humanized CD47-neutralizing antibody generated by mouse immunization and phage display technology. Its efficacy and safety were evaluated using Results: Discussion: These findings suggest that 1B2-10 demonstrates a favorable efficacy and safety profile, indicating great therapeutic potential for cancer. Based on these studies, 1B2-10 has been renamed as DS003 and is currently advancing through Phase I clinical trials in China to further evaluate its safety profile and preliminary efficacy in human subjects.

Indexed as

CD47hematotoxicitymacrophagesmonoclonal antibodyN-linked glycosylation

Identifiers

PMID41383500
PMCPMC12690563

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.