Evidence map›Paper›PMID 37077474›Full record

ArticleAntibody therapeutics2023

Preclinical evaluation of ISH0339, a tetravalent broadly neutralizing bispecific antibody against SARS-CoV-2 with long-term protection.

Huabing Yang, Yuxin Chen, Dongcheng Jiang, Xiaoli Feng, Ying Xu, Jiayu Wei, Qingcui Zou, Qiaojiang Yang, Jihong Chen, Xiaoling Jiang and 6 more

Open access · goldAbstract read
In one paragraph

Article in Antibody therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 97% 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

2 citing papers in PubMed, 0 citations in OpenAlex.

  1. Article
  2. 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

16 authors at 3 institutions in 1 country.

Huabing YangSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Yuxin ChenDepartment of Laboratory Medicine, Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing 210008, Jiangsu, China.
Dongcheng JiangSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Xiaoli FengKunming National High-level Biosafety Research Center for Non-Human Primates, Center for Biosafety Mega-Science, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650107, Yunnan, China.
Ying XuCollege of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China.
Jiayu WeiCollege of Life Sciences, Nanjing Agricultural University, Nanjing 210095, Jiangsu, China.
Qingcui ZouKunming National High-level Biosafety Research Center for Non-Human Primates, Center for Biosafety Mega-Science, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650107, Yunnan, China.
Qiaojiang YangKunming National High-level Biosafety Research Center for Non-Human Primates, Center for Biosafety Mega-Science, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650107, Yunnan, China.
Jihong ChenSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Xiaoling JiangSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Chunling QinSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Zhenzhen HuangSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Chongbing WuSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Ying ZhouSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Minghua LiKunming National High-level Biosafety Research Center for Non-Human Primates, Center for Biosafety Mega-Science, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650107, Yunnan, China.
Liusong YinSunHo (China) BioPharmaceutical Co., Ltd., No.5 Xingjian Road, Economic and Technological Development Zone, Nanjing 210046, Jiangsu, China.
Kunming Institute of Zoology · CNNanjing Agricultural University · CNNanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnding the global COVID-19 pandemic requires efficacious therapies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Nevertheless, the emerging Omicron sublineages largely escaped the neutralization of current authorized monoclonal antibody therapies. Here we report a tetravalent bispecific antibody ISH0339, as a potential candidate for long-term and broad protection against COVID-19.

methodsWe report here the making of ISH0339, a novel tetravalent bispecific antibody composed of a pair of non-competing neutralizing antibodies that binds specifically to two different neutralizing epitopes of SARS-CoV-2 receptor-binding domain (RBD) and contains an engineered Fc region for prolonged antibody half-life. We describe the preclinical characterization of ISH0339 and discuss its potential as a novel agent for both prophylactic and therapeutic purposes against SARS-CoV-2 infection.

resultsISH0339 bound to SARS-CoV-2 RBD specifically with high affinity and potently blocked the binding of RBD to the host receptor hACE2. ISH0339 demonstrated greater binding, blocking and neutralizing efficiency than its parental monoclonal antibodies, and retained neutralizing ability to all tested SARS-CoV-2 variants of concern. Single dosing of ISH0339 showed potent neutralizing activity for treatment via intravenous injection and for prophylaxis via nasal spray. Preclinical studies following single dosing of ISH0339 showed favorable pharmacokinetics and well-tolerated toxicology profile.

conclusionISH0339 has demonstrated a favorable safety profile and potent anti-SARS-CoV-2 activities against all current variants of concern. Furthermore, prophylactic and therapeutic application of ISH0339 significantly reduced the viral titer in lungs. Investigational New Drug studies to evaluate the safety, tolerability and preliminary efficacy of ISH0339 for both prophylactic and therapeutic purposes against SARS-CoV-2 infection have been filed.

Indexed as

bispecificCOVID-19ISH0339long-protectionneutralizingomicronSARS-CoV-2tetravalent

Identifiers

PMID37077474
PMCPMC10108555
OpenAlexW4323352010

What OpenQuestion holds

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LicenceCC BY-NC
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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.