Evidence map›Paper›PMID 35264679›Full record

ArticleScientific reports2022

First-in-class trispecific VHH-Fc based antibody with potent prophylactic and therapeutic efficacy against SARS-CoV-2 and variants.

Allison Titong, Sachith Gallolu Kankanamalage, Jianbo Dong, Betty Huang, Nicholas Spadoni, Bo Wang, Meredith Wright, Keegan L J Pham, Anh Hai Le, Yue Liu

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

10 authors.

Allison TitongAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Sachith Gallolu KankanamalageAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Jianbo DongAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Betty HuangAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Nicholas SpadoniAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Bo WangAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Meredith WrightAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Keegan L J PhamAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Anh Hai LeAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA.
Yue LiuAb Studio Inc., 3541 Investment Blvd., Suite 3, Hayward, CA, 94545, USA. yue.liu@antibodystudio.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 and its variants have persisted in this ongoing COVID-19 pandemic. While the vaccines have greatly reduced the COVID-19 cases, hospitalizations, and death, about half of the world remain unvaccinated due to various reasons. Furthermore, the duration of the immunity gained from COVID-19 vaccination is still unclear. Therefore, there is a need for innovative prophylactic and treatment measures. In response to this need, we previously reported on the successful computer-aided development of potent VHH-based multispecific antibodies that were characterized in vitro. Here, we evaluated in vivo efficacy and safety of the lead trispecific VHH-Fc, ABS-VIR-001. Importantly, our data showed that ABS-VIR-001 treatment prevented SARS-CoV-2 infection and death when provided as an intranasal prophylaxis in a humanized ACE-2 mouse model. In addition, ABS-VIR-001 post-exposure treatment was shown to greatly reduce viral loads by as much as 50-fold. A detailed panel of metabolic and cellular parameters demonstrated that ABS-VIR-001 treatment was overall comparable to the PBS treatment, indicating a favorable safety profile. Notably, our inhibition studies show that ABS-VIR-001 continued to demonstrate unwavering efficacy against SARS-CoV-2 mutants, associated with key variants including Delta and Omicron, owing to its multiple epitope design. Lastly, we rigorously tested and confirmed the excellent thermostability of ABS-VIR-001 when heated to 45 °C for up to 4 weeks. Taken together, our study suggests that ABS-VIR-001 is an efficacious and durable prophylaxis and post-exposure treatment for COVID-19 with promising safety and manufacturability features for global distribution.

Indexed as

COVID-19 Drug TreatmentAngiotensin-Converting Enzyme 2AnimalsAntigen-Antibody ReactionsBiomarkersCOVID-19Drug StabilityHumansImmunocompromised HostMiceMice, TransgenicSARS-CoV-2Single-Domain AntibodiesSpike Glycoprotein, CoronavirusViral LoadACE2 protein, humanAngiotensin-Converting Enzyme 2BiomarkersSingle-Domain AntibodiesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID35264679
PMCPMC8905027

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LicenceCC BY
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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.