Evidence map›Paper›PMID 35655326›Full record

ReviewJournal of medical virology2022

Transchromosomic bovines-derived broadly neutralizing antibodies as potent biotherapeutics to counter important emerging viral pathogens with a special focus on SARS-CoV-2, MERS-CoV, Ebola, Zika, HIV-1, and influenza A virus.

AbdulRahman A Saied, Manuela Sales Lima Nascimento, Adriano Henrique do Nascimento Rangel, Krzysztof Skowron, Katarzyna Grudlewska-Buda, Kuldeep Dhama, Jaffer Shah, Ahmed Abdeen, Fouad S El-Mayet, Hassan Ahmed and 1 more

Open access · greenAbstract readReview
In one paragraph

Review in Journal of medical virology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

11 authors at 8 institutions in 6 countries.

AbdulRahman A SaiedNational Food Safety Authority (NFSA), Aswan, Egypt.ORCID 0000-0001-8616-5874
Manuela Sales Lima NascimentoDepartment of Microbiology and Parasitology, Biosciences Center, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Adriano Henrique do Nascimento RangelSpecialized Academic Unit in Agricultural Sciences, Federal University of Rio Grande do Norte, Natal, Macaíba-Rio Grande do Norte, Brazil.
Krzysztof SkowronDepartment of Microbiology, Nicolaus Copernicus University in Toruń, L. Rydygier Collegium Medicum in Bydgoszcz, Bydgoszcz, Poland.
Katarzyna Grudlewska-BudaDepartment of Microbiology, Nicolaus Copernicus University in Toruń, L. Rydygier Collegium Medicum in Bydgoszcz, Bydgoszcz, Poland.
Kuldeep DhamaDivision of Pathology, ICAR-Indian Veterinary Research Institute (IVRI), Izatnagar, Uttar Pradesh, India.ORCID 0000-0001-7469-4752
Jaffer ShahMedical Research Center, Kateb University, Kabul, Afghanistan.
Ahmed AbdeenDepartment of Forensic Medicine and Toxicology, Faculty of Veterinary Medicine, Benha University, Toukh, Egypt.
Fouad S El-MayetDepartment of Virology, Faculty of Veterinary Medicine, Benha University, Toukh, Egypt.
Hassan AhmedDepartment of Physiology, Faculty of Veterinary Medicine, South Valley University, Qena, Egypt.
Asmaa A MetwallyDepartment of Surgery, Anesthesiology, and Radiology, Faculty of Veterinary Medicine, Aswan University, Aswan, Egypt.ORCID 0000-0001-8565-8220
Benha University · EGNicolaus Copernicus University · PLUniversidade Federal do Rio Grande do Norte · BRAswan University · EGIndian Veterinary Research Institute · INMinistry of Antiquities · EGNew York State Department of Health · USSouth Valley University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Historically, passive immunotherapy is an approved approach for protecting and treating humans against various diseases when other alternative therapeutic options are unavailable. Human polyclonal antibodies (hpAbs) can be made from convalescent human donor serum, although it is considered limited due to pandemics and the urgent requirement. Additionally, polyclonal antibodies (pAbs) could be generated from animals, but they may cause severe immunoreactivity and, once "humanized," may have lower neutralization efficiency. Transchromosomic bovines (TcBs) have been developed to address these concerns by creating robust neutralizing hpAbs, which are useful in preventing and/or curing human infections in response to hyperimmunization with vaccines holding adjuvants and/or immune stimulators over an extensive period. Unlike other animal-derived pAbs, potent hpAbs could be promptly produced from TcB in large amounts to assist against an outbreak scenario. Some of these highly efficacious TcB-derived antibodies have already neutralized and blocked diseases in clinical studies. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has numerous variants classified into variants of concern (VOCs), variants of interest (VOIs), and variants under monitoring. Although these variants possess different mutations, such as N501Y, E484K, K417N, K417T, L452R, T478K, and P681R, SAB-185 has shown broad neutralizing activity against VOCs, such as Alpha, Beta, Gamma, Delta, and Omicron variants, and VOIs, such as Epsilon, Iota, Kappa, and Lambda variants. This article highlights recent developments in the field of bovine-derived biotherapeutics, which are seen as a practical platform for developing safe and effective antivirals with broad activity, particularly considering emerging viral infections such as SARS-CoV-2, Ebola, Middle East respiratory syndrome coronavirus, Zika, human immunodeficiency virus type 1, and influenza A virus. Antibodies in the bovine serum or colostrum, which have been proved to be more protective than their human counterparts, are also reviewed.

Indexed as

COVID-19Hemorrhagic Fever, EbolaHIV-1Influenza A virusMiddle East Respiratory Syndrome CoronavirusZika VirusZika Virus InfectionAnimalsAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesHumansImmunoglobulin GSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralBroadly Neutralizing AntibodiesImmunoglobulin GSAB-185Spike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibody-based therapiesbovine-derived biotherapeuticsEbolaemerging virusesHIV-1influenza A virusMERS-CoVSARS-CoV-2transchromosomic bovinesZika

Identifiers

PMID35655326
PMCPMC9347534
OpenAlexW4281967975

What OpenQuestion holds

Textmetadata
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.