Evidence map›Paper›PMID 34260218›Full record

ArticleACS infectious diseases2021

Immunogenicity and Protective Efficacy of a Highly Thermotolerant, Trimeric SARS-CoV-2 Receptor Binding Domain Derivative.

Sameer Kumar Malladi, Unnatiben Rajeshbhai Patel, Raju S Rajmani, Randhir Singh, Suman Pandey, Sahil Kumar, Sara Khaleeq, Petrus Jansen van Vuren, Shane Riddell, Sarah Goldie and 24 more

Open access · bronzeAbstract read
In one paragraph

Article in ACS infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 47 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

34 authors at 6 institutions in 3 countries.

Sameer Kumar MalladiMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Unnatiben Rajeshbhai PatelMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Raju S RajmaniMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Randhir SinghMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Suman PandeyMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Sahil KumarVirology Unit, Institute of Microbial Technology, Council of Scientific and Industrial Research (CSIR), Sector 39-A, Chandigarh 160036, India.
Sara KhaleeqMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Petrus Jansen van VurenAustralian Centre for Disease Preparedness (ACDP), Commonwealth Scientific and Industrial Research Organisation (CSIRO), 5 Portarlington Road, Geelong 3220, Victoria, Australia.
Shane RiddellAustralian Centre for Disease Preparedness (ACDP), Commonwealth Scientific and Industrial Research Organisation (CSIRO), 5 Portarlington Road, Geelong 3220, Victoria, Australia.
Sarah GoldieAustralian Centre for Disease Preparedness (ACDP), Commonwealth Scientific and Industrial Research Organisation (CSIRO), 5 Portarlington Road, Geelong 3220, Victoria, Australia.
Savitha GayathriMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Debajyoti ChakrabortyMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Parismita KalitaMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Ishika PramanickMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Nupur AgarwalMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Poorvi ReddyMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Nidhi GirishMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Aditya UpadhyayaMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Mohammad Suhail KhanMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Kawkab KanjoMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Madhuraj BhatMynvax Private Limited, ES12, Entrepreneurship Centre, SID, Indian Institute of Science, Bengaluru 560012, India.
Shailendra ManiTranslational Health Science and Technology Institute, NCR Biotech Science Cluster, Third Milestone, Gurugram-Faridabad Expressway, Faridabad 121001, India.
Sankar BhattacharyyaTranslational Health Science and Technology Institute, NCR Biotech Science Cluster, Third Milestone, Gurugram-Faridabad Expressway, Faridabad 121001, India.
Samreen SiddiquiMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, Delhi 1100017, India.
Akansha TyagiMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, Delhi 1100017, India.
Sujeet JhaMax Super Speciality Hospital (A Unit of Devki Devi Foundation), Max Healthcare, Delhi 1100017, India.
Rajesh PandeyIntegrative Genomics of Host-Pathogen (INGEN-HOPE) Laboratory, CSIR-Institute of Genomics and Integrative Biology (CSIR-IGIB), Mall Road, Delhi 110007, India.
Shashank TripathiDepartment of Microbiology & Cell Biology, Indian Institute of Science, Bengaluru 560012, India.
Somnath DuttaMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.
Alexander J McAuleyAustralian Centre for Disease Preparedness (ACDP), Commonwealth Scientific and Industrial Research Organisation (CSIRO), 5 Portarlington Road, Geelong 3220, Victoria, Australia.
Nagendrakumar Balasubramanian SinganallurAustralian Centre for Disease Preparedness (ACDP), Commonwealth Scientific and Industrial Research Organisation (CSIRO), 5 Portarlington Road, Geelong 3220, Victoria, Australia.
Seshadri S VasanAustralian Centre for Disease Preparedness (ACDP), Commonwealth Scientific and Industrial Research Organisation (CSIRO), 5 Portarlington Road, Geelong 3220, Victoria, Australia.
Rajesh P RingeVirology Unit, Institute of Microbial Technology, Council of Scientific and Industrial Research (CSIR), Sector 39-A, Chandigarh 160036, India.
Raghavan VaradarajanMolecular Biophysics Unit (MBU), Indian Institute of Science, Bengaluru 560012, India.ORCID 0000-0002-2693-5248
Indian Institute of Science Bangalore · INCommonwealth Scientific and Industrial Research Organisation · AUMax Super Speciality Hospital · INInstitute of Microbial Technology · INTranslational Health Science and Technology Institute · INInstitute of Genomics and Integrative Biology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The receptor binding domain (RBD) of SARS-CoV-2 is the primary target of neutralizing antibodies. We designed a trimeric, highly thermotolerant glycan engineered RBD by fusion to a heterologous, poorly immunogenic disulfide linked trimerization domain derived from cartilage matrix protein. The protein expressed at a yield of ∼80-100 mg/L in transiently transfected Expi293 cells, as well as CHO and HEK293 stable cell lines and formed homogeneous disulfide-linked trimers. When lyophilized, these possessed remarkable functional stability to transient thermal stress of up to 100 °C and were stable to long-term storage of over 4 weeks at 37 °C unlike an alternative RBD-trimer with a different trimerization domain. Two intramuscular immunizations with a human-compatible SWE adjuvanted formulation elicited antibodies with pseudoviral neutralizing titers in guinea pigs and mice that were 25-250 fold higher than corresponding values in human convalescent sera. Against the beta (B.1.351) variant of concern (VOC), pseudoviral neutralization titers for RBD trimer were ∼3-fold lower than against wildtype B.1 virus. RBD was also displayed on a designed ferritin-like Msdps2 nanoparticle. This showed decreased yield and immunogenicity relative to trimeric RBD. Replicative virus neutralization assays using mouse sera demonstrated that antibodies induced by the trimers neutralized all four VOC to date, namely B.1.1.7, B.1.351, P.1, and B.1.617.2 without significant differences. Trimeric RBD immunized hamsters were protected from viral challenge. The excellent immunogenicity, thermotolerance, and high yield of these immunogens suggest that they are a promising modality to combat COVID-19, including all SARS-CoV-2 VOC to date.

Indexed as

COVID-19ThermotoleranceAnimalsAntibodies, ViralCOVID-19 SerotherapyGuinea PigsHEK293 CellsHumansImmunization, PassiveMiceSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, ViralSpike Glycoprotein, Coronavirusglycosylationoligomerizationthermostablevaccinevariant of concern

Identifiers

PMID34260218
PMCPMC8996237
OpenAlexW3180190017

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.