Evidence map›Paper›PMID 36851133›Full record

ArticleVaccines2023

A Live Attenuated COVID-19 Candidate Vaccine for Children: Protection against SARS-CoV-2 Challenge in Hamsters.

Rajeev Mehla, Prasad Kokate, Sarika R Bhosale, Vivek Vaidya, Shridhar Narayanan, Radha K Shandil, Mayas Singh, Gudepalya R Rudramurthy, Chakenahalli N Naveenkumar, Kumaraswamy Bharathkumar and 4 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 14 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

14 authors at 3 institutions in 2 countries.

Rajeev MehlaSerum Institute of India Pvt. Ltd., Pune 411028, Maharashtra, India.
Prasad KokateSerum Institute of India Pvt. Ltd., Pune 411028, Maharashtra, India.
Sarika R BhosaleSerum Institute of India Pvt. Ltd., Pune 411028, Maharashtra, India.
Vivek VaidyaSerum Institute of India Pvt. Ltd., Pune 411028, Maharashtra, India.
Shridhar NarayananFoundation for Neglected Disease Research, Bengaluru 561203, Karnataka, India.
Radha K ShandilFoundation for Neglected Disease Research, Bengaluru 561203, Karnataka, India.
Mayas SinghFoundation for Neglected Disease Research, Bengaluru 561203, Karnataka, India.
Gudepalya R RudramurthyFoundation for Neglected Disease Research, Bengaluru 561203, Karnataka, India.ORCID 0000-0002-0179-5138
Chakenahalli N NaveenkumarFoundation for Neglected Disease Research, Bengaluru 561203, Karnataka, India.
Kumaraswamy BharathkumarFoundation for Neglected Disease Research, Bengaluru 561203, Karnataka, India.
Rob ColemanCodagenix, Inc., Farmingdale, New York, NY 11735, USA.
Steffen MuellerCodagenix, Inc., Farmingdale, New York, NY 11735, USA.
Rajeev M DhereSerum Institute of India Pvt. Ltd., Pune 411028, Maharashtra, India.
Leena R YeolekarSerum Institute of India Pvt. Ltd., Pune 411028, Maharashtra, India.
Foundation for Neglected Disease Research · INSerum Institute of India (India) · INCodagenix (United States) · US

Funding

Gilead Sciences, inc. 000
6 · The paper itself

Abstract

Children are at risk of infection from severe acute respiratory syndrome coronavirus-2 virus (SARS-CoV-2) resulting in coronavirus disease (COVID-19) and its more severe forms. New-born infants are expected to receive short-term protection from passively transferred maternal antibodies from their mothers who are immunized with first-generation COVID-19 vaccines. Passively transferred antibodies are expected to wane within first 6 months of infant's life, leaving them vulnerable to COVID-19. Live attenuated vaccines, unlike inactivated or viral-protein-based vaccines, offer broader immune engagement. Given effectiveness of live attenuated vaccines in controlling infectious diseases such as mumps, measles and rubella, we undertook development of a live attenuated COVID-19 vaccine with an aim to vaccinate children beyond 6 months of age. An attenuated vaccine candidate (dCoV), engineered to express sub-optimal codons and deleted polybasic furin cleavage sites in the spike protein of the SARS-CoV-2 WA/1 strain, was developed and tested in hamsters. Hamsters immunized with dCoV via intranasal or intramuscular routes induced high levels of neutralizing antibodies and exhibited complete protection against the SARS-CoV-2 wild-type isolates, i.e., the Wuhan-like (USA-WA1/2020) and Delta variants (B.1.617.2) in a challenge study. In addition, the dCoV formulated with the marketed measles-rubella (MR) vaccine, designated as MR-dCoV, administered to hamsters via intramuscular route, also protected against both SARS-CoV-2 challenges, and dCoV did not interfere with the MR vaccine-mediated immune response. The safety and efficacy of the dCoV and the MR-dCoV against both variants of SARS-CoV-2 opens the possibility of early immunization in children without an additional injection.

Indexed as

codon de-optimized vaccinecoronavirus combination vaccineCOVID-19 in childrenhamster challenge studylive-attenuatedmeaslesrubellaSARS-CoV-2vaccine efficacy

Identifiers

PMID36851133
PMCPMC9965573
OpenAlexW4318042613

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.