Evidence map›Paper›PMID 35589003›Full record

ArticleEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V2022

RBD decorated PLA nanoparticle admixture with aluminum hydroxide elicit robust and long lasting immune response against SARS-CoV-2.

Jairam Meena, Priyank Singhvi, Sudeepa Srichandan, Jyotsna Dandotiya, Juhi Verma, Mamta Singh, Rahul Ahuja, Neha Panwar, Tabiya Qayoom Wani, Ritika Khatri and 4 more

Abstract read
In one paragraph

Article in European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Frontiers in cellular and infection microbiology · 2026
    Article
  3. Article
  4. International journal of nanomedicine · 2025
    Article
  5. Article
  6. Overview of Antimicrobial Biodegradable Polyester-Based Formulations.International journal of molecular sciences · 2023
    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

14 authors.

Jairam MeenaProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India; Department of Pharmaceutical Engineering and Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi, Uttar Pradesh 221005, India. Electronic address: jairam.meena20@gmail.com.
Priyank SinghviProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Sudeepa SrichandanProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Jyotsna DandotiyaProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Juhi VermaProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Mamta SinghProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Rahul AhujaProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Neha PanwarProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Tabiya Qayoom WaniProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Ritika KhatriInfection and Immunology Laboratory, Translational Health Science & Technology Institute, Gurgaon-Faridabad, India.
Gazala SiddiquiInfection and Immunology Laboratory, Translational Health Science & Technology Institute, Gurgaon-Faridabad, India.
Anuradha GuptaProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India.
Sweety SamalInfection and Immunology Laboratory, Translational Health Science & Technology Institute, Gurgaon-Faridabad, India.
Amulya Kumar PandaProduct Development Cell, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India. Electronic address: amulya@nii.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoparticles-based multivalent antigen display has the capability of mimicking natural virus infection characteristics, making it useful for eliciting potent long-lasting immune response. Several vaccines are developed against global pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However these subunit vaccines use mammalian expression system, hence mass production with rapid pace is a bigger challenge. In contrast E. coli based subunit vaccine production circumvents these limitations. The objective of the present investigation was to develop nanoparticle vaccine with multivalent display of receptor binding domain (RBD) of SARS-CoV-2 expressed in E. coli. Results showed that RBD entrapped PLA (Poly lactic acid) nanoparticle in combination with aluminum hydroxide elicited 9-fold higher immune responses as compared to RBD adsorbed aluminum hydroxide, a common adjuvant used for human immunization. It was interesting to note that RBD entrapped PLA nanoparticle with aluminum hydroxide not only generated robust and long-lasting antibody response but also provided Th1 and Th2 balanced immune response. Moreover, challenge with 1 µg of RBD alone was able to generate secondary antibody response, suggesting that immunization with RBD-PLA nanoparticles has the ability to elicit memory antibody against RBD. Plaque assay revealed that the antibody generated using the polymeric formulation was able to neutralize SARS-CoV-2. The RBD entrapped PLA nanoparticles blended with aluminum hydroxide thus has potential to develop asa subunit vaccine against COVID-19.

Indexed as

COVID-19NanoparticlesAluminum HydroxideAnimalsAntibodies, NeutralizingAntibodies, ViralAntibody FormationCOVID-19 VaccinesEscherichia coliHumansMammalsPolyestersSARS-CoV-2Spike Glycoprotein, CoronavirusVaccines, SubunitAluminum HydroxideAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesPolyestersSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vaccines, SubunitCOVID-19 vaccineMemory antibody responsePolymeric nanoparticlesProtein-subunit vaccineReceptor binding domainSARS-CoV-2 vaccineVirus neutralization

Identifiers

PMID35589003
PMCPMC9110063

What OpenQuestion holds

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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.