Evidence map›Paper›PMID 36087216›Full record

ArticleMolecular biotechnology2023

Seed-Based System for Cost-Effective Production of Vaccine Against Chronic Respiratory Disease in Chickens.

Yao Shi, Peyman Habibi, Ayesha Naveed Ul Haq, Madiha Saeed, Namra Gulghutay Amjad, Imran Khan

Abstract read
In one paragraph

Article in Molecular biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Immune Evasion ofInternational journal of molecular sciences · 2024
    Review
  2. Review
  3. 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

6 authors.

Yao ShiDepartment of Basic and Translational Sciences, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Peyman HabibiDepartment of Pathology and Laboratory Medicine and Center for Cellular Immunotherapies, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Ayesha Naveed Ul HaqSA-Center for Interdisciplinary Research in Basic Sciences, International Islamic University, Islamabad, Pakistan.
Madiha SaeedSA-Center for Interdisciplinary Research in Basic Sciences, International Islamic University, Islamabad, Pakistan.
Namra Gulghutay AmjadDepartment of Community Medicine and Public Health, Khyber Girls Medical College, KPK, Peshawar, Pakistan.
Imran KhanDepartment of Chemical Engineering, School of Engineering, University of California, Davis, Davis, CA, USA. ikhan@ucdavis.edu.ORCID http://orcid.org/0000-0002-9521-5359

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The production of vaccines in plant cells, termed plant-made pharmaceuticals or molecular farming, is a promising technology for scalable production. Compared to mammalian cell lines, like Chinese Hamster Ovary (CHO) or bacterial cells, plants can be grown with less cost on a large scale to make vaccines antigens and therapeutics affordable and accessible worldwide. An innovative application of this alternative system is the production of vaccines in edible tissues that can be consumed orally to deliver protein antigen without any further processing. In this project, we report stable expression of amino acid sequences corresponding to the TM-1 gene of Mycoplasma gallisepticum as a candidate vaccine antigen against Chronic Respiratory Disease (CRD) in chickens using wheat seed's tissues as a production host. Molecular and immunoblotting analysis confirmed the ubiquitous expression of a recombinant 41.8-kDa protein with an expression level of 1.03 mg/g dry weight in the endosperm tissues. When orally delivered, the plant-made vaccine was effective in terms of developing antibody response in animal model i.e., chicken without any detectable weight loss. Two doses of orally delivered plant-made TM-1 vaccine candidate elicited the immune response and protective effect against MG virus challenge at the level comparable to commercially available inactivated vaccine against CRD. Our study demonstrates that plant-made vaccines are not only safe but also scalable and cost-effective with prolonged stability at room temperature.

Indexed as

ChickensVaccinesAnimalsCHO CellsCost-Benefit AnalysisCricetinaeCricetulusPlantsRecombinant ProteinsSeedsRecombinant ProteinsVaccinesChronic respiratory diseaseGreen vaccineImmunizationMolecular farmingOral delivery oral vaccineRecombinant proteinSeed-based expressionVeterinary vaccine

Identifiers

PMID36087216
PMCPMC9463513

What OpenQuestion holds

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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.