Evidence map›Paper›PMID 42752847›Full record

ReviewBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2026

Plant-Based Systems for Producing Therapeutic Proteins: Current Status and Future Prospects.

Qiang Chen

Abstract readReview
In one paragraph

Review in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Qiang ChenThe Biodesign Institute and School of Life Sciences, Arizona State University, Mail Zone 5401, 1001 S. McAllister Avenue, Tempe, AZ, 85287, USA. qiang.chen.4@asu.edu.ORCID http://orcid.org/0000-0003-1498-7013

Funding

Plant-derived MAb therapeutics for west nile virusU01AI075549 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CHEN, QIANG · 2007 to 2010
$1.6M
Bifunctional antibodies with targeted CNS delivery against West Nile VirusR33AI101329 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CHEN, QIANG · 2014 to 2016
$1.3M
Bifunctional antibodies with targeted CNS delivery against West Nile virusR21AI101329 · NIAID · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI CHEN, QIANG · 2012 to 2013
$428k
Division of Intramural Research, National Institute of Allergy and Infectious Diseases R21/R33AI101329Division of Intramural Research, National Institute of Allergy and Infectious Diseases U01 AI075549NIAID NIH HHS R21 AI101329NIAID NIH HHS R33 AI101329NIAID NIH HHS U01 AI075549
6 · The paper itself

Abstract

Protein-based therapeutics have transformed modern disease treatment and now constitute a rapidly expanding segment of the pharmaceutical market. In this context, plant-based expression systems have emerged as a versatile alternative to conventional mammalian cell platforms for the production of recombinant proteins. Beyond their well-established advantages in cost, scalability, and biosafety, recent advances in transient expression technologies and plant cell culture systems have enabled rapid, high-yield production of complex biologics with increasing control over product quality. In particular, deconstructed viral vectors and Agrobacterium-mediated transient expression in plants enable rapid recombinant protein production, supporting their potential for applications requiring flexible and accelerated manufacturing. Concurrently, progress in host glycoengineering has enabled the generation of humanized and functionally tailored glycoforms, including antibody glycovariants with enhanced Fc-mediated effector functions. These advances have expanded the applicability of plant-based platforms to the production of monoclonal antibodies, antibody fragments, and emerging antibody-based modalities. In parallel, a broad range of single-chain therapeutic proteins, including enzymes, antimicrobial and antiviral agents, and proteins for inducing immune tolerance, have been successfully produced in plant systems as biologically active and functional therapeutics, demonstrating the broad utility of plant-based platforms across multiple therapeutic classes. This review provides a comprehensive overview of current plant-based production platforms, including whole-plant and plant cell suspension systems, and evaluates their comparative advantages and limitations relative to mammalian expression technologies. Recent progress in the development of therapeutic proteins, with an emphasis on monoclonal antibodies for passive immunization, is highlighted. Finally, the remaining technical, regulatory, and commercial challenges are discussed, along with future prospects for integrating plant-based systems into mainstream biopharmaceutical manufacturing.

Identifiers

PMID42752847
PMCPMC13632707

What OpenQuestion holds

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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.