Evidence map›Paper›PMID 42240905›Full record

ArticleApplied biochemistry and biotechnology2026

Improving In Vitro Antibody Production Using Synthetic Peptide Derived from RhD Loops.

Faezeh Kheiri Ardahaei, Fatemeh Yari, Amir Teimourpour

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Article in Applied biochemistry and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Faezeh Kheiri ArdahaeiBlood Transfusion Research Center, High Institute for research and Education in Transfusion Medicine, Tehran, Iran.
Fatemeh YariBlood Transfusion Research Center, High Institute for research and Education in Transfusion Medicine, Tehran, Iran. f.yari@ibto.ir.ORCID http://orcid.org/0000-0003-1036-3801
Amir TeimourpourBlood Transfusion Research Center, High Institute for research and Education in Transfusion Medicine, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimthe RhD antigen is highly immunogenic, and poses a significant clinical risk of hemolytic transfusion reactions (HTRs), rendering it a critical factor in safe blood transfusion. Conventional immunization strategies relying on full-length RhD protein are limited by restricted antigen availability, high production costs, and ethical concerns associated with in vivo antibody generation. To address these challenges, we evaluated an in vitro immunization platform using human peripheral blood mononuclear cells (PBMCs) stimulated with either full length RhD protein or a designed synthetic RhD peptide, aiming to establish a rapid, ethical, and reproducible biotechnological alternative for in vitro antibody production. MATERIALS AND

methodsPBMCs from O-negative blood units were isolated by Ficoll density gradient, and treated with L-leucine methyl ester to deplete immunosuppressive cells. PBMCs were stimulated with full length RhD protein, synthetic peptide, or peptide conjugated to Keyhole Limpet Hemocyanin (KLH). Conjugation efficiency was confirmed via ELISA and spectrophotometry (280/412 nm). Cultures were supplemented with IL-4, IFN-γ, and conditioned medium, and then incubated at 37°C for one week. Antibody production in culture supernatants was quantified by ELISA.

resultsPeptide-KLH induced higher antibody levels (84.87±13.6 ng/mL) than free peptide (52.4±9.8 ng/mL), while RhD protein elicited (108.7±10.4 ng/mL). Combined stimulation with peptide-KLH and RhD protein further enhanced antibody levels (157.9±23.6 ng/mL). Two-step immunization significantly enhanced responses (P=0.006). The combination of IL-4 and IFN-γ yielded the highest cytokine-driven enhancement.

conclusionSynthetic RhD peptide, especially when conjugated to KLH, provides an attractive and convenient alternative to full-length protein for in vitro antibody production. This approach has practical applications in biotechnology, including the generation of antibodies and antibody producing clones, reducing reliance on in vivo immunization.

Indexed as

Antibody FormationLeukocytes, MononuclearPeptidesRh-Hr Blood-Group SystemHemocyaninsHumansHemocyaninskeyhole-limpet hemocyaninPeptidesRh-Hr Blood-Group SystemRho(D) antigenCarrier proteinHuman antibodyIn vitro techniquesProtein conjugationRhD antigenSynthetic peptides

Identifiers

PMID42240905

What Socratic holds

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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 Socratic graph.