Rapid generation of human recombinant monoclonal antibodies from antibody-secreting cells using ferrofluid-based technology.

CD138-ferrofluid COVID-19 antibody secreting cells (ASCs) antigen-specific ASCs functional selection human monoclonal antibodies single cell PCR transcriptionally active PCR (TAP)

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2024
Historique:
received: 20 11 2023
accepted: 06 03 2024
medline: 3 5 2024
pubmed: 3 5 2024
entrez: 3 5 2024
Statut: epublish

Résumé

Monoclonal antibodies (mAbs) are one of the most important classes of biologics with high therapeutic and diagnostic value, but traditional methods for mAbs generation, such as hybridoma screening and phage display, have limitations, including low efficiency and loss of natural chain pairing. To overcome these challenges, novel single B cell antibody technologies have emerged, but they also have limitations such as

Identifiants

pubmed: 38698845
doi: 10.3389/fimmu.2024.1341389
pmc: PMC11064063
doi:

Substances chimiques

Antibodies, Monoclonal 0
Recombinant Proteins 0
Antibodies, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1341389

Informations de copyright

Copyright © 2024 Strazza, Rossi, Avati, Tiseo, Falcone, Cusi, Menichetti, Ricciardi-Castagnoli, Tinti and Pileri.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Veronica Strazza (V)

Hyper Antibody Research & Development (HARD) -Lab, Toscana Life Sciences Foundation, Siena, Italy.
Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.

Marco Rossi (M)

Hyper Antibody Research & Development (HARD) -Lab, Toscana Life Sciences Foundation, Siena, Italy.

Andrea Avati (A)

Hyper Antibody Research & Development (HARD) -Lab, Toscana Life Sciences Foundation, Siena, Italy.

Giusy Tiseo (G)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliero Universitaria Pisana, University of Pisa, Pisa, Italy.

Marco Falcone (M)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliero Universitaria Pisana, University of Pisa, Pisa, Italy.

Maria Grazia Cusi (MG)

Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Francesco Menichetti (F)

Infectious Diseases Unit, Department of Clinical and Experimental Medicine, Azienda Ospedaliero Universitaria Pisana, University of Pisa, Pisa, Italy.

Paola Ricciardi-Castagnoli (P)

Hyper Antibody Research & Development (HARD) -Lab, Toscana Life Sciences Foundation, Siena, Italy.

Cristina Tinti (C)

Hyper Antibody Research & Development (HARD) -Lab, Toscana Life Sciences Foundation, Siena, Italy.

Piero Pileri (P)

Hyper Antibody Research & Development (HARD) -Lab, Toscana Life Sciences Foundation, Siena, Italy.

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Classifications MeSH