An oligoclonal combination of human monoclonal antibodies able to neutralize tetanus toxin

Epitope mapping Ganglioside Neuron receptor Neutralizing antibody Peptide array Tetanus toxin

Journal

Toxicon: X
ISSN: 2590-1710
Titre abrégé: Toxicon X
Pays: England
ID NLM: 101741983

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 26 10 2018
revised: 27 12 2018
accepted: 10 01 2019
entrez: 19 6 2020
pubmed: 18 1 2019
medline: 18 1 2019
Statut: epublish

Résumé

The use of antibody-based therapy to treat a variety of diseases and conditions is well documented. The use of antibodies as an antidote to treat tetanus infections was one of the first examples of immunotherapy and remains the standard of care for cases involving potential infections. Plasma-derived immunoglobulins obtained from human or horse pose risks of infection from undetectable emergent viruses or may cause anaphylaxis. Further, there is a lack of consistency between lots. In the search for new formulations, we obtained a series of clonally related human monoclonal antibodies (mAbs) derived from B cells sorted from donors that presented anti-tetanus neutralizing titers. Donors were revaccinated prior to blood collection. Different strategies were used for single-cell sorting, since it was challenging to identify cells at a very low frequency: memory B cell sorting using fluorescent-labeled tetanus toxoid and toxin as baits, and plasmablast sorting done shortly after revaccination. Screening of the recombinant mAbs with the whole tetanus toxin allowed us to select candidates with therapeutic potential, since mAbs to different domains can contribute additively to the neutralizing effect. Because of selective binding to different domains, we tested mAbs individually, or in mixtures of two or three, in the neutralizing

Identifiants

pubmed: 32550563
doi: 10.1016/j.toxcx.2019.100006
pii: S2590-1710(19)30003-7
pii: 100006
pmc: PMC7285915
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100006

Informations de copyright

© 2019 The Author(s).

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Auteurs

Eduardo Aliprandini (E)

Laboratory of Biopharmaceuticals in Animal Cells, Instituto Butantan, São Paulo, Brazil.
Interunits Graduate Program in Biotechnology, University of São Paulo, Brazil.

Daniela Yumi Takata (DY)

Laboratory of Biopharmaceuticals in Animal Cells, Instituto Butantan, São Paulo, Brazil.
Interunits Graduate Program in Biotechnology, University of São Paulo, Brazil.

Ana Lepique (A)

Dept of Immunology, Biomedical Sciences Institute, University of São Paulo, Brazil.

Jorge Kalil (J)

Laboratory of Immunology, School of Medicine, University of São Paulo, São Paulo, Brazil.
Institute for Investigation in Immunology, iii - INCT (National Institute of Science and Technology), São Paulo, Brazil.

Silvia Beatriz Boscardin (SB)

Dept of Parasitology, Biomedical Sciences Institute, University of São Paulo, Brazil.
Institute for Investigation in Immunology, iii - INCT (National Institute of Science and Technology), São Paulo, Brazil.

Ana Maria Moro (AM)

Laboratory of Biopharmaceuticals in Animal Cells, Instituto Butantan, São Paulo, Brazil.
Institute for Investigation in Immunology, iii - INCT (National Institute of Science and Technology), São Paulo, Brazil.

Classifications MeSH