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Centaur antibodies: Engineered chimeric equine-human recombinant antibodies

Hyper-immune antisera from large mammals, in particular horses, are routinely used for life-saving anti-intoxication intervention. While highly efficient, the use of these immunotherapeutics is complicated by possible recipient reactogenicity and limited availability. Accordingly, there is an urgent...

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Autores principales: Rosenfeld, Ronit, Alcalay, Ron, Zvi, Anat, Ben-David, Alon, Noy-Porat, Tal, Chitlaru, Theodor, Epstein, Eyal, Israeli, Ofir, Lazar, Shirley, Caspi, Noa, Barnea, Ada, Dor, Eyal, Chomsky, Inbar, Pitel, Shani, Makdasi, Efi, Zichel, Ran, Mazor, Ohad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437483/
https://www.ncbi.nlm.nih.gov/pubmed/36059507
http://dx.doi.org/10.3389/fimmu.2022.942317
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author Rosenfeld, Ronit
Alcalay, Ron
Zvi, Anat
Ben-David, Alon
Noy-Porat, Tal
Chitlaru, Theodor
Epstein, Eyal
Israeli, Ofir
Lazar, Shirley
Caspi, Noa
Barnea, Ada
Dor, Eyal
Chomsky, Inbar
Pitel, Shani
Makdasi, Efi
Zichel, Ran
Mazor, Ohad
author_facet Rosenfeld, Ronit
Alcalay, Ron
Zvi, Anat
Ben-David, Alon
Noy-Porat, Tal
Chitlaru, Theodor
Epstein, Eyal
Israeli, Ofir
Lazar, Shirley
Caspi, Noa
Barnea, Ada
Dor, Eyal
Chomsky, Inbar
Pitel, Shani
Makdasi, Efi
Zichel, Ran
Mazor, Ohad
author_sort Rosenfeld, Ronit
collection PubMed
description Hyper-immune antisera from large mammals, in particular horses, are routinely used for life-saving anti-intoxication intervention. While highly efficient, the use of these immunotherapeutics is complicated by possible recipient reactogenicity and limited availability. Accordingly, there is an urgent need for alternative improved next-generation immunotherapies to respond to this issue of high public health priority. Here, we document the development of previously unavailable tools for equine antibody engineering. A novel primer set, EquPD v2020, based on equine V-gene data, was designed for efficient and accurate amplification of rearranged horse antibody V-segments. The primer set served for generation of immune phage display libraries, representing highly diverse V-gene repertoires of horses immunized against botulinum A or B neurotoxins. Highly specific scFv clones were selected and expressed as full-length antibodies, carrying equine V-genes and human Gamma1/Lambda constant genes, to be referred as “Centaur antibodies”. Preliminary assessment in a murine model of botulism established their therapeutic potential. The experimental approach detailed in the current report, represents a valuable tool for isolation and engineering of therapeutic equine antibodies.
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spelling pubmed-94374832022-09-03 Centaur antibodies: Engineered chimeric equine-human recombinant antibodies Rosenfeld, Ronit Alcalay, Ron Zvi, Anat Ben-David, Alon Noy-Porat, Tal Chitlaru, Theodor Epstein, Eyal Israeli, Ofir Lazar, Shirley Caspi, Noa Barnea, Ada Dor, Eyal Chomsky, Inbar Pitel, Shani Makdasi, Efi Zichel, Ran Mazor, Ohad Front Immunol Immunology Hyper-immune antisera from large mammals, in particular horses, are routinely used for life-saving anti-intoxication intervention. While highly efficient, the use of these immunotherapeutics is complicated by possible recipient reactogenicity and limited availability. Accordingly, there is an urgent need for alternative improved next-generation immunotherapies to respond to this issue of high public health priority. Here, we document the development of previously unavailable tools for equine antibody engineering. A novel primer set, EquPD v2020, based on equine V-gene data, was designed for efficient and accurate amplification of rearranged horse antibody V-segments. The primer set served for generation of immune phage display libraries, representing highly diverse V-gene repertoires of horses immunized against botulinum A or B neurotoxins. Highly specific scFv clones were selected and expressed as full-length antibodies, carrying equine V-genes and human Gamma1/Lambda constant genes, to be referred as “Centaur antibodies”. Preliminary assessment in a murine model of botulism established their therapeutic potential. The experimental approach detailed in the current report, represents a valuable tool for isolation and engineering of therapeutic equine antibodies. Frontiers Media S.A. 2022-08-19 /pmc/articles/PMC9437483/ /pubmed/36059507 http://dx.doi.org/10.3389/fimmu.2022.942317 Text en Copyright © 2022 Rosenfeld, Alcalay, Zvi, Ben-David, Noy-Porat, Chitlaru, Epstein, Israeli, Lazar, Caspi, Barnea, Dor, Chomsky, Pitel, Makdasi, Zichel and Mazor https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Rosenfeld, Ronit
Alcalay, Ron
Zvi, Anat
Ben-David, Alon
Noy-Porat, Tal
Chitlaru, Theodor
Epstein, Eyal
Israeli, Ofir
Lazar, Shirley
Caspi, Noa
Barnea, Ada
Dor, Eyal
Chomsky, Inbar
Pitel, Shani
Makdasi, Efi
Zichel, Ran
Mazor, Ohad
Centaur antibodies: Engineered chimeric equine-human recombinant antibodies
title Centaur antibodies: Engineered chimeric equine-human recombinant antibodies
title_full Centaur antibodies: Engineered chimeric equine-human recombinant antibodies
title_fullStr Centaur antibodies: Engineered chimeric equine-human recombinant antibodies
title_full_unstemmed Centaur antibodies: Engineered chimeric equine-human recombinant antibodies
title_short Centaur antibodies: Engineered chimeric equine-human recombinant antibodies
title_sort centaur antibodies: engineered chimeric equine-human recombinant antibodies
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437483/
https://www.ncbi.nlm.nih.gov/pubmed/36059507
http://dx.doi.org/10.3389/fimmu.2022.942317
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