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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9437483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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