Cargando…
Nanovesicles released by OKT3 hybridoma express fully active antibodies
Recent findings have shown that nanovesicles preparations from either primary immune cells culture supernatants or plasma contain immunoglobulins, suggesting that a natural way of antibody production may be through exosome release. To verify this hypothesis, we used the OKT3 hybridoma clone, which p...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801098/ https://www.ncbi.nlm.nih.gov/pubmed/33404266 http://dx.doi.org/10.1080/14756366.2020.1852401 |
_version_ | 1783635500260655104 |
---|---|
author | Logozzi, Mariantonia Di Raimo, Rossella Properzi, Francesca Barca, Stefano Angelini, Daniela F. Mizzoni, Davide Falchi, Mario Battistini, Luca Fais, Stefano |
author_facet | Logozzi, Mariantonia Di Raimo, Rossella Properzi, Francesca Barca, Stefano Angelini, Daniela F. Mizzoni, Davide Falchi, Mario Battistini, Luca Fais, Stefano |
author_sort | Logozzi, Mariantonia |
collection | PubMed |
description | Recent findings have shown that nanovesicles preparations from either primary immune cells culture supernatants or plasma contain immunoglobulins, suggesting that a natural way of antibody production may be through exosome release. To verify this hypothesis, we used the OKT3 hybridoma clone, which produces a murine IgG2a monoclonal antibody used to reduce rejection in patients undergoing organ transplantation. We showed exosome-associated immunoglobulins in hybridoma supernatants, by Western blot, nanoscale flow cytometry and immunocapture-based ELISA. The OKT3-exo was also being able to trigger cytokines production in both CD4 and CD8 T cells. These results show that nanovesicles contain immunoglobulin and could be used for immunotherapy. These data could lead to a new approach to improve the effectiveness of therapeutic antibodies by exploiting their natural property to be expressed on nanovesicle membrane, that probably render them more stable and as a consequence more capable to interact with their specific ligand in the best way. |
format | Online Article Text |
id | pubmed-7801098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-78010982021-01-21 Nanovesicles released by OKT3 hybridoma express fully active antibodies Logozzi, Mariantonia Di Raimo, Rossella Properzi, Francesca Barca, Stefano Angelini, Daniela F. Mizzoni, Davide Falchi, Mario Battistini, Luca Fais, Stefano J Enzyme Inhib Med Chem Research Paper Recent findings have shown that nanovesicles preparations from either primary immune cells culture supernatants or plasma contain immunoglobulins, suggesting that a natural way of antibody production may be through exosome release. To verify this hypothesis, we used the OKT3 hybridoma clone, which produces a murine IgG2a monoclonal antibody used to reduce rejection in patients undergoing organ transplantation. We showed exosome-associated immunoglobulins in hybridoma supernatants, by Western blot, nanoscale flow cytometry and immunocapture-based ELISA. The OKT3-exo was also being able to trigger cytokines production in both CD4 and CD8 T cells. These results show that nanovesicles contain immunoglobulin and could be used for immunotherapy. These data could lead to a new approach to improve the effectiveness of therapeutic antibodies by exploiting their natural property to be expressed on nanovesicle membrane, that probably render them more stable and as a consequence more capable to interact with their specific ligand in the best way. Taylor & Francis 2021-01-06 /pmc/articles/PMC7801098/ /pubmed/33404266 http://dx.doi.org/10.1080/14756366.2020.1852401 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Logozzi, Mariantonia Di Raimo, Rossella Properzi, Francesca Barca, Stefano Angelini, Daniela F. Mizzoni, Davide Falchi, Mario Battistini, Luca Fais, Stefano Nanovesicles released by OKT3 hybridoma express fully active antibodies |
title | Nanovesicles released by OKT3 hybridoma express fully active antibodies |
title_full | Nanovesicles released by OKT3 hybridoma express fully active antibodies |
title_fullStr | Nanovesicles released by OKT3 hybridoma express fully active antibodies |
title_full_unstemmed | Nanovesicles released by OKT3 hybridoma express fully active antibodies |
title_short | Nanovesicles released by OKT3 hybridoma express fully active antibodies |
title_sort | nanovesicles released by okt3 hybridoma express fully active antibodies |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801098/ https://www.ncbi.nlm.nih.gov/pubmed/33404266 http://dx.doi.org/10.1080/14756366.2020.1852401 |
work_keys_str_mv | AT logozzimariantonia nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT diraimorossella nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT properzifrancesca nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT barcastefano nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT angelinidanielaf nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT mizzonidavide nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT falchimario nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT battistiniluca nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies AT faisstefano nanovesiclesreleasedbyokt3hybridomaexpressfullyactiveantibodies |