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Investigation of Cas9 antibodies in the human eye
Preexisting immunity against Cas9 proteins in humans represents a safety risk for CRISPR–Cas9 technologies. However, it is unclear to what extent preexisting Cas9 immunity is relevant to the eye as it is targeted for early in vivo CRISPR–Cas9 clinical trials. While the eye lacks T-cells, it contains...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881612/ https://www.ncbi.nlm.nih.gov/pubmed/35217666 http://dx.doi.org/10.1038/s41467-022-28674-1 |
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author | Toral, Marcus A. Charlesworth, Carsten T. Ng, Benjamin Chemudupati, Teja Homma, Shota Nakauchi, Hiromitsu Bassuk, Alexander G. Porteus, Matthew H. Mahajan, Vinit B. |
author_facet | Toral, Marcus A. Charlesworth, Carsten T. Ng, Benjamin Chemudupati, Teja Homma, Shota Nakauchi, Hiromitsu Bassuk, Alexander G. Porteus, Matthew H. Mahajan, Vinit B. |
author_sort | Toral, Marcus A. |
collection | PubMed |
description | Preexisting immunity against Cas9 proteins in humans represents a safety risk for CRISPR–Cas9 technologies. However, it is unclear to what extent preexisting Cas9 immunity is relevant to the eye as it is targeted for early in vivo CRISPR–Cas9 clinical trials. While the eye lacks T-cells, it contains antibodies, cytokines, and resident immune cells. Although precise mechanisms are unclear, intraocular inflammation remains a major cause of vision loss. Here, we used immunoglobulin isotyping and ELISA platforms to profile antibodies in serum and vitreous fluid biopsies from human adult subjects and Cas9-immunized mice. We observed high prevalence of preexisting Cas9-reactive antibodies in serum but not in the eye. However, we detected intraocular antibodies reactive to S. pyogenes-derived Cas9 after S. pyogenes intraocular infection. Our data suggest that serum antibody concentration may determine whether specific intraocular antibodies develop, but preexisting immunity to Cas9 may represent a lower risk in human eyes than systemically. |
format | Online Article Text |
id | pubmed-8881612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88816122022-03-17 Investigation of Cas9 antibodies in the human eye Toral, Marcus A. Charlesworth, Carsten T. Ng, Benjamin Chemudupati, Teja Homma, Shota Nakauchi, Hiromitsu Bassuk, Alexander G. Porteus, Matthew H. Mahajan, Vinit B. Nat Commun Article Preexisting immunity against Cas9 proteins in humans represents a safety risk for CRISPR–Cas9 technologies. However, it is unclear to what extent preexisting Cas9 immunity is relevant to the eye as it is targeted for early in vivo CRISPR–Cas9 clinical trials. While the eye lacks T-cells, it contains antibodies, cytokines, and resident immune cells. Although precise mechanisms are unclear, intraocular inflammation remains a major cause of vision loss. Here, we used immunoglobulin isotyping and ELISA platforms to profile antibodies in serum and vitreous fluid biopsies from human adult subjects and Cas9-immunized mice. We observed high prevalence of preexisting Cas9-reactive antibodies in serum but not in the eye. However, we detected intraocular antibodies reactive to S. pyogenes-derived Cas9 after S. pyogenes intraocular infection. Our data suggest that serum antibody concentration may determine whether specific intraocular antibodies develop, but preexisting immunity to Cas9 may represent a lower risk in human eyes than systemically. Nature Publishing Group UK 2022-02-25 /pmc/articles/PMC8881612/ /pubmed/35217666 http://dx.doi.org/10.1038/s41467-022-28674-1 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Toral, Marcus A. Charlesworth, Carsten T. Ng, Benjamin Chemudupati, Teja Homma, Shota Nakauchi, Hiromitsu Bassuk, Alexander G. Porteus, Matthew H. Mahajan, Vinit B. Investigation of Cas9 antibodies in the human eye |
title | Investigation of Cas9 antibodies in the human eye |
title_full | Investigation of Cas9 antibodies in the human eye |
title_fullStr | Investigation of Cas9 antibodies in the human eye |
title_full_unstemmed | Investigation of Cas9 antibodies in the human eye |
title_short | Investigation of Cas9 antibodies in the human eye |
title_sort | investigation of cas9 antibodies in the human eye |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881612/ https://www.ncbi.nlm.nih.gov/pubmed/35217666 http://dx.doi.org/10.1038/s41467-022-28674-1 |
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