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A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis

BACKGROUND: GM1 gangliosidosis is a rare, fatal, neurodegenerative disease caused by mutations in the GLB1 gene and deficiency in β-galactosidase. Delay of symptom onset and increase in lifespan in a GM1 gangliosidosis cat model after adeno-associated viral (AAV) gene therapy treatment provide the b...

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Autores principales: Kell, Pamela, Sidhu, Rohini, Qian, Mingxing, Mishra, Sonali, Nicoli, Elena-Raluca, D'Souza, Precilla, Tifft, Cynthia J., Gross, Amanda L., Gray-Edwards, Heather L., Martin, Douglas R., Sena- Esteves, Miguel, Dietzen, Dennis J., Singh, Manmilan, Luo, Jingqin, Schaffer, Jean E., Ory, Daniel S., Jiang, Xuntian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277919/
https://www.ncbi.nlm.nih.gov/pubmed/37267847
http://dx.doi.org/10.1016/j.ebiom.2023.104627
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author Kell, Pamela
Sidhu, Rohini
Qian, Mingxing
Mishra, Sonali
Nicoli, Elena-Raluca
D'Souza, Precilla
Tifft, Cynthia J.
Gross, Amanda L.
Gray-Edwards, Heather L.
Martin, Douglas R.
Sena- Esteves, Miguel
Dietzen, Dennis J.
Singh, Manmilan
Luo, Jingqin
Schaffer, Jean E.
Ory, Daniel S.
Jiang, Xuntian
author_facet Kell, Pamela
Sidhu, Rohini
Qian, Mingxing
Mishra, Sonali
Nicoli, Elena-Raluca
D'Souza, Precilla
Tifft, Cynthia J.
Gross, Amanda L.
Gray-Edwards, Heather L.
Martin, Douglas R.
Sena- Esteves, Miguel
Dietzen, Dennis J.
Singh, Manmilan
Luo, Jingqin
Schaffer, Jean E.
Ory, Daniel S.
Jiang, Xuntian
author_sort Kell, Pamela
collection PubMed
description BACKGROUND: GM1 gangliosidosis is a rare, fatal, neurodegenerative disease caused by mutations in the GLB1 gene and deficiency in β-galactosidase. Delay of symptom onset and increase in lifespan in a GM1 gangliosidosis cat model after adeno-associated viral (AAV) gene therapy treatment provide the basis for AAV gene therapy trials. The availability of validated biomarkers would greatly improve assessment of therapeutic efficacy. METHODS: The liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to screen oligosaccharides as potential biomarkers for GM1 gangliosidosis. The structures of pentasaccharide biomarkers were determined with mass spectrometry, as well as chemical and enzymatic degradations. Comparison of LC-MS/MS data of endogenous and synthetic compounds confirmed the identification. The study samples were analyzed with fully validated LC-MS/MS methods. FINDINGS: We identified two pentasaccharide biomarkers, H3N2a and H3N2b, that were elevated more than 18-fold in patient plasma, cerebrospinal fluid (CSF), and urine. Only H3N2b was detectable in the cat model, and it was negatively correlated with β-galactosidase activity. Following intravenous (IV) AAV9 gene therapy treatment, reduction of H3N2b was observed in central nervous system, urine, plasma, and CSF samples from the cat model and in urine, plasma, and CSF samples from a patient. Reduction of H3N2b accurately reflected normalization of neuropathology in the cat model and improvement of clinical outcomes in the patient. INTERPRETATIONS: These results demonstrate that H3N2b is a useful pharmacodynamic biomarker to evaluate the efficacy of gene therapy for GM1 gangliosidosis. H3N2b will facilitate the translation of gene therapy from animal models to patients. FUNDING: This work was supported by grants U01NS114156, R01HD060576, ZIAHG200409, and P30 DK020579 from the 10.13039/100000002National Institutes of Health (NIH) and a grant from 10.13039/100003189National Tay-Sachs and Allied Diseases Association Inc.
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spelling pubmed-102779192023-06-20 A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis Kell, Pamela Sidhu, Rohini Qian, Mingxing Mishra, Sonali Nicoli, Elena-Raluca D'Souza, Precilla Tifft, Cynthia J. Gross, Amanda L. Gray-Edwards, Heather L. Martin, Douglas R. Sena- Esteves, Miguel Dietzen, Dennis J. Singh, Manmilan Luo, Jingqin Schaffer, Jean E. Ory, Daniel S. Jiang, Xuntian eBioMedicine Articles BACKGROUND: GM1 gangliosidosis is a rare, fatal, neurodegenerative disease caused by mutations in the GLB1 gene and deficiency in β-galactosidase. Delay of symptom onset and increase in lifespan in a GM1 gangliosidosis cat model after adeno-associated viral (AAV) gene therapy treatment provide the basis for AAV gene therapy trials. The availability of validated biomarkers would greatly improve assessment of therapeutic efficacy. METHODS: The liquid chromatography-tandem mass spectrometry (LC-MS/MS) was used to screen oligosaccharides as potential biomarkers for GM1 gangliosidosis. The structures of pentasaccharide biomarkers were determined with mass spectrometry, as well as chemical and enzymatic degradations. Comparison of LC-MS/MS data of endogenous and synthetic compounds confirmed the identification. The study samples were analyzed with fully validated LC-MS/MS methods. FINDINGS: We identified two pentasaccharide biomarkers, H3N2a and H3N2b, that were elevated more than 18-fold in patient plasma, cerebrospinal fluid (CSF), and urine. Only H3N2b was detectable in the cat model, and it was negatively correlated with β-galactosidase activity. Following intravenous (IV) AAV9 gene therapy treatment, reduction of H3N2b was observed in central nervous system, urine, plasma, and CSF samples from the cat model and in urine, plasma, and CSF samples from a patient. Reduction of H3N2b accurately reflected normalization of neuropathology in the cat model and improvement of clinical outcomes in the patient. INTERPRETATIONS: These results demonstrate that H3N2b is a useful pharmacodynamic biomarker to evaluate the efficacy of gene therapy for GM1 gangliosidosis. H3N2b will facilitate the translation of gene therapy from animal models to patients. FUNDING: This work was supported by grants U01NS114156, R01HD060576, ZIAHG200409, and P30 DK020579 from the 10.13039/100000002National Institutes of Health (NIH) and a grant from 10.13039/100003189National Tay-Sachs and Allied Diseases Association Inc. Elsevier 2023-05-31 /pmc/articles/PMC10277919/ /pubmed/37267847 http://dx.doi.org/10.1016/j.ebiom.2023.104627 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Kell, Pamela
Sidhu, Rohini
Qian, Mingxing
Mishra, Sonali
Nicoli, Elena-Raluca
D'Souza, Precilla
Tifft, Cynthia J.
Gross, Amanda L.
Gray-Edwards, Heather L.
Martin, Douglas R.
Sena- Esteves, Miguel
Dietzen, Dennis J.
Singh, Manmilan
Luo, Jingqin
Schaffer, Jean E.
Ory, Daniel S.
Jiang, Xuntian
A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis
title A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis
title_full A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis
title_fullStr A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis
title_full_unstemmed A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis
title_short A pentasaccharide for monitoring pharmacodynamic response to gene therapy in GM1 gangliosidosis
title_sort pentasaccharide for monitoring pharmacodynamic response to gene therapy in gm1 gangliosidosis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277919/
https://www.ncbi.nlm.nih.gov/pubmed/37267847
http://dx.doi.org/10.1016/j.ebiom.2023.104627
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