Cargando…

Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease

BACKGROUND: Neuroinflammation plays a pathogenic role in Parkinson's disease (PD). Immunotherapies that restore brain homeostasis can mitigate neurodegeneration by transforming T cell phenotypes. Sargramostim has gained considerable attention as an immune transformer through laboratory bench to...

Descripción completa

Detalles Bibliográficos
Autores principales: Olson, Katherine E., Namminga, Krista L., Lu, Yaman, Schwab, Aaron D., Thurston, Mackenzie J., Abdelmoaty, Mai M., Kumar, Vikas, Wojtkiewicz, Melinda, Obaro, Helen, Santamaria, Pamela, Mosley, R. Lee, Gendelman, Howard E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138485/
https://www.ncbi.nlm.nih.gov/pubmed/34000620
http://dx.doi.org/10.1016/j.ebiom.2021.103380
_version_ 1783695820915212288
author Olson, Katherine E.
Namminga, Krista L.
Lu, Yaman
Schwab, Aaron D.
Thurston, Mackenzie J.
Abdelmoaty, Mai M.
Kumar, Vikas
Wojtkiewicz, Melinda
Obaro, Helen
Santamaria, Pamela
Mosley, R. Lee
Gendelman, Howard E.
author_facet Olson, Katherine E.
Namminga, Krista L.
Lu, Yaman
Schwab, Aaron D.
Thurston, Mackenzie J.
Abdelmoaty, Mai M.
Kumar, Vikas
Wojtkiewicz, Melinda
Obaro, Helen
Santamaria, Pamela
Mosley, R. Lee
Gendelman, Howard E.
author_sort Olson, Katherine E.
collection PubMed
description BACKGROUND: Neuroinflammation plays a pathogenic role in Parkinson's disease (PD). Immunotherapies that restore brain homeostasis can mitigate neurodegeneration by transforming T cell phenotypes. Sargramostim has gained considerable attention as an immune transformer through laboratory bench to bedside clinical studies. However, its therapeutic use has been offset by dose-dependent adverse events. Therefore, we performed a reduced drug dose regimen to evaluate safety and to uncover novel disease-linked biomarkers during 5 days/week sargramostim treatments for one year. METHODS: Five PD subjects were enrolled in a Phase 1b, unblinded, open-label study to assess safety and tolerability of 3 μg/kg/day sargramostim. Complete blood counts and chemistry profiles, physical examinations, adverse events (AEs), immune profiling, Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) scores, T cell phenotypes/function, DNA methylation, and gene and protein patterns were evaluated. FINDINGS: Sargramostim administered at 3 μg/kg/day significantly reduced numbers and severity of AEs/subject/month compared to 6 μg/kg/day treatment. While MDS-UPDRS Part III score reductions were recorded, peripheral blood immunoregulatory phenotypes and function were elevated. Hypomethylation of upstream FOXP3 DNA elements was also increased. INTERPRETATION: Long-term sargramostim treatment at 3 μg/kg/day is well-tolerated and effective in restoring immune homeostasis. There were decreased numbers and severity of AEs and restored peripheral immune function coordinate with increased numbers and function of Treg. MDS-UPDRS Part III scores did not worsen. Larger patient numbers need be evaluated to assess conclusive drug efficacy (ClinicalTrials.gov NCT03790670). FUNDING: The research was supported by community funds to the University of Nebraska Foundation and federal research support from 5 R01NS034239-25.
format Online
Article
Text
id pubmed-8138485
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-81384852021-05-24 Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease Olson, Katherine E. Namminga, Krista L. Lu, Yaman Schwab, Aaron D. Thurston, Mackenzie J. Abdelmoaty, Mai M. Kumar, Vikas Wojtkiewicz, Melinda Obaro, Helen Santamaria, Pamela Mosley, R. Lee Gendelman, Howard E. EBioMedicine Research Paper BACKGROUND: Neuroinflammation plays a pathogenic role in Parkinson's disease (PD). Immunotherapies that restore brain homeostasis can mitigate neurodegeneration by transforming T cell phenotypes. Sargramostim has gained considerable attention as an immune transformer through laboratory bench to bedside clinical studies. However, its therapeutic use has been offset by dose-dependent adverse events. Therefore, we performed a reduced drug dose regimen to evaluate safety and to uncover novel disease-linked biomarkers during 5 days/week sargramostim treatments for one year. METHODS: Five PD subjects were enrolled in a Phase 1b, unblinded, open-label study to assess safety and tolerability of 3 μg/kg/day sargramostim. Complete blood counts and chemistry profiles, physical examinations, adverse events (AEs), immune profiling, Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) scores, T cell phenotypes/function, DNA methylation, and gene and protein patterns were evaluated. FINDINGS: Sargramostim administered at 3 μg/kg/day significantly reduced numbers and severity of AEs/subject/month compared to 6 μg/kg/day treatment. While MDS-UPDRS Part III score reductions were recorded, peripheral blood immunoregulatory phenotypes and function were elevated. Hypomethylation of upstream FOXP3 DNA elements was also increased. INTERPRETATION: Long-term sargramostim treatment at 3 μg/kg/day is well-tolerated and effective in restoring immune homeostasis. There were decreased numbers and severity of AEs and restored peripheral immune function coordinate with increased numbers and function of Treg. MDS-UPDRS Part III scores did not worsen. Larger patient numbers need be evaluated to assess conclusive drug efficacy (ClinicalTrials.gov NCT03790670). FUNDING: The research was supported by community funds to the University of Nebraska Foundation and federal research support from 5 R01NS034239-25. Elsevier 2021-05-14 /pmc/articles/PMC8138485/ /pubmed/34000620 http://dx.doi.org/10.1016/j.ebiom.2021.103380 Text en 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 Research Paper
Olson, Katherine E.
Namminga, Krista L.
Lu, Yaman
Schwab, Aaron D.
Thurston, Mackenzie J.
Abdelmoaty, Mai M.
Kumar, Vikas
Wojtkiewicz, Melinda
Obaro, Helen
Santamaria, Pamela
Mosley, R. Lee
Gendelman, Howard E.
Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease
title Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease
title_full Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease
title_fullStr Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease
title_full_unstemmed Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease
title_short Safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of Parkinson's disease
title_sort safety, tolerability, and immune-biomarker profiling for year-long sargramostim treatment of parkinson's disease
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138485/
https://www.ncbi.nlm.nih.gov/pubmed/34000620
http://dx.doi.org/10.1016/j.ebiom.2021.103380
work_keys_str_mv AT olsonkatherinee safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT nammingakristal safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT luyaman safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT schwabaarond safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT thurstonmackenziej safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT abdelmoatymaim safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT kumarvikas safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT wojtkiewiczmelinda safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT obarohelen safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT santamariapamela safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT mosleyrlee safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease
AT gendelmanhowarde safetytolerabilityandimmunebiomarkerprofilingforyearlongsargramostimtreatmentofparkinsonsdisease