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Amyotrophic Lateral Sclerosis Volume 12, 2011 - Issue 6
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Research Article

Anti-superoxide dismutase antibodies are associated with survival in patients with sporadic amyotrophic lateral sclerosis

Marka van BlitterswijkDepartment of Neurology, University of Massachusetts Medical Center, Worcester, Massachusetts; Current Address for MVB: Department of Neurology, University Medical Center Utrecht, Heidelberglaan 100, 3508 GA Utrecht, the Netherlands
,
Sunita GulatiDivision of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts
,
Elizabeth SmootDepartment of Biostatistics, Massachusetts General Hospital, Boston, Massachusetts
,
Matthew JaffaNeurology Clinical Trials Unit, Massachusetts General Hospital, Charlestown, Massachusetts
,
Nancy MaherBrigham and Women’s Hospital, Harvard NeuroDiscovery Biomarker Program, Cambridge, Massachusetts
,
Bradley T. HymanHarvard NeuroDiscovery Center Biomarker Program, Harvard Medical School, Cambridge, Massachusetts
,
Adrian J. IvinsonHarvard NeuroDiscovery Center Biomarker Program, Harvard Medical School, Cambridge, Massachusetts
,
Clemens R. ScherzerHarvard NeuroDiscovery Center Biomarker Program, Harvard Medical School, Cambridge, Massachusetts;Center for Neurologic Diseases, Brigham and Women’s Hospital, Cambridge, Massachusetts
,
David A. SchoenfeldDepartment of Biostatistics, Massachusetts General Hospital, Boston, Massachusetts
,
Merit E. CudkowiczNeurology Clinical Trials Unit, Massachusetts General Hospital, Charlestown, Massachusetts
,
Robert H. Brown JrDepartment of Neurology, University of Massachusetts Medical Center, Worcester, Massachusetts
&
Daryl A. BoscoDepartment of Neurology, University of Massachusetts Medical Center, Worcester, MassachusettsCorrespondence[email protected]
 show all
Pages 430-438 | Received 18 Feb 2011, Accepted 21 Apr 2011, Published online: 24 Oct 2011

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. (2014) THEME 1 IMPROVING DIAGNOSIS, PROGNOSIS AND DISEASE PROGRESSION. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 15:sup1, pages 57-67.
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Stefan Mimic, Başak Aru, Cemil Pehlivanoğlu, Hadi Sleiman, Pavle R. Andjus & Gülderen Yanıkkaya Demirel. (2023) Immunology of amyotrophic lateral sclerosis – role of the innate and adaptive immunity. Frontiers in Neuroscience 17.
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Hélèna L. Denis, Melanie Alpaugh, Claudia P. Alvarez, Alexis Fenyi, Roger A. Barker, Sylvain Chouinard, Cheryl H. Arrowsmith, Ronald Melki, Richard Labib, Rachel J. Harding & Francesca Cicchetti. (2023) Detection of antibodies against the huntingtin protein in human plasma. Cellular and Molecular Life Sciences 80:2.
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Meenakshi Sundaram Kumar, Megan E. Fowler-Magaw, Daniel Kulick, Sivakumar Boopathy, Del Hayden Gadd, Melissa Rotunno, Catherine Douthwright, Diane Golebiowski, Issa Yusuf, Zuoshang Xu, Robert H. BrownJr.Jr., Miguel Sena-Esteves, Alison L. O'Neil & Daryl A. Bosco. (2022) Anti-SOD1 Nanobodies That Stabilize Misfolded SOD1 Proteins Also Promote Neurite Outgrowth in Mutant SOD1 Human Neurons. International Journal of Molecular Sciences 23:24, pages 16013.
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Giuseppe Schirò, Vincenzo Di Stefano, Salvatore Iacono, Antonino Lupica, Filippo Brighina, Roberto Monastero & Carmela Rita Balistreri. (2022) Advances on Cellular Clonotypic Immunity in Amyotrophic Lateral Sclerosis. Brain Sciences 12:10, pages 1412.
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Yoshiaki Furukawa & Eiichi Tokuda. (2020) Does wild-type Cu/Zn-superoxide dismutase have pathogenic roles in amyotrophic lateral sclerosis?. Translational Neurodegeneration 9:1.
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Eiichi Tokuda, Yo-ichi Takei, Shinji Ohara, Noriko Fujiwara, Isao Hozumi & Yoshiaki Furukawa. (2019) Wild-type Cu/Zn-superoxide dismutase is misfolded in cerebrospinal fluid of sporadic amyotrophic lateral sclerosis. Molecular Neurodegeneration 14:1.
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Sid E. O'Bryant, Melissa Edwards, Fan Zhang, Leigh A. Johnson, James Hall, Yuliya Kuras & Clemens R. Scherzer. (2019) Potential two‐step proteomic signature for Parkinson's disease: Pilot analysis in the Harvard Biomarkers Study. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring 11:1, pages 374-382.
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Gareth S. A. Wright, Svetlana V. Antonyuk & S. Samar Hasnain. (2019) The biophysics of superoxide dismutase-1 and amyotrophic lateral sclerosis. Quarterly Reviews of Biophysics 52.
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Marcel Maier, Tobias Welt, Fabian WirthFabio Montrasio, Daniel PreisigJordan McAfooseFernando G. Vieira, Luka Kulic, Claudia Späni, Thilo StehleSteve PerrinMarkus WeberChristoph HockRoger M. NitschJan Grimm. (2018) A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis. Science Translational Medicine 10:470.
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W. Allison, Michèle DuVal, Kim Nguyen-Phuoc & Patricia Leighton. (2017) Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology. International Journal of Molecular Sciences 18:10, pages 2223.
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Charles Schutt, Howard E. Gendelman & R. Lee Mosley. 2017. Neuroimmune Pharmacology. Neuroimmune Pharmacology 767 797 .
Owen M. Peters, Mehdi Ghasemi & Robert H. BrownJr.Jr.. (2015) Emerging mechanisms of molecular pathology in ALS. Journal of Clinical Investigation 125:5, pages 1767-1779.
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Andrea Malaspina, Fabiola Puentes & Sandra Amor. (2015) Disease origin and progression in amyotrophic lateral sclerosis: an immunology perspective. International Immunology 27:3, pages 117-129.
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Monica Bucchia, Agnese Ramirez, Valeria Parente, Chiara Simone, Monica Nizzardo, Francesca Magri, Sara Dametti & Stefania Corti. (2015) Therapeutic Development in Amyotrophic Lateral Sclerosis. Clinical Therapeutics 37:3, pages 668-680.
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F. Puentes, J. Topping, J. Kuhle, B. J. van der Star, A. Douiri, G. Giovannoni, D. Baker, S. Amor & A. Malaspina. (2013) Immune reactivity to neurofilament proteins in the clinical staging of amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery & Psychiatry 85:3, pages 274-278.
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Kevin D Foust, Desirée L Salazar, Shibi Likhite, Laura Ferraiuolo, Dara Ditsworth, Hristelina Ilieva, Kathrin Meyer, Leah Schmelzer, Lyndsey Braun, Don W Cleveland & Brian K Kaspar. (2013) Therapeutic AAV9-mediated Suppression of Mutant SOD1 Slows Disease Progression and Extends Survival in Models of Inherited ALS. Molecular Therapy 21:12, pages 2148-2159.
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Inhee Choi, Elizabeth Lee & Luke P. Lee. (2014) Current nano/biotechnological approaches in amyotrophic lateral sclerosis. Biomedical Engineering Letters 3:4, pages 209-222.
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Teresa J. Broering, Hongyan Wang, Naomi K. Boatright, Yang Wang, Katherine Baptista, Gilda Shayan, Kerry A. Garrity, Can Kayatekin, Daryl A. Bosco, C. Robert Matthews, Donna M. Ambrosino, Zuoshang Xu & Gregory J. Babcock. (2013) Identification of Human Monoclonal Antibodies Specific for Human SOD1 Recognizing Distinct Epitopes and Forms of SOD1. PLoS ONE 8:4, pages e61210.
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Vikram Khipple Mulligan, Aaron Kerman, Rob C. Laister, Priya Roy Sharda, Pharhad Eli Arslan & Avijit Chakrabartty. (2012) Early Steps in Oxidation-Induced SOD1 Misfolding: Implications for Non-Amyloid Protein Aggregation in Familial ALS. Journal of Molecular Biology 421:4-5, pages 631-652.
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