Skip to main content
Top
Published in: Neurology and Therapy 1/2019

Open Access 01-06-2019 | Review

Emerging Immunotherapies for Parkinson Disease

Authors: Samis M. A. Zella, Judith Metzdorf, Emine Ciftci, Friederike Ostendorf, Siegfried Muhlack, Ralf Gold, Lars Tönges

Published in: Neurology and Therapy | Issue 1/2019

Login to get access

Abstract

Symptomatic treatment options for Parkinson disease have steadily improved, and individualized therapeutic approaches are becoming established for every stage of the disease. However, disease-modifying therapy with a causal approach is still unavailable. The central causative role of alpha-synuclein pathology, including its progressive spread to most areas of the CNS, has been widely recognized, and a strong involvement of immune responses has recently been discovered. New immunologic technologies have been shown to effectively prevent the progression of alpha-synuclein pathology in animal models. These approaches have recently been translated into the first human clinical trials, representing a novel starting point for the causal therapy of Parkinson disease. In this review, the pathomechanistic role of alpha-synuclein and its influence on the surrounding cellular environment are analyzed with a strong focus on immune responses and neuroinflammation. The potential of novel immunotherapeutic approaches that reduce the burden of alpha-synuclein pathology in the CNS is critically evaluated, and currently ongoing human clinical trials are presented. The clinical development of these new immunotherapies is progressing rapidly and gives reason to hope that a causal therapy of Parkinson disease could be possible in the foreseeable future.
Literature
1.
go back to reference Poewe W, Seppi K, Tanner CM, Halliday GM, Brundin P, Volkmann J, et al. Parkinson disease. Nat Rev Dis Primers. 2017;3:17013.CrossRef Poewe W, Seppi K, Tanner CM, Halliday GM, Brundin P, Volkmann J, et al. Parkinson disease. Nat Rev Dis Primers. 2017;3:17013.CrossRef
2.
go back to reference Braak H, Del Tredici K, Rub U, De Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging. 2003;24(2):197–211.CrossRef Braak H, Del Tredici K, Rub U, De Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging. 2003;24(2):197–211.CrossRef
3.
go back to reference Klingelhoefer L, Reichmann H. Pathogenesis of Parkinson disease—the gut-brain axis and environmental factorS. NAT REV NEUROL. 2015;11(11):625–36.CrossRef Klingelhoefer L, Reichmann H. Pathogenesis of Parkinson disease—the gut-brain axis and environmental factorS. NAT REV NEUROL. 2015;11(11):625–36.CrossRef
4.
go back to reference Walsh DM, Selkoe DJ. A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration. Nat Rev Neurosci. 2016;17(4):251–60.CrossRef Walsh DM, Selkoe DJ. A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration. Nat Rev Neurosci. 2016;17(4):251–60.CrossRef
6.
go back to reference Chitnis T, Weiner HL. CNS inflammation and neurodegeneration. J Clin Invest. 2017;127(10):3577–87.CrossRef Chitnis T, Weiner HL. CNS inflammation and neurodegeneration. J Clin Invest. 2017;127(10):3577–87.CrossRef
7.
go back to reference Bendor JT, Logan TP, Edwards RH. The function of alpha-synuclein. Neuron. 2013;79(6):1044–66.CrossRef Bendor JT, Logan TP, Edwards RH. The function of alpha-synuclein. Neuron. 2013;79(6):1044–66.CrossRef
8.
go back to reference Braak H, del Tredici K. Neuropathological staging of brain pathology in sporadic Parkinson’s disease: separating the wheat from the chaff. J Parkinsons Dis. 2017;7(S1):S71–85.CrossRef Braak H, del Tredici K. Neuropathological staging of brain pathology in sporadic Parkinson’s disease: separating the wheat from the chaff. J Parkinsons Dis. 2017;7(S1):S71–85.CrossRef
9.
go back to reference Barbour R, Kling K, Anderson JP, Banducci K, Cole T, Diep L, et al. Red blood cells are the major source of alpha-synuclein in blood. Neurodegener Dis. 2008;5(2):55–9.CrossRef Barbour R, Kling K, Anderson JP, Banducci K, Cole T, Diep L, et al. Red blood cells are the major source of alpha-synuclein in blood. Neurodegener Dis. 2008;5(2):55–9.CrossRef
10.
go back to reference Doppler K, Jentschke HM, Schulmeyer L, Vadasz D, Janzen A, Luster M, et al. Dermal phospho-alpha-synuclein deposits confirm rem sleep behaviour disorder as prodromal Parkinson’s disease. Acta Neuropathol. 2017;133(4):535–45.CrossRef Doppler K, Jentschke HM, Schulmeyer L, Vadasz D, Janzen A, Luster M, et al. Dermal phospho-alpha-synuclein deposits confirm rem sleep behaviour disorder as prodromal Parkinson’s disease. Acta Neuropathol. 2017;133(4):535–45.CrossRef
11.
go back to reference Dauer W, Przedborski S. Parkinson’s disease: mechanisms and models. Neuron. 2003;39(6):889–909.CrossRef Dauer W, Przedborski S. Parkinson’s disease: mechanisms and models. Neuron. 2003;39(6):889–909.CrossRef
12.
go back to reference Baba M, Nakajo S, Tu PH, Tomita T, Nakaya K, Lee VM, et al. Aggregation of alpha-synuclein in lewy bodies of sporadic Parkinson’s disease and dementia with lewy bodies. Am J Pathol. 1998;152(4):879–84.PubMedPubMedCentral Baba M, Nakajo S, Tu PH, Tomita T, Nakaya K, Lee VM, et al. Aggregation of alpha-synuclein in lewy bodies of sporadic Parkinson’s disease and dementia with lewy bodies. Am J Pathol. 1998;152(4):879–84.PubMedPubMedCentral
13.
go back to reference Trinh J, Farrer M. Advances in the genetics of Parkinson disease. Nat Rev Neurol. 2013;9(8):445–54.CrossRef Trinh J, Farrer M. Advances in the genetics of Parkinson disease. Nat Rev Neurol. 2013;9(8):445–54.CrossRef
14.
go back to reference Burré J, Sharma M, Tsetsenis T, Buchman V, Etherton MR, Südhof TC. Alpha-synuclein promotes snare-complex assembly in vivo and in vitro. Science. 2010;329(5999):1663–7.CrossRef Burré J, Sharma M, Tsetsenis T, Buchman V, Etherton MR, Südhof TC. Alpha-synuclein promotes snare-complex assembly in vivo and in vitro. Science. 2010;329(5999):1663–7.CrossRef
15.
go back to reference Wong YC, Krainc D. Alpha-synuclein toxicity in neurodegeneration: mechanism and therapeutic strategies. Nat Med. 2017;23(2):1–13.CrossRef Wong YC, Krainc D. Alpha-synuclein toxicity in neurodegeneration: mechanism and therapeutic strategies. Nat Med. 2017;23(2):1–13.CrossRef
16.
go back to reference Bridi JC, Hirth F. Mechanisms, of alpha-synuclein induced synaptopathy in Parkinson’s disease. Front Neurosci. 2018;12:80.CrossRef Bridi JC, Hirth F. Mechanisms, of alpha-synuclein induced synaptopathy in Parkinson’s disease. Front Neurosci. 2018;12:80.CrossRef
17.
go back to reference Sudhof TC. A molecular machine for neurotransmitter release: synaptotagmin and beyond. Nat Med. 2013;19(10):1227–31.CrossRef Sudhof TC. A molecular machine for neurotransmitter release: synaptotagmin and beyond. Nat Med. 2013;19(10):1227–31.CrossRef
18.
go back to reference Lashuel HA, Overk CR, Oueslati A, Masliah E. The, many faces, of alpha-synuclein: from structure and toxicity to therapeutic target. Nat Rev Neurosci. 2013;14(1):38–48.CrossRef Lashuel HA, Overk CR, Oueslati A, Masliah E. The, many faces, of alpha-synuclein: from structure and toxicity to therapeutic target. Nat Rev Neurosci. 2013;14(1):38–48.CrossRef
19.
20.
go back to reference Bergstrom AL, Kallunki P, Fog K. Development, of passive immunotherapies for synucleinopathies. Mov Disord. 2016;31(2):203–13.CrossRef Bergstrom AL, Kallunki P, Fog K. Development, of passive immunotherapies for synucleinopathies. Mov Disord. 2016;31(2):203–13.CrossRef
21.
go back to reference Burre J, Sharma M, Sudhof TC. Definition of a molecular pathway mediating alpha-synuclein neurotoxicity. J Neurosci. 2015;35(13):5221–32.CrossRef Burre J, Sharma M, Sudhof TC. Definition of a molecular pathway mediating alpha-synuclein neurotoxicity. J Neurosci. 2015;35(13):5221–32.CrossRef
22.
go back to reference Marques O, Outeiro TF. Alpha-synuclein: from secretion to dysfunction and death. Cell Death Dis. 2012;3:E350.CrossRef Marques O, Outeiro TF. Alpha-synuclein: from secretion to dysfunction and death. Cell Death Dis. 2012;3:E350.CrossRef
23.
go back to reference Volpicelli-Daley LA, Luk KC, Patel TP, Tanik SA, Riddle DM, Stieber A, et al. Exogenous alpha-synuclein fibrils induce lewy body pathology leading to synaptic dysfunction and neuron death. Neuron. 2011;72(1):57–71.CrossRef Volpicelli-Daley LA, Luk KC, Patel TP, Tanik SA, Riddle DM, Stieber A, et al. Exogenous alpha-synuclein fibrils induce lewy body pathology leading to synaptic dysfunction and neuron death. Neuron. 2011;72(1):57–71.CrossRef
24.
go back to reference Volpicelli-Daley LA, Luk KC, Lee VM. Addition, of exogenous alpha-synuclein preformed fibrils to primary neuronal cultures to seed recruitment of endogenous alpha-synuclein to lewy body and lewy neurite-like aggregates. Nat Protoc. 2014;9(9):2135–46.CrossRef Volpicelli-Daley LA, Luk KC, Lee VM. Addition, of exogenous alpha-synuclein preformed fibrils to primary neuronal cultures to seed recruitment of endogenous alpha-synuclein to lewy body and lewy neurite-like aggregates. Nat Protoc. 2014;9(9):2135–46.CrossRef
25.
go back to reference Brahic M, Bousset L, Bieri G, Melki R, Gitler AD. Axonal transport and secretion of fibrillar forms of alpha-synuclein, ABETA42 peptide and httexon 1. Acta Neuropathol. 2016;131(4):539–48.CrossRef Brahic M, Bousset L, Bieri G, Melki R, Gitler AD. Axonal transport and secretion of fibrillar forms of alpha-synuclein, ABETA42 peptide and httexon 1. Acta Neuropathol. 2016;131(4):539–48.CrossRef
26.
go back to reference Mao X, Ou MT, Karuppagounder SS, Kam TI, Yin X, Xiong Y, et al. Pathological alpha-synuclein transmission initiated by binding lymphocyte-activation gene 3. Science. 2016;353(6307):aah3374.CrossRef Mao X, Ou MT, Karuppagounder SS, Kam TI, Yin X, Xiong Y, et al. Pathological alpha-synuclein transmission initiated by binding lymphocyte-activation gene 3. Science. 2016;353(6307):aah3374.CrossRef
27.
go back to reference Zhang Y, Chen K, Sloan SA, Bennett ML, Scholze AR, O’Keeffe S, et al. An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex. J Neurosci. 2014;34(36):11929–47.CrossRef Zhang Y, Chen K, Sloan SA, Bennett ML, Scholze AR, O’Keeffe S, et al. An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex. J Neurosci. 2014;34(36):11929–47.CrossRef
28.
go back to reference Diogenes MJ, Dias RB, Rombo DM, Vicente Miranda H, Maiolino F, Guerreiro P, et al. Extracellular alpha-synuclein oligomers modulate synaptic transmission and impair LTP via NMDA-receptor activation. J Neurosci. 2012;32(34):11750–62.CrossRef Diogenes MJ, Dias RB, Rombo DM, Vicente Miranda H, Maiolino F, Guerreiro P, et al. Extracellular alpha-synuclein oligomers modulate synaptic transmission and impair LTP via NMDA-receptor activation. J Neurosci. 2012;32(34):11750–62.CrossRef
29.
go back to reference Peelaerts W, Bousset L, van der Perren A, Moskalyuk A, Pulizzi R, Giugliano M, et al. Alpha-synuclein strains cause distinct synucleinopathies after local and systemic administration. Nature. 2015;522(7556):340–4.CrossRef Peelaerts W, Bousset L, van der Perren A, Moskalyuk A, Pulizzi R, Giugliano M, et al. Alpha-synuclein strains cause distinct synucleinopathies after local and systemic administration. Nature. 2015;522(7556):340–4.CrossRef
30.
go back to reference Luk KC, Kehm V, Carroll J, Zhang B, O’Brien P, Trojanowski JQ, et al. Pathological alpha-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice. Science. 2012;338(6109):949–53.CrossRef Luk KC, Kehm V, Carroll J, Zhang B, O’Brien P, Trojanowski JQ, et al. Pathological alpha-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice. Science. 2012;338(6109):949–53.CrossRef
31.
go back to reference Tonges L, Szego EM, Hause P, Saal KA, Tatenhorst L, Koch JC, et al. Alpha-synuclein mutations impair axonal regeneration in models of Parkinson’s disease. Front Aging Neurosci. 2014;6:239.PubMedPubMedCentral Tonges L, Szego EM, Hause P, Saal KA, Tatenhorst L, Koch JC, et al. Alpha-synuclein mutations impair axonal regeneration in models of Parkinson’s disease. Front Aging Neurosci. 2014;6:239.PubMedPubMedCentral
32.
go back to reference Herculano-Houzel S. The human brain in numbers: a linearly scaled-up primate brain. Front Hum Neurosci. 2009;3:31.CrossRef Herculano-Houzel S. The human brain in numbers: a linearly scaled-up primate brain. Front Hum Neurosci. 2009;3:31.CrossRef
33.
go back to reference Sofroniew MV, Vinters HV. Astrocytes: biology and pathology. Acta Neuropathol. 2010;119(1):7–35.CrossRef Sofroniew MV, Vinters HV. Astrocytes: biology and pathology. Acta Neuropathol. 2010;119(1):7–35.CrossRef
34.
go back to reference Rostami J, Holmqvist S, Lindstrom V, Sigvardson J, Westermark GT, Ingelsson M, et al. Human astrocytes transfer aggregated alpha-synuclein via tunneling nanotubes. J Neurosci. 2017;37(49):11835–53.CrossRef Rostami J, Holmqvist S, Lindstrom V, Sigvardson J, Westermark GT, Ingelsson M, et al. Human astrocytes transfer aggregated alpha-synuclein via tunneling nanotubes. J Neurosci. 2017;37(49):11835–53.CrossRef
35.
go back to reference Dexter DT, Jenner P. Parkinson disease: from pathology to molecular disease mechanisms. Free Radic Biol Med. 2013;62:132–44.CrossRef Dexter DT, Jenner P. Parkinson disease: from pathology to molecular disease mechanisms. Free Radic Biol Med. 2013;62:132–44.CrossRef
36.
go back to reference Gustafsson G, Lindstrom V, Rostami J, Nordstrom E, Lannfelt L, Bergstrom J, et al. Alpha-synuclein oligomer-selective antibodies reduce intracellular accumulation and mitochondrial impairment in alpha-synuclein exposed astrocytes. J Neuroinflammation. 2017;14(1):241.CrossRef Gustafsson G, Lindstrom V, Rostami J, Nordstrom E, Lannfelt L, Bergstrom J, et al. Alpha-synuclein oligomer-selective antibodies reduce intracellular accumulation and mitochondrial impairment in alpha-synuclein exposed astrocytes. J Neuroinflammation. 2017;14(1):241.CrossRef
37.
38.
go back to reference Wolf SA, Boddeke HW, Kettenmann H. Microglia in physiology and diseaSE. Annu Rev Physiol. 2017;79:619–43.CrossRef Wolf SA, Boddeke HW, Kettenmann H. Microglia in physiology and diseaSE. Annu Rev Physiol. 2017;79:619–43.CrossRef
39.
go back to reference Hoffmann A, Ettle B, Bruno A, Kulinich A, Hoffmann AC, Von Wittgenstein J, et al. Alpha-synuclein activates BV2 microglia dependent on its aggregation state. Biochem Biophys Res Commun. 2016;479(4):881–6.CrossRef Hoffmann A, Ettle B, Bruno A, Kulinich A, Hoffmann AC, Von Wittgenstein J, et al. Alpha-synuclein activates BV2 microglia dependent on its aggregation state. Biochem Biophys Res Commun. 2016;479(4):881–6.CrossRef
40.
go back to reference Kim C, Ho DH, Suk JE, You S, Michael S, Kang J, et al. Neuron-released oligomeric alpha-synuclein is an endogenous agonist of TLR2 for paracrine activation of microglia. Nat Commun. 2013;4:1562.CrossRef Kim C, Ho DH, Suk JE, You S, Michael S, Kang J, et al. Neuron-released oligomeric alpha-synuclein is an endogenous agonist of TLR2 for paracrine activation of microglia. Nat Commun. 2013;4:1562.CrossRef
41.
go back to reference Hoenen C, Gustin A, Birck C, Kirchmeyer M, Beaume N, Felten P, et al. Alpha-synuclein proteins promote pro-inflammatory cascades in microglia: stronger effects of the A53T mutant. PLoS One. 2016;11(9):E0162717.CrossRef Hoenen C, Gustin A, Birck C, Kirchmeyer M, Beaume N, Felten P, et al. Alpha-synuclein proteins promote pro-inflammatory cascades in microglia: stronger effects of the A53T mutant. PLoS One. 2016;11(9):E0162717.CrossRef
42.
go back to reference Bergström AL, Kallunki P, Fog K. Development, of passive immunotherapies for synucleinopathies. Mov Disord. 2016;31(2):203–13.CrossRef Bergström AL, Kallunki P, Fog K. Development, of passive immunotherapies for synucleinopathies. Mov Disord. 2016;31(2):203–13.CrossRef
43.
go back to reference Bruck D, Wenning GK, Stefanova N, Fellner L. Glia and alpha-synuclein in neurodegeneration: a complex interaction. Neurobiol Dis. 2016;85:262–74.CrossRef Bruck D, Wenning GK, Stefanova N, Fellner L. Glia and alpha-synuclein in neurodegeneration: a complex interaction. Neurobiol Dis. 2016;85:262–74.CrossRef
44.
go back to reference Games D, Valera E, Spencer B, Rockenstein E, Mante M, Adame A, et al. Reducing C-TERMINAL-truncated alpha-synuclein by immunotherapy attenuates neurodegeneration and propagation in Parkinson’s disease-like models. J Neurosci. 2014;34(28):9441–54.CrossRef Games D, Valera E, Spencer B, Rockenstein E, Mante M, Adame A, et al. Reducing C-TERMINAL-truncated alpha-synuclein by immunotherapy attenuates neurodegeneration and propagation in Parkinson’s disease-like models. J Neurosci. 2014;34(28):9441–54.CrossRef
45.
go back to reference Mandler M, Valera E, Rockenstein E, Mante M, Weninger H, Patrick C, et al. Active immunization against alpha-synuclein ameliorates the degenerative pathology and prevents demyelination in a model of multiple system atrophy. Mol Neurodegener. 2015;10:10.CrossRef Mandler M, Valera E, Rockenstein E, Mante M, Weninger H, Patrick C, et al. Active immunization against alpha-synuclein ameliorates the degenerative pathology and prevents demyelination in a model of multiple system atrophy. Mol Neurodegener. 2015;10:10.CrossRef
46.
go back to reference Sardi SP, Cedarbaum JM, Brundin P. Targeted therapies for Parkinson’s disease: from genetics to the clinic. Mov Disord. 2018;33(5):684–96.CrossRef Sardi SP, Cedarbaum JM, Brundin P. Targeted therapies for Parkinson’s disease: from genetics to the clinic. Mov Disord. 2018;33(5):684–96.CrossRef
47.
go back to reference Rockenstein E, Mallory M, Hashimoto M, Song D, Shults CW, Lang I, et al. Differential neuropathological alterations in transgenic mice expressing alpha-synuclein from the platelet-derived growth factor and Thy-1 promoters. J Neurosci Res. 2002;68(5):568–78.CrossRef Rockenstein E, Mallory M, Hashimoto M, Song D, Shults CW, Lang I, et al. Differential neuropathological alterations in transgenic mice expressing alpha-synuclein from the platelet-derived growth factor and Thy-1 promoters. J Neurosci Res. 2002;68(5):568–78.CrossRef
48.
go back to reference Masliah E, Rockenstein E, Adame A, Alford M, Crews L, Hashimoto M, et al. Effects of alpha-synuclein immunization in a mouse model of Parkinson’s disease. Neuron. 2005;46(6):857–68.CrossRef Masliah E, Rockenstein E, Adame A, Alford M, Crews L, Hashimoto M, et al. Effects of alpha-synuclein immunization in a mouse model of Parkinson’s disease. Neuron. 2005;46(6):857–68.CrossRef
50.
go back to reference Ghochikyan A, Petrushina I, Davtyan H, Hovakimyan A, Saing T, Davtyan A, et al. Immunogenicity of epitope vaccines targeting differenT B cell antigenic determinants of human α-synuclein: feasibility study. Neurosci Lett. 2014;560:86–91.CrossRef Ghochikyan A, Petrushina I, Davtyan H, Hovakimyan A, Saing T, Davtyan A, et al. Immunogenicity of epitope vaccines targeting differenT B cell antigenic determinants of human α-synuclein: feasibility study. Neurosci Lett. 2014;560:86–91.CrossRef
51.
go back to reference Mandler M, Valera E, Rockenstein E, Weninger H, Patrick C, Adame A, et al. Next-generation active immunization approach for synucleinopathies: implications for parkinson’s disease clinical trials. Acta Neuropathol. 2014;127(6):861–79.CrossRef Mandler M, Valera E, Rockenstein E, Weninger H, Patrick C, Adame A, et al. Next-generation active immunization approach for synucleinopathies: implications for parkinson’s disease clinical trials. Acta Neuropathol. 2014;127(6):861–79.CrossRef
52.
go back to reference Villadiego J, Labrador-Garrido A, Franco JM, Leal-Lasarte M, De Genst EJ, Dobson CM, et al. Immunization with Α-Synuclein/Grp94 reshapes peripheral immunity and suppresses microgliosis in a chronic Parkinsonism model. GLIA. 2018;66(1):191–205.CrossRef Villadiego J, Labrador-Garrido A, Franco JM, Leal-Lasarte M, De Genst EJ, Dobson CM, et al. Immunization with Α-Synuclein/Grp94 reshapes peripheral immunity and suppresses microgliosis in a chronic Parkinsonism model. GLIA. 2018;66(1):191–205.CrossRef
53.
go back to reference Kingwell K. Zeroing in on neurodegenerative Α-synuclein. Nat Rev Drug Discov. 2017;16(6):371–3.CrossRef Kingwell K. Zeroing in on neurodegenerative Α-synuclein. Nat Rev Drug Discov. 2017;16(6):371–3.CrossRef
54.
go back to reference Valera E, Masliah E. Immunotherapy for neurodegenerative diseases: focus on Α-synucleinopathies. Pharmacol Ther. 2013;138(3):311–22.CrossRef Valera E, Masliah E. Immunotherapy for neurodegenerative diseases: focus on Α-synucleinopathies. Pharmacol Ther. 2013;138(3):311–22.CrossRef
55.
go back to reference Affiris announces encouraging long-term data from a series of first-in-human studies using Affitope® PD01A targeting oligomeric alpha-synuclein in early Parkinson’s disease Patients [Press Release]. 2018. Affiris announces encouraging long-term data from a series of first-in-human studies using Affitope® PD01A targeting oligomeric alpha-synuclein in early Parkinson’s disease Patients [Press Release]. 2018.
57.
go back to reference Masliah E, Rockenstein E, Mante M, Crews L, Spencer B, Adame A, et al. Passive immunization reduces behavioral and neuropathological deficits in an alpha-synuclein transgenic model of lewy body disease. PLoS One. 2011;6(4):E19338.CrossRef Masliah E, Rockenstein E, Mante M, Crews L, Spencer B, Adame A, et al. Passive immunization reduces behavioral and neuropathological deficits in an alpha-synuclein transgenic model of lewy body disease. PLoS One. 2011;6(4):E19338.CrossRef
58.
go back to reference Mishizen-Eberz AJ, Norris EH, Giasson BI, Hodara R, Ischiropoulos H, Lee VM, et al. Cleavage of alpha-synuclein by calpain: potential role in degradation of fibrillized and nitrated species of alpha-synuclein. Biochemistry. 2005;44(21):7818–29.CrossRef Mishizen-Eberz AJ, Norris EH, Giasson BI, Hodara R, Ischiropoulos H, Lee VM, et al. Cleavage of alpha-synuclein by calpain: potential role in degradation of fibrillized and nitrated species of alpha-synuclein. Biochemistry. 2005;44(21):7818–29.CrossRef
59.
go back to reference Tofaris GK, Garcia Reitböck P, Humby T, Lambourne SL, O’Connell M, Ghetti B, et al. Pathological changes in dopaminergic nerve cells of the substantia nigra and olfactory bulb in mice transgenic for truncated human alpha-synuclein(1-120): implications for lewy body disorders. J Neurosci. 2006;26(15):3942–50.CrossRef Tofaris GK, Garcia Reitböck P, Humby T, Lambourne SL, O’Connell M, Ghetti B, et al. Pathological changes in dopaminergic nerve cells of the substantia nigra and olfactory bulb in mice transgenic for truncated human alpha-synuclein(1-120): implications for lewy body disorders. J Neurosci. 2006;26(15):3942–50.CrossRef
60.
go back to reference Bae EJ, Lee HJ, Rockenstein E, Ho DH, Park EB, Yang NY, et al. Antibody-aided clearance of extracellular Α-synuclein prevents cell-to-cell aggregate transmission. J Neurosci. 2012;32(39):13454–69.CrossRef Bae EJ, Lee HJ, Rockenstein E, Ho DH, Park EB, Yang NY, et al. Antibody-aided clearance of extracellular Α-synuclein prevents cell-to-cell aggregate transmission. J Neurosci. 2012;32(39):13454–69.CrossRef
61.
go back to reference Fleming SM, Salcedo J, Fernagut PO, Rockenstein E, Masliah E, Levine MS, et al. Early and progressive sensorimotor anomalies in mice overexpressing wild-type human alpha-synuclein. J Neurosci. 2004;24(42):9434–40.CrossRef Fleming SM, Salcedo J, Fernagut PO, Rockenstein E, Masliah E, Levine MS, et al. Early and progressive sensorimotor anomalies in mice overexpressing wild-type human alpha-synuclein. J Neurosci. 2004;24(42):9434–40.CrossRef
62.
go back to reference Shahaduzzaman M, Nash K, Hudson C, Sharif M, Grimmig B, Lin X, et al. anti-human Α-synuclein N-terminal peptide antibody protects against dopaminergic cell death and ameliorates behavioral deficits in an aav-α-synuclein rat model of Parkinson’s Disease. PLoS One. 2015;10(2):E0116841.CrossRef Shahaduzzaman M, Nash K, Hudson C, Sharif M, Grimmig B, Lin X, et al. anti-human Α-synuclein N-terminal peptide antibody protects against dopaminergic cell death and ameliorates behavioral deficits in an aav-α-synuclein rat model of Parkinson’s Disease. PLoS One. 2015;10(2):E0116841.CrossRef
63.
go back to reference Tran HT, Chung CH, Iba M, Zhang B, Trojanowski JQ, Luk KC, et al. Α-synuclein immunotherapy blocks uptake and templated propagation of misfolded α-synuclein and neurodegeneration. Cell Rep. 2014;7(6):2054–65.CrossRef Tran HT, Chung CH, Iba M, Zhang B, Trojanowski JQ, Luk KC, et al. Α-synuclein immunotherapy blocks uptake and templated propagation of misfolded α-synuclein and neurodegeneration. Cell Rep. 2014;7(6):2054–65.CrossRef
64.
go back to reference Kahle PJ, Neumann M, Ozmen L, Muller V, Jacobsen H, Schindzielorz A, et al. Subcellular localization of wild-type and Parkinson’s disease-associated mutant alpha-synuclein in human and transgenic mouse brain. J Neurosci. 2000;20(17):6365–73.CrossRef Kahle PJ, Neumann M, Ozmen L, Muller V, Jacobsen H, Schindzielorz A, et al. Subcellular localization of wild-type and Parkinson’s disease-associated mutant alpha-synuclein in human and transgenic mouse brain. J Neurosci. 2000;20(17):6365–73.CrossRef
65.
go back to reference Lindström V, Fagerqvist T, Nordström E, Eriksson F, Lord A, Tucker S, et al. Immunotherapy targeting α-synuclein protofibrils reduced pathology iN (THY-1)-H[A30P] α-synuclein mice. Neurobiol Dis. 2014;69:134–43.CrossRef Lindström V, Fagerqvist T, Nordström E, Eriksson F, Lord A, Tucker S, et al. Immunotherapy targeting α-synuclein protofibrils reduced pathology iN (THY-1)-H[A30P] α-synuclein mice. Neurobiol Dis. 2014;69:134–43.CrossRef
66.
go back to reference Gustafsson G, Eriksson F, Möller C, Da Fonseca TL, Outeiro TF, LannfelT L, et al. Cellular uptake of α-synuclein oligomer-selective antibodies is enhanced by the extracellular presence of α-synuclein and mediated via Fcγ ReceptorS. Cell Mol Neurobiol. 2017;37(1):121–31.CrossRef Gustafsson G, Eriksson F, Möller C, Da Fonseca TL, Outeiro TF, LannfelT L, et al. Cellular uptake of α-synuclein oligomer-selective antibodies is enhanced by the extracellular presence of α-synuclein and mediated via Fcγ ReceptorS. Cell Mol Neurobiol. 2017;37(1):121–31.CrossRef
67.
go back to reference El-Agnaf O, Overk C, Rockenstein E, Mante M, Florio J, Adame A, et al. Differential effects of immunotherapy with antibodies targeting α-synuclein oligomers and fibrils in a transgenic model of synucleinopathy. Neurobiol Dis. 2017;104:85–96.CrossRef El-Agnaf O, Overk C, Rockenstein E, Mante M, Florio J, Adame A, et al. Differential effects of immunotherapy with antibodies targeting α-synuclein oligomers and fibrils in a transgenic model of synucleinopathy. Neurobiol Dis. 2017;104:85–96.CrossRef
68.
go back to reference Schenk DB, Koller M, Ness DK, Griffith SG, Grundman M, Zago W, et al. First-in-human assessment of PRX002, an anti-alpha-synuclein monoclonal antibody, in healthy volunteers. Mov Disord. 2017;32(2):211–8.CrossRef Schenk DB, Koller M, Ness DK, Griffith SG, Grundman M, Zago W, et al. First-in-human assessment of PRX002, an anti-alpha-synuclein monoclonal antibody, in healthy volunteers. Mov Disord. 2017;32(2):211–8.CrossRef
70.
go back to reference Weihofen A, Patel H, Huy C, Liu C, Combaluzier I, Mueller-Steiner S, et al. Binding and functional characterization of human-derived anti-alpha-synuclein antibody BIIB054. Neurodeg Dis. 2017;17 (SUPPL 1)(8):59. Weihofen A, Patel H, Huy C, Liu C, Combaluzier I, Mueller-Steiner S, et al. Binding and functional characterization of human-derived anti-alpha-synuclein antibody BIIB054. Neurodeg Dis. 2017;17 (SUPPL 1)(8):59.
71.
go back to reference Brys M, Hung S, Fanning L, Penner N, Yang M, Welch M, et al. Randomized, double- blind, placebo-controlled, single ascending dose study of antialpha-synuclein antibody biib054 in patients with Parkinson disease. Neurology. 2018;90(15 15 SUPPLEMENT):S26.001. Brys M, Hung S, Fanning L, Penner N, Yang M, Welch M, et al. Randomized, double- blind, placebo-controlled, single ascending dose study of antialpha-synuclein antibody biib054 in patients with Parkinson disease. Neurology. 2018;90(15 15 SUPPLEMENT):S26.001.
73.
go back to reference Wisniewski T, Goni F. Immunotherapeutic approaches for Alzheimer’s disease. Neuron. 2015;85(6):1162–76.CrossRef Wisniewski T, Goni F. Immunotherapeutic approaches for Alzheimer’s disease. Neuron. 2015;85(6):1162–76.CrossRef
74.
75.
go back to reference Guy B. The perfect mix: recent progress in adjuvant research. Nat Rev Microbiol. 2007;5(7):505–17.CrossRef Guy B. The perfect mix: recent progress in adjuvant research. Nat Rev Microbiol. 2007;5(7):505–17.CrossRef
76.
go back to reference Tabira T. Immunization therapy for alzheimer disease: a comprehensive review of active immunization strategies. Tohoku J Exp Med. 2010;220(2):95–106.CrossRef Tabira T. Immunization therapy for alzheimer disease: a comprehensive review of active immunization strategies. Tohoku J Exp Med. 2010;220(2):95–106.CrossRef
77.
go back to reference Penninkilampi R, Brothers HM, Eslick GD. Safety and efficacy of anti-amyloid-beta immunotherapy in Alzheimer’s disease: a systematic review and meta-analysis. J Neuroimmune Pharmacol. 2017;12(1):194–203.CrossRef Penninkilampi R, Brothers HM, Eslick GD. Safety and efficacy of anti-amyloid-beta immunotherapy in Alzheimer’s disease: a systematic review and meta-analysis. J Neuroimmune Pharmacol. 2017;12(1):194–203.CrossRef
Metadata
Title
Emerging Immunotherapies for Parkinson Disease
Authors
Samis M. A. Zella
Judith Metzdorf
Emine Ciftci
Friederike Ostendorf
Siegfried Muhlack
Ralf Gold
Lars Tönges
Publication date
01-06-2019
Publisher
Springer Healthcare
Published in
Neurology and Therapy / Issue 1/2019
Print ISSN: 2193-8253
Electronic ISSN: 2193-6536
DOI
https://doi.org/10.1007/s40120-018-0122-z

Other articles of this Issue 1/2019

Neurology and Therapy 1/2019 Go to the issue