Literature DB >> 19788637

Continuous intraventricular infusion of pentosan polysulfate: clinical trial against prion diseases.

Yoshio Tsuboi1, Katsumi Doh-Ura, Tatsuo Yamada.   

Abstract

Prion diseases are progressive neurological disorders due to abnormal prion protein (PrP(Sc)) deposition in the central nervous system. At present, there is no effective treatment available for any form of prion disease. Pentosan polysulfate (PPS) has been shown to prolong significantly the incubation period in mice with PrP(Sc) infection when administered to the cerebral ventricles in preclinical trials. In human studies conducted in European countries and Japan, intraventricular PPS was administered to patients with different forms of prion disease and was well tolerated. We report 11 patients with prion disease treated with intraventricular PPS at Fukuoka University from 2004. Cases included three familial CJD (two with V180I mutation, one GSS with P102L mutation), two iatrogenic CJD, and six sporadic CJD cases. At present, average survival period after treatment was 24.2 months (range, 4-49). Seven cases died of sepsis and pneumonia. Subdural effusion with various degrees was seen on CT scan in most cases. Except for these, adverse effects did not occur in the treatment period. Although our preliminary study of the new treatment with PPS by continuous intraventricular infusion showed no apparent improvement of clinical features in patients with prion disease, the possibility of extended survival in some patients receiving long-term PPS was suggested.

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Year:  2009        PMID: 19788637     DOI: 10.1111/j.1440-1789.2009.01058.x

Source DB:  PubMed          Journal:  Neuropathology        ISSN: 0919-6544            Impact factor:   1.906


  38 in total

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Authors:  Kazuchika Nishitsuji; Kenji Uchimura
Journal:  Glycoconj J       Date:  2017-04-11       Impact factor: 2.916

Review 2.  Rapidly progressive dementias and the treatment of human prion diseases.

Authors:  Brian S Appleby; Constantine G Lyketsos
Journal:  Expert Opin Pharmacother       Date:  2010-11-23       Impact factor: 3.889

3.  PRION-1 scales analysis supports use of functional outcome measures in prion disease.

Authors:  S Mead; M Ranopa; G S Gopalakrishnan; A G B Thompson; P Rudge; S Wroe; A Kennedy; F Hudson; A MacKay; J H Darbyshire; J Collinge; A S Walker
Journal:  Neurology       Date:  2011-10-19       Impact factor: 9.910

4.  The crystal structure of an octapeptide repeat of the prion protein in complex with a Fab fragment of the POM2 antibody.

Authors:  Mridula Swayampakula; Pravas Kumar Baral; Adriano Aguzzi; Nat N V Kav; Michael N G James
Journal:  Protein Sci       Date:  2013-05-31       Impact factor: 6.725

5.  Validation of Poly(Propylene Imine) Glycodendrimers Towards Their Anti-prion Conversion Efficiency.

Authors:  Matthias Schmitz; Niccolo Candelise; Eirini Kanata; Franc Llorens; Katrin Thüne; Anna Villar-Piqué; Susana Margarida da Silva Correia; Dimitra Dafou; Theodoros Sklaviadis; Dietmar Appelhans; Inga Zerr
Journal:  Mol Neurobiol       Date:  2019-12-17       Impact factor: 5.590

6.  Efficacy and mechanism of a glycoside compound inhibiting abnormal prion protein formation in prion-infected cells: implications of interferon and phosphodiesterase 4D-interacting protein.

Authors:  Keiko Nishizawa; Ayumi Oguma; Maki Kawata; Yuji Sakasegawa; Kenta Teruya; Katsumi Doh-ura
Journal:  J Virol       Date:  2014-01-22       Impact factor: 5.103

Review 7.  Developing Therapeutics for PrP Prion Diseases.

Authors:  Kurt Giles; Steven H Olson; Stanley B Prusiner
Journal:  Cold Spring Harb Perspect Med       Date:  2017-04-03       Impact factor: 6.915

8.  Specific glycosaminoglycan chain length and sulfation patterns are required for cell uptake of tau versus α-synuclein and β-amyloid aggregates.

Authors:  Barbara E Stopschinski; Brandon B Holmes; Gregory M Miller; Victor A Manon; Jaime Vaquer-Alicea; William L Prueitt; Linda C Hsieh-Wilson; Marc I Diamond
Journal:  J Biol Chem       Date:  2018-05-11       Impact factor: 5.157

Review 9.  Therapies for human prion diseases.

Authors:  Peter K Panegyres; Elizabeth Armari
Journal:  Am J Neurodegener Dis       Date:  2013-09-18

10.  Calcineurin inhibition at the clinical phase of prion disease reduces neurodegeneration, improves behavioral alterations and increases animal survival.

Authors:  Abhisek Mukherjee; Diego Morales-Scheihing; Dennisse Gonzalez-Romero; Kristi Green; Giulio Taglialatela; Claudio Soto
Journal:  PLoS Pathog       Date:  2010-10-07       Impact factor: 6.823

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