СОВРЕМЕННЫЙ ВЗГЛЯД НА ПРОБЛЕМУ РАННЕЙ ДИАГНОСТИКИ ПРИОННЫХ ЗАБОЛЕВАНИЙ (ОБЗОР ЛИТЕРАТУРЫ)
Аннотация
Прионные заболевания составляют группу смертельных нейродегенеративных болезней человека. Уникальность заболеваний заключается в ятрогенном, спорадическом или наследственном способе передачи. В связи с возможностью ятрогенного способа возникает вопрос о ранней доклинической диагностике прионных болезней для последующего уменьшения рисков возможного инфицирования здоровых людей. В результате длительного инкубационного периода и трансмиссивности прионного белка невозможно определить уровень распространенности заболевания и принять адекватные профилактические мероприятия. Существует вероятность заражения любого из пациентов, получавших компоненты крови, трансплантацию тканей головного мозга. Постепенная разработка новых неинвазивных методов диагностики позволяет выявить наличие прионного белка до появления клинических симптомов и предотвратить дальнейшее заражение.
Литература
1. Prion-Related Diseases Tarakad S Ramachandran, MBBS, MBA, MPH, FAAN, FACP, FAHA, FRCP, FRCPC, FRS, LRCP, MRCP, MRCS. Dec 18, 2017
Available at: https://emedicine.medscape.com/article/1168941overview#a6
(accessed 15.05.2018)
2. Казаков В.Н., Шлопов В.Г. Прионные болезни: Монография – 2009. – 444с.
3. Prusiner S.B. Novel proteinaceous infectious particles cause scrapie. Science. 1982. 216(4542):136–144
4. Collinge, J; Prion diseases. In: Ledingham, JGG and Warrell, DA, (eds.) Concise Oxford textbook of medicine. 2000(pp. 1307-1311).
5. K M Pan, M Baldwin, J Nguyen, M Gasset, A Serban, D Groth, I Mehlhorn, Z Huang, R J Fletterick, F E Cohen and Prusiner S.B. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. Dec 1, 1993. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC47901/ (accessed 13.05.2018)
6. Collinge J. Prion diseases of humans and animals: their causes and molecular basis. Annu. Rev. Neurosci. 2001. 24:519–550
7. URL: http://www.prion.ucl.ac.uk/clinic-services/ (accessed 13.05.2018)
8. Bernoulli C, Siegfried J, Baumgartner G, Regli F, Rabinowicz T, Gajdusek DC, Gibbs CJ Jr. Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery. Lancet. 1977 Feb 26; 1(8009):478-9.
9. Powell-Jackson J, Weller RO, Kennedy P, Preece MA, Whitcombe EM, Newsom-Davis J. Creutzfeldt-Jakob disease after administration of human growth hormone. Lancet. 1985 Aug 3; 2(8449):244-6
10. Brown P, Brandel JP, Sato T, Nakamura Y, MacKenzie J, Will RG, Ladogana A, Pocchiari M, Leschek EW, Schonberger LB Emerg Infect Dis. Iatrogenic Creutzfeldt-Jakob disease, final assessment. 2012 Jun; 18(6):901-7. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358170/#R-2-2 (accessed 20.05.2018)
11. Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW. Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient.Lancet. 2004 Aug 7-13; 364(9433):527-9.
12. Wadsworth, JD, Joiner, S, Fox, K et al. Prion infectivity in variant Creutzfeldt-Jakob disease rectum. Gut. 2007; 56: 90–94 Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1856674/ (accessed 17.05.2018)
13. Tattum, MH, Jones, S, Pal, S, Collinge, J, and Jackson, GS. Discrimination between prion-infected and normal blood samples by protein misfolding cyclic amplification. Transfusion. 2010; 50: 996–1002
14. Wang L.H., Bucelli R.C., Patrick E., Rajderkar D., Alvarez Iii E., Lim M.M., Debruin G., Sharma V., Dahiya S., Schmidt R.E., Benzinger T.S., Ward B.A., Ances B.M. Role of magnetic resonance imaging, cerebrospinal fluid, and electroencephalogram in diagnosis of sporadic Creutzfeldt-Jakob disease. J. Neurol. 2013;260(2):498–506.
15. Lynne I. McGuire, Alexander H. Peden, Christina D. Orrú, Jason M. Wilham, Nigel E. Appleford, Gary Mallinson, Mary Andrews, Mark W. Head, Byron Caughey, Robert G. Will, Richard S.G. Knight, and Alison J.E. Green. RT-QuIC analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease. 2013
Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458796/
(accessed 15.05.2018).
16.. Franko E, Wehner T, Joly O, Lowe J, Porter MC, Kenny J, Thompson A, Rudge P, Collinge J, Mead S. J Neurol Neurosurg Psychiatry. Quantitative EEG parameters correlate with the progression of human prion diseases .2016 Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036210/ (accessed 16.05.2018)
17. Sawyer EB, Edgeworth JA, Thomas C, Collinge J, Jackson GS. Sci Rep. Preclinical detection of infectivity and disease-specific PrP in blood throughout the incubation period of prion disease. 2015 Dec 3;5:17742.
Available at: https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(10)62308-2/fulltext (accessed 20.05.2018) doi: 10.1038/srep17742
18. Luk C, Jones S, Thomas C, Fox NC, Mok TH, Mead S, Collinge J, Jackson GS. JAMA Neurol. Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine. 2016 Oct 3.
Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701732/#R14
(accessed 20.05.2018). doi:10.1001/jamaneurol.2016.3733 PubMed PMID: 27699415.
Available at: https://emedicine.medscape.com/article/1168941overview#a6
(accessed 15.05.2018)
2. Казаков В.Н., Шлопов В.Г. Прионные болезни: Монография – 2009. – 444с.
3. Prusiner S.B. Novel proteinaceous infectious particles cause scrapie. Science. 1982. 216(4542):136–144
4. Collinge, J; Prion diseases. In: Ledingham, JGG and Warrell, DA, (eds.) Concise Oxford textbook of medicine. 2000(pp. 1307-1311).
5. K M Pan, M Baldwin, J Nguyen, M Gasset, A Serban, D Groth, I Mehlhorn, Z Huang, R J Fletterick, F E Cohen and Prusiner S.B. Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. Dec 1, 1993. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC47901/ (accessed 13.05.2018)
6. Collinge J. Prion diseases of humans and animals: their causes and molecular basis. Annu. Rev. Neurosci. 2001. 24:519–550
7. URL: http://www.prion.ucl.ac.uk/clinic-services/ (accessed 13.05.2018)
8. Bernoulli C, Siegfried J, Baumgartner G, Regli F, Rabinowicz T, Gajdusek DC, Gibbs CJ Jr. Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery. Lancet. 1977 Feb 26; 1(8009):478-9.
9. Powell-Jackson J, Weller RO, Kennedy P, Preece MA, Whitcombe EM, Newsom-Davis J. Creutzfeldt-Jakob disease after administration of human growth hormone. Lancet. 1985 Aug 3; 2(8449):244-6
10. Brown P, Brandel JP, Sato T, Nakamura Y, MacKenzie J, Will RG, Ladogana A, Pocchiari M, Leschek EW, Schonberger LB Emerg Infect Dis. Iatrogenic Creutzfeldt-Jakob disease, final assessment. 2012 Jun; 18(6):901-7. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358170/#R-2-2 (accessed 20.05.2018)
11. Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW. Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient.Lancet. 2004 Aug 7-13; 364(9433):527-9.
12. Wadsworth, JD, Joiner, S, Fox, K et al. Prion infectivity in variant Creutzfeldt-Jakob disease rectum. Gut. 2007; 56: 90–94 Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1856674/ (accessed 17.05.2018)
13. Tattum, MH, Jones, S, Pal, S, Collinge, J, and Jackson, GS. Discrimination between prion-infected and normal blood samples by protein misfolding cyclic amplification. Transfusion. 2010; 50: 996–1002
14. Wang L.H., Bucelli R.C., Patrick E., Rajderkar D., Alvarez Iii E., Lim M.M., Debruin G., Sharma V., Dahiya S., Schmidt R.E., Benzinger T.S., Ward B.A., Ances B.M. Role of magnetic resonance imaging, cerebrospinal fluid, and electroencephalogram in diagnosis of sporadic Creutzfeldt-Jakob disease. J. Neurol. 2013;260(2):498–506.
15. Lynne I. McGuire, Alexander H. Peden, Christina D. Orrú, Jason M. Wilham, Nigel E. Appleford, Gary Mallinson, Mary Andrews, Mark W. Head, Byron Caughey, Robert G. Will, Richard S.G. Knight, and Alison J.E. Green. RT-QuIC analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease. 2013
Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458796/
(accessed 15.05.2018).
16.. Franko E, Wehner T, Joly O, Lowe J, Porter MC, Kenny J, Thompson A, Rudge P, Collinge J, Mead S. J Neurol Neurosurg Psychiatry. Quantitative EEG parameters correlate with the progression of human prion diseases .2016 Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036210/ (accessed 16.05.2018)
17. Sawyer EB, Edgeworth JA, Thomas C, Collinge J, Jackson GS. Sci Rep. Preclinical detection of infectivity and disease-specific PrP in blood throughout the incubation period of prion disease. 2015 Dec 3;5:17742.
Available at: https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(10)62308-2/fulltext (accessed 20.05.2018) doi: 10.1038/srep17742
18. Luk C, Jones S, Thomas C, Fox NC, Mok TH, Mead S, Collinge J, Jackson GS. JAMA Neurol. Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine. 2016 Oct 3.
Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701732/#R14
(accessed 20.05.2018). doi:10.1001/jamaneurol.2016.3733 PubMed PMID: 27699415.
Опубликована
2018-12-03
Как цитировать
СТАТИНОВА, Е. А.; КОЦЕНКО, Ю. И.; ЗОРИЛО, А. В..
СОВРЕМЕННЫЙ ВЗГЛЯД НА ПРОБЛЕМУ РАННЕЙ ДИАГНОСТИКИ ПРИОННЫХ ЗАБОЛЕВАНИЙ (ОБЗОР ЛИТЕРАТУРЫ).
Университетская клиника, [S.l.], n. 4(29), p. 84-87, дек. 2018.
ISSN 1819-0464. Доступно на: <http://journal.dnmu.ru/index.php/UC/article/view/210>. Дата доступа: 26 апр. 2024
doi: https://doi.org/10.26435/uc.v0i4(29).210.
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