ARTYKUŁ PRZEGLĄDOWY
Analiza związku polimorfizmu pojedynczego nukleotydu w zakresie CD209, IL-10, IL-28 i CCR5 D32 z predyspozycją do rozwoju kleszczowe zapalenie mózgu
Piotr Czupryna 1 , Miłosz Parczewski 2 , Sambor Grygorczuk 1 , Sławomir Pancewicz 1 , Joanna Zajkowska 1 , Justyna Dunaj 1 , Maciej Kondrusik 1 , Katarzyna Krawczuk 3 , Anna Moniuszko-Malinowska 11. Department of Infectious Diseases and Neuroinfections, Medical University in Białystok, Poland
2. Department of Infectious, Tropical Diseases and Immune Deficiency, Pomeranian Medical University, Szczecin, Poland
3. Pediatric Observation Unit, University Hospital of Bialystok, Poland
Opublikowany: 2017-01-04
DOI: 10.5604/01.3001.0010.3856
GICID: 01.3001.0010.3856
Dostępne wersje językowe: pl en
Wydanie: Postepy Hig Med Dosw 2017; 71 : 788-796
Abstrakt
Przypisy
- 1. Atrasheuskaya A.V., Fredeking T.M., Ignatyev G.M.: Changes inimmune parameters and their correction in human cases of tick–borne encephalitis. Clin. Exp. Immunol., 2003; 131: 148-154
Google Scholar - 2. Barkhash A.V., Perelygin A.A., Babenko V.N., Brinton M.A., VoevodaM.I.: Single nucleotide polymorphism in the promoter regionof the CD209 gene is associated with human predisposition to severeforms of tick- borne encephalitis. Antiviral Res., 2012; 93: 64-68
Google Scholar - 3. Czupryna P., Moniuszko A., Pancewicz S.A., Grygorczuk S., KondrusikM., Zajkowska J.: Tick-borne encephalitis in Poland in years1993-2008 – epidemiology and clinical presentation. A retrospectivestudy of 687 patients. Eur. J. Neurol., 2011; 18: 673-679
Google Scholar - 4. Ge D., Fellay J., Thompson A.J., Simon J.S., Shianna K.V., UrbanT.J., Heinzen E.L., Qiu P., Bertelsen A.H., Muir A.J., Sulkowski M.,McHutchison J.G., Goldstein D.B.: Genetic variation in IL28B predictshepatitis C treatment-induced viral clearance. Nature, 2009;461: 399-401 5 Glass W.G., McDermott D.H., Lim J.K., Lekhong S., Yu S.F., Frank W.A.,Pape J., Cheshier R.C., Murphy P.M.: CCR5 deficiency increases risk ofsymptomatic West Nile virus infection. J. Exp. Med., 2006; 203: 35-40
Google Scholar - 5. (CCR5) gene is associated with tickborne encephalitis. J. Infect.Dis., 2008; 1975: 266-269
Google Scholar - 6. Grebely J., Petoumenos K., Hellard M., Matthews G.V., SuppiahV., Applegate T., Yeung B., Marks P., Rawlinson W., Lloyd A.R., BoothD., Kaldor J.M., George J., Dore G.J., ATAHC Study Group: Potentialrole for interleukin-28B genotype in treatment decision-making inrecent hepatitis C virus infection. Hepatology, 2010; 52: 1216-1224
Google Scholar - 7. Günther G., Haglund M., Lindquist L., Forsgren M., Andersson J.,Andersson B., Sköldenberg B.: Tick-borne encephalitis is associatedwith low levels of interleukin-10 in cerebrospinal fluid. Infect. Ecol.Epidemiol., 2011; 1: 6029
Google Scholar - 8. Ignat’ev G.M., Otrashevskaia E.V., Vorob’eva M.C.: Cytokine productionduring experimental infection of mice with tick-borne encephalitisvirus. Vopr. Virusol., 2003; 48: 18-21
Google Scholar - 9. Kaiser R.: Tick-borne encephalitis: Clinical findings and prognosisin adults. Wien. Med. Wochenschr., 2012; 162: 239-243
Google Scholar - 10. Kindberg E., Mickiene A., Ax C., Akerlind B., Vene S., LindquistL., Lundkvist A., Svensson L.: A deletion in the chemokine receptor
Google Scholar - 11. Kristiansen T.B., Knudsen T.B., Ohlendorff S., Eugen-Olsen J.:A new multiplex PCR strategy for the simultaneous determinationof four genetic polymorphisms affecting HIV-1 disease progression.J. Immunol. Methods, 2001; 252: 147-151
Google Scholar - 12. Labuda M., Austyn J.M., Zuffova E., Kozuch O., Fuchsberger N.,Lysy J., Nuttall P.A.: Importance of localized skin infection in tickborneencephalitis virus transmission. Virology, 1996; 219: 357-366
Google Scholar - 13. Li J., Liu Y., Xu F., Chen J., Chen Y.: Three polymorphisms in theIL-10 gene and the risk of HCV infection: a meta-analysis plus a ChineseAssociation Study involving 1140 subjects. Epidemiol. Infect.,2013; 141: 893-904
Google Scholar - 14. Libraty D.H., Endy T.P., Houng H.S., Green S., Kalayanarooj S.,Suntayakorn S., Chansiriwongs W., Vaughn D.W., Nisalak A., EnnisF.A., Rothman A.L.: Differing influences of virus burden and immuneactivation on disease severity in secondary dengue-3 virus infections.J. Infect. Dis., 2002; 185: 1213-1221
Google Scholar - 15. Lim J.K., Louie C.Y., Glaser C., Jean C., Johnson B., Johnson H.,McDermott D.H., Murphy P.M.: Genetic deficiency of chemokine receptorCCR5 is a strong risk factor for symptomatic West Nile Virusinfection: a meta-analysis of 4 cohorts in the US epidemics. J. Infect.Dis., 2008; 197: 262-265
Google Scholar - 16. Lim J.K., McDermott D.H., Lisco A., Foster G.A., Krysztof D., FollmannD., Stramer S.L., Murphy P.M.: CCR5 deficiency is a risk factorfor early clinical manifestations of West Nile virus infection but notfor viral transmission. J. Infect. Dis., 2010; 201: 178-185
Google Scholar - 17. Liu R., Paxton W.A., Choe S., Ceradini D., Martin S.R., Horuk R.,MacDonald M.E., Stuhlmann H., Koup R.A., Landau N.R.: Homozygousdefect in HIV-1 coreceptor accounts for resistance of some multiply-exposedindividuals to HIV-1 infection. Cell, 1996; 86: 367-377
Google Scholar - 18. Loeb M., Eskandarian S., Rupp M., Fishman N., Gasink L., PattersonJ., Bramson J., Hudson T.J., Lemire M.: Genetic variants andsusceptibility to neurological complications following West Nilevirus infection. J. Infect. Dis., 2011; 204: 1031-1037
Google Scholar - 19. Lucotte G.: Frequencies of 32 base pair deletion of the (Δ32) alleleof the CCR5 HIV-1 co-receptor gene in Caucasians: a comparativeanalysis. Infect. Genet. Evol., 2002; 1: 201-205
Google Scholar - 20. Mege J.L., Meghari S., Honstettre A., Capo C., Raoult D.: The twofaces of interleukin 10 in human infectious diseases. Lancet Infect.Dis., 2006; 6: 557-569
Google Scholar - 21. Patterson B.K., Czerniewski M., Andersson J., Sullivan Y., Su F.,Jiyamapa D., Burki Z., Landay A.: Regulation of CCR5 and CXCR4 expressionby type 1 and type 2 cytokines: CCR5 expression is downregulatedby IL-10 in CD4-positive lymphocytes. Clin. Immunol.,1999; 91: 254-262
Google Scholar - 22. PZH, www. pzh. gov.pl (20.10.2015)
Google Scholar - 23. Ryan E.J., Dring M., Ryan C.M., McNulty C., Stevenson N.J., LawlessM.W., Crowe J., Nolan N., Hegarty J.E., O’Farrelly C.: Variant inCD209 promoter is associated with severity of liver disease in chronichepatitis C virus infection. Hum. Immunol., 2010; 71: 829-832
Google Scholar - 24. SNPedia. rs 2287886. www.snpedia.com/index.php/Rs2287886(18.07.2015)
Google Scholar - 25. Sun X.R., Wu J., Shi K.Q., Tang K.F.: Relationship between IL-10gene -1082A/G and -592C/A polymorphisms and the risk of hepatitisC infection: a meta-analysis. J. Viral. Hepat., 2013; 20: 602-611
Google Scholar - 26. Tanaka Y., Nishida N., Sugiyama M., Kurosaki M., Matsuura K.,Sakamoto N., Nakagawa M., Korenaga M., Hino K., Hige S., Ito Y., MitaE., Tanaka E., Mochida S., Murawaki Y., et al.: Genome-wide associationof IL-28B with response to pegylated interferon-α and ribavirintherapy for chronic hepatitis C. Nat. Genet., 2009; 41: 1105-1109
Google Scholar - 27. Ubol S., Masrinoul P., Chaijaruwanich J., Kalayanarooj S., CharoensirisuthikulT., Kasisith J.: Differences in global gene expressionin peripheral blood mononuclear cells indicate a significant role ofthe innate responses in progression of dengue fever but not denguehaemorrhagic fever. J. Infect. Dis., 2008; 197: 1459-1467
Google Scholar - 28. Wang L., Chen R.F., Liu J.W., Lee I.K., Lee C.P., Kuo H.C., HuangS.K., Yang K.D.: DC-SIGN (CD209) Promoter -336 A/G polymorphismis associated with dengue hemorrhagic fever and correlated to DCSIGNexpression and immune augmentation. PLoS Negl. Trop. Dis.,2011; 5: e934
Google Scholar - 29. Zambito Marsala S., Pistacchi M., Gioulis M., Mel R., Marchini C.,Francavilla E.: Neurological complications of tick borne encephalitis:the experience of 89 patients studied and literature review. Neurol.Sci., 2014; 35: 15-21
Google Scholar