-
Something wrong with this record ?
The assessment of pathogenic prions in the brains of eye tissue donors: 2-years experience in the Czech Republic
K. Jirsova, I. Krabcova, J. Novakova, I. Hnathova, F. Koukolik, B. Kubesova, M. Netukova, R. Matej,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Frontal Lobe chemistry MeSH
- Creutzfeldt-Jakob Syndrome diagnosis transmission MeSH
- Tissue Donors MeSH
- Humans MeSH
- Brain Chemistry MeSH
- Eye Banks MeSH
- Disease Transmission, Infectious prevention & control MeSH
- Prion Diseases transmission MeSH
- Prions analysis MeSH
- Corneal Transplantation MeSH
- Blotting, Western MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
PURPOSE: The aim of this study was to assess the presence of pathogenic prions in the brain tissue of eye donors and to evaluate the benefits of 2-year obligatory testing in the Czech Republic. METHODS: Brain tissue was retrieved during autopsies of eye donors of 3 tissue banks in the Czech Republic. The frozen specimens obtained from the frontal lobe were transported to the Czech National Reference Laboratory for the diagnosis of human prion disorders. The presence of pathogenic prions was tested using the Prionics-Check WESTERN kit. Confirmative Western blotting using 1 of 2 different clones of monoclonal anti-PrP antibody was performed as well. RESULTS: No pathogenic prions were found in any of the 1142 tested specimens. One specimen revealed weak positivity at initial screening; however, repeated examination of the specimen and other specimens from different locations in the brain of the same donor did not confirm the presence of pathogenic prions. The negative result was confirmed by the National CJD Surveillance Unit, University of Edinburgh, United Kingdom. CONCLUSION: The absence of pathogenic prions from all of the 1142 tested specimens corresponds to the presumed very low risk of transmission of Creutzfeldt-Jakob disease through corneal graft transplantation. As a result of this disorder's rarity, a larger series of tested samples should be evaluated to obtain statistically significant findings. Although such testing increases the safety of donor eye tissue, it also increases the expense, causes organizational difficulties, and may extend the time needed to release the tissue for grafting.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12026365
- 003
- CZ-PrNML
- 005
- 20121207092721.0
- 007
- ta
- 008
- 120817s2010 xxu f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1097/ico.0b013e3181cc7b37 $2 doi
- 035 __
- $a (PubMed)20520532
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Jirsova, Katerina $u Ocular Tissue Bank General Teaching Hospital, Charles University, Prague, Czech Republic.
- 245 14
- $a The assessment of pathogenic prions in the brains of eye tissue donors: 2-years experience in the Czech Republic / $c K. Jirsova, I. Krabcova, J. Novakova, I. Hnathova, F. Koukolik, B. Kubesova, M. Netukova, R. Matej,
- 520 9_
- $a PURPOSE: The aim of this study was to assess the presence of pathogenic prions in the brain tissue of eye donors and to evaluate the benefits of 2-year obligatory testing in the Czech Republic. METHODS: Brain tissue was retrieved during autopsies of eye donors of 3 tissue banks in the Czech Republic. The frozen specimens obtained from the frontal lobe were transported to the Czech National Reference Laboratory for the diagnosis of human prion disorders. The presence of pathogenic prions was tested using the Prionics-Check WESTERN kit. Confirmative Western blotting using 1 of 2 different clones of monoclonal anti-PrP antibody was performed as well. RESULTS: No pathogenic prions were found in any of the 1142 tested specimens. One specimen revealed weak positivity at initial screening; however, repeated examination of the specimen and other specimens from different locations in the brain of the same donor did not confirm the presence of pathogenic prions. The negative result was confirmed by the National CJD Surveillance Unit, University of Edinburgh, United Kingdom. CONCLUSION: The absence of pathogenic prions from all of the 1142 tested specimens corresponds to the presumed very low risk of transmission of Creutzfeldt-Jakob disease through corneal graft transplantation. As a result of this disorder's rarity, a larger series of tested samples should be evaluated to obtain statistically significant findings. Although such testing increases the safety of donor eye tissue, it also increases the expense, causes organizational difficulties, and may extend the time needed to release the tissue for grafting.
- 650 _2
- $a western blotting $7 D015153
- 650 _2
- $a mozek - chemie $7 D001923
- 650 _2
- $a transplantace rohovky $7 D016039
- 650 _2
- $a Creutzfeldtova-Jakobova nemoc $x diagnóza $x přenos $7 D007562
- 650 _2
- $a přenos infekční nemoci $x prevence a kontrola $7 D018562
- 650 _2
- $a oční banky $7 D005125
- 650 _2
- $a čelní lalok $x chemie $7 D005625
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a prionové nemoci $x přenos $7 D017096
- 650 _2
- $a priony $x analýza $7 D011328
- 650 _2
- $a dárci tkání $7 D014019
- 651 _2
- $a Česká republika $7 D018153
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Krabcova, Ivana
- 700 1_
- $a Novakova, Jana
- 700 1_
- $a Hnathova, Iveta
- 700 1_
- $a Koukolik, Frantisek
- 700 1_
- $a Kubesova, Barbara
- 700 1_
- $a Netukova, Magdalena
- 700 1_
- $a Matej, Radoslav
- 773 0_
- $w MED00006006 $t Cornea $x 1536-4798 $g Roč. 29, č. 9 (2010), s. 996-9
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/20520532 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m
- 990 __
- $a 20120817 $b ABA008
- 991 __
- $a 20121207092756 $b ABA008
- 999 __
- $a ok $b bmc $g 948407 $s 783711
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2010 $b 29 $c 9 $d 996-9 $i 1536-4798 $m Cornea $n Cornea $x MED00006006
- LZP __
- $a Pubmed-20120817/10/04