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Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype
The MV1 and MV2 subtypes of sporadic Creutzfeldt–Jakob disease (sCJD) are linked to the heterozygous methionine (M)/valine (V) polymorphism at codon 129 of the prion protein (PrP) gene. MV2 is phenotypically heterogeneous, whereas MV1, due to its low prevalence, is one of the least well characterize...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469800/ https://www.ncbi.nlm.nih.gov/pubmed/37653534 http://dx.doi.org/10.1186/s40478-023-01631-9 |
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author | Cracco, Laura Puoti, Gianfranco Cornacchia, Antonio Glisic, Katie Lee, Seong‑Ki Wang, Zerui Cohen, Mark L. Appleby, Brian S. Cali, Ignazio |
author_facet | Cracco, Laura Puoti, Gianfranco Cornacchia, Antonio Glisic, Katie Lee, Seong‑Ki Wang, Zerui Cohen, Mark L. Appleby, Brian S. Cali, Ignazio |
author_sort | Cracco, Laura |
collection | PubMed |
description | The MV1 and MV2 subtypes of sporadic Creutzfeldt–Jakob disease (sCJD) are linked to the heterozygous methionine (M)/valine (V) polymorphism at codon 129 of the prion protein (PrP) gene. MV2 is phenotypically heterogeneous, whereas MV1, due to its low prevalence, is one of the least well characterized subtypes. In this study, we investigated the biochemical properties of PrP(Sc) and phenotypic expression of cases diagnosed as sCJD MV1 and MV2. We describe four MV2 histotypes: 2C, with cortical (C) coarse pathology; 2K, with kuru (K) plaque deposits; 2C-K, with co-existing C and K histotypic features; and the novel histotype 2C-PL that mimics 2C in the cerebral cortex and cerebellum, but exhibits plaque-like (PL) PrP deposits in subcortical regions (e.g., basal nuclei, thalamus and midbrain). Histotype prevalence is highest for 2C-K (55%), intermediate for 2C (31%), and lowest for 2C-PL and 2K (7%). Nearly every MV2 case expressed both PrP(Sc) types, with T2 being the predominant type (“MV2-1”). MV1 cases typically show a rapid disease course (≤ 4 months), and feature the 1C histotype, phenotypically identical to sCJDMM1. Co-existing PrP(Sc) types, with T1 significantly exceeding T2 (“MV1-2”), are detected in patients diagnosed as MV1 with longer disease courses. We observed four histotypes among MV1-2 cases, including two novel histotypes: 1V, reminiscent of sCJDVV1; 1C-2C, resembling sCJDMM1-2 with predominant MM1 histotypic component; and novel histotypes 1C-2PL and 1C-2K, overall mimicking 1C in the cerebral cortex, but harboring T2 and plaque-like PrP deposits in subcortical regions (1C-2PL), and T2 and kuru plaques in the cerebellum (1C-2K). Lesion profiles of 1C, 1V, and 1C-2C are similar, but differ from 1C-2PL and 1C-2K, as the latter two groups show prominent hippocampal and nigral degeneration. We believe that the novel “C-PL” histotypes are distinct entities rather than intermediate forms between “C” and “C-K” groups, and that 1C-2PL and 1C-2K histotypes may be characterized by different T1 variants of the same size. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01631-9. |
format | Online Article Text |
id | pubmed-10469800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104698002023-09-01 Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype Cracco, Laura Puoti, Gianfranco Cornacchia, Antonio Glisic, Katie Lee, Seong‑Ki Wang, Zerui Cohen, Mark L. Appleby, Brian S. Cali, Ignazio Acta Neuropathol Commun Research The MV1 and MV2 subtypes of sporadic Creutzfeldt–Jakob disease (sCJD) are linked to the heterozygous methionine (M)/valine (V) polymorphism at codon 129 of the prion protein (PrP) gene. MV2 is phenotypically heterogeneous, whereas MV1, due to its low prevalence, is one of the least well characterized subtypes. In this study, we investigated the biochemical properties of PrP(Sc) and phenotypic expression of cases diagnosed as sCJD MV1 and MV2. We describe four MV2 histotypes: 2C, with cortical (C) coarse pathology; 2K, with kuru (K) plaque deposits; 2C-K, with co-existing C and K histotypic features; and the novel histotype 2C-PL that mimics 2C in the cerebral cortex and cerebellum, but exhibits plaque-like (PL) PrP deposits in subcortical regions (e.g., basal nuclei, thalamus and midbrain). Histotype prevalence is highest for 2C-K (55%), intermediate for 2C (31%), and lowest for 2C-PL and 2K (7%). Nearly every MV2 case expressed both PrP(Sc) types, with T2 being the predominant type (“MV2-1”). MV1 cases typically show a rapid disease course (≤ 4 months), and feature the 1C histotype, phenotypically identical to sCJDMM1. Co-existing PrP(Sc) types, with T1 significantly exceeding T2 (“MV1-2”), are detected in patients diagnosed as MV1 with longer disease courses. We observed four histotypes among MV1-2 cases, including two novel histotypes: 1V, reminiscent of sCJDVV1; 1C-2C, resembling sCJDMM1-2 with predominant MM1 histotypic component; and novel histotypes 1C-2PL and 1C-2K, overall mimicking 1C in the cerebral cortex, but harboring T2 and plaque-like PrP deposits in subcortical regions (1C-2PL), and T2 and kuru plaques in the cerebellum (1C-2K). Lesion profiles of 1C, 1V, and 1C-2C are similar, but differ from 1C-2PL and 1C-2K, as the latter two groups show prominent hippocampal and nigral degeneration. We believe that the novel “C-PL” histotypes are distinct entities rather than intermediate forms between “C” and “C-K” groups, and that 1C-2PL and 1C-2K histotypes may be characterized by different T1 variants of the same size. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01631-9. BioMed Central 2023-08-31 /pmc/articles/PMC10469800/ /pubmed/37653534 http://dx.doi.org/10.1186/s40478-023-01631-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Cracco, Laura Puoti, Gianfranco Cornacchia, Antonio Glisic, Katie Lee, Seong‑Ki Wang, Zerui Cohen, Mark L. Appleby, Brian S. Cali, Ignazio Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype |
title | Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype |
title_full | Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype |
title_fullStr | Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype |
title_full_unstemmed | Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype |
title_short | Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype |
title_sort | novel histotypes of sporadic creutzfeldt–jakob disease linked to 129mv genotype |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469800/ https://www.ncbi.nlm.nih.gov/pubmed/37653534 http://dx.doi.org/10.1186/s40478-023-01631-9 |
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