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Deconstructing the liquid architecture of human herpesvirus 8 diseases

Human herpesvirus 8 (HHV‐8), also called Kaposi sarcoma herspesvirus (KSHV), causes several human tumours, which may be associated with systemic inflammation and body cavity effusions, including a form of multicentric Castleman disease (MCD) and a novel inflammatory syndrome, KSHV inflammatory cytok...

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Autor principal: Polizzotto, Mark N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099195/
https://www.ncbi.nlm.nih.gov/pubmed/36397674
http://dx.doi.org/10.1111/bjh.18546
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author Polizzotto, Mark N.
author_facet Polizzotto, Mark N.
author_sort Polizzotto, Mark N.
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description Human herpesvirus 8 (HHV‐8), also called Kaposi sarcoma herspesvirus (KSHV), causes several human tumours, which may be associated with systemic inflammation and body cavity effusions, including a form of multicentric Castleman disease (MCD) and a novel inflammatory syndrome, KSHV inflammatory cytokine syndrome (KICS). In this issue, Zhou et al. demonstrate that HHV‐8‐infected lambda‐restricted plasmablasts can be detected in these effusions and can be used to distinguish MCD from other HHV‐8 tumours as well as to categorise KICS into distinct clinicopathological groups. These findings open a path to an integrated clinicopathological approach to HHV‐8‐associated inflammatory diseases and may have clinical implications. Commentary on: Zhou et al. A novel approach for characterisation of KSHV‐associated multicentric Castleman disease from effusions. Br J Haematol 2023;200:462‐475.
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spelling pubmed-100991952023-04-14 Deconstructing the liquid architecture of human herpesvirus 8 diseases Polizzotto, Mark N. Br J Haematol Commentaries Human herpesvirus 8 (HHV‐8), also called Kaposi sarcoma herspesvirus (KSHV), causes several human tumours, which may be associated with systemic inflammation and body cavity effusions, including a form of multicentric Castleman disease (MCD) and a novel inflammatory syndrome, KSHV inflammatory cytokine syndrome (KICS). In this issue, Zhou et al. demonstrate that HHV‐8‐infected lambda‐restricted plasmablasts can be detected in these effusions and can be used to distinguish MCD from other HHV‐8 tumours as well as to categorise KICS into distinct clinicopathological groups. These findings open a path to an integrated clinicopathological approach to HHV‐8‐associated inflammatory diseases and may have clinical implications. Commentary on: Zhou et al. A novel approach for characterisation of KSHV‐associated multicentric Castleman disease from effusions. Br J Haematol 2023;200:462‐475. John Wiley and Sons Inc. 2022-11-17 2023-02 /pmc/articles/PMC10099195/ /pubmed/36397674 http://dx.doi.org/10.1111/bjh.18546 Text en © 2022 The Author. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Commentaries
Polizzotto, Mark N.
Deconstructing the liquid architecture of human herpesvirus 8 diseases
title Deconstructing the liquid architecture of human herpesvirus 8 diseases
title_full Deconstructing the liquid architecture of human herpesvirus 8 diseases
title_fullStr Deconstructing the liquid architecture of human herpesvirus 8 diseases
title_full_unstemmed Deconstructing the liquid architecture of human herpesvirus 8 diseases
title_short Deconstructing the liquid architecture of human herpesvirus 8 diseases
title_sort deconstructing the liquid architecture of human herpesvirus 8 diseases
topic Commentaries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099195/
https://www.ncbi.nlm.nih.gov/pubmed/36397674
http://dx.doi.org/10.1111/bjh.18546
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