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CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever

Primary immunodeficiencies with selective susceptibility to EBV infection are rare conditions associated with severe lymphoproliferation. We followed a patient, son of consanguineous parents, referred to our center for recurrent periodic episodes of fever associated with tonsillitis and adenitis sta...

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Autores principales: Caorsi, Roberta, Rusmini, Marta, Volpi, Stefano, Chiesa, Sabrina, Pastorino, Claudia, Sementa, Angela Rita, Uva, Paolo, Grossi, Alice, Lanino, Edoardo, Faraci, Maura, Minoia, Francesca, Signa, Sara, Picco, Paolo, Martini, Alberto, Ceccherini, Isabella, Gattorno, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796890/
https://www.ncbi.nlm.nih.gov/pubmed/29434583
http://dx.doi.org/10.3389/fimmu.2017.02015
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author Caorsi, Roberta
Rusmini, Marta
Volpi, Stefano
Chiesa, Sabrina
Pastorino, Claudia
Sementa, Angela Rita
Uva, Paolo
Grossi, Alice
Lanino, Edoardo
Faraci, Maura
Minoia, Francesca
Signa, Sara
Picco, Paolo
Martini, Alberto
Ceccherini, Isabella
Gattorno, Marco
author_facet Caorsi, Roberta
Rusmini, Marta
Volpi, Stefano
Chiesa, Sabrina
Pastorino, Claudia
Sementa, Angela Rita
Uva, Paolo
Grossi, Alice
Lanino, Edoardo
Faraci, Maura
Minoia, Francesca
Signa, Sara
Picco, Paolo
Martini, Alberto
Ceccherini, Isabella
Gattorno, Marco
author_sort Caorsi, Roberta
collection PubMed
description Primary immunodeficiencies with selective susceptibility to EBV infection are rare conditions associated with severe lymphoproliferation. We followed a patient, son of consanguineous parents, referred to our center for recurrent periodic episodes of fever associated with tonsillitis and adenitis started after an infectious mononucleosis and responsive to oral steroid. An initial diagnosis of periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome was done. In the following months, recurrent respiratory infections and episodes of keratitis were also observed, together with a progressive reduction of immunoglobulin levels and an increase of CD20(+) cells. Cell sorting and EBV PCR showed 25,000 copies for 100,000 leukocytes with predominant infection of B lymphocytes. Lymph node’s biopsy revealed reactive lymphadenopathy with paracortical involvement consistent with a chronic EBV infection. Molecular analysis of XIAP, SHA2D1A, ITK, and CD27 genes did not detect any pathogenic mutation. The patients underwent repeated courses of anti-CD20 therapy with only a partial control of the disease, followed by stem cell transplantation with a complete normalization of clinical and immunological features. Whole exome sequencing of the trio was performed. Among the variants identified, a novel loss of function homozygous c.163-2A>G mutation of the CD70 gene, affecting the exon 2 AG-acceptor splice site, fit the expected recessive model of inheritance. Indeed, deficiency of both CD27, and, more recently, of its ligand CD70, has been reported as a cause of EBV-driven lymphoproliferation and hypogammaglobulinemia. Cell surface analysis of patient-derived PHA-T cell blasts and EBV-transformed lymphoblastoid cell lines confirmed absence of CD70 expression. In conclusion, we describe a case of severe chronic EBV infection caused by a novel mutation of CD70 presenting with recurrent periodic fever.
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spelling pubmed-57968902018-02-12 CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever Caorsi, Roberta Rusmini, Marta Volpi, Stefano Chiesa, Sabrina Pastorino, Claudia Sementa, Angela Rita Uva, Paolo Grossi, Alice Lanino, Edoardo Faraci, Maura Minoia, Francesca Signa, Sara Picco, Paolo Martini, Alberto Ceccherini, Isabella Gattorno, Marco Front Immunol Immunology Primary immunodeficiencies with selective susceptibility to EBV infection are rare conditions associated with severe lymphoproliferation. We followed a patient, son of consanguineous parents, referred to our center for recurrent periodic episodes of fever associated with tonsillitis and adenitis started after an infectious mononucleosis and responsive to oral steroid. An initial diagnosis of periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome was done. In the following months, recurrent respiratory infections and episodes of keratitis were also observed, together with a progressive reduction of immunoglobulin levels and an increase of CD20(+) cells. Cell sorting and EBV PCR showed 25,000 copies for 100,000 leukocytes with predominant infection of B lymphocytes. Lymph node’s biopsy revealed reactive lymphadenopathy with paracortical involvement consistent with a chronic EBV infection. Molecular analysis of XIAP, SHA2D1A, ITK, and CD27 genes did not detect any pathogenic mutation. The patients underwent repeated courses of anti-CD20 therapy with only a partial control of the disease, followed by stem cell transplantation with a complete normalization of clinical and immunological features. Whole exome sequencing of the trio was performed. Among the variants identified, a novel loss of function homozygous c.163-2A>G mutation of the CD70 gene, affecting the exon 2 AG-acceptor splice site, fit the expected recessive model of inheritance. Indeed, deficiency of both CD27, and, more recently, of its ligand CD70, has been reported as a cause of EBV-driven lymphoproliferation and hypogammaglobulinemia. Cell surface analysis of patient-derived PHA-T cell blasts and EBV-transformed lymphoblastoid cell lines confirmed absence of CD70 expression. In conclusion, we describe a case of severe chronic EBV infection caused by a novel mutation of CD70 presenting with recurrent periodic fever. Frontiers Media S.A. 2018-01-29 /pmc/articles/PMC5796890/ /pubmed/29434583 http://dx.doi.org/10.3389/fimmu.2017.02015 Text en Copyright © 2018 Caorsi, Rusmini, Volpi, Chiesa, Pastorino, Sementa, Uva, Grossi, Lanino, Faraci, Minoia, Signa, Picco, Martini, Ceccherini and Gattorno. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Caorsi, Roberta
Rusmini, Marta
Volpi, Stefano
Chiesa, Sabrina
Pastorino, Claudia
Sementa, Angela Rita
Uva, Paolo
Grossi, Alice
Lanino, Edoardo
Faraci, Maura
Minoia, Francesca
Signa, Sara
Picco, Paolo
Martini, Alberto
Ceccherini, Isabella
Gattorno, Marco
CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever
title CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever
title_full CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever
title_fullStr CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever
title_full_unstemmed CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever
title_short CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever
title_sort cd70 deficiency due to a novel mutation in a patient with severe chronic ebv infection presenting as a periodic fever
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796890/
https://www.ncbi.nlm.nih.gov/pubmed/29434583
http://dx.doi.org/10.3389/fimmu.2017.02015
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