Plerixafor for the Treatment of WHIM Syndrome
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.17/4730 |
Resumo: | WHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis), a primary immunodeficiency disorder involving panleukopenia, is caused by autosomal dominant gain-of-function mutations in CXC chemokine receptor 4 (CXCR4). Myelokathexis is neutropenia caused by neutrophil retention in bone marrow. Patients with WHIM syndrome are often treated with granulocyte colony-stimulating factor (G-CSF), which can increase neutrophil counts but does not affect cytopenias other than neutropenia. In this investigator-initiated, open-label study, three severely affected patients with WHIM syndrome who could not receive G-CSF were treated with low-dose plerixafor, a CXCR4 antagonist, for 19 to 52 months. Myelofibrosis, panleukopenia, anemia, and thrombocytopenia were ameliorated, the wart burden and frequency of infection declined, human papillomavirus-associated oropharyngeal squamous-cell carcinoma stabilized, and quality of life improved markedly. Adverse events were mainly infections attributable to the underlying immunodeficiency. One patient died from complications of elective reconstructive surgery. (Funded by the National Institutes of Health.). |
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Plerixafor for the Treatment of WHIM SyndromeBenzylaminesBone Marrow / pathology*Bone Marrow ExaminationCyclamsFatal OutcomeHeterocyclic Compounds / therapeutic use*Immunologic Deficiency Syndromes / drug therapy*Immunologic Deficiency Syndromes / pathologyMiddle AgedNeoplasms, Squamous Cell / drug therapyNeoplasms, Squamous Cell / geneticsPhenotypePrimary Immunodeficiency DiseasesPrimary Myelofibrosis / drug therapyPrimary Myelofibrosis / pathologyReceptors, CXCR4 / antagonists & inhibitors*Receptors, CXCR4 / geneticsWarts / drug therapy*Warts / pathologyHDE INF PEDWHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis), a primary immunodeficiency disorder involving panleukopenia, is caused by autosomal dominant gain-of-function mutations in CXC chemokine receptor 4 (CXCR4). Myelokathexis is neutropenia caused by neutrophil retention in bone marrow. Patients with WHIM syndrome are often treated with granulocyte colony-stimulating factor (G-CSF), which can increase neutrophil counts but does not affect cytopenias other than neutropenia. In this investigator-initiated, open-label study, three severely affected patients with WHIM syndrome who could not receive G-CSF were treated with low-dose plerixafor, a CXCR4 antagonist, for 19 to 52 months. Myelofibrosis, panleukopenia, anemia, and thrombocytopenia were ameliorated, the wart burden and frequency of infection declined, human papillomavirus-associated oropharyngeal squamous-cell carcinoma stabilized, and quality of life improved markedly. Adverse events were mainly infections attributable to the underlying immunodeficiency. One patient died from complications of elective reconstructive surgery. (Funded by the National Institutes of Health.).NEJM GroupRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEMcDermott, DHPastrana, DVCalvo, KRPittaluga, SVelez, DCho, ELiu, QTrout, HHFarela Neves, JGardner, PJBianchi, DABlair, EALandon, EMSilva, SLBuck, CBMurphy, PM2023-11-03T11:33:48Z20192019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4730engN Engl J Med . 2019 Jan 10;380(2):163-17010.1056/NEJMoa1808575info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-05T06:33:13Zoai:repositorio.chlc.min-saude.pt:10400.17/4730Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:26:50.106621Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Plerixafor for the Treatment of WHIM Syndrome |
title |
Plerixafor for the Treatment of WHIM Syndrome |
spellingShingle |
Plerixafor for the Treatment of WHIM Syndrome McDermott, DH Benzylamines Bone Marrow / pathology* Bone Marrow Examination Cyclams Fatal Outcome Heterocyclic Compounds / therapeutic use* Immunologic Deficiency Syndromes / drug therapy* Immunologic Deficiency Syndromes / pathology Middle Aged Neoplasms, Squamous Cell / drug therapy Neoplasms, Squamous Cell / genetics Phenotype Primary Immunodeficiency Diseases Primary Myelofibrosis / drug therapy Primary Myelofibrosis / pathology Receptors, CXCR4 / antagonists & inhibitors* Receptors, CXCR4 / genetics Warts / drug therapy* Warts / pathology HDE INF PED |
title_short |
Plerixafor for the Treatment of WHIM Syndrome |
title_full |
Plerixafor for the Treatment of WHIM Syndrome |
title_fullStr |
Plerixafor for the Treatment of WHIM Syndrome |
title_full_unstemmed |
Plerixafor for the Treatment of WHIM Syndrome |
title_sort |
Plerixafor for the Treatment of WHIM Syndrome |
author |
McDermott, DH |
author_facet |
McDermott, DH Pastrana, DV Calvo, KR Pittaluga, S Velez, D Cho, E Liu, Q Trout, HH Farela Neves, J Gardner, PJ Bianchi, DA Blair, EA Landon, EM Silva, SL Buck, CB Murphy, PM |
author_role |
author |
author2 |
Pastrana, DV Calvo, KR Pittaluga, S Velez, D Cho, E Liu, Q Trout, HH Farela Neves, J Gardner, PJ Bianchi, DA Blair, EA Landon, EM Silva, SL Buck, CB Murphy, PM |
author2_role |
author author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE |
dc.contributor.author.fl_str_mv |
McDermott, DH Pastrana, DV Calvo, KR Pittaluga, S Velez, D Cho, E Liu, Q Trout, HH Farela Neves, J Gardner, PJ Bianchi, DA Blair, EA Landon, EM Silva, SL Buck, CB Murphy, PM |
dc.subject.por.fl_str_mv |
Benzylamines Bone Marrow / pathology* Bone Marrow Examination Cyclams Fatal Outcome Heterocyclic Compounds / therapeutic use* Immunologic Deficiency Syndromes / drug therapy* Immunologic Deficiency Syndromes / pathology Middle Aged Neoplasms, Squamous Cell / drug therapy Neoplasms, Squamous Cell / genetics Phenotype Primary Immunodeficiency Diseases Primary Myelofibrosis / drug therapy Primary Myelofibrosis / pathology Receptors, CXCR4 / antagonists & inhibitors* Receptors, CXCR4 / genetics Warts / drug therapy* Warts / pathology HDE INF PED |
topic |
Benzylamines Bone Marrow / pathology* Bone Marrow Examination Cyclams Fatal Outcome Heterocyclic Compounds / therapeutic use* Immunologic Deficiency Syndromes / drug therapy* Immunologic Deficiency Syndromes / pathology Middle Aged Neoplasms, Squamous Cell / drug therapy Neoplasms, Squamous Cell / genetics Phenotype Primary Immunodeficiency Diseases Primary Myelofibrosis / drug therapy Primary Myelofibrosis / pathology Receptors, CXCR4 / antagonists & inhibitors* Receptors, CXCR4 / genetics Warts / drug therapy* Warts / pathology HDE INF PED |
description |
WHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis), a primary immunodeficiency disorder involving panleukopenia, is caused by autosomal dominant gain-of-function mutations in CXC chemokine receptor 4 (CXCR4). Myelokathexis is neutropenia caused by neutrophil retention in bone marrow. Patients with WHIM syndrome are often treated with granulocyte colony-stimulating factor (G-CSF), which can increase neutrophil counts but does not affect cytopenias other than neutropenia. In this investigator-initiated, open-label study, three severely affected patients with WHIM syndrome who could not receive G-CSF were treated with low-dose plerixafor, a CXCR4 antagonist, for 19 to 52 months. Myelofibrosis, panleukopenia, anemia, and thrombocytopenia were ameliorated, the wart burden and frequency of infection declined, human papillomavirus-associated oropharyngeal squamous-cell carcinoma stabilized, and quality of life improved markedly. Adverse events were mainly infections attributable to the underlying immunodeficiency. One patient died from complications of elective reconstructive surgery. (Funded by the National Institutes of Health.). |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019 2019-01-01T00:00:00Z 2023-11-03T11:33:48Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.17/4730 |
url |
http://hdl.handle.net/10400.17/4730 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
N Engl J Med . 2019 Jan 10;380(2):163-170 10.1056/NEJMoa1808575 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
NEJM Group |
publisher.none.fl_str_mv |
NEJM Group |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799134150211403776 |