Increasing microenvironment complexity in HL
- Autores
- Chabay, Paola Andrea
- Año de publicación
- 2023
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- cHL is unique among lymphoid malignancies, given that malignant HRSC comprise less than 1% of the total cell population. HRSC secrete chemokines and cytokines that drive the formation of a complex microenvironment of nontumor cells. This microenvironment consists of both innate as well as adaptive immune cells.2 The extensive but ineffective immune cell infiltrates found in cHL suggest that HRSC have developed mechanisms to escape immunosurveillance. Furthermore, HRSC depend on microenvironmental signals for survival and growth. Even though many cHL patients are cured with current treatment regimens, 20% to 30% fail to respond or experience a relapse after treatment. Moreover, especially in adolescents and young adults, treatment-related toxicity and long-term morbidity are persistent challenges requiring more basic research to identify new therapeutic targets, particularly within this unique microenvironment.3,4 Stewart et al provide evidence for the first time of the expression of immunoregulatory checkpoints and the secretion of chemokines from previously uncharacterized cells that contribute to the exhaustion of T cells and contribute to immune evasion in cHL.
Fil: Chabay, Paola Andrea. Gobierno de la Ciudad de Buenos Aires. Instituto Multidisciplinario de Investigaciones en Patologías Pediátricas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto Multidisciplinario de Investigaciones en Patologías Pediátricas; Argentina - Materia
-
Hodgkin lymphoma
microenvironment - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/227646
Ver los metadatos del registro completo
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Increasing microenvironment complexity in HLChabay, Paola AndreaHodgkin lymphomamicroenvironmenthttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3cHL is unique among lymphoid malignancies, given that malignant HRSC comprise less than 1% of the total cell population. HRSC secrete chemokines and cytokines that drive the formation of a complex microenvironment of nontumor cells. This microenvironment consists of both innate as well as adaptive immune cells.2 The extensive but ineffective immune cell infiltrates found in cHL suggest that HRSC have developed mechanisms to escape immunosurveillance. Furthermore, HRSC depend on microenvironmental signals for survival and growth. Even though many cHL patients are cured with current treatment regimens, 20% to 30% fail to respond or experience a relapse after treatment. Moreover, especially in adolescents and young adults, treatment-related toxicity and long-term morbidity are persistent challenges requiring more basic research to identify new therapeutic targets, particularly within this unique microenvironment.3,4 Stewart et al provide evidence for the first time of the expression of immunoregulatory checkpoints and the secretion of chemokines from previously uncharacterized cells that contribute to the exhaustion of T cells and contribute to immune evasion in cHL.Fil: Chabay, Paola Andrea. Gobierno de la Ciudad de Buenos Aires. Instituto Multidisciplinario de Investigaciones en Patologías Pediátricas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto Multidisciplinario de Investigaciones en Patologías Pediátricas; ArgentinaAmerican Society of Hematology2023-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/227646Chabay, Paola Andrea; Increasing microenvironment complexity in HL; American Society of Hematology; Blood; 141; 19; 5-2023; 2290-22910006-4971CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1182/blood.2023019661info:eu-repo/semantics/altIdentifier/url/https://ashpublications.org/blood/article/141/19/2290/495579/Increasing-microenvironment-complexity-in-HLinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:22:30Zoai:ri.conicet.gov.ar:11336/227646instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:22:30.973CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Increasing microenvironment complexity in HL |
title |
Increasing microenvironment complexity in HL |
spellingShingle |
Increasing microenvironment complexity in HL Chabay, Paola Andrea Hodgkin lymphoma microenvironment |
title_short |
Increasing microenvironment complexity in HL |
title_full |
Increasing microenvironment complexity in HL |
title_fullStr |
Increasing microenvironment complexity in HL |
title_full_unstemmed |
Increasing microenvironment complexity in HL |
title_sort |
Increasing microenvironment complexity in HL |
dc.creator.none.fl_str_mv |
Chabay, Paola Andrea |
author |
Chabay, Paola Andrea |
author_facet |
Chabay, Paola Andrea |
author_role |
author |
dc.subject.none.fl_str_mv |
Hodgkin lymphoma microenvironment |
topic |
Hodgkin lymphoma microenvironment |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
cHL is unique among lymphoid malignancies, given that malignant HRSC comprise less than 1% of the total cell population. HRSC secrete chemokines and cytokines that drive the formation of a complex microenvironment of nontumor cells. This microenvironment consists of both innate as well as adaptive immune cells.2 The extensive but ineffective immune cell infiltrates found in cHL suggest that HRSC have developed mechanisms to escape immunosurveillance. Furthermore, HRSC depend on microenvironmental signals for survival and growth. Even though many cHL patients are cured with current treatment regimens, 20% to 30% fail to respond or experience a relapse after treatment. Moreover, especially in adolescents and young adults, treatment-related toxicity and long-term morbidity are persistent challenges requiring more basic research to identify new therapeutic targets, particularly within this unique microenvironment.3,4 Stewart et al provide evidence for the first time of the expression of immunoregulatory checkpoints and the secretion of chemokines from previously uncharacterized cells that contribute to the exhaustion of T cells and contribute to immune evasion in cHL. Fil: Chabay, Paola Andrea. Gobierno de la Ciudad de Buenos Aires. Instituto Multidisciplinario de Investigaciones en Patologías Pediátricas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto Multidisciplinario de Investigaciones en Patologías Pediátricas; Argentina |
description |
cHL is unique among lymphoid malignancies, given that malignant HRSC comprise less than 1% of the total cell population. HRSC secrete chemokines and cytokines that drive the formation of a complex microenvironment of nontumor cells. This microenvironment consists of both innate as well as adaptive immune cells.2 The extensive but ineffective immune cell infiltrates found in cHL suggest that HRSC have developed mechanisms to escape immunosurveillance. Furthermore, HRSC depend on microenvironmental signals for survival and growth. Even though many cHL patients are cured with current treatment regimens, 20% to 30% fail to respond or experience a relapse after treatment. Moreover, especially in adolescents and young adults, treatment-related toxicity and long-term morbidity are persistent challenges requiring more basic research to identify new therapeutic targets, particularly within this unique microenvironment.3,4 Stewart et al provide evidence for the first time of the expression of immunoregulatory checkpoints and the secretion of chemokines from previously uncharacterized cells that contribute to the exhaustion of T cells and contribute to immune evasion in cHL. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-05 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/227646 Chabay, Paola Andrea; Increasing microenvironment complexity in HL; American Society of Hematology; Blood; 141; 19; 5-2023; 2290-2291 0006-4971 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/227646 |
identifier_str_mv |
Chabay, Paola Andrea; Increasing microenvironment complexity in HL; American Society of Hematology; Blood; 141; 19; 5-2023; 2290-2291 0006-4971 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1182/blood.2023019661 info:eu-repo/semantics/altIdentifier/url/https://ashpublications.org/blood/article/141/19/2290/495579/Increasing-microenvironment-complexity-in-HL |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Society of Hematology |
publisher.none.fl_str_mv |
American Society of Hematology |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844614216810496000 |
score |
13.070432 |