CAR-T Immunotherapy in oncological treatment: literature review
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/27709 |
Resumo: | Introduction: Immunotherapies are developed to overcome limitations of conventional cancer therapy through stimulating innate immune response against tumor antigen. Objective: Elaborate a review on CAR-T Immunotherapy (Chimeric T Cell Antigen Receptor) in cancer treatment. Methods: Bibliographic survey of systematic reviews published in PubMed in the last 5 years. Results: 21 studies were selected. Antitumor effect occurs through cell lysis, due to CAR-T lymphocytes release of cytokines. Tumor escape is related to tumor's ability to not expose its Major Histocompatibility Complex (MHC) and/or inability of the adaptive immune system to recognize tumor antigens. These molecular targets may be proteins, carbohydrates, or glycolipids, with CD19 standing out as target of this therapy and in neoplasms as leukemia and lymphoma. Four generations of CARs have been described, which differ in terms of co-stimulatory domains and consequent functional efficiency. The therapy is indicated for cases of recurrence/refractoriness of hematological neoplasms, however applicability in solid tumors has been studied. Adverse events of CAR-T immunotherapy described were: cytokine release syndrome, neurotoxicity, anaphylactic shock, autoimmune reactions, B cell aplasia, tumor lysis syndrome and graft-versus-host disease. Conclusions: CAR-T immunotherapy is a promising therapy against relapsed/refractory cancer. It’s mainly used in leukemias and lymphomas. Choice of dose and generation of CARs should be cautious, considering specific molecular targets of each neoplasm and its presence in healthy tissues, avoiding adverse events. |
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CAR-T Immunotherapy in oncological treatment: literature reviewInmunoterapia CAR-T en tratamiento oncológico: revisión de la literaturaImunoterapia CAR-T no tratamento oncológico: revisão de literaturaNeoplasiasInmunoterapia adoptiva.Receptores de antígenos quiméricosLinfocitosSistema inmunitario.NeoplasiasImunoterapia AdotivaReceptores de antígenos quiméricosLinfócitosSistema imunitário.NeoplasmsAdoptive ImmunotherapyChimeric Antigen ReceptorsLymphocytesImmune system.Introduction: Immunotherapies are developed to overcome limitations of conventional cancer therapy through stimulating innate immune response against tumor antigen. Objective: Elaborate a review on CAR-T Immunotherapy (Chimeric T Cell Antigen Receptor) in cancer treatment. Methods: Bibliographic survey of systematic reviews published in PubMed in the last 5 years. Results: 21 studies were selected. Antitumor effect occurs through cell lysis, due to CAR-T lymphocytes release of cytokines. Tumor escape is related to tumor's ability to not expose its Major Histocompatibility Complex (MHC) and/or inability of the adaptive immune system to recognize tumor antigens. These molecular targets may be proteins, carbohydrates, or glycolipids, with CD19 standing out as target of this therapy and in neoplasms as leukemia and lymphoma. Four generations of CARs have been described, which differ in terms of co-stimulatory domains and consequent functional efficiency. The therapy is indicated for cases of recurrence/refractoriness of hematological neoplasms, however applicability in solid tumors has been studied. Adverse events of CAR-T immunotherapy described were: cytokine release syndrome, neurotoxicity, anaphylactic shock, autoimmune reactions, B cell aplasia, tumor lysis syndrome and graft-versus-host disease. Conclusions: CAR-T immunotherapy is a promising therapy against relapsed/refractory cancer. It’s mainly used in leukemias and lymphomas. Choice of dose and generation of CARs should be cautious, considering specific molecular targets of each neoplasm and its presence in healthy tissues, avoiding adverse events.Introducción: Inmunoterapias están diseñadas para superar limitaciones de la terapia convencional contra el cáncer mediante estimulación de la respuesta inmunitaria innata al antígeno tumoral. Objetivo: Elaborar una revisión sobre inmunoterapia CAR-T (receptor de antígeno quimérico en células T) en el tratamiento oncológico. Métodos: Levantamiento bibliográfico de revisiones sistemáticas publicadas en PubMed en los últimos 5 años. Resultados: Se seleccionaron 21 estudios. El efecto antitumoral se produce a través de la lisis celular, con la liberación de citoquinas por los linfocitos CAR-T. El escape del tumor está relacionado con la capacidad a no exponer su complejo principal de histocompatibilidad y/o la incapacidad del sistema inmunitario adaptativo para reconocer los antígenos tumorales. Estas dianas moleculares pueden ser proteínas, carbohidratos, o glicolípidos, destacándose el CD19 como diana de esta terapia y en neoplasias como leucemias y linfomas. Se describieron cuatro generaciones de CARs que presentan diferencias en los dominios coestimuladores y eficiencia funcional. La terapia está indicada para casos de recurrencia o refractariedad de neoplasias hematológicas, pero se ha estudiado su aplicabilidad en tumores sólidos. Los eventos adversos de la inmunoterapia CAR-T descritos fueron: síndrome de liberación de citoquinas, neurotoxicidad, shock anafiláctico, reacciones autoinmunes, aplasia de células B, síndrome de lisis tumoral y enfermedad de injerto contra huésped. Conclusiones: Inmunoterapia CAR-T es una terapia prometedora contra el cáncer en recaída o refractario. Actualmente se utiliza principalmente en leucemias y linfomas. La elección de la dosis y generación de CARs debe ser juiciosa, considerando las dianas moleculares específicas de cada neoplasia y su presencia en tejidos sanos, evitando eventos adversos.Introdução: Imunoterapias são desenvolvidas para superar limitações da terapia convencional contra o câncer através do estímulo da resposta imune inata ao antígeno tumoral. Objetivo: Elaborar revisão sobre a Imunoterapia CAR-T (receptor quimérico de antígeno em células T) no tratamento oncológico. Métodos: Levantamento bibliográfico de revisões sistemáticas publicadas no PubMed nos últimos 5 anos. Resultados: Foram selecionados 21 estudos. O efeito antitumoral ocorre através da lise de células, a partir da liberação de citocinas pelos linfócitos CAR-T. O escape tumoral está relacionado à capacidade do tumor em não expor seu complexo principal de histocompatibilidade (MHC) e/ou incapacidade do sistema imune adaptativo em reconhecer antígenos tumorais. Esses alvos moleculares podem ser proteínas, carboidratos, ou glicolipídeos, sendo que o CD19 se destaca como alvo dessa terapia e em neoplasias como leucemias e linfoma. Foram descritas quatro gerações de CARs que apresentam diferenças quanto aos domínios co-estimulatórios e consequente eficiência funcional. A terapia é indicada para casos de recidivas ou refratariedade de neoplasias hematológicas, porém a aplicabilidade em tumores sólidos vem sendo estudada. Os eventos adversos da imunoterapia CAR-T descritos foram: síndrome de liberação de citocinas, neurotoxicidade, choque anafilático, reações autoimunes, aplasia de células B, síndrome de lise tumoral e doença do enxerto contra o hospedeiro. Conclusões: A imunoterapia CAR-T é uma terapia promissora contra o câncer recidivado ou refratário. Atualmente é utilizada principalmente em leucemias e linfomas. A escolha da dose e geração dos CARs deve ser criteriosa, considerando os alvos moleculares específicos de cada neoplasia e sua presença em tecidos saudáveis, evitando eventos adversos.Research, Society and Development2022-03-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2770910.33448/rsd-v11i4.27709Research, Society and Development; Vol. 11 No. 4; e57411427709Research, Society and Development; Vol. 11 Núm. 4; e57411427709Research, Society and Development; v. 11 n. 4; e574114277092525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/27709/24264Copyright (c) 2022 Gabriela Barge Azzam; Edson Gabriel de Oliveira; Rimon Sobhi Azzam; Francisco Sandro Menezes-Rodrigueshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessAzzam, Gabriela Barge Oliveira, Edson Gabriel de Azzam, Rimon Sobhi Menezes-Rodrigues, Francisco Sandro 2022-03-27T17:17:09Zoai:ojs.pkp.sfu.ca:article/27709Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:45:20.721996Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
CAR-T Immunotherapy in oncological treatment: literature review Inmunoterapia CAR-T en tratamiento oncológico: revisión de la literatura Imunoterapia CAR-T no tratamento oncológico: revisão de literatura |
title |
CAR-T Immunotherapy in oncological treatment: literature review |
spellingShingle |
CAR-T Immunotherapy in oncological treatment: literature review Azzam, Gabriela Barge Neoplasias Inmunoterapia adoptiva. Receptores de antígenos quiméricos Linfocitos Sistema inmunitario. Neoplasias Imunoterapia Adotiva Receptores de antígenos quiméricos Linfócitos Sistema imunitário. Neoplasms Adoptive Immunotherapy Chimeric Antigen Receptors Lymphocytes Immune system. |
title_short |
CAR-T Immunotherapy in oncological treatment: literature review |
title_full |
CAR-T Immunotherapy in oncological treatment: literature review |
title_fullStr |
CAR-T Immunotherapy in oncological treatment: literature review |
title_full_unstemmed |
CAR-T Immunotherapy in oncological treatment: literature review |
title_sort |
CAR-T Immunotherapy in oncological treatment: literature review |
author |
Azzam, Gabriela Barge |
author_facet |
Azzam, Gabriela Barge Oliveira, Edson Gabriel de Azzam, Rimon Sobhi Menezes-Rodrigues, Francisco Sandro |
author_role |
author |
author2 |
Oliveira, Edson Gabriel de Azzam, Rimon Sobhi Menezes-Rodrigues, Francisco Sandro |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Azzam, Gabriela Barge Oliveira, Edson Gabriel de Azzam, Rimon Sobhi Menezes-Rodrigues, Francisco Sandro |
dc.subject.por.fl_str_mv |
Neoplasias Inmunoterapia adoptiva. Receptores de antígenos quiméricos Linfocitos Sistema inmunitario. Neoplasias Imunoterapia Adotiva Receptores de antígenos quiméricos Linfócitos Sistema imunitário. Neoplasms Adoptive Immunotherapy Chimeric Antigen Receptors Lymphocytes Immune system. |
topic |
Neoplasias Inmunoterapia adoptiva. Receptores de antígenos quiméricos Linfocitos Sistema inmunitario. Neoplasias Imunoterapia Adotiva Receptores de antígenos quiméricos Linfócitos Sistema imunitário. Neoplasms Adoptive Immunotherapy Chimeric Antigen Receptors Lymphocytes Immune system. |
description |
Introduction: Immunotherapies are developed to overcome limitations of conventional cancer therapy through stimulating innate immune response against tumor antigen. Objective: Elaborate a review on CAR-T Immunotherapy (Chimeric T Cell Antigen Receptor) in cancer treatment. Methods: Bibliographic survey of systematic reviews published in PubMed in the last 5 years. Results: 21 studies were selected. Antitumor effect occurs through cell lysis, due to CAR-T lymphocytes release of cytokines. Tumor escape is related to tumor's ability to not expose its Major Histocompatibility Complex (MHC) and/or inability of the adaptive immune system to recognize tumor antigens. These molecular targets may be proteins, carbohydrates, or glycolipids, with CD19 standing out as target of this therapy and in neoplasms as leukemia and lymphoma. Four generations of CARs have been described, which differ in terms of co-stimulatory domains and consequent functional efficiency. The therapy is indicated for cases of recurrence/refractoriness of hematological neoplasms, however applicability in solid tumors has been studied. Adverse events of CAR-T immunotherapy described were: cytokine release syndrome, neurotoxicity, anaphylactic shock, autoimmune reactions, B cell aplasia, tumor lysis syndrome and graft-versus-host disease. Conclusions: CAR-T immunotherapy is a promising therapy against relapsed/refractory cancer. It’s mainly used in leukemias and lymphomas. Choice of dose and generation of CARs should be cautious, considering specific molecular targets of each neoplasm and its presence in healthy tissues, avoiding adverse events. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-03-28 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/27709 10.33448/rsd-v11i4.27709 |
url |
https://rsdjournal.org/index.php/rsd/article/view/27709 |
identifier_str_mv |
10.33448/rsd-v11i4.27709 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/27709/24264 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 11 No. 4; e57411427709 Research, Society and Development; Vol. 11 Núm. 4; e57411427709 Research, Society and Development; v. 11 n. 4; e57411427709 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052708362911744 |