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1.
Rev Med Chil ; 150(1): 93-99, 2022 Jan.
Artigo em Espanhol | MEDLINE | ID: mdl-35856970

RESUMO

Professors James P. Allison and Tasuku Honjo were awarded with the 2018 Nobel Prize in Medicine for their contributions in cancer immunotherapy. The latter is a breakthrough in cancer therapy, aimed to overcome tumor-induced immunosuppression, leading to the reactivation of the immune system against cancer cells. Under physiological conditions, the CTLA-4 and PD-1 proteins expressed on T-cells and discovered by the awarded scientists, lead to immune tolerance. Cancer cells exploit these control points to enhance the inhibition of T-cells. The expression of PD ligands (PD-L1) in tumor cells and CTLA-4 ligands in antigen presenting cells, which bind the PD-1 receptor and CTLA-4 respectively, block anti-tumor immunity. This situation led to a biotechnological race focused on the development of effective antibodies able to "turn-on" the immune system cheated by the tumor. Anti-CTLA-4 and anti-PD-1 antibodies improve life-expectancy in cancer patients. In this review, we perform an historical overview of Professors Allison and Honjo contribution, as well as the immunological basis of this new and powerful therapeutic strategy, highlighting the clinical benefits of such intervention.


Assuntos
Inibidores de Checkpoint Imunológico , Neoplasias , Antígeno CTLA-4/uso terapêutico , Humanos , Imunoterapia , Neoplasias/tratamento farmacológico , Prêmio Nobel , Receptor de Morte Celular Programada 1/uso terapêutico
2.
Hum Mol Genet ; 23(7): 1771-82, 2014 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-24218365

RESUMO

Potocki-Lupski syndrome (PTLS) is a genomic disorder associated with an ∼3 Mb duplication in 17p11.2. Clinical features include leanness, intellectual disability, autistic features and developmental deficits. RAI1 gene dosage is associated with the PTLS phenotypes. To understand where and when Rai1 overexpression is detrimental, we generated a mouse that over-expresses Rai1 conditionally in forebrain neurons (I-Rai1). Phenotypic characterization of I-Rai1 mice showed significant underweight, hyperactivity and impaired learning and memory ability compared with wild-type littermates. Doxycycline administration can turn off the transgene expression allowing the restoration of Rai1 normal expression levels. When the transgene was turned off from conception to 3 months of age, no phenotypic differences were observed between I-Rai1 and their wild-type littermates. Surprisingly, we found that turning off the transgene expression before the onset of the phenotypes (1-3 months) or after the onset of the phenotypes (3-5 months) cannot prevent nor reverse the phenotypic outcomes. Our results indicate that Rai1 dosage in forebrain neurons is critical during the development and is related to body weight regulation, activity levels and learning and memory.


Assuntos
Dosagem de Genes/genética , Hipercinese/genética , Aprendizagem em Labirinto/fisiologia , Prosencéfalo/metabolismo , Transativadores/genética , Anormalidades Múltiplas , Animais , Antibacterianos/farmacologia , Peso Corporal/genética , Transtornos Cromossômicos , Duplicação Cromossômica , Modelos Animais de Doenças , Doxiciclina/farmacologia , Deficiência Intelectual/genética , Memória/fisiologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos CBA , Camundongos Transgênicos , Atividade Motora/genética , Síndrome de Smith-Magenis/genética , Transativadores/biossíntese , Transgenes/efeitos dos fármacos , Transgenes/genética
3.
Rev. méd. Chile ; 150(1): 93-99, ene. 2022. ilus, tab
Artigo em Espanhol | LILACS | ID: biblio-1389623

RESUMO

Professors James P. Allison and Tasuku Honjo were awarded with the 2018 Nobel Prize in Medicine for their contributions in cancer immunotherapy. The latter is a breakthrough in cancer therapy, aimed to overcome tumor-induced immunosuppression, leading to the reactivation of the immune system against cancer cells. Under physiological conditions, the CTLA-4 and PD-1 proteins expressed on T-cells and discovered by the awarded scientists, lead to immune tolerance. Cancer cells exploit these control points to enhance the inhibition of T-cells. The expression of PD ligands (PD-L1) in tumor cells and CTLA-4 ligands in antigen presenting cells, which bind the PD-1 receptor and CTLA-4 respectively, block anti-tumor immunity. This situation led to a biotechnological race focused on the development of effective antibodies able to "turn-on" the immune system cheated by the tumor. Anti-CTLA-4 and anti-PD-1 antibodies improve life-expectancy in cancer patients. In this review, we perform an historical overview of Professors Allison and Honjo contribution, as well as the immunological basis of this new and powerful therapeutic strategy, highlighting the clinical benefits of such intervention.


Assuntos
Humanos , Inibidores de Checkpoint Imunológico , Neoplasias/tratamento farmacológico , Antígeno CTLA-4/uso terapêutico , Receptor de Morte Celular Programada 1/uso terapêutico , Imunoterapia , Prêmio Nobel
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