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| Autor(es): Mostrar menos - |
Silvestre, Renata Nacasaki
;
Eitler, Jiri
;
de Azevedo, Julia Teixeira Cottas
;
Tirapelle, Mariane Cariati
;
Fantacini, Daianne Maciely Carvalho
;
de Souza, Lucas Eduardo Botelho
;
Swiech, Kamilla
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Covas, Dimas Tadeu
;
Calado, Rodrigo T.
;
Montero, Paola Ortiz
;
Malmegrim, Kelen Cristina Ribeiro
;
Figueiredo, Marxa L.
;
Tonn, Torsten
;
Picanco-Castro, Virginia
Número total de Autores: 14
|
| Tipo de documento: | Artigo Científico |
| Fonte: | FRONTIERS IN IMMUNOLOGY; v. 14, p. 15-pg., 2023-09-25. |
| Resumo | |
Introduction: Natural killer 92 (NK-92) cells are an attractive therapeutic approach as alternative chimeric antigen receptor (CAR) carriers, different from T cells, once they can be used in the allogeneic setting. The modest in vivo outcomes observed with NK-92 cells continue to present hurdles in successfully translating NK-92 cell therapies into clinical applications. Adoptive transfer of CAR-NK-92 cells holds out the promise of therapeutic benefit at a lower rate of adverse events due to the absence of GvHD and cytokine release syndrome. However, it has not achieved breakthrough clinical results yet, and further improvement of CAR-NK-92 cells is necessary.Methods: In this study, we conducted a comparative analysis between CD19-targeted CAR (CAR.19) co-expressing IL-15 (CAR.19-IL15) with IL-15/IL-15R alpha (CAR.19-IL15/IL15R alpha) to promote NK cell proliferation, activation, and cytotoxic activity against B-cell leukemia. CAR constructs were cloned into lentiviral vector and transduced into NK-92 cell line. Potency of CAR-NK cells were assessed against CD19-expressing cell lines NALM-6 or Raji in vitro and in vivo in a murine model. Tumor burden was measured by bioluminescence.Results: We demonstrated that a fourth- generation CD19-targeted CAR (CAR.19) co-expressing IL-15 linked to its receptor IL-15/IL-15R alpha (CAR.19-IL-15/IL-15R alpha) significantly enhanced NK-92 cell proliferation, proinflammatory cytokine secretion, and cytotoxic activity against B-cell cancer cell lines in vitro and in a xenograft mouse model.Conclusion: Together with the results of the systematic analysis of the transcriptome of activated NK-92 CAR variants, this supports the notion that IL-15/IL-15R alpha comprising fourth-generation CARs may overcome the limitations of NK-92 cell-based targeted tumor therapies in vivo by providing the necessary growth and activation signals. (AU) | |
| Processo FAPESP: | 13/08135-2 - CTC - Centro de Terapia Celular |
| Beneficiário: | Dimas Tadeu Covas |
| Modalidade de apoio: | Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs |
| Processo FAPESP: | 19/25309-0 - NK-CAR (off-the-shelf) para o tratamento de Leucemias e Linfomas |
| Beneficiário: | Virginia Picanço e Castro |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 20/08279-8 - Estabelecimento de uma plataforma para geração de células NK-CAR com maior eficácia terapêutica in vitro e in vivo |
| Beneficiário: | Júlia Teixeira Cottas de Azevedo |
| Modalidade de apoio: | Bolsas no Brasil - Pós-Doutorado |
| Processo FAPESP: | 20/07055-9 - Núcleo de Terapia Celular - NuTeC |
| Beneficiário: | Rodrigo do Tocantins Calado de Saloma Rodrigues |
| Modalidade de apoio: | Auxílio à Pesquisa - Núcleos de Pesquisa Orientada a Problemas em São Paulo |