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1.
J Gene Med ; 25(5): e3484, 2023 05.
Artículo en Inglés | MEDLINE | ID: mdl-36781390

RESUMEN

Chimeric antigen receptor (CAR) T-cell therapy is an immunotherapy approach that has played a tremendous role in the battle against cancer for years. Since the CAR T lymphocytes are unrestricted-major histocompatibility complex T lymphocytes, they could identify more targets than natural T cells, resulting in practical and widespread functions. The good prospects of CAR T-cell therapy in oncology can be additionally applied to treat other diseases such as autoimmune and infectious diseases. CAR-T cell-derived immunotherapy for autoimmune disorders can be allocated to CAR-Tregs and chimeric autoantibody receptor T cells. Other generations of CARs target human immunodeficiency virus (HIV) proteins. In this review, we summarize CAR-T cell therapies in autoimmune disorders and HIV infection.


Asunto(s)
Enfermedades Autoinmunes , Infecciones por VIH , Receptores Quiméricos de Antígenos , Humanos , Linfocitos T , Infecciones por VIH/terapia , Inmunoterapia Adoptiva/métodos , Enfermedades Autoinmunes/metabolismo , Receptores de Antígenos de Linfocitos T/metabolismo
2.
Int Immunopharmacol ; 113(Pt A): 109365, 2022 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-36332452

RESUMEN

Immune checkpoint inhibitors (ICIs) targeting programmed cell death-1 (PD-1 or CD279) have noticeably improved the treatment landscape of advanced cancer patients. Nivolumab, the most well-known genetically engineered anti-PD-1 monoclonal antibody (mAb), promotes anti-tumor immunity and shows excellent capability for treating various cancers, particularly lung cancer, renal cancer, and melanoma. Systemic administration of nivolumab could inspire durable therapeutic responses not typically seen with traditional cytotoxic anti-cancer agents. However, nivolumab monotherapy is ineffective in 60-70 percent of patients. The mechanisms leading to both primary and acquired resistance to PD-1/PD-L1 inhibition are varied and multifactorial. Recently, the rationality of adding other conventional therapies such as chemo-radiotherapy and targeted therapies such as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and VEGF/VEGFR inhibitors to nivolumab has strongly been verified. These regimens overcome cancer resistance and thus boost nivolumab efficacy in cancer patients. Herein, we discuss the current status of the combination therapy with nivolumab in cancer patients, with a particular focus on the recent clinical reports.


Asunto(s)
Antineoplásicos , Neoplasias Pulmonares , Humanos , Nivolumab/uso terapéutico , Inhibidores de Puntos de Control Inmunológico , Inmunoterapia , Anticuerpos Monoclonales/uso terapéutico , Antineoplásicos/uso terapéutico
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