MX2021008121A - Metodos y composiciones farmaceuticas para mejorar las respuestas inmunitarias dependientes de celulas t cd8+ en sujetos que sufren de cancer. - Google Patents

Metodos y composiciones farmaceuticas para mejorar las respuestas inmunitarias dependientes de celulas t cd8+ en sujetos que sufren de cancer.

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Publication number
MX2021008121A
MX2021008121A MX2021008121A MX2021008121A MX2021008121A MX 2021008121 A MX2021008121 A MX 2021008121A MX 2021008121 A MX2021008121 A MX 2021008121A MX 2021008121 A MX2021008121 A MX 2021008121A MX 2021008121 A MX2021008121 A MX 2021008121A
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cells
nrp1
tumor
cell
cancer
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MX2021008121A
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English (en)
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Olivier Hermine
Julien Rossignol
Zakia Belaid-Choucair
Guillemette Fouquet
Lucile Couronne
Michael Dussiot
Rachel Rignault-Bricard
Tereza Coman
Flavia Guillem
Yves Lepelletier
Amédée Renand
Pierre Milpied
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Inst Nat Sante Rech Med
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Publication of MX2021008121A publication Critical patent/MX2021008121A/es

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    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/574Immunoassay; Biospecific binding assay; Materials therefor for cancer
    • G01N33/57484Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites
    • G01N33/57492Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites involving compounds localized on the membrane of tumor or cancer cells
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    • C07K16/2863Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
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    • A61K39/4611T-cells, e.g. tumor infiltrating lymphocytes [TIL], lymphokine-activated killer cells [LAK] or regulatory T cells [Treg]
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Abstract

Dirigirse a los puntos de control inmunitarios, como la Muerte Celular Programada 1 (PD1), ha mejorado la supervivencia en los pacientes con cáncer al liberar células T CD8+ agotadas, restaurando así las respuestas inmunitarias anti-tumorales. La mayoría de los pacientes, sin embargo, recaen o son refractarios a terapias de bloqueo de puntos de control inmunitarios. Aquí, se muestra que NRP1 es reclutada en la sinapsis citolítica de las células T PD1+CD8+, interactúa y mejora la actividad de PD-1. En ratones, la deleción específica de células T CD8+ de Nrp1 mejora las respuestas inmunitarias anti-tumorales espontáneas y de anticuerpos anti-PD1. De igual manera, en melanoma metastásico humano, la expresión de NRP1 en células T CD8+ infiltrantes de tumor predice un mal resultado de pacientes tratados con anti PD1 (por ejemplo, pembrolizumab). Finalmente, la combinación de anticuerpos anti-NRP1 y anti-PD1 es sinérgica en la respuesta anti-tumoral específicamente de células T CD8+ humanas. Por lo tanto, la inhibición terapéutica de NRP1 por sí sola o combinada con un inhibidor de puntos de control inmunitarios (por ejemplo, anticuerpo anti-PD1) podría reprimir de manera eficiente el crecimiento de tumor en cáncer humano. La presente invención también está relacionada con anticuerpos multiespecíficos que comprenden al menos un sitio de unión que se une específicamente a una molécula de punto de control inmunitario (por ejemplo, PD-1), y al menos un sitio de unión que se une específicamente a NRP-1. La presente invención también está relacionada con una población de células diseñadas para expresar un receptor de antígeno quimérico (CAR) y en donde la expresión de NRP-1 en dichas células es reprimida.
MX2021008121A 2019-01-03 2020-01-02 Metodos y composiciones farmaceuticas para mejorar las respuestas inmunitarias dependientes de celulas t cd8+ en sujetos que sufren de cancer. MX2021008121A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19305003 2019-01-03
PCT/EP2020/050039 WO2020141199A1 (en) 2019-01-03 2020-01-02 Methods and pharmaceutical compositions for enhancing cd8+ t cell-dependent immune responses in subjects suffering from cancer

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MX2021008121A true MX2021008121A (es) 2021-12-10

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Country Status (12)

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US (1) US20220073626A1 (es)
EP (2) EP4059569A1 (es)
JP (1) JP2022517324A (es)
KR (1) KR20220008253A (es)
CN (1) CN113574386A (es)
AU (1) AU2020205150A1 (es)
BR (1) BR112021013157A8 (es)
CA (1) CA3125476A1 (es)
IL (1) IL284556A (es)
MX (1) MX2021008121A (es)
SG (1) SG11202107257UA (es)
WO (1) WO2020141199A1 (es)

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WO2022192353A1 (en) * 2021-03-09 2022-09-15 Mayo Foundation For Medical Education And Research Biomarkers for identifying and treating cancer patients
WO2024052233A1 (en) * 2022-09-07 2024-03-14 Novigenix Sa Methods to predict response to immunotherapy in metastatic melanoma
WO2024055010A1 (en) * 2022-09-08 2024-03-14 Board Of Regents, The University Of Texas System Compositions for treating cancer and methods of using the same
CN116041539B (zh) * 2022-10-31 2023-07-21 山东博安生物技术股份有限公司 Il-2突变体免疫缀合物

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