AR108035A1 - Tratamientos contra el cáncer de útero - Google Patents

Tratamientos contra el cáncer de útero

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Publication number
AR108035A1
AR108035A1 ARP170100576A ARP170100576A AR108035A1 AR 108035 A1 AR108035 A1 AR 108035A1 AR P170100576 A ARP170100576 A AR P170100576A AR P170100576 A ARP170100576 A AR P170100576A AR 108035 A1 AR108035 A1 AR 108035A1
Authority
AR
Argentina
Prior art keywords
peptide
seq
fragment
variant
lymphocytes
Prior art date
Application number
ARP170100576A
Other languages
English (en)
Inventor
Harpreet Singh
Jens Fritsche
Oliver Schoor
Colette Song
Toni Weinschenk
Andrea Mahr
Original Assignee
Immatics Biotechnologies Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Immatics Biotechnologies Gmbh filed Critical Immatics Biotechnologies Gmbh
Publication of AR108035A1 publication Critical patent/AR108035A1/es

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    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
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Abstract

Reivindicación 1: Péptido que comprende una secuencia de aminoácidos seleccionada entre el grupo consistente en la SEQ ID Nº 1 y a la SEQ ID Nº 54, y secuencias variantes de las mismas que son como mínimo homólogas en un 88% a las SEQ ID Nº 1 a la SEQ ID Nº 54, y en que dicha variante se une a una o varias moléculas del complejo mayor de histocompatibilidad (MHC) y/o induce la reacción cruzada de linfocitos T con dicho péptido variante; y una sal farmacéuticamente aceptable del mismo, en que dicho péptido no es un polipéptido entero. Reivindicación 8: Un receptor de células T, preferiblemente soluble o unido a membrana, o un fragmento del mismo, que es reactivo con un ligando HLA, en donde dicho ligando es el péptido o una variante del mismo de acuerdo con cualquiera de las reivindicaciones 1 a 5, preferiblemente el péptido o una variante del mismo de acuerdo con cualquiera de las reivindicaciones 1 a 5 cuando se une a una molécula MHC. Reivindicación 14: Método in vitro para producir linfocitos T activados, método que comprende la puesta en contacto de linfocitos T in vitro con antígeno cargado en moléculas MHC de clase I o II humanas que se expresan en la superficie de una célula presentadora de antígeno adecuada o en un constructo artificial que emula a una célula presentadora de antígeno durante un periodo de tiempo suficiente para activar dichos linfocitos T de un modo específico de antígeno, siendo dicho antígeno un péptido acorde con la cualquiera de las reivindicaciones 1 a 4. Reivindicación 20: El péptido acorde con cualquiera de las reivindicaciones 1 a 6 el anticuerpo o un fragmento del mismo de acuerdo con la reivindicación 7, el receptor de células T o un fragmento del mismo de acuerdo con la reivindicación 8 ó 9, el aptámero de acuerdo con la reivindicación 11, el ácido nucleico o el vector de expresión de acuerdo con la reivindicación 12, la célula huésped de acuerdo con la reivindicación 13 o el linfocito T activado acorde con la reivindicación 15 destinado al uso en el diagnóstico y/o el tratamiento del cáncer o a al uso en la fabricación de un medicamento contra el cáncer. Reivindicación 22: Un equipo que comprende: a) un envase que comprende una composición farmacéutica que contiene el o los péptidos a la o las variantes acordes con cualquiera de las reivindicaciones 1 a 6, el anticuerpo o un fragmento del mismo de acuerdo con la reivindicación 7, el receptor de células T o un fragmento del mismo de acuerdo con la reivindicación 8 ó 9, el aptámero de acuerdo con la reivindicación 11, el ácido nucleico o el vector de expresión de acuerdo con la reivindicación 12, la célula huésped de acuerdo con la reivindicación 13, o el linfocito T activado acorde con la reivindicación 15, en solución o en forma liofilizada; b) opcionalmente, un segundo envase que contiene un diluyente o solución de reconstitución para la formulación liofilizada; c) opcionalmente, al menos un péptido más seleccionado del grupo consistente en las SEQ ID Nº 1 a SEQ ID Nº 71, y d) opcionalmente, instrucciones para (I) el uso de la solución o (II) la reconstitución y/o el uso de la formulación liofilizada.
ARP170100576A 2016-03-08 2017-03-08 Tratamientos contra el cáncer de útero AR108035A1 (es)

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