WO2024141790 - GENETICALLY MODIFIED CELLS COMPRISING A NUCLEIC ACID ENCODING A CD40L BINDING AGENT AND USES THEREOF

National phase entry is expected:
Publication Number WO/2024/141790
Publication Date 04.07.2024
International Application No. PCT/IB2023/000797
International Filing Date 29.12.2023
Title **
[English] GENETICALLY MODIFIED CELLS COMPRISING A NUCLEIC ACID ENCODING A CD40L BINDING AGENT AND USES THEREOF
[French] CELLULES GÉNÉTIQUEMENT MODIFIÉES COMPRENANT UN ACIDE NUCLÉIQUE CODANT POUR UN AGENT DE LIAISON CD40L ET LEURS UTILISATIONS
Applicants **
AFFYXELL THERAPEUTICS CO., LTD.
Inventors
ANH, Kyong-Hoon
CHOI, Sung Hyun
KIM, Kinam
RYU, Jong Sang
JEON, Sengho
Priority Data
10-2022-0188961   29.12.2022   KR
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting5575
EPO Filing, Examination, Granting61934
Japan Filing, Examination, Granting4002
South Korea Filing, Examination, Granting4158
USA Filing, Examination, Granting21340
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Total: 97,009

The term for entry into the National Phase has expired. This quotation is for informational purposes only

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Abstract[English] Disclosed are a genetically modified cell in which a nucleic acid encoding a CD40L binding agent (e.g., a stefin A protein variant specifically binding to CD40L or a fusion protein including the same ) is introduced into a host cell and uses thereof. Provided are genetically modified cells expressing a CD40L binding agent enabling secretion thereof, expression thereof on a cell membrane, and/or intracellular localization thereof, and are thereby capable of reducing or inhibiting the activity of CD40L. Provided genetically modified cells may inhibit T-cell activity and B-cell activity and exhibit an immunosuppressive effect, and may be thus useful for the prevention or treatment of immune diseases such as autoimmune diseases or inflammatory diseases.[French] Est divulguée une cellule génétiquement modifiée dans laquelle un acide nucléique codant pour un agent de liaison CD40L (par exemple, un variant de protéine se liant spécifiquement à CD40L ou une protéine de fusion le comprenant) est introduit dans une cellule hôte et ses utilisations. L'invention propose des cellules génétiquement modifiées exprimant un agent de liaison à CD40L permettant leur sécrétion, leur expression sur une membrane cellulaire, et/ou leur localisation intracellulaire, et pouvant ainsi réduire ou inhiber l'activité de CD40L. L'invention propose des cellules génétiquement modifiées pouvant inhiber l'activité des cellules T et l'activité des cellules B et présentant un effet immunosuppresseur, et pouvant ainsi être utiles pour la prévention ou le traitement de maladies immunitaires telles que des maladies auto-immunes ou des maladies inflammatoires.