US2020247898A1PendingUtilityA1

Human immune therapies using a cd27 agonist alone or in combination with other immune modulators

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Assignee: UNIV SOUTHAMPTONPriority: Oct 20, 2006Filed: Feb 5, 2020Published: Aug 6, 2020
Est. expiryOct 20, 2026(~0.3 yrs left)· nominal 20-yr term from priority
A61P 1/00A61P 19/02A61P 37/06Y02A50/30A61P 33/04A61K 2039/505A61P 25/00C07K 16/2875A61P 37/02A61P 31/06A61P 31/00A61P 33/00A61P 17/06A61P 29/00A61P 31/20A61P 7/06A61P 31/12A61P 17/00A61P 33/02A61P 31/14A61P 35/02A61P 1/04A61P 35/00A61P 3/10A61K 2039/507A61P 5/40A61P 37/00A61P 7/04C07K 2317/24A61P 35/04C07K 2317/74A61P 31/16A61K 45/06A61P 31/22C07K 2317/75C07K 16/2878A61K 39/3955A61P 5/14A61P 25/28C07K 2317/21A61P 21/04A61P 37/04A61P 37/08A61P 31/18A61P 31/10A61P 31/04Y02A50/466Y02A50/41Y02A50/403Y02A50/412
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Claims

Abstract

Methods of inducing T cell proliferation and expansion in vivo for treating conditions wherein antigen-specific T cell immune response are therapeutically desirable such as cancer, infection, inflammation, allergy and autoimmunity and for enhancing the efficacy of vaccines are provided. These methods comprise the administration of at least one CD27 agonist, preferably an agonistic CD27 antibody, alone or in association with another moiety such as immune stimulant or immune modulator such as an anti-CD40, OX-40, 4-1BB, or CTLA-4 antibody or an agent that depletes regulatory cells, or a cytokine. These mono and combination therapies may also optionally include the administration of a desired antigen such as a tumor antigen, an allergen, an autoantigen, or an antigen specific to an infectious agent or pathogen against which a T cell response (often CD8+) is desirably elicited.

Claims

exact text as granted — not AI-modified
1 . An agonistic anti-human CD27 antibody or an antigen binding fragment thereof. 
     
     
         2 - 104 . (canceled)

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