IP Library Granted Patent US 12,084,508
Granted Patent B2
US 12,084,508 · App. 17/410,832 · Granted Sep 10, 2024

TRAILshort antibody and methods of use

Inventor: Andrew D. Badley (Rochester, MN)
Assignee: Mayo Foundation for Medical Education and Research
C07K16/2875A61K39/39558C07K16/2878A61K38/191C07K2317/24C07K2317/73C07K2317/75C07K2317/76
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Quick Facts
Patent No.
US 12,084,508
App. No.
17/410,832
Granted
Sep 10, 2024
Kind
B2
Abstract

This document provides antibodies against tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) short, and more particularly to humanized TRAILshort antibodies that can neutralize TRAILshort. For example, materials and methods for using one or more humanized TRAILshort antibodies to induce apoptosis (e.g., via TRAIL mediated cell death, natural killer (NK) cytotoxicity, and/or CD8+ T cell killing) are provided.

Claims (10)

1. A method of treating a viral infection, said method comprising:

administering to a mammal having said viral infection a humanized antibody that binds tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) short, said antibody comprising a heavy chain variable region (VH) domain comprising the complementarity-determining regions (CDRs) set forth in SEQ ID NO:1, SEQ ID NO:2, and SEQ ID NO:3 and having at least 85% sequence identity to SEQ ID NO:6; and a light chain variable region (VL) domain comprising the CDRs set forth in SEQ ID NO:14, SEQ ID NO:15, and SEQ ID NO:16 and having at least 85% sequence identity to SEQ ID NO:20;

wherein said antibody increases natural killer (NK) cytotoxicity.

2. The method of claim 1 , wherein said viral infection is a chronic infection.

3. The method of claim 2 , wherein said viral infection is selected from the group consisting of human immunodeficiency virus infection, hepatitis B virus infection, and hepatitis C virus infection.

4. The method of claim 1 , wherein said mammal is a human.

5. The method of claim 1 , further comprising administering to said mammal a TRAIL agonist.

6. The method of claim 5 , wherein said TRAIL agonist is selected from the group consisting of recombinant TRAIL, an anti-TRAIL-R1 antibody, an anti-TRAIL-R2 antibody, and a TRAIL oligomer.

7. The method of claim 1 , further comprising administering to said mammal an antiretroviral therapy.

8. The method of claim 7 , wherein said antiretroviral therapy is selected from the group consisting of abacavir, didanosine, emtricitabine, entecavir, lamivudine, stavudine, tenofovir disoproxil fumarate, zalcitabine, zidovudine, delavirdine, efavirenz, etravirine, nevirapine, rilpivirine, adefovir, tenofovir, enfuvirtide, maraviroc, dolutegravir, elvitegravir, raltegravir, bevirimat, amprenavir, fosamprenavir, indinavir, lopinavir, nelfinavir, ritonavir, saquinavir, atazanavir, darunavir, tipranavir, TRIM5alpha, a tat antagonists, trichosanthin, pegylated interferon alfa (PEG-IFN-a), daclatasvir, elbasvir, grazoprevir, glecaprevir, pibrentasvir, ledipasvir, sofosbuvir, ombitasvir, paritaprevir, ritonavir, dasabuvir, simeprevir, velpatasvir, and voxilaprevir.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 26, 2023
From: MAYO CLINIC ROCHESTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 064388/0398 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2021
From: BADLEY, ANDREW D.
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 057667/0071 →
Continuity (4)
Continuation 16485056
Provisional Application 62512627 · May 30, 2017
Provisional Application 62457614 · Feb 10, 2017
Related Publication 20220127370A1 · Apr 28, 2022