IP Library › Granted Patent US 9,297,803
Granted Patent B2
US 9,297,803 · App. 12/447,620 · Granted Mar 29, 2016

Compositions and methods for immunodominant antigens

Inventors: Philip Felgner (Rancho Santa Fe, CA); David Huw Davies (Long Beach, CA); Xiaowu Liang (La Jolla, CA); Maria Laura Gennaro (New York, NY)
Assignees: Immport Therapeutics, Inc.; Rutgers, The State University of New Jersey
G01N33/5695A61K39/015A61K39/0208A61K39/0225A61K39/04A61K39/098A61K39/118A61K39/12A61K39/245A61K39/285A61K39/385C07K14/005G01N33/566G01N33/56911A61K2039/60C12N2710/16621C12N2710/16622C12N2710/16634C12N2710/24122C12N2710/24134G01N2469/20
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Quick Facts
Patent No.
US 9,297,803
App. No.
12/447,620
Granted
Mar 29, 2016
Kind
B2
Abstract

Contemplated compositions, devices, and methods comprise immunodominant antigens from selected human pathogens ( Burkholderia pseudomallei, Borrelia burgdorferi, Brucella melitensis, Chlamydia muridarum, Coxiella burnetii, Francisella tularensis , human Herpes virus 1 and 2, Mycobacterium tuberculosis, Plasmodium falciparum , and Vaccinia virus) can be used as a vaccine, as diagnostic markers, and as therapeutic agents. In particularly preferred aspects, the antigens have quantified and known relative reactivities with respect to sera of a population infected with the pathogen, and have a known association with a disease parameter.

Claims (8)

1. An isolated antigen composition comprising:

a plurality of immunodominant antigens of a pathogenic organism disposed on a solid carrier; and

wherein the plurality of antigens are encoded by nucleic acids selected from the group consisting of SEQ ID NO:503 and SEQ ID NO:512, or fragments thereof.

2. The isolated antigen composition of claim 1 further comprising at least one additional antigen of Brucella melitensis , encoded by nucleic acids selected from the group consisting of SEQ ID NO:446 to SEQ ID NO:545.

3. The isolated antigen composition of claim 1 wherein the plurality of antigens is disposed on the carrier in an array.

4. The isolated antigen composition of claim 3 wherein each of the antigens are present in a purity of greater than 60%.

5. The isolated antigen composition of claim 3 wherein the antigens or fragments thereof are recombinant.

6. The isolated antigen composition of claim 3 wherein the antigens or fragments thereof are purified.

Assignments (1)
NUNC PRO TUNC ASSIGNMENT Recorded Sep 6, 2013
From: THE UNIVERSITY OF MEDICINE AND DENTISTRY OF NEW JERSEY
To: RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY
Reel/Frame 031152/0452 →
Continuity (2)
Provisional Application 60856217 · Nov 1, 2006
Related Publication 20100119535A1 · May 13, 2010