IP Library Granted Patent US 7,087,236
Granted Patent B1
US 7,087,236 · App. 09/386,266 · Granted Aug 8, 2006

Method for inducing a cell-mediated immune response and improved parenteral vaccine formulations thereof

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Quick Facts
Patent No.
US 7,087,236
App. No.
09/386,266
Granted
Aug 8, 2006
Kind
B1
Abstract

A method of inducing either a T H 1 polarized immune response, a T H 2 polarized immune response or a combined T H 1 and T H 2 response to an antigen and associated vaccine formulations are disclosed. A method is provided for inducing a polarized T H 1 response by parenteral administration of microparticles sized such that at least 50% of the microparticles are less than 5 μm. The microparticles containing antigen entrapped or encapsulated by a biodegradable polymer. Additionally, a method is provided for inducing a polarized T H 2 response by parenteral administration of nanoparticles sized such that at least 50% of the nanoparticles are less than 600 nm, the nanoparticles containing antigen entrapped or encapsulated by a biodegradable polymer. Vaccine formulations containing the B. pertussis antigens PTd, FHA or a combination of PTd and FHA are provided.

Claims (10)

1. A method of inducing a T H 1 polarized immune response to at least one antigen comprising parenterally administering to a subject microparticles comprising said at least one antigen entrapped or encapsulated in a biodegradable polymer, wherein said biodegradable polymer comprises a copolymer of lactic acid and glycolic acid or enantiomers thereof, and wherein said microparticles are sized such that the average diameter of said microparticles is from 2.4 μm to 4.3 μm and at least 50% of the microparticles are less than 5 μm.

2. The method of claim 1 , wherein the microparticles are sized such that at least 50% of the microparticles are less than 3 μm.

3. The method of claim 1 , wherein the microparticles are formed using a solvent evaporation method.

4. The method of claim 1 , wherein the at least one antigen comprises a B. pertussis antigen.

5. The method of claim 1 , wherein the parenteral administration is selected from the group consisting of intraperitoneal administration, subcutaneous administration and intramuscular administration.

6. A vaccine formulation for enhancing a T H 1 immune response to at least one antigen and adapted for parenteral administration comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of microparticles comprising said at least one antigen entrapped or encapsulated in a biodegradable polymer, wherein said biodegradable polymer comprises a copolymer of lactic acid and glycolic acid or enantiomers thereof, and wherein said microparticles are sized such that average diameter of said microparticles is from 2.4 μm to 4.3 μm and at least 50% of the microparticles are less than 5 μm.

7. The vaccine formulation of claim 6 , wherein the microparticles are sized such that at least 50% of the microparticles are less than 3 μm.

8. The vaccine formulation of claim 6 , wherein the microparticles are formed using a solvent evaporation method.

9. The vaccine formulation of claim 6 , wherein the at least one antigen comprises a B. pertussis antigen.

10. A vaccine formulation for enhancing a T H 1 immune response to at least one antigen and adapted for parenteral administration comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of microparticles comprising at least 2 subpopulations of microparticles, each subpopulation comprising a different antigen, each antigen entrapped or encapsulated by a biodegradable polymer, comprises a copolymer of lactic acid and glycolic acid of enantiomers thereof, and wherein said microparticles are sized such that the average diameter of said microparticles is from 2.4 μm to 4.3 μm and at least 50% of the microparticles are less than 5 μm.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2016
From: MERRION RESEARCH III LIMITED
To: NOVO NORDISK A/S
Reel/Frame 038292/0131 →
CHANGE OF NAME Recorded Jun 27, 2008
From: MERRION RESEARCH II LIMITED
To: MERRION RESEARCH III LIMITED
Reel/Frame 021189/0291 →
CHANGE OF NAME Recorded Jun 24, 2008
From: MERRION RESEARCH I LIMITED
To: MERRION RESEARCH II LIMITED
Reel/Frame 021141/0871 →
CHANGE OF NAME Recorded Dec 8, 2004
From: ADAPTIV BIOPHARMA LIMITED
To: MERRION BIOPHARMA LIMITED
Reel/Frame 016046/0109 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 8, 2004
From: MERRION BIOPHARMA LIMITED (FORMERLY KNOWN AS ADAPTIV BIOPHARMA LIMITED)
To: MERRION RESEARCH I LIMITED (FORMERY KNOWN AS ADAPTIV RESEARCH I LIMITED)
Reel/Frame 016061/0289 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2004
From: ELAN CORPORATION, PLC
To: ADAPTIV BIOPHARMA LIMITED
Reel/Frame 016043/0684 →