IP Library Granted Patent US 8,088,397
Granted Patent B2
US 8,088,397 · App. 12/824,577 · Granted Jan 3, 2012

Human lymphocyte vaccine adjuvant

Assignees: Hasumi, LLC; University of Maryland, Baltimore
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Quick Facts
Patent No.
US 8,088,397
App. No.
12/824,577
Granted
Jan 3, 2012
Kind
B2
Abstract

The present invention relates to an adjuvant derived from human lymphocytes. The adjuvant can be used in combination with traditional vaccines or cancer immunotherapy, to enhance the response of the patient's immune system to the vaccine or other immunotherapeutic agent. The adjuvant is derived from the supernatant collected from cultured activated lymphocytes.

Claims (12)

1. A composition for enhancing an immune response to an antigen in a mammal, comprising an antigen in combination with lymphocyte conditioned medium, said lymphocyte conditioned medium is the supernatant derived from cultures of peripheral blood mononuclear cells activated with anti-CD3- and anti-CD28-coated beads, wherein said composition when administered to a mammal facilitates and enhances dendritic cell maturation and antigen-presenting cell function which results in enhanced immunologic responses to said antigen in the mammal.

2. The composition of claim 1 , wherein said antigen is HIV-1 or HIV-2.

3. The composition of claim 1 , wherein said antigen is hepatitis-B.

4. The composition of claim 1 , wherein said antigen is tetanus toxoid.

5. The composition of claim 1 , wherein said antigen is prostate-specific antigen.

6. The composition of claim 1 , wherein said antigen is hepatitis-A.

7. The composition of claim 1 , wherein said antigen is diptheria.

8. The composition of claim 1 , wherein said antigen is selected from the group consisting of viruses, bacteria, fungi, proteins, peptides, DNA fragments, other molecular species found on surfaces or within cancer cells and combinations thereof.”

9. The composition of claim 1 , wherein the dosage administered to the mammal is about 10 μg to about 500 μg.

10. The composition of claim 1 , wherein route of administration is selected from the group consisting of intracutaneous, subcutaneous and intramuscular injection and combinations thereof.

11. The composition of claim 1 , wherein timing of administration is selected from the group consisting of weekly, biweekly, monthly, yearly and combinations thereof.

12. A composition for enhancing an immune response to an antigen in a mammal, comprising a vaccine comprised of an antigen and lymphocyte conditioned medium, said lymphocyte conditioned medium is the supernatant derived from cultures of peripheral blood mononuclear cells activated with anti-CD3- and anti-CD28-coated beads, wherein said composition when administered to a mammal facilitates and enhances dendritic cell maturation and antigen-presenting cell function which results in enhanced immunologic responses to said antigen in the mammal.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 8, 2020
From: HASUMI, LLC
To: HASUMI, KENICHIRO
Reel/Frame 052340/0945 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2010
From: HASUMI, KENICHIRO
To: HASUMI, LLC
Reel/Frame 024919/0017 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2010
From: MANN, DEAN L; GRAULICH HANKEY, KIM; HOLT, KRISTINA MICHELLE
To: UNIVERSITY OF MARYLAND
Reel/Frame 024919/0196 →
Continuity (2)
Division 10783259 · Feb 20, 2004
Related Publication 20100266534A1 · Oct 21, 2010