IP Library Granted Patent US 10,232,026
Granted Patent B2
US 10,232,026 · App. 15/377,291 · Granted Mar 19, 2019

Vaccine for mycoplasma infection

Inventors: Kazuhiro Matsuda (Tokyo, JP); Koji Ichiyama (Tokyo, JP); Sachie Matsuda (Tokyo, JP); Yuko Sasaki (Kokubunji, JP); Yoshichika Arakawa (Nagoya, JP); Ryo Harasawa (Morioka, JP); Yoshihiro Nishida (Matsudo, JP); Norio Katayama (Sakura, JP); Yasuo Endo (Miyagi, JP); Nobuo Nomura (Tokyo, JP)
Assignees: NATIONAL INSTITUTE OF INFECTIOUS DISEASES; M BIO TECHNOLOGY INC.
A61K39/0241A61K9/127A61K9/1272A61K39/12A61K39/145A61K39/39A61K2039/55555A61K2039/55594Y02A50/403
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Quick Facts
Patent No.
US 10,232,026
App. No.
15/377,291
Granted
Mar 19, 2019
Kind
B2
Abstract

Disclosed is a vaccine which has a high therapeutic effect on mycoplasma infection and is highly safe. For the purpose of developing effective therapeutic methods for mycoplasma infection, mycoplasma -mimic particles which are effective as a vaccine for mycoplasma infection are provided, and also provided are bacterium-mimic particles including common bacteria. Bacterium-mimic particles such as mycoplasma -mimic particles can be provided by producing liposome particles in which a lipid antigen specific to a pathogenic bacterium such as mycoplasma is contained as a liposome-constituting lipid component. The administration of the mycoplasma -mimic particles enables the induction of a potent immunological activity in living bodies. The mycoplasma -mimic particles can be used as an excellent vaccine for the prevention or treatment of mycoplasma infection.

Claims (15)

1. Pathogenic bacterium-mimic particles, comprising:

liposome particles including at least one purified lipid antigen specific to a pathogenic bacterium as a liposome-constituting lipid component,

wherein the lipid component consists of the purified lipid antigen alone or a mixture of the purified lipid antigen, phospholipid and cholesterol, and

wherein the pathogenic bacterium-mimic particles can cause immune response in the immune system in an organism which is susceptible of being infected with the pathogenic bacterium.

2. Mycoplasma -mimic particles, comprising:

liposome particles including at least one purified mycoplasma -specific glycolipid antigen as a liposome-constituting lipid component,

wherein the at least one purified mycoplasma -specific glycolipid antigen is chemically or enzymatically synthesized, and then separated and purified.

3. The mycoplasma -mimic particles according to claim 2 , wherein the at least one purified mycoplasma -specific glycolipid antigen is a Mycoplasma pneumoniae -specific glycolipid antigen, or a Mycoplasma fermentans -specific glycolipid antigen.

4. The mycoplasma -mimic particles according to claim 2 , further comprising:

phosphatidyl choline, phosphoglycerol, and/or cholesterol as a second liposome-constituting lipid component.

5. The mycoplasma -mimic particles according to claim 2 , wherein the liposome-constituting lipid components containing the purified mycoplasma -specific glycolipid antigen are mixed in a solvent, and then prepared as particles under conditions in which the particle diameter is in a range of 30 to 300 nm, and 80% or more thereof is in a range of 40 to 200 nm by ultrasonic wave treatment.

6. A vaccine for prevention or treatment of a disease caused by a mycoplasma infection, comprising the mycoplasma -mimic particles according to claim 2 as an active ingredient and a pharmaceutically acceptable excipient.

7. The vaccine for prevention or treatment of a disease caused by a mycoplasma infection according to claim 6 , wherein the mycoplasma -mimic particles are Mycoplasma pneumoniae -mimic particles or Mycoplasma fermentans -mimic particles.

8. The pathogenic bacterium-mimic particles according to claim 1 , wherein the pathogenic bacterium is selected from the group consisting of Helicobacter pylori bacterium, chlamydia, rickettsia , tuberculosis bacterium, and pneumococcus.

9. The mycoplasma -mimic particles according to claim 3 , wherein the at least one purified mycoplasma -specific glycolipid antigen is selected from the group consisting of GGPL-I, GGPL-III, GGL Glc-type, and GGL Gal-type.

Assignments (2)
MERGER Recorded Nov 4, 2025
From: NATIONAL INSTITUTE OF INFECTIOUS DISEASES
To: JAPAN INSTITUTE FOR HEALTH SECURITY
Reel/Frame 073511/0398 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 7, 2017
From: MATSUDA, KAZUHIRO; ICHIYAMA, KOJI; MATSUDA, SACHIE; SASAKI, YUKO; ARAKAWA, YOSHIICHIKA; HARASAWA, RYO; NISHIDA, YOSHIHIRO; KATAYAMA, NORIO; ENDO, YASUO; NOMURA, NOBUO
To: NATIONAL INSTITUTE OF INFECTIOUS DISEASES; M BIO TECHNOLOGY INC.
Reel/Frame 041930/0334 →
Priority Claims (2)
JP 2009-135592 · Jun 4, 2009 · national
JP 2009-271633 · Nov 30, 2009 · national
Continuity (2)
Continuation 13376009
Related Publication 20170165343A1 · Jun 15, 2017