US2020338185A1PendingUtilityA1
Ostrich antibody for bacterial infectious diseases
Est. expiryNov 2, 2037(~11.3 yrs left)· nominal 20-yr term from priority
Inventors:Yasuhiro Tsukamoto
Y02A50/30C07K 16/1278C07K 2317/23C07K 16/1282C07K 16/1239A61K 2039/505C07K 2317/76C07K 2317/11C07K 2317/94A23G 3/364A23L 33/135A61K 2039/542A61K 39/08A23G 3/366A61K 39/107A61K 39/395A61P 31/04A61K 39/085
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Claims
Abstract
The present invention provides an ostrich antibody-containing composition for treating a bacterial infectious disease, and a method for treating a bacterial infectious disease by using the ostrich antibody. The present invention further provides a method for producing this ostrich antibody. The infectious disease can be a gastrointestinal infection. The ostrich antibody can be produced by using a component derived from a bacterium as an immunogen. The bacterium can be Clostridium difficile, Vibrio cholera, Staphylococcus aureus, or the like. Further, the bacterium can be a drug-resistant bacterium.
Claims
exact text as granted — not AI-modified1 . A method of treating an infectious disease of a gastrointestinal tract infectious bacterium, comprising administering ostrich antibodies to a subject, wherein immunogens of the antibodies are components derived from the bacterium.
2 . The method of claim 1 , wherein the bacterium is selected from the group consisting of Clostridium difficile, Vibrio cholera, Staohylococcus aureus, Pseudomonas aeruginosa, Enterobacteriaceae, Enterococcus faecium, Helicobacter pylori, Campylobacter, Salmonella, and Shigella.
3 . The method of claim 1 , wherein the infectious disease is a gastrointestinal tract infectious disease.
4 . The method of claim 1 , wherein the infectious disease includes an infectious disease in at least one location of a stomach, a duodenum, a small intestine, a large intestine, a rectum, and an anus.
5 . The method of claim 1 , wherein the components derived from the bacterium include a microbial cell, a homogenate, a toxin, an enzyme, a polysaccharide, a pigment, a cell wall, a cytoplasm, a spore, a flagellum, a fimbria of the bacterium, or a part thereof, or any combination thereof.
6 . The method of claim 1 , wherein the bacterium includes Clostridium difficile.
7 . The method of claim 6 , wherein the immunogens include at least one of Clostridium difficile toxin A and toxin B.
8 . The method of claim 1 , wherein the bacterium includes Vibrio cholera.
9 . The method of claim 8 , wherein the immunogens include Vibrio cholera toxin.
10 . The method of claim 1 , wherein the bacterium includes Staphylococcus aureus.
11 . The method of claim 10 , wherein the immunogens include a homogenate of Staphylococcus aureus.
12 . The method of claim 1 , wherein the infectious disease is due to an agent-resistant bacterium of the bacterium.
13 . The method of claim 12 , wherein the components derived from the bacterium include a homogenate of the bacterium.
14 . The method of claim 8 ,
wherein the components derived from the bacterium include a homogenate of the bacterium; and wherein the bacterium includes methicillin-resistant Staphylococcus aureus.
15 . The method of claim 1 , wherein the ostrich antibodies are administered as a pharmaceutical composition.
16 . The method of claim 15 , wherein the ostrich antibodies are administered as a pharmaceutical composition for oral administration.
17 . The method of claim 1 , wherein the ostrich antibodies are administered as a food composition.
18 . The method of claim 1 , wherein the ostrich antibodies are administered as a candyCited by (0)
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