US2011135684A1PendingUtilityA1
Use of L-alpha-lysophosphatidylcholine to obtain the differentiation of monocytes in mature dendritic cells in vitro
Est. expiryMar 11, 2022(expired)· nominal 20-yr term from priority
A61P 43/00A61P 37/00A61P 37/04A61P 31/18A61K 47/24A61P 35/00A61P 31/10A61P 33/00A61P 31/14A61P 35/02A61P 31/00A61K 47/10A61K 31/4439A61P 29/00A61P 33/06A61P 31/04A61P 31/12A61K 9/0019A61P 31/20
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Claims
Abstract
A method for treating and/or preventing certain ailments by administering to a person in need thereof L-α-lysophosphatidylcholine as an agent for activating the immune system of the person. Also, vaccine compositions that include L-α-lysophosphatidylcholine.
Claims
exact text as granted — not AI-modified1 . A method of treating and/or preventing, in a person, an infection of bacterial, viral, fungal or parasitic origin or an infection caused by a yeast, said method comprising administering L-α-lysophosphatidylcholine as an agent for activating the immune system of the person.
2 . A method of treating or preventing cancer in a person, said method comprising administering L-α-lysophosphatidylcholine as an agent for activating the immune system of the person.
3 . A method for preventing an inflammation and/or for combating an inflammatory disease and/or an autoimmune disease in a person, said method comprising:
administering to the person an inhibitor of L-α-lysophosphatidylcholine, in which the inhibitor is a lipid emulsion comprising triglycerides, phospholipids and glycerol.
4 . The method of claim 3 , wherein the lipid emulsion comprises:
from 15 to 25% of triglycerides, from 0.5 to 1.5% of phospholipids, and from 1.8 to 2.6% of glycerol.
5 . A method for preventing an inflammation and/or for combating an inflammatory disease and/or an autoimmune disease in a person, said method comprising administering to the person an inhibitor of L-α-lysophosphatidylcholine, wherein the inhibitor is a PPARgamma agonist.
6 . A vaccine composition, comprising:
L-α-lysophosphatidylcholine as an agent for activating the immune system, and a biological agent selected from the group consisting of an antigen, a nucleic acid that encodes an antigen, and a lysate of autologous or heterologous tumor cells.
7 . The vaccine composition of claim 6 , wherein said biological agent is an antigen selected from the group consisting of a bacterial antigen, a viral antigen, a yeast antigen, a parasite antigen, a fungal antigen, and a tumor antigen.
8 . The vaccine composition of claim 6 , wherein said biological agent is a nucleic acid that encodes an antigen selected from the group consisting of a bacterial antigen, a viral antigen, a yeast antigen, a parasite antigen, a fungal antigen, and a tumor antigen.
9 . The vaccine composition of claim 6 , wherein said biological agent is a lysate of autologous or of heterologous tumor cells.
10 . The vaccine composition of claim 6 , wherein said vaccine composition is formulated for parenteral, subcutaneous, intramuscular, intravenous, intradermal, topical, intratracheal, rectal, or transdermal administration.
11 . The vaccine composition of claim 10 , wherein said biological agent is an antigen selected from the group consisting of a bacterial antigen, a viral antigen, a yeast antigen, a parasite antigen, a fungal antigen, and a tumor antigen.
12 . The vaccine composition of claim 10 , wherein said biological agent is a nucleic acid that encodes an antigen selected from the group consisting of a bacterial antigen, a viral antigen, a yeast antigen, a parasite antigen, a fungal antigen, and a tumor antigen.
13 . The vaccine composition of claim 10 , wherein said biological agent is a lysate of autologous or of heterologous tumor cells.
14 . The vaccine composition of claim 10 , wherein said vaccine composition is formulated for parenteral administration.Join the waitlist — get patent alerts
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