US2008118945A1PendingUtilityA1
Use of gelsolin to treat infections
Est. expiryMay 12, 2024(expired)· nominal 20-yr term from priority
A61P 31/18A61P 31/20A61P 31/00A61P 31/22A61P 31/14A61P 31/10A61P 31/04A61P 33/00A61P 31/16A61P 39/02A61P 31/12A61P 7/00A61K 38/1709A61K 39/085A61K 39/002A61K 38/16Y02A50/30
60
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Claims
Abstract
The invention relates to the use of gelsolin to treat infections and to monitor the treatment of infections. The invention also provides methods up-regulating interleukin expression and methods for down-regulating pro-inflammatory cytokine expression.
Claims
exact text as granted — not AI-modified1 . A method for characterizing a subject's risk profile of developing a gram-positive bacterium infection, comprising:
comparing a level of gelsolin from the subject to a predetermined value, and characterizing the subject's risk profile of developing the gram-positive bacterium infection based upon the level of gelsolin in comparison to the predetermined value, wherein the level of gelsolin below the predetermined value indicates the subject has an elevated risk of developing the gram-positive bacterium infection.
2 . The method of claim 1 , wherein the predetermined value is about 2.4 μM/L of plasma.
3 . The method of claim 1 , wherein the subject is an apparently healthy subject.
4 . The method of claim 1 , further comprising obtaining the level of gelsolin from the subject.
5 . The method of claim 1 , wherein the gram-positive bacterium is a Pasteurella species, Staphylococcus species, Streptococcus species, Bacillus anthracis, Corynebacterium species, Diphtheroids species, Listeria species, Erysipelothrix species or Clostridium species.
6 . A method for characterizing a subject's risk profile of developing a future gram-negative bacterium infection, comprising:
comparing a level of gelsolin from the subject to a predetermined value, and characterizing the subject's risk profile of developing the gram-negative bacterium infection based upon the level of gelsolin in comparison to the predetermined value, wherein the level of gelsolin below the predetermined value indicates the subject has an elevated risk of developing the gram-negative bacterium infection.
7 . The method of claim 6 , wherein the predetermined value is about 2.4 μM/L of plasma.
8 . The method of claim 6 , wherein the subject is an apparently healthy subject.
9 . The method of claim 6 , further comprising obtaining the level of gelsolin from the subject.
10 . The method of claim 6 , wherein the gram-negative bacterium is a Neisseria species, Branhamella species, Escherichia species, Enterobacter species, Proteus species, Pseudomonas species, Klebsiella species, Salmonella species, Shigella species, Serratia species, Acinetobacter species, Haemophilus species, Brucella species, Yersinia species, Francisella species, Pasturella species, Vibrio cholera species, Flavobacterium species, Pseudomonas species, Campylobacter species, Bacteroides species, Fusobacterium species, Calymmatobacterium species, Streptobacillus species, or Legionella species.
11 . A method for characterizing a risk profile of a subject developing a virus, fungus, or parasite infection, comprising:
comparing a level of gelsolin from the subject to a predetermined value, and characterizing the risk profile of the subject developing the infection based upon the level of gelsolin in comparison to the predetermined value, wherein the level of gelsolin below the predetermined value indicates the subject has an elevated risk of developing the infection.
12 . The method of claim 11 , wherein the predetermined value is about 2.4 μM/L of plasma.
13 . The method of claim 11 , further comprising obtaining the level of gelsolin from the subject.
14 . The method of claim 11 , wherein the virus infection is selected from the group consisting of a Retro virus, human immunodeficiency virus, Cytomegalovirus, Picoma virus, Polio virus, hepatitis A virus, enterovirus, Coxsackie virus, rhinovirus, echovirus, Calcivirus, Toga virus, equine encephalitis virus, rubella virus, Flavivirus, dengue virus, encephalitis virus, yellow fever virus, coronavirus, Rhabdovirus, vesicular stomatitis virus, rabies virus, Filovirus, ebola virus, Paramyxo virus, parainfluenza virus, mumps virus, measles virus, respiratory syncytial virus, Orthomyxovirus, influenza virus, Hantaan virus, bunga virus, phlebovirus, Nairo virus, Arena virus, hemorrhagic fever virus, reovirus, orbivirus, rotavirus, Bimavirus, Hepadnavirus, Hepatitis B virus, parvovirus, Papovaviruses, papilloma virus, polyoma virus, Adenovirus, Herpes virus, varicella zoster virus, Pox viruses, variola virus, vaccinia virus, Iridovirus, African swine fever virus, delta hepatitis virus, non-A, non-B hepatitis virus, Hepatitis C, Norwalk virus, astrovirus, and an unclassified virus.
15 . The method of claim 11 , wherein the fungus infection is selected from the group consisting of a Cryptococcus species, Histoplasma species, Coccidioides species, Paracoccidioides species, Blastomyces species, Chlamydia species, Candida species, Sporothrix species, Aspergillus species and fungus of mucormycosis
16 . The method of claim 11 , wherein the parasite infection is selected from the group consisting of a Plasmodium species, Toxoplasma species, Babesia species, Leishmania species and Trypanosoma species.
17 . A method for characterizing a risk of developing a secondary infection, comprising:
comparing a level of gelsolin from a subject known to have a primary infection to a predetermined value, and characterizing the risk of the subject developing the secondary infection based upon the level of gelsolin in comparison to the predetermined value, wherein the level of gelsolin below the predetermined value indicates the subject has an elevated risk of developing the secondary infection.
18 . The method of claim 17 , wherein the predetermined value is about 2.4 μM/L of plasma.
19 . The method of claim 17 , further comprising obtaining the level of gelsolin from the subject.
20 . The method of claim 17 , wherein the primary infection is a bacterial, viral, fungal, parasitic, or protozoal infection.
21 . A method for characterizing a risk of a subject developing a more severe infection, comprising:
comparing a level of the gelsolin from the subject to a predetermined value, and characterizing the risk of the subject developing the severe infection based upon the level of gelsolin in comparison to the predetermined value, wherein the level of gelsolin below the predetermined value indicates the subject has an elevated risk of developing the more severe infection.
22 . The method of claim 21 , wherein the predetermined value is about 2.4 μM/L of plasma.
23 . The method of claim 21 , further comprising obtaining the level of gelsolin from the subject.
24 . The method of claim 21 , wherein the subject is known to have an infection.
25 . The method of claim 21 , wherein the more severe infection is lethal sepsis.Cited by (0)
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