COMBINED FUNGAL COMPOSITION FOR MODULATING AN INFLAMMATORY RESPONSE
Described herein are combined fungal compositions for treating, prophylaxis of, or ameliorating symptoms of one or more adverse reactions triggered by an infectious disease or condition that causes an inflammatory response. In one aspect the composition comprises an aqueous or solid fraction of Trametes versicolor and Fomitopsis officinalis mycelium, fermented substrates thereof, or combinations thereof.
1 . A composition for treating, prophylaxis of, or ameliorating symptoms of one or more adverse reactions triggered by an infectious disease or condition that increases an anti-inflammatory response in a subject, the composition comprising:
an aqueous or solid fraction of a mushroom mycelium and/or fruit body mixture;
one or more buffering agents;
ethanol; and
water.
2 . The composition of claim 1 , wherein the aqueous or solid fraction comprises beta-glucans.
3 . The composition of claim 1 , wherein the buffering agent comprises phosphate buffered saline.
4 . The composition of claim 1 , wherein the composition comprises an aqueous or solid fraction of Trametes versicolor mycelium.
5 . The composition of claim 1 , wherein the composition comprises about 200 mg to about 10 g of Trametes versicolor mycelium.
6 . The composition of claim 1 , wherein the composition further comprises one or more preservatives, flavorings, colorings, stabilizers, emulsifiers, or other pharmaceutically acceptable excipients.
7 . The composition of claim 1 , wherein the infectious disease or condition increases expression of growth factors.
8 . The composition of claim 7 , wherein the growth factors comprise one or more of basic fibroblast growth factor, or vascular endothelial growth factor.
9 . The composition of claim 1 , wherein the mushroom mycelium and/or fruit body mixture comprises one or more of Agaricus brasiliensis f. blazei, Cordyceps militaris, Flammulina velutipes, Fomes fomentarius, Fomitopsis officinalis, Ganoderma applanatum, Ganoderma lucidum s.l., Ganoderma oregonense s.l., Grifola frondosa, Hericium erinaceus, Inonotus obliquus, Lentinula edodes, Phellinus linteus, Piptoporus betulinus, Pleurotus ostreatus, Schizophyllum commune , or Trametes versicolor.
10 . A composition for treating, prophylaxis of, or ameliorating symptoms of one or more adverse reactions triggered by an infectious disease or condition that increases an anti-inflammatory response in a subject, the composition comprising:
an aqueous or solid fraction of Trametes versicolor mycelium, a fermented substrate thereof, or a combination thereof;
one or more buffering agents;
ethanol; and
water.
11 . The composition of claim 10 , wherein the aqueous or solid fraction comprises beta-glucans.
12 . The composition of claim 10 , wherein the buffering agent comprises phosphate buffered saline.
13 . The composition of claim 10 , wherein the infectious disease or condition increases expression of growth factors.
14 . The composition of claim 13 , wherein the growth factors comprise one or more of basic fibroblast growth factor or vascular endothelial growth factor.
15 . The composition of claim 10 , wherein the composition comprises about 200 mg to about 10 g of Trametes versicolor mycelium.
16 . The composition of claim 10 , wherein the infectious disease comprises a bacterial infection.
17 . The composition of claim 16 , wherein the bacterial infection comprises one or more of Streptococcus pneumoniae, Mycobacterium tuberculosis, Bordetella pertussis, Haemophilus influenzae, Moraxella catarrhalis, Pseudomonas aeruginosa, Stenotrophomonas maltophila, Staphylococcus aureus, Streptococcus pyogenes, Neisseria meningitidis, Klebsiella pneumoniae , or Non-tuberculosis Mycobacterium.
18 . The composition of claim 10 , wherein the infectious disease comprises a viral infection.
19 . The composition of claim 18 , wherein the viral infection comprises one or more of Paramyxoviridae (respiratory syncytial virus (RSV), parainfluenza virus (PIV), metapneumovirus (MPV), enteroviruses), Picornaviridae (Rhinovirus, RV), Coronaviridae (CoV), Adenoviridae (Adenovirus), Parvoviridae (HBOV), Orthomyxoviridae (influenza A, B, C, D, Isavirus, Thogotovirus, Quaranjavirus), or Herpesviridae (human herpes viruses, Varicella zoster virus, Epstein-Barr virus, cytomegalovirus).
20 . The composition of claim 19 , wherein the CoV comprises one or more of Severe Acute Respiratory Syndrome (SARS-COV), Middle East Respiratory Syndrome (MERS-COV), COVID-19 (2019-nCOV, SARS-COV-2), 229E, NL63, OC43, or HKU1.
21 . A composition comprising an aqueous, hydroethanolic, or ethanolic extract of Trametes versicolor mycelium.
22 . Use of the composition of any one of the preceding claims for modulating an inflammatory response comprising administering an effective amount of the composition to a subject in need thereof.
23 . The use of claim 22 , wherein the inflammatory response comprises release of anti-inflammatory and pro-inflammatory cytokines.
24 . The use of claim 23 , wherein the pro-inflammatory cytokines comprise one or more of interleukin-1β, interleukin-2, interleukin-4, interleukin-5, interleukin-6, interleukin-7, interleukin-8, interleukin-9, interleukin-12p70, interleukin-13, interleukin-15, interleukin-17A, tumor necrosis factor-α, interferon-γ, monocyte chemoattractant protein 1, eotaxin, interferon gamma-induced protein 10, granulocyte colony-stimulating factor, macrophage inflammatory protein 1α, macrophage inflammatory protein 1β, or RANTES.
25 . The use of claim 23 , wherein the anti-inflammatory cytokines comprise one or more of interleukin-1 receptor antagonist, interleukin-2, interleukin-4, interleukin-7, interleukin-9 interleukin-10, or interleukin-15.
26 . A means for modulating an inflammatory response comprising administering to a subject in need thereof an effective amount of the composition of any one of the preceding claims .
27 . The means of claim 26 , wherein the inflammatory response comprises release of anti-inflammatory and pro-inflammatory cytokines.
28 . A method for treating, prophylaxis of, or ameliorating symptoms of an infectious disease comprising:
administering to a subject in need thereof an effective amount of a composition comprising:
an aqueous or solid fraction of a mycelium, a fermented substrate thereof, or a combination thereof;
one or more buffering agents;
ethanol; and
water.
29 . The method claim 28 , wherein the mycelium comprises one or more of Agaricus brasiliensis f. blazei, Cordyceps militaris, Flammulina velutipes, Fomes fomentarius, Fomitopsis officinalis, Ganoderma applanatum, Ganoderma lucidum s.l., Ganoderma oregonense s.l., Grifola frondosa, Hericium erinaceus, Inonotus obliquus, Lentinula edodes, Phellinus linteus, Piptoporus betulinus, Pleurotus ostreatus, Schizophyllum commune , or Trametes versicolor.
30 . The method of claim 28 , wherein the mycelium is Trametes versicolor mycelium.
31 . The composition of claim 28 , wherein the composition comprises about 200 mg to about 10 g of Trametes versicolor mycelium.
32 . The method of claim 28 , wherein the aqueous or solid fraction comprises beta-glucans.
33 . The method of claim 28 , wherein the composition comprises an aqueous or solid fraction of Trametes versicolor mycelium.
34 . The method of claim 28 , wherein the composition further comprises one or more preservatives, flavorings, colorings, stabilizers, emulsifiers, or other pharmaceutically acceptable excipients.
35 . The method of claim 28 , wherein the infectious disease comprises one or more symptoms comprising shortness of breath, wheezing, coughing, yellow mucus, green mucus, blood-tinged mucus, chest pain, breathlessness, rapid breathing, hypoxia, inflammation of the lung tissue, rapid heart rate, or increased blood pressure, or decreased blood pressure.
36 . The method of claim 28 , wherein the infectious disease comprises a bacterial infection.
37 . The method of claim 36 , wherein the bacterial infection comprises one or more of Streptococcus pneumoniae, Mycobacterium tuberculosis, Bordetella pertussis, Haemophilus influenzae, catarrhalis, Moraxella Pseudomonas aeruginosa, Stenotrophomonas maltophila, Staphylococcus aureus, Streptococcus pyogenes, Neisseria meningitidis, Klebsiella pneumoniae , or Non-tuberculosis Mycobacterium.
38 . The method of claim 28 , wherein the infectious disease comprises a viral infection.
39 . The method of claim 38 , wherein the viral infection comprises one or more of Paramyxoviridae (respiratory syncytial virus (RSV), parainfluenza virus (PIV), metapneumovirus (MPV), enteroviruses), Picornaviridae (Rhinovirus, RV), Coronaviridae (CoV), Adenoviridae (Adenovirus), Parvoviridae (HBOV), Orthomyxoviridae (influenza A, B, C, D, Isavirus, Thogotovirus, Quaranjavirus), or Herpesviridae (human herpes viruses, Varicella zoster virus, Epstein-Barr virus, cytomegalovirus).
40 . The method of claim 39 , wherein the CoV comprises one or more of Severe Acute Respiratory Syndrome (SARS-COV), Middle East Respiratory Syndrome (MERS-COV), COVID-19 (2019-nCOV, SARS-COV-2), 229E, NL63, OC43, or HKU1.
41 . A method for treating, prophylaxis of, or ameliorating symptoms of a bacterial or viral infection comprising administering an effective amount of an aqueous or solid extract of Trametes versicolor.
42 . A method for modulating an inflammatory response associated with a bacterial or viral infection comprising administering an effective amount of an aqueous or solid extract of Trametes versicolor.
43 . A method of manufacturing the composition of any one of the preceding claims , the method comprising:
growing a mushroom on a substrate; and,
separating the mushroom mycelium from a fruitbody and the substrate.
44 . The method of claim 43 , wherein the method further comprises incubating the mycelium with a solvent, forming a solution;
extracting an aqueous fraction from the solution; and
extracting a solid fraction from the solution.
45 . The method of claim 43 , wherein the method further comprises freeze-drying the mycelium; and
grinding the dried mycelium into a powder.
46 . The method of claim 45 , wherein a pressure of about 1,500 mbar to about 2,000 mbar is applied to the mycelium during freeze-drying.
47 . The method of any one of claims 45-46 , wherein a temperature of about 75° C. to 95° C. is applied to the mycelium.
48 . The method of any one of claims 43-47 , wherein the substrate comprises one or more of rice, oat, straw, or sawdust.
49 . The method of any one of claims 43-47 , wherein the mushroom is grown on a substrate at about 15° C. to about 30° C. for about 20 to about 120 days.
50 . The method of any one of claims 43-47 , wherein the mushroom is grown on a substrate at about 20° C. to about 25° C. for about 40 days.
51 . The method of claim 44 , wherein the solvent is cold water.
52 . A method for manufacturing the composition of claim 1 , the method comprising:
incubating a powder of the mushroom mycelium and/or fruit body mixture in a solvent, forming a solution;
extracting aqueous compounds from the solution in a buffered solution;
extracting non-aqueous compounds from the solution in an ethanol solution; and
extracting a solid fraction from the solution.
53 . The method of claim 52 , wherein the buffered solution comprises phosphate buffered saline.
54 . The method of claim 52 , wherein the ethanol solution comprises about 95% ethanol.
55 . The method of claim 52 , wherein the solid fraction comprises insoluble fractions of the powder of the mushroom mycelium and/or fruit body mixture.
56 . A method for treating or lessening the severity of any type of pain in a subject in need thereof comprising:
administering to the subject an effective amount of a composition comprising:
an aqueous or solid fraction of a mycelium, a fermented substrate thereof, or a combination thereof;
one or more buffering agents;
ethanol; and
water.
57 . The method claim 56 , wherein the mycelium comprises one or more of Agaricus brasiliensis f. blazei, Cordyceps militaris, Flammulina velutipes, Fomes fomentarius, Fomitopsis officinalis, Ganoderma applanatum, Ganoderma lucidum s.l., Ganoderma oregonense s.l., Grifola frondosa, Hericium erinaceus, Inonotus obliquus, Lentinula edodes, Phellinus linteus, Piptoporus betulinus, Pleurotus ostreatus, Schizophyllum commune , or Trametes versicolor.
58 . The method of claim 56 , wherein the mycelium is Trametes versicolor mycelium.
59 . The method of claim 56 , wherein the composition comprises about 200 mg to about 10 g of Trametes versicolor mycelium.
60 . The method of claim 56 , wherein the aqueous or solid fraction comprises beta-glucans.
61 . The method of claim 56 , wherein the composition comprises an aqueous or solid fraction of Trametes versicolor mycelium.
62 . The method of claim 56 , wherein the composition further comprises one or more preservatives, flavorings, colorings, stabilizers, emulsifiers, or other pharmaceutically acceptable excipients.
63 . The method of claim 56 , wherein the pain comprises one or more types of neuropathic pain, somatic pain, visceral pain, and other types of pain.
64 . A method for enhancing a viral therapy comprising:
administering to a subject an effective amount of a composition comprising:
an aqueous or solid fraction of a mycelium, a fermented substrate thereof, or a combination thereof;
one or more buffering agents;
ethanol; and
water.
65 . The method of claim 64 , wherein the viral therapy comprises a vaccine, an antiviral drug, or a combination thereof.
66 . The method claim 64 , wherein the mycelium comprises one or more of Agaricus brasiliensis f. blazei, Cordyceps militaris, Flammulina velutipes, Fomes fomentarius, Fomitopsis officinalis, Ganoderma applanatum, Ganoderma lucidum s.l., Ganoderma oregonense s.l., Grifola frondosa, Hericium erinaceus, Inonotus obliquus, Lentinula edodes, Phellinus linteus, Piptoporus betulinus, Pleurotus ostreatus, Schizophyllum commune , or Trametes versicolor.
67 . The method of claim 64 , wherein the mycelium is Trametes versicolor mycelium.
68 . The composition of claim 64 , wherein the composition comprises about 200 mg to about 10 g of Trametes versicolor mycelium.