US2018256738A1PendingUtilityA1
Beta-glucan compounds, compositions, and methods
Est. expiryMay 9, 2031(~4.8 yrs left)· nominal 20-yr term from priority
Inventors:Nandita BoseAnissa S.H. ChanMichael E. DanielsonMary A. AntonysamyJohn VasilakosKeith B. GordenSteven LeonardoWilliam J. Grossman
A61K 47/643A61K 31/716A61K 39/39
56
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Claims
Abstract
Described herein are beta-glucan compounds, compositions, and methods. Generally, the methods exploit the observation that beta-glucan compounds can bind to B cells. Thus, the methods generally include administering a beta-glucan compound to a subject in an amount effective for the beta-glucan compound to bind to a B cell and modulate at least one biological function of the B cell.
Claims
exact text as granted — not AI-modified1 . A method comprising:
administering to a subject an amount of a β-glucan compound effective to bind to B cells and modulate at least one biological function of the B cells, the composition comprising: a β-glucan moiety; and an active moiety coupled to the β-glucan moiety, the active moiety comprising a danger-associated molecular pattern.
2 - 18 . (canceled)
19 . The method of claim 1 wherein the β-glucan moiety comprises a soluble β-glucan or a particulate β-glucan.
20 . The method of claim 1 wherein the β-glucan moiety comprises a derivatized β-glucan.
21 . The method of claim 1 wherein the β-glucan moiety is isolated from yeast.
22 . The method of claim 21 wherein the yeast comprises Saccharomyces cerevisiae.
23 . The method of claim 1 wherein the danger-associated molecular pattern comprises a heat-shock protein, high-mobility group box 1 protein, a protein generated following tissue injury, a hyaluronan fragment, ATP, uric acid, heparin sulfate or DNA.
24 . The method of claim 1 wherein the β-glucan moiety and the active moiety are coupled through a covalent linkage.
25 . The method of claim 1 wherein the β-glucan moiety and the active moiety are coupled through an affinity linkage.
26 . The method of claim 1 wherein at least one biological function of the B cells comprises making an immunoglobulin involved in cancer therapy.
27 . The method of claim 1 wherein modulating at least one biological function of the B cells comprises making an immunoglobulin involved in infectious disease treatment.
28 . A β-glucan compound comprising:
a β-glucan moiety; and
an active moiety coupled to the β-glucan moiety, the active moiety comprising a danger-associated molecular pattern.
29 . The β-glucan compound of claim 28 wherein the active moiety comprises a heat-shock protein, high-mobility group box 1 protein, a protein generated following tissue injury, a hyaluronan fragment, ATP, uric acid, heparin sulfate or DNA.
30 . The β-glucan moiety of claim 28 wherein the β-glucan moiety is isolated from yeast.
31 . The β-glucan moiety of claim 30 wherein the yeast comprises Saccharomyces cerevisiae.
32 . The β-glucan moiety of claim 28 wherein the β-glucan moiety and the active moiety are coupled through a covalent linkage or an affinity linkage.
33 . A pharmaceutical composition comprising:
a β-glucan compound comprising:
a β-glucan moiety; and
an active moiety coupled to the β-glucan moiety, the active moiety comprising a danger-associated molecular pattern; and
a pharmaceutically acceptable carrier.
34 . The pharmaceutical composition of claim 33 wherein the active moiety comprises a heat-shock protein, high-mobility group box 1 protein, a protein generated following tissue injury, a hyaluronan fragment, ATP, uric acid, heparin sulfate or DNA.
35 . The pharmaceutical composition of claim 33 wherein the β-glucan moiety is isolated from yeast.
36 . The pharmaceutical composition of claim 35 wherein the yeast comprises Saccharomyces cerevisiae.
37 . The pharmaceutical composition of claim 33 wherein the β-glucan moiety and the active moiety are coupled through a covalent linkage or an affinity linkage.Cited by (0)
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