US2017368166A1PendingUtilityA1
Tissue Targeted Antigenic Activation of the Immune Response to Treat Cancers
Est. expiryJun 7, 2024(expired)· nominal 20-yr term from priority
Inventors:Harold David Gunn
A61K 39/092G01N 33/5055A61K 2039/5252A61K 39/0266A61K 31/405A61K 39/235A61K 2039/521A61K 39/0241A61K 39/0258A61K 39/1045A61K 39/085A61K 2039/5254A61K 2039/70C12N 2760/16032C12N 2710/10032A61K 31/635A61K 39/0275G01N 33/5088A61K 2039/585C12N 2760/18532A61K 39/155C12N 2760/18632A61K 2039/522A61K 2039/545A61K 39/145A61K 2039/575A61K 39/102A61P 35/00A61K 31/192A61K 33/24C12R 1/445A61K 39/0011A61K 40/46A61K 40/24A61K 40/19A61K 2239/58A61K 2239/49A61K 2239/54C12N 1/205C12R 2001/445A61K 33/243Y02A50/30
67
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Claims
Abstract
The invention provides in part methods of treating cancers of a specific organ or tissue by administering a composition that is antigenically specific for one or more microbes that are pathogenic in the specific organ or tissue in which the cancer is situated.
Claims
exact text as granted — not AI-modified1 - 97 . (canceled)
98 . A method for treating a human patient for a cancer situated in a lung tissue, the method comprising:
administering to the patient a medicament comprising an effective amount of an antigenic composition comprising antigenic determinants characteristic of Klebsiella pneumoniae , the antigenic determinants together being specific for Klebsiella pneumoniae so that the composition elicits an immune response in the patient that is specific for Klebsiella pneumoniae.
99 . The method according to claim 98 , wherein the method comprises administering the medicament in successive doses given at a dosage interval of between one hour and one month, over a dosage duration of at least two weeks.
100 . The method according to claim 99 , wherein the method comprises administering the medicament in a dose so that each dose is effective to cause a localized inflammatory immune response at an administration site.
101 . The method according to claim 100 , wherein the administration site is distant from the lung.
102 . The method of claim 101 , wherein the method comprises administering the medicament in a manner such that visible localized inflammation at the administration site occurs within 1 to 48 hours.
103 . The method according to claim 98 , wherein the method comprises administering the medicament intradermally or subcutaneously.
104 . The method according to claim 102 , wherein the method comprises administering the medicament intradermally or subcutaneously.
105 . The method according to claim 98 , wherein the method comprises intranasal, inhalational, or aerosol, administration of the medicament.
106 . The method according to claim 99 , wherein the method comprises intranasal, inhalational, or aerosol, administration of the medicament.
107 . The method according to claim 98 , wherein the method further comprises administering to the patient an effective amount of cisplatin.
108 . The method according to claim 99 , wherein the method further comprises administering to the patient an effective amount of cisplatin.
109 . The method according to claim 104 , wherein the method further comprises administering to the patient an effective amount of cisplatin.
110 . The method according to claim 106 , wherein the method further comprises administering to the patient an effective amount of cisplatin.
111 . The method of claim 98 , wherein the patient is a patient that has been diagnosed as having suffered from a prior pathogenic exposure to Klebsiella pneumoniae.
112 . The method according to claim 98 , wherein the medicament is administered to the subject in an amount and for a time that is effective to modulate an immune response.
113 . The method of claim 112 , wherein the modulation of the immune response comprises a shift in the activation state of macrophages.
114 . The method of claim 113 , wherein the modulation of the immune response comprises shifting from a M2-like macrophage response to a M1-like macrophage response.
115 . The method of claim 112 , wherein the method further comprises measuring a characteristic of the immune response.
116 . The method of claim 115 , wherein measuring the characteristic of the immune response comprises comparing an indication of the numbers of any one or more of the following cells: inflammatory monocytes, macrophages, CD11b + Gr-1 + cells, dendritic cells, CD11c + MHC class II + cells, CD4 + T cells, CD8 + T cells, or NK cells.
117 . A method for treating a human patient for a cancer situated in a lung tissue, the method comprising:
administering to the patient a medicament comprising an effective amount of an antigenic composition comprising antigenic determinants characteristic of Klebsiella pneumoniae , the antigenic determinants together being specific for Klebsiella pneumoniae so that the composition elicits an immune response in the patient that is specific for Klebsiella pneumoniae; administering the medicament in successive doses given at a dosage interval of between one hour and one month, over a dosage duration of at least two weeks in an amount and for a time that is effective to modulate an immune response, and the modulation of the immune response comprises a shift in the activation state of macrophages from a M2-like macrophage response to a M1-like macrophage response; and, administering to the patient an effective amount of cisplatin.Join the waitlist — get patent alerts
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