US 11,992,495 B2
Enhancing GABA's ability to modulate immune responses
Daniel Kaufman, Los Angeles, CA (US); and Jide Tian, Los Angeles, CA (US)
Assigned to THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, Oakland, CA (US)
Appl. No. 16/625,181
Filed by THE REGENTS OF THE UNIVERSITY OF CALIFORNIA, Oakland, CA (US)
PCT Filed Jun. 20, 2018, PCT No. PCT/US2018/038428
§ 371(c)(1), (2) Date Dec. 20, 2019,
PCT Pub. No. WO2018/236955, PCT Pub. Date Dec. 27, 2018.
Claims priority of provisional application 62/524,338, filed on Jun. 23, 2017.
Prior Publication US 2020/0138830 A1, May 7, 2020
Int. Cl. A61K 31/5517 (2006.01); A61K 9/20 (2006.01); A61K 31/5513 (2006.01); A61K 31/57 (2006.01); A61P 29/00 (2006.01); A61P 37/02 (2006.01)
CPC A61K 31/5517 (2013.01) [A61K 9/20 (2013.01); A61K 31/5513 (2013.01); A61K 31/57 (2013.01); A61P 29/00 (2018.01); A61P 37/02 (2018.01)] 15 Claims
 
1. A method of reducing an inflammatory immune response and/or promoting a regulatory immune response in a mammal, said method comprising administering to said mammal the GABAA receptor positive allosteric modulator (PAM) alprazolam and the GABA receptor activating ligand GABA, wherein the dose of GABA would be sufficient to achieve a reduction of an inflammatory immune response and/or promotion of a regulatory immune response when used alone, and the dose of alprazolam is sufficient to increase the reduction of an inflammatory immune response and/or promotion of a regulatory immune response, and wherein the combination of said alprazolam and GABA is more effective to reduce an inflammatory immune response and/or to promote a regulatory immune response in said mammal than when either agent is administered alone.