| CPC A61K 39/39583 (2013.01) [A61K 31/716 (2013.01); A61K 39/39 (2013.01); A61K 39/39558 (2013.01); A61K 39/39575 (2013.01); A61K 45/06 (2013.01); A61K 47/6835 (2017.08); C07K 16/12 (2013.01); C07K 16/14 (2013.01); G01N 33/5047 (2013.01); G01N 33/554 (2013.01); G01N 33/56966 (2013.01); A61K 2039/55583 (2013.01); G01N 2400/24 (2013.01)] | 9 Claims |
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1. A method of improving β-glucan immunotherapy for a subject who is a low-binder of β-glucan, the method comprising:
identifying a subject who is a low binder of β-glucan; and
administering to said subject an antibody preparation comprising an anti-β-glucan antibody and a β-glucan immunotherapy, wherein the β-glucan immunotherapy comprises soluble β(1,6)-[poly-(1,3)-D-glucopyranosyl]-poly-β(1,3)-D-glucopyranose and one or more tumor-related monoclonal antibodies;
wherein a subject is identified as a low-binder of β-glucan if β(1,6)-[poly-(1,3)-D-glucopyranosyl]-poly-β(1,3)-D-glucopyranose is bound to no more than 10% of the subject's immune cells, or wherein a subject is identified as a low binder of β-glucan if the anti-β-glucan IgG antibody titer of the subject is less than 20,000.
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