| CPC A61K 31/436 (2013.01) [A61K 9/0019 (2013.01); A61K 9/127 (2013.01); A61K 9/5115 (2013.01); A61K 9/5153 (2013.01); A61K 9/5192 (2013.01); A61K 31/192 (2013.01); A61K 38/19 (2013.01); A61K 38/21 (2013.01); A61K 38/37 (2013.01); A61K 38/43 (2013.01); A61K 38/47 (2013.01); A61K 39/39533 (2013.01); A61K 39/3955 (2013.01); A61K 45/06 (2013.01); A61K 47/6923 (2017.08); A61K 47/6929 (2017.08); A61K 47/6935 (2017.08); A61K 47/6937 (2017.08); C07K 16/18 (2013.01); C07K 16/241 (2013.01); C07K 16/40 (2013.01); A61K 2039/505 (2013.01); C12Y 305/01001 (2013.01)] | 20 Claims |
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1. A method comprising:
providing a therapeutic dose of a therapeutic macromolecule, wherein the therapeutic macromolecule is not attached to synthetic nanocarriers;
providing a composition comprising synthetic nanocarriers that are attached to immunosuppressants; and
administering the composition and the therapeutic dose of the therapeutic macromolecule to a subject concomitantly,
and
wherein the concomitant administration of the composition and the therapeutic dose of the therapeutic macromolecule reduces both Type 1 hypersensitivity and Type IV hypersensitivity in the subject.
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