CPC A61K 39/0008 (2013.01) [A61K 39/0005 (2013.01); A61K 39/0007 (2013.01); A61P 25/16 (2018.01); A61P 37/06 (2018.01); A61K 2039/545 (2013.01); A61K 2039/55505 (2013.01); A61K 2039/577 (2013.01); A61K 2039/6037 (2013.01); A61K 2039/6081 (2013.01); A61K 2039/627 (2013.01)] | 10 Claims |
1. A method for vaccination against a self-antigen in a human patient wherein a dose with an effective amount of a self-antigen is administered to the patient to elicit a primary immune response, wherein the patient is subjected to a boost administration of said self-antigen, wherein the amount of the self-antigen in the dose for the boost administration is at least 50 μg and is at least 200% higher than the amount of the self-antigen in the dose used in the administration for the primary immune response, wherein the self-antigen is selected from the group consisting of proprotein convertase subtilisin/kexin type 9 (PCSK9), and an alpha synuclein antigen, and wherein the boost administration is administered at least 6 months after the first administration of the self-antigen for eliciting the primary immune response.
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