CPC A61K 31/575 (2013.01) [A61K 31/7088 (2013.01); A61K 31/713 (2013.01); A61K 35/76 (2013.01); A61K 38/00 (2013.01); A61K 45/00 (2013.01); A61K 45/06 (2013.01); A61K 48/00 (2013.01); A61P 37/06 (2018.01); C07K 14/47 (2013.01)] | 9 Claims |
1. A method for regulating Rac-activating activity of DOCK2, the method comprising at least one of:
(i) forming an immune-privileged site by administering to a patient in need of treatment an effective amount of cholesterol 3-sulfate, a pharmacologically acceptable salt thereof, or a solvate thereof, to regulate DOCK2-mediated Rac activation;
(ii) forming an immune-privileged site by administering to a patient in need of treatment an effective amount of a SULT2B1b protein, or an expression vector of the SULT2B1b protein; and
(iii) destroying an immune-privileged site by administering to a patient in need of treatment an effective amount of an expression inhibition substance of the SULT2B1b protein,
wherein:
the SULT2B1b protein is a protein which comprises the amino acid sequence of SEQ ID NO: 2, or a protein which comprises an amino acid sequence formed by the deletion, substitution, or addition of 1 to 3 amino acids in the amino acid sequence of SEQ ID NO: 2, and acts to add a sulfonic acid group to the carbon at position 3 of cholesterol and generate cholesterol 3-sulfate, and
the expression inhibition substance of the SULT2B1b protein is siRNA or shRNA.
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