ERAAP modulators regulate immune responses
View Patent ↗An immune response is modulated by selectively inhibiting ERAAP (an acronym for ER aminopeptidase associated with antigen processing) and confirming a resultant immune response modulation. More particularly, the method comprises contacting a patient determined to be in need of immune response modulation with a physiologically acceptable dosage composition comprising an effective amount of an inhibitor of ERAAP activity; confirming a resultant inhibition of said ERAAP activity and confirming a resultant immune response modulation in the patient. A variety of selective inhibitors are shown to be effective, including amino thiols, such as leucine thiol, ERAAP-specific antibody complementarity-determining region, and an ERAAP-specific siRNA.
1. A method of inhibiting MHC class I antigen processing by ERAAP, wherein ERAAP is an acronym for ER aminopeptidase associated with antigen processing, the method comprising the steps of:
administering to a host cell in vitro, expressing said ERAAP, and predetermined to be in need of suppression of antigen processing or antigen presentation an effective amount of an ERAAP inhibitor, and wherein the inhibitor is selected from the group consisting of leucine-thiol, lysine-thiol and isoleucine-thiol; and
confirming a resultant inhibition of said ERAAP and inhibition of said MHC class I antigen processing.
2. The method of claim 1 , wherein the inhibitor is leucine-thiol.
3. The method of claim 1 , wherein the inhibitor is lysine-thiol.
4. The method of claim 1 , wherein the inhibitor is isoleucine-thiol.
5. A method of inhibiting MHC class I antigen processing by ERAAP, wherein ERAAP is an acronym for ER aminopeptidase associated with antigen processing, the method comprising the steps of:
administering to a host cell in vitro, expressing said ERAAP and predetermined to be in need of suppression of antigen processing or antigen presentation an effective amount of an ERAAP inhibitor, and wherein the inhibitor is a pharmacophore selected from the group consisting of L-bis(1-thio-2-amino-4-methylpentane)dihydrochloride (TAMP), L-bis(1-thio-2-amino-3-phenylpropane)dihydrochloride (TAPP) and an alpha-thiolbestatin; and
confirming a resultant inhibition of said ERAAP and inhibition of the MHC class I antigen processing.
6. The method of claim 5 , wherein the pharmacophore is L-bis(1-thio-2-amino-4-methylpentane)dihydrochloride (TAMP).
7. The method of claim 5 , wherein the pharmacophore is L-bis(1-thio-2-amino-3-phenylpropane)dihydrochloride (TAPP).
8. The method of claim 5 , wherein the pharmacophore is an alpha-thiolbestatin.