TOLERIZING TREATMENTS FOR AUTOIMMUNE DISEASE
The disclosure relates to methods of identifying a compound that comprises an epitope that induces immune tolerance in a patient suffering from an autoimmune disease. The disclosure further relates to methods of treating an autoimmune disease by administering (i) a compound identified by the methods described herein, (ii) regulatory T-cells from the patient or a compatible donor, or (iii) a combination of regulatory T-cells and a compound identified by the methods described herein. The disclosure further relates to methods of treating age-related macular degeneration and uveitis.
1 . An in vitro cellular composition, comprising:
human regulatory T-cells cultured in vitro in the presence of synthetic peptide GEPIPVTVDVTNNTEKTVKK (SEQ ID NO:1).
2 . The in vitro cellular composition of claim 1 , wherein the regulatory T-cells are selected from the group consisting of CD4 + CD25 + T-cells, CD4 + Foxp3 + T-cells, and CD4 + CD25 + Foxp3 + T-cells.
3 . The in vitro cellular composition of claim 1 , consisting essentially of:
human regulatory T-cells cultured in vitro in the presence of synthetic peptide GEPIPVTVDVTNNTEKTVKK (SEQ ID NO:1).
4 . The in vitro cellular composition of claim 3 , wherein the regulatory T-cells are selected from the group consisting of CD4 + CD25 + T-cells, CD4 + Foxp3 + T-cells, and CD4 + CD25 + Foxp3 + T-cells.
5 . The in vitro cellular composition of claim 1 , comprising:
human regulatory T-cells cultured in vitro in the presence of
(i) synthetic peptide GEPIPVTVDVTNNTEKTVKK (SEQ ID NO:1), and
(ii) at least one enhancer of the immune suppressive activity of regulatory T-cells selected from the group consisting of high molecular weight hyaluronic acid, IL-2, IL-15, TGF-β, all-trans retinoic acid, rapamycin, anti-CD3, anti-CD28, vitamin D3, dexamethasone, IL-10, idolamine-2,3-dioxygenase, FTY720, a sphingosine kinase 1 inhibitor, cholera toxin B subunit, ovalbumin, Flt2L, sirolimus and anti-thymocyte globulin, and CTLA-4/Ig.
6 . The in vitro cellular composition of claim 5 , wherein the regulatory T-cells are selected from the group consisting of CD4 + CD25 + T-cells, CD4 + Foxp3 + T-cells, and CD4 + CD25 + Foxp3 + T-cells.
7 . The in vitro cellular composition of claim 5 , consisting essentially of:
human regulatory T-cells cultured in vitro in the presence of
(i) synthetic peptide GEPIPVTVDVTNNTEKTVKK (SEQ ID NO:1), and
(ii) at least one enhancer of the immune suppressive activity of regulatory T-cells selected from the group consisting of high molecular weight hyaluronic acid, IL-2, IL-15, TGF-β, all-trans retinoic acid, rapamycin, anti-CD3, anti-CD28, vitamin D3, dexamethasone, IL-10, idolamine-2,3-dioxygenase, FTY720, a sphingosine kinase 1 inhibitor, cholera toxin B subunit, ovalbumin, Flt2L, sirolimus and anti-thymocyte globulin, and CTLA-4/Ig.
8 . The in vitro cellular composition of claim 7 , wherein the regulatory T-cells are selected from the group consisting of CD4 + CD25 + T-cells, CD4 + Foxp3 + T-cells, and CD4 + CD25 + Foxp3 + T-cells.
9 . A method for treating age-related macular degeneration, comprising the step of:
administering the human cellular composition of claim 1 to a human patient having age-related macular degeneration.
10 . The method of claim 9 , wherein the human cellular composition is autologous to the human patient.
11 . A method for treating age-related macular degeneration, comprising the step of:
administering the human cellular composition of claim 5 to a human patient having age-related macular degeneration.
12 . The method of claim 11 , wherein the human cellular composition is autologous to the human patient.
13 . A method of producing an in vitro cellular composition comprising regulatory T-cells trained with an epitope, comprising the steps of:
providing, in vitro, purified human regulatory T-cells that have not been trained by in vitro culture in the presence of synthetic peptide GEPIPVTVDVTNNTEKTVKK (SEQ ID NO:1); and
culturing the purified human regulatory T-cells in vitro in the presence of synthetic peptide GEPIPVTVDVTNNTEKTVKK (SEQ ID NO:1), thereby training the human regulatory T-cells.
14 . The method of claim 13 , wherein the purified human regulatory T-cells are selected from the group consisting of CD4 + CD25 + T-cells, CD4 + Foxp3 + T-cells, and CD4 + CD25 + Foxp3 + T-cells.
15 . The method of claim 13 , further comprising the step of:
after the culturing step, administering the cultured purified human regulatory T-cells to a human patient having age-related macular degeneration.
16 . The method of claim 15 , wherein the human regulatory T-cells are autologous to the human patient.
17 . The method of claim 13 , wherein the step of culturing the purified human regulatory T-cells is further performed in the presence of at least one enhancer of the immune suppressive activity of regulatory T-cells selected from the group consisting of: high molecular weight hyaluronic acid, IL-2, IL-15, TGF-β, all-trans retinoic acid, rapamycin, anti-CD3, anti-CD28, vitamin D3, dexamethasone, IL-10, idolamine-2,3-dioxygenase, FTY720, a sphingosine kinase 1 inhibitor, cholera toxin B subunit, ovalbumin, Flt2L, sirolimus and anti-thymocyte globulin, and CTLA-4/Ig.
18 . The method of claim 17 , wherein the purified human regulatory T-cells are selected from the group consisting of CD4 + CD25 + T-cells, CD4 + Foxp3 + T-cells, and CD4 + CD25 + Foxp3 + T-cells.
19 . The method of claim 17 , further comprising the step of:
after the culturing step, administering the cultured purified human regulatory T-cells to a human patient having age-related macular degeneration.
20 . The method of claim 19 , wherein the purified human regulatory T-cells are autologous to the human patient.