Methods to cause differentiation of T-cells for use in cell therapy
A method resulting in differentiation of T-cells for use in cell therapy includes labeling the T-cells with a first array of antibodies specific for T-cell surface antigens; applying a universal cross-linking agent to the labeled T-cells with the first array of antibodies; labeling the T-cells with a second array of antibodies specific for T-cell surface antigens; and applying a universal cross-linking agent to the labeled T-cells with the second array of antibodies.
1. A method to cause differentiation of T-cells for use in cell therapy comprising:
labeling the T-cells with a first array of antibodies specific for T-cell surface antigens;
applying a universal cross-linking agent to the labeled T-cells with the first array of antibodies;
labeling the T-cells with a second array of antibodies specific for T-cell surface antigens; and
applying a universal cross-linking agent to the labeled T-cells with the second array of antibodies.
2. The method of claim 1 wherein labeling the T-cells with a second array of antibodies specific for T-cell surface antigens and applying a universal cross-linking agent to the labeled T-cells is repeated one or more times.
3. The method of claim 1 where the first or second array of antibodies is selected from one or more of the following: anti-CD3, -CD28, -B7-H3, -PD-L1, -PD-L2, -IL-15R, -CD2, -CD48, -LFA-1, -CD43, -CD45, -CD4, -CD8, -CD7, -GM1, -LIGHT, -CD27, -OX40, -4-1BB, -CD30, -CD44, -CD31, -CD18/CD 11 a , -CD29, -CD54, -CD62L, -VLA4, -IL-2R, -IL-4R, IL-10R, -type II IFNR1 and R2, -type I IFNR, -IL-12beta1l and beta2, -IL-15R, - TNFR1, -TNFR2, and -IL-1R.
4. The method of claim 1 where the first or second array of antibodies include anti-chemokine receptors.
5. The method of claim 4 where the anti-chemokine receptors include C-C and C-X-C categories.
6. The method of claim 5 where the anti-chemokine receptors include one or more of the following: CCR1, CCR2, CCR3, CCR4, CCR5 and CXCR3.
7. The method of claim 1 wherein the universal cross-linking agent is attached to a biodegradable support.
8. The method of claim 1 wherein the T-cells are used to stimulate immunity.
9. The method of claim 1 wherein the T-cells are used to suppress immunity.