Compositions and methods for modulating an immune response
The invention provides methods of modulating follicular regulatory T (TFR) cell-mediated immune responses, follicular helper T (TFH) cell-mediated immune responses or both, and the use of those methods in the treatment of diseases or conditions mediated by TFR or TFH cells. The invention also provides novel methods for identifying TFR and TFH cells in a population of cells. The invention also provides compositions comprising TFR cells that have enhanced suppressive activity as compared wild type TFR cells. The invention also provides compositions comprising T follicular regulatory (TFR) cells isolated from the peripheral blood of a subject wherein the composition is enriched for TFR cells. Methods of making and using the compositions of the invention to modulate an immune response are also provided.
1. A method of preparing a composition comprising TFR cells having enhanced immune suppressive activity comprising the steps of:
a) obtaining an initial population of cells comprising TFR cells, T regulatory (Treg) progenitor cells or both;
b) activating the cells ex vivo in the presence of a PD-1 antagonist or PD-1 ligand antagonist, or both; and
c) isolating activated TFR cells from the population wherein the isolated TFR cells have enhanced immune suppressive activity.
2. The method of claim 1 , wherein the initial population of cells is isolated from the peripheral blood, tissues or organs of one or more subjects.
3. The method of claim 1 , further comprising sorting TFR cells and Treg progenitor cells from the cell population prior to activation of the cell population or after activation of the cell population.
4. The method of claim 1 , wherein the activation step comprises expanding the cell population.
5. The method of claim 1 , wherein the activation step comprises contacting the cell population with a stimulatory composition.
6. The method of claim 5 , wherein the stimulatory composition comprises an anti-CD3 antibody, physiological antigen presenting cells (APCs), purified CD19+ B cells, and anti-CD28 antibody.
7. The method of claim 5 , wherein stimulatory composition comprises beads coated with CD3 antibody, the anti-CD28 antibody or any combination thereof.
8. The method of claim 1 , wherein the PD-1 antagonist or PD-1ligand antagonist is selected from: a PD1-ligand antibody, an anti-PD-1 antibody, a peptide or a small molecule or any combination thereof, wherein the antagonist inhibits the interaction between PD-1 and a PD-1 ligand.
9. The method of claim 1 , wherein the isolating step comprises sorting TFR cells based on surface markers of CD4 + CXCR5 + ICOS + GITR + or CD4 + CXCR5 + ICOS + CD25 hi .
10. A composition comprising T follicular regulatory (TFR) cells having enhanced immune suppressive activity prepared by the method of claim 1 .
11. The composition of claim 10 , wherein the TFR cells are characterized by their ability to more potently inhibit antibody production in vitro and in vivo.
12. The composition of claim 11 , wherein the TFR cells are characterized by their ability to more potently inhibit T follicular helper (TFH) cell-mediated antibody production in vitro and in vivo.
13. The composition of claim 10 , wherein the TFR cells are characterized by their ability to more potently inhibit T-follicular helper (TFH) cell function in vitro and in vivo.
14. The composition of claim 10 , wherein the TFR cells having enhanced suppressive activity are characterized by their ability to more potently inhibit an antibody response in vitro and in vivo as compared to native TFR cells.
15. The composition of claim 10 , wherein the TFR cells are at least two-fold more potent than native TFR.