Hydrogel for engineered immune response to D-chirality peptides
An immune-modulating biomaterial comprising a hydrogel scaffold coupled to D-amino acid containing peptides having unexpected properties in vivo is described. For example, certain inflammatory reactions in vivo are significantly increased around the D-peptide containing particles of hydrogel scaffold as compared to particles that contain both L and D peptides or L peptides alone. In addition, these D-peptide compositions are further observed to enhance wound healing and improve the tensile strength of healed tissues. For these and other reasons, the D-amino acid hydrogel materials disclosed herein are useful in a number of methodologies that seek to modulate the immune response and/or wound healing.
1. A composition comprising:
a polymeric hydrogel scaffold coupled to an adjuvant peptide comprising at least one D amino acid; and
an immunogenic peptide comprising a viral, bacterial or cancer immunogen recognized by human immune cells, wherein:
the adjuvant peptide and the immunogenic peptide are disposed in the polymeric hydrogel scaffold such that an in vivo immune reaction observed in human immune cells exposed to the immunogenic peptide is greater than an immune reaction observed in response to a control polymeric hydrogel scaffold composition that is identical to said polymeric hydrogel scaffold composition except that said control polymeric hydrogel scaffold composition comprises peptides formed only from L amino acids.
2. The composition of claim 1 , wherein the polymeric hydrogel scaffold surrounds and encapsulates the immunogenic peptide.
3. The composition of claim 1 , wherein the polymeric hydrogel scaffold forms pores in the composition, and the pores are between 1 μm and 50 μm such that immune cells can infiltrate the composition.
4. The composition of claim 1 , wherein the hydrogel scaffold comprises at least one of:
polyethylene glycol polymers;
hyaluronic acid polymers;
an RGD peptide;
a Q peptide;
a K peptide; or
a Matrix Metallo-protease (MMP) peptide.
5. The composition of claim 1 , wherein the adjuvant peptide comprises a crosslinker forming part of a backbone structure of the hydrogel scaffold.
6. The composition of claim 1 , wherein the immunogenic peptide is disposed in the polymeric hydrogel scaffold such that a titer of IgG1 antibodies generated against the immunogenic peptide is at least 50% greater than a titer of IgG1 antibodies generated in response to the control polymeric hydrogel scaffold composition.
7. A method of modulating an immune response comprising contacting human immune cells with a composition of claim 1 , so that the cells recognize the immunogenic peptide and initiate an immune response to the immunogenic peptide.
8. The method of claim 7 , wherein the immune response comprises an infiltration of CD11b + cells to the site of the composition.
9. The method of claim 8 , wherein an amount of CD11b + immune cells that infiltrate into the composition in vivo is at least 50% greater than an amount of CD11b + immune cells observed in response to the control polymeric hydrogel scaffold composition.
10. The method of claim 7 , wherein the immune response comprises generating a titer of IgG1 antibodies that is at least 50% greater than a titer of IgG1 antibodies generated in response to the control polymeric hydrogel scaffold composition.
11. The method of claim 7 , wherein the composition is disposed in a wound.
12. A method of increasing the tensile strength of new tissue forming in a wound comprising contacting the wound with a composition comprising a polymeric hydrogel scaffold and a peptide comprising at least one D amino acid, wherein said peptide comprises 16 amino acids.
13. The method of claim 12 , wherein the tensile strength of tissue in the healed wound as measured by a tensiometer is at least 50% greater than a wound contacted with a control composition comprising the polymeric hydrogel scaffold coupled to a peptide having an identical amino acid sequence to the peptide of claim 12 but which comprises only L amino acids.