Tolerogenic synthetic nanocarriers for allergy therapy
Disclosed are synthetic nanocarrier compositions, and related methods, comprising immunosuppressants and MHC Class II-restricted epitopes of an allergen that provide tolerogenic immune responses specific to the allergen.
1. A composition comprising:
(i) a first population of polymeric synthetic nanocarriers that are coupled to rapamycin, and
(ii) a second population of polymeric synthetic nanocarriers that are coupled to antigens that comprise Major Histocompatibility Complex (MHC) Class II-restricted epitopes of an allergen, wherein the composition comprises substantially no B cell epitopes of the allergen, and
wherein the load of the rapamycin on average across the first population of polymeric synthetic nanocarriers is at least 2% but no more than 25% (weight/weight), wherein the load of the antigens on average across the second population of polymeric synthetic nanocarriers is between 1% and 10% weight/weight,
wherein the composition is in an amount effective to reduce the generation of an undesired immune response against the allergen,
wherein at least 75% of the polymeric synthetic nanocarriers of the first population of synthetic nanocarriers have a minimum dimension, obtained using dynamic light scattering, that is greater than 110 nm and a maximum dimension, obtained using dynamic light scattering, that is equal to or less than 500 nm.
2. The composition of claim 1 , wherein the first population and second population are the same population.
3. The composition of claim 1 , wherein the allergen induces an undesired immune response in a subject.
4. The composition of claim 3 , wherein the undesired immune response is allergen-specific antibody production.
5. The composition of claim 3 , wherein the undesired immune response is allergen-specific CD4+ T cell proliferation and/or activity.
6. The composition of claim 1 , wherein the aspect ratio of the maximum to minimum dimension of the synthetic nanocarriers of the first population or second population is greater than 1:1, 1:1.2, 1:1.5, 1:2, 1:3, 1:5, 1:7 or 1:10.
7. The composition of claim 1 , wherein the composition further comprises a pharmaceutically acceptable excipient.
8. A dosage form comprising the composition of claim 1 .