IP Library Granted Patent US 11,779,641
Granted Patent B2
US 11,779,641 · App. 15/061,204 · Granted Oct 10, 2023

Tolerogenic synthetic nanocarriers for allergy therapy

Inventors: Takashi Kei Kishimoto (Lexington, MA); Christopher Fraser (Arlington, MA); Roberto A. Maldonado (Jamaica Plain, MA)
Assignee: Selecta Biosciences, Inc.
A61K39/385A61K9/127A61K9/14A61K9/51A61K9/5115A61K9/5146A61K9/5153A61K31/192A61K38/13A61K38/1816A61K38/38A61K39/00A61K39/001A61K39/0008A61K39/35A61K39/36A61K47/50A61K47/52A61K47/544A61K47/593A61K47/643A61K47/69A61K47/6923A61K47/6929A61K47/6937B82Y5/00G01N33/505G01N33/56972A61K2039/5154A61K2039/55511A61K2039/55555A61K2039/577B82Y40/00G01N2333/7051G01N2333/70514G01N2333/70517Y02A50/30
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Quick Facts
Patent No.
US 11,779,641
App. No.
15/061,204
Granted
Oct 10, 2023
Kind
B2
Abstract

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.

Claims (38)

1. A method comprising administering to a subject, a composition comprising:

(i) a first population of polymeric synthetic nanocarriers that are coupled to rapamycin or a rapamycin analog and

(ii) a second population of polymeric synthetic nanocarriers that are coupled to MHC Class II-restricted epitopes of an 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, and

wherein the composition comprises substantially no B cell epitopes of the allergen, and wherein the load of the rapamycin or a rapamycin analog on average across the first population of synthetic nanocarriers is at least 2% but no more than 25% (weight/weight).

2. A method comprising:

administering to a subject a composition comprising:

(i) a first population of polymeric synthetic nanocarriers that are coupled to rapamycin or a rapamycin analog, and

(ii) a second population of polymeric synthetic nanocarriers that are coupled to MHC Class II-restricted epitopes of an 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, and

wherein the composition comprises substantially no B cell epitopes of the allergen, wherein the load of the rapamycin or a rapamycin analog on average across the first population of synthetic nanocarriers is at least 2% but no more than 25% (weight/weight), wherein the composition is in an amount effective to reduce an undesired immune response to the allergen in the subject, and wherein the subject is experiencing or is at risk of experiencing the undesired immune response to the allergen.

3. A method comprising:

reducing an undesired immune response to an allergen in a subject by administering a composition comprising:

(i) a first population of polymeric synthetic nanocarriers that are coupled to rapamycin or a rapamycin analog, and

(ii) a second population of polymeric synthetic nanocarriers that are coupled to MHC Class II-restricted epitopes of 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, and

wherein the composition comprises substantially no B cell epitopes of the allergen, wherein the load of the rapamycin or a rapamycin analog on average across the first population of synthetic nanocarriers is at least 2% but no more than 25% (weight/weight), wherein the composition is in an amount effective to reduce the undesired immune response to the allergen in the subject, and wherein the subject is experiencing or is at risk of experiencing the undesired immune response to the allergen.

4. A method comprising:

administering a composition to a subject according to a protocol that was previously shown to reduce an undesired immune response to an allergen in one or more test subjects;

wherein the composition comprises:

(i) a first population of polymeric synthetic nanocarriers that are coupled to rapamycin or a rapamycin analog, and

(ii) a second population of polymeric synthetic nanocarriers that are coupled to MHC Class II-restricted epitopes of 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, and

wherein the composition comprises substantially no B cell epitopes of the allergen, wherein the load of the rapamycin or a rapamycin analog on average across the first population of synthetic nanocarriers is at least 2% but no more than 25% (weight/weight), wherein the composition is in an amount effective to reduce the undesired immune response to the allergen in the subject, and wherein the subject is experiencing or is at risk of experiencing the undesired immune response to the allergen.

5. The method of claim 1 , wherein the allergen induces allergen-specific antibody production and/or allergen-specific CD4+ T cell proliferation and/or activity in the subject.

6. The method of claim 2 , wherein the undesired immune response is allergen-specific antibody production and/or allergen-specific CD4+ T cell proliferation and/or activity.

7. The method of claim 3 , wherein the undesired immune response is allergen-specific antibody production and/or allergen-specific CD4+ T cell proliferation and/or activity.

8. The method of claim 4 , wherein the undesired immune response is allergen-specific antibody production and/or allergen-specific CD4+ T cell proliferation and/or activity.

9. The method of claim 1 , wherein the allergen comprises an asthma antigen, a hay fever antigen, a hives antigen, an eczema antigen, a plant allergen, an insect sting allergen, an insect allergen, an animal allergen, a fungal allergen, a drug allergen, a pet allergen, a latex allergen, a mold allergen, a cosmetic allergen or a food allergen.

10. The method of claim 2 , wherein the allergen comprises an asthma antigen, a hay fever antigen, a hives antigen, an eczema antigen, a plant allergen, an insect sting allergen, an insect allergen, an animal allergen, a fungal allergen, a drug allergen, a pet allergen, a latex allergen, a mold allergen, a cosmetic allergen or a food allergen.

11. The method of claim 3 , wherein the allergen comprises an asthma antigen, a hay fever antigen, a hives antigen, an eczema antigen, a plant allergen, an insect sting allergen, an insect allergen, an animal allergen, a fungal allergen, a drug allergen, a pet allergen, a latex allergen, a mold allergen, a cosmetic allergen or a food allergen.

12. The method of claim 4 , wherein the allergen comprises an asthma antigen, a hay fever antigen, a hives antigen, an eczema antigen, a plant allergen, an insect sting allergen, an insect allergen, an animal allergen, a fungal allergen, a drug allergen, a pet allergen, a latex allergen, a mold allergen, a cosmetic allergen or a food allergen.

13. The method of claim 1 , wherein the polymeric synthetic nanocarriers comprise a polyester, a polyester coupled to a polyether, polyamino acid, polycarbonate, polyacetal, polyketal, polysaccharide, polyethyloxazoline or polyethyleneimine.

14. The method of claim 13 , wherein the polyester comprises a poly(lactic acid), poly(glycolic acid), poly(lactic-co-glycolic acid) or polycaprolactone.

15. The method of claim 13 , wherein the polymeric synthetic nanocarriers comprise a polyester and a polyester coupled to a polyether.

16. The method of claim 13 , wherein the polyether comprises polyethylene glycol or polypropylene glycol.

17. The method 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.

18. The method of claim 1 , wherein at least 80%, at least 90%, or at least 95% of the first and/or second population of synthetic nanocarriers have a minimum dimension or maximum dimension that falls within 5%, 10%, or 20% of the mean diameter of the synthetic nanocarriers.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2016
From: KISHIMOTO, TAKASHI KEI; FRASER, CHRISTOPHER; MALDONADO, ROBERTO A.
To: SELECTA BIOSCIENCES, INC.
Reel/Frame 038376/0375 →
Continuity (14)
Division 13457977 · Apr 27, 2012
Provisional Application 61531147 · Sep 6, 2011
Provisional Application 61531153 · Sep 6, 2011
Provisional Application 61531164 · Sep 6, 2011
Provisional Application 61531168 · Sep 6, 2011
Provisional Application 61531175 · Sep 6, 2011
Provisional Application 61531180 · Sep 6, 2011
Provisional Application 61531194 · Sep 6, 2011
Provisional Application 61531204 · Sep 6, 2011
Provisional Application 61531209 · Sep 6, 2011
Provisional Application 61531215 · Sep 6, 2011
Provisional Application 61513514 · Jul 29, 2011
Provisional Application 61480946 · Apr 29, 2011
Related Publication 20160279234A1 · Sep 29, 2016
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