IP Library Granted Patent US 12,576,123
Granted Patent B2
US 12,576,123 · App. 17/438,515 · Granted Mar 17, 2026

Epitope-based approach for allergy treatments and inhibitors for Crohn's disease

Inventors: Zachary Apte (San Francisco, CA); Jessica Richman (San Francisco, CA); Daniel Almonacid (San Francisco, CA); Mario Saavedra (San Francisco, CA); Ingrid Araya (San Francisco, CA)
Assignee: Psomagen, Inc.
A61K38/00A61P37/08C07K7/08A61K39/35G01N2800/24
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,576,123
App. No.
17/438,515
Granted
Mar 17, 2026
Kind
B2
Abstract

The present disclosure relates to pharmaceutical compounds and compositions and methods for treating an allergy and Crohn's disease. Methods for treating an allergy can include (a) predicting potential epitopes based proteomes of microbiome and that of an allergen, (b) filtering the potential epitopes obtained in step a) to result in a list of epitopes; and (c) reengineering the list of epitopes obtained in step b) to result in the new epitope. Methods for treating Crohn's disease can include (a), identifying one or more binding regions of an HLA class II protein and/or hemagglutinin to I2 superantigen; (b) determining a first peptide sequence corresponding to the one or more binding regions, and (c) producing a peptide inhibitor having a second peptide sequence that is a mutation of the first peptide sequence, wherein the second peptide sequence has a stronger binding affinity to the I2 superantigen than the first peptide sequence.

Claims (27)

1 . A peptide comprising a sequence of X 1 X 2 X 3 X 4 X 5 X 6 X 7 X 8 X 9 X 10 X 11 X 12 X 13 X 14 X 15 (SEQ ID NO: 1); wherein:

X 1 is E;

X 2 is T;

X 3 is Q or P;

X 4 is G;

X 5 is A or W;

X 6 is I;

X 7 is V;

X 8 is T;

X 9 is V;

X 10 is K;

X 11 is G or Q;

X 12 is G;

X 13 is L;

X 14 is R; and

X 15 is I, H or W.

2 . A pharmaceutical composition comprising the peptide of claim 1 .

3 . The peptide of claim 1 , wherein X 3 is Q.

4 . The peptide of claim 1 , wherein X 3 is P.

5 . The peptide of claim 1 , wherein X 5 is A.

6 . The peptide of claim 1 , wherein X 5 is W.

7 . The peptide of claim 1 , wherein X 11 is G.

8 . The peptide of claim 1 , wherein X 11 is Q.

9 . The peptide of claim 1 , wherein X 15 is I.

10 . The peptide of claim 1 , wherein X 15 is H.

11 . The peptide of claim 1 , wherein X 15 is W.

12 . The peptide of claim 1 , wherein X 3 is P, X 5 is W, X 11 is Q and X 15 is H.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2024
From: PSOMAGEN INC.
To: MACROGEN INC.
Reel/Frame 068067/0415 →
Continuity (6)
Provisional Application 62832811 · Apr 11, 2019
Provisional Application 62828074 · Apr 2, 2019
Provisional Application 62824095 · Mar 26, 2019
Provisional Application 62817564 · Mar 13, 2019
Provisional Application 62817621 · Mar 13, 2019
Related Publication 20220233686A1 · Jul 28, 2022
References Cited (19)
US 20160375130A1 · O'Hehir et al. · 2016 [cited by applicant]
US 20170304432A1 · Hearl et al. · 2017 [cited by applicant]
JP 2002501748A · 2002 [cited by applicant]
JP 2017521064A · 2017 [cited by applicant]
WO 2013187906A1 · 2013 [cited by applicant]
WO 2017186808A1 · 2017 [cited by applicant]
Thakur, R. and Shankar, J. (2016). In silico Identification of Potential Peptides or Allergen Shot Candidates Against Aspergillus fumigatus. BioResearch Open Access 5(1): 330-341. (Year: 2016). [cited by examiner]
Prickett et al. (2013). “Ara h 1 CD4+ T cell epitope-based peptides: candidates for a peanut allergy therapeutic.” Clin. Exp. Allergy, 43(6):684-697. (Year: 2013). [cited by examiner]
Lundegaard et al. (2012). “Predictions versus high-throughput experiments in T-cell epitope discovery: competition or synergy?” Expert Rev. Vaccines, 11(1): 43-54. (Year: 2012). [cited by examiner]
Hayes et al. (2015). “In silico tools for exploring potential human allergy to proteins.” Drug Discov. Today Dis. Models, 17-18:3-11. (Year: 2015). [cited by examiner]
Jiang et al. (2010). “GenBank ADQ53859.1: Ara h 3 allergen [ [cited by examiner]
Office Action issued in corresponding European Patent Application No. 20769559.4 dated Nov. 18, 2022. [cited by applicant]
Office Action issued in corresponding Japanese Patent Application No. 2021-552937 dated Sep. 16, 2022 with English Translation. [cited by applicant]
Piersam et al: “Proteolytic processing of the peanut allergen Ara h 3” (Mol. Nutr. Food Res. 2005, vol. 49, p. 744-755). [cited by applicant]
S. R. Prickett et al: “Ara h 1 CD4+ T cell epitope-based peptides: candidates for a peanut allergy therapeutic” (Clinical & Experimental Allergy, 2013 vol. 43, p. 684-697). [cited by applicant]
Manish Ramesh et al: “Peanut T-cell epitope discovery: Ara h 1” (Journal of Allergy and Clinical Immunology vol. 137, Issue 6, Jun. 2016, pp. 1764-1771.e4). [cited by applicant]
International Search Report issued in corresponding International Patent Application No. PCT/US2020/022701 dated Sep. 18, 2020. [cited by applicant]
Jiang et al., Ara h 3 allergen [ [cited by applicant]
Prickett et al., “Safety and Tolerability of a Novel Peptide-Based Immunotherapy for Peanut Allergy,” Journal of Allergy and Clinical Immunology, 143 (2): AB431 (Feb. 1, 2019). [cited by applicant]