Granted Patent B2

US 12,545,948 · App. 16/318,720 · Granted Feb 10, 2026

Inventors: Hakon Hakonarson (Malvern, PA); Berta Almoguera (Philadelphia, PA); Lyam M. Vazquez (Philadelphia, PA); Patrick M.A. Sleiman (Philadelphia, PA)

Assignee: The Children'S Hospital of Philadelphia

C12Q1/6827A61K45/06A61P11/06C12Q1/6883A61K31/343A61K31/353A61K31/46A61K31/4704A61K31/522A61K31/56A61K39/395C12Q2600/106C12Q2600/156G01N2800/122

Abstract

Claims (31)

1 . A method for identifying a human subject of European descent having a predisposition for asthma, comprising,

a) identifying a risk allele indicative of a predisposition for asthma present in a single nucleotide polymorphism (SNP) containing nucleic acid isolated from biological sample obtained from said subject, selected from:

an A allele at rs72721168 in SEQ ID NO: 1;

a T allele at rs72721166 in SEQ ID NO: 2;

an A allele at rs72721164 in SEQ ID NO: 3;

a C allele at rs72721158 in SEQ ID NO: 4;

a T allele at rs35632171 in SEQ ID NO: 14;

an A allele at rs36080042 in SEQ ID NO: 15; and

an A allele at rs75446656 in SEQ ID NO: 162 in the subject of European descent; and

b) administering at least one agent useful to treat asthma to the subject, wherein said agent is selected from one or more of a PGE synthetic agonist, an oral steroid, an anti-IgE, a β1 agonist, a β2 agonist, a mast cell stabilizer, a leukotriene antagonist, Ipratropium bromide, and a phosphodiesterase inhibitor.

2 . The method of claim 1 , wherein said agent is selected from Epoprostenol, Iloprost, Treprostinil, Methylprednisolone, Prednisone, Prednisolone, Triamcinolone, Omalizumab, Beclomethasone, Budesonide, Ciclesonide, Flunisolide, Fluticasone, Fluticasone propionate HFA, Fluticasone Propionate inhaled, Momethasone, Triamcinolone Acetonide, Triamcinolone, Dobutamine, Epinephrine, Racepinephrine Isoproterenol β1, Isoproterenol β2, Methylxanthine, Theophylline, Arformoterol, Albuterol, Albuterol Sulfate, Clenbuterol, Fenoterol, Formoterol, Isoetarine, Levalbuterol, Levalbuterol HCL, Levalbuterol Tartrate, Metaproterenol, Pirbuterol, Procaterol, Ritodrine, Salmeterol, Terbutaline, Cromolyn, Cromolyn Sodium, Nedocromi, Montelukast, Zafirlukast, Zileuton, Ipratropium Bromide, and Ibudilast.

3 . The method of claim 1 , wherein a combination of drugs is administered, said combination selected from

i) a PGE-agonist and a leukotriene inhibitor;

ii) a PGE-agonist and low dose inhaled steroid;

iii) a PGE-agonist and a beta adrenergic agonist;

iv) a PGE-agonist and a phosphodiesterase inhibitor;

v) a PGE-agonist and an anti-IgE antibody;

vi) a PGE-agonist and anticholinergic agent; and

vii) a PGE-agonist and a mast cell stabilizer.

4 . The method of claim 3 , wherein combinations i-vi further comprise a mast cell stabilizer.

5 . The method of claim 3 , wherein said PGE-agonist is selected from epoprostenol, iloprost and treprostinil, said leukotriene inhibitor is montelukast; said inhaled steroid is fluticasone; said phospdiesterase inhibitor is theophylline, said anti-IgE antibody is omalizumab, said anticholinergic agent is ipratropium bromide, and said mast cell stabilizer is chromolyn.

6 . The method of claim 1 , wherein the risk allele is identified by contacting the nucleic acid sample with a collection of probes or primers of sufficient length and composition to detect said asthma-associated SNP, wherein said probes or primers hybridize to, or amplify SEQ ID NO: 1-4, 14, 15, and 162.

7 . The method of claim 1 , wherein the step of identifying said risk allele in said SNP containing nucleic acid is performed using a process selected from detection of specific hybridization, measurement of allele size, restriction fragment length polymorphism analysis, allele-specific hybridization analysis, single base primer extension reaction, and sequencing of an amplified polynucleotide.

8 . The method of claim 1 , wherein the nucleic acid in the sample is DNA or RNA.

9 . The method of claim 1 , wherein the nucleic acid sample is from blood, urine, serum, gastric lavage, cerebral spinal fluid, brain cells, mononuclear cells, fetal cells in maternal circulation, or body tissue.

10 . The method of claim 1 , wherein the SNP containing nucleic acids are selected from:

a T allele at rs72721166 in SEQ ID NO: 2;

an A allele at rs72721164 in SEQ ID NO: 3;

a C allele at rs72721158 in SEQ ID NO: 4;

an A allele at rs36080042 in SEQ ID NO: 15; and

an A allele at rs75446656 in SEQ ID NO: 162.

Assignments (2)

Continuity (2)

References Cited (46)