Labeled probe and methods of use
View Patent ↗The present disclosure provides for methods and compositions useful for imaging inflammation and inflammatory disease markers with an affinity for TREM-1 antibodies. The methods and compositions can include a labeled probe having a TREM-1 antibody and a radiolabel.
1. An in vivo method of imaging neurological tissue inflammation from a neurological disease in a subject using a Positron Emission Tomography (PET) imaging system, comprising:
administering to a subject a labeled probe, wherein the labeled probe comprises a TREM-1 antibody and a radiolabel;
wherein the radiolabel is selected from 64 Cu, 18 F, and 89 Zr;
imaging at least a portion of the subject; and
detecting a signal from the labeled probe, wherein the detection of the signal corresponds to the tissue inflammation from the neurological disease;
wherein the neurological disease is selected from the group consisting of Alzheimer's disease, multiple sclerosis, epilepsy, traumatic brain injury, Huntington's disease, amyotrophic lateral sclerosis, Parkinson's disease, sepsis, stroke, chronic fatigue syndrome, depression, and schizophrenia.
2. The method of claim 1 , wherein the neurological disease is Alzheimer's disease.
3. The method of claim 1 , wherein the neurological disease is sepsis.
4. The method of claim 1 , wherein the radiolabel is conjugated to the TREM-1 antibody using a chelator selected from the group consisting of: (1,4,7,10-tetraazacyclododecane-1,4,7,1 0-tetraacetic acid); NOTA (1,4,7-Triazacyclononane-1,4,7-triacetic acid); EDTA (Ethylenediaminetetraacetic acid); Df (Desferrioxamine); DTPA (Diethylenetriaminepentaacetic acid; and TETA (Triethylenetetramine).
5. A method of monitoring the progress of tissue inflammation from a neurological disease in a subject, the method comprising:
administering to a subject a labeled probe, wherein the labeled probe includes TREM-1 antibody and a radiolabel,
imaging at least a portion of the subject; and
detecting a signal from the labeled probe, wherein detection of the signal corresponds to the tissue inflammation from the neurological disease, wherein dimensions of the signal are monitored over time and the neurological disease is selected from the group consisting of Alzheimer's disease, multiple sclerosis, epilepsy, traumatic brain injury, Huntington's disease, amyotrophic lateral sclerosis, Parkinson's disease, sepsis, stroke, chronic fatigue syndrome, depression, and schizophrenia.
6. The method of claim 5 , wherein a level of uptake of the labeled probe in a tissue corresponds to a level of inflammation in the tissue.
7. The method of claim 5 , wherein the detection of the signal is performed in vitro using Positron Emission Tomography (PET), Computerized Tomography (CT), or a combination thereof.
8. The method of claim 1 , wherein a level of uptake of the labeled probe in the tissue corresponds to a level of inflammation in the tissue.
9. An in vivo method of imaging neurological tissue inflammation from a neurological disease in a subject using a Positron Emission Tomography (PET) imaging system, comprising:
administering to a subject a labeled probe, wherein the labeled probe comprises a TREM-1 antibody and a radiolabel;
wherein the radiolabel is selected from 64 Cu, 18 F, and 89 Zr;
imaging at least a portion of the subject's brain; and
detecting a signal from the labeled probe, wherein the detection of the signal corresponds to the neurological tissue inflammation from the neurological disease;
wherein the neurological disease is selected from the group consisting of Alzheimer's disease, multiple sclerosis, epilepsy, traumatic brain injury, Huntington's disease, amyotrophic lateral sclerosis, Parkinson's disease, sepsis, stroke, chronic fatigue syndrome, depression, and schizophrenia.
10. The method of claim 9 , wherein the radiolabel is conjugated to the TREM-1 antibody using a chelator selected from the group consisting of: (1,4,7,10-tetraazacyclododecane-1,4,7,1 0-tetraacetic acid); NOTA (1,4,7-Triazacyclononane-1,4,7-triacetic acid); EDTA (Ethylenediaminetetraacetic acid); Df (Desferrioxamine); DTPA (Diethylenetriaminepentaacetic acid; and TETA (Triethylenetetramine).