IP Library Granted Patent US 10,041,945
Granted Patent B2
US 10,041,945 · App. 15/309,403 · Granted Aug 7, 2018

Methods of diagnosing and treating tuberculosis

Inventors: Jyothi Rengarajan (Decatur, GA); Toidi Adekambi (Atlanta, GA); Christian C. Ibegbu (Stockbridge, GA)
Assignee: Emory University
G01N33/56972A61K31/133A61K31/4409A61K31/496A61K31/4965A61K45/06G01N33/5091G01N2333/35G01N2333/47G01N2333/57G01N2333/70514G01N2333/70539G01N2333/70596G01N2800/26
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Quick Facts
Patent No.
US 10,041,945
App. No.
15/309,403
Granted
Aug 7, 2018
Kind
B2
Abstract

This disclosure relates to methods of treating and diagnosing a tuberculosis infection as pulmonary active or latent based on biomarkers expressed on pools of CD4 + cells. In certain embodiments, the disclosure relates to methods of treatment of a subject diagnosed with tuberculosis comprising the steps of, measuring a pool of CD4 IFN-γ cells for cells that also express CD38, HLA-DR, and/or Ki-67 providing a measurement; associating an increased measurement of CD4 IFN-γ cells that also express CD38, HLA-DR, Ki-67, compared to a control, as an indication that the subject has active tuberculosis; and treating the subject with an aggressive tuberculosis treatment.

Claims (18)

1. A method of diagnosing and treating a subject with tuberculosis comprising the steps of,

measuring a pool of CD4 IFN-γ cells for cells that also express CD38, HLA-DR, and Ki-67 providing a measurement;

associating an increased measurement of CD4 IFN-γ cells that also express CD38, HLA-DR, Ki-67, compared to a control, as an indication that the subject has active tuberculosis infection, providing a subject diagnosed with an active tuberculosis infection,

wherein the increased measurement of CD4 IFN-γ cells that also express CD38, HLA-DR, Ki-67, compared to a control is a quantification that,

greater than 18% of the CD4 IFN-γ cells also express CD38;

greater than 60% of the CD4 IFN-γ cells also express HLA-DR; and

greater than 5% of the CD4 IFN-γ cells also express Ki-67; and

administering to the subject diagnosed with an active tuberculosis infection an aggressive tuberculosis treatment.

2. The method of claim 1 , wherein the aggressive tuberculosis treatment comprises administering a combination of more than two antibacterial agents.

3. The method of claim 1 , wherein the aggressive tuberculosis treatment comprises administering a combination of isoniazid, rifampicin, pyrazinamide, and ethambutol.

4. The method of claim 1 , further comprising the steps of,

measuring a second pool of CD4 IFN-γ cells for the quantity of cells that also express CD38, HLA-DR, and Ki-67;

associating a deceased measurement of CD4 IFN-γ cells that also express CD38, HLA-DR, Ki-67, compared to the increased measurement, as an indication that the subject has a latent tuberculosis infection, providing a subject diagnosed with a latent tuberculosis infection; and

administering to the subject diagnosed with a latent tuberculosis infection a less aggressive tuberculosis treatment.

5. The method of claim 4 , wherein the less aggressive tuberculosis treatment is only one or not more than a combination of two antibacterial agents.

6. The method of claim 4 , wherein the less aggressive tuberculosis treatment is a combination of only isoniazid and rifampicin.

7. The method of claim 1 , wherein the measurement, quantification, or indication is recorded on a computer readable medium.

8. The method of claim 7 , wherein the measurement, quantification, or indication is communicated to a medical professional or the subject.

Assignments (1)
CONFIRMATORY LICENSE Recorded Dec 14, 2016
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040732/0283 →
Continuity (2)
Provisional Application 61988406 · May 5, 2014
Related Publication 20170082623A1 · Mar 23, 2017