Tuberculosis (TB), caused by the intracellular bacteria Mycobacterium tuberculosis (Mtb), is the second-leading cause of death worldwide from infection. Following inhalation, Mtb are phagocytosed by macrophages at the epithelial barrier of the lung, eliciting an inflammatory response and recruitment of other immune cells from the blood. While in the circulation, infected phagocytes can disseminate throughout the body, leading to infection at extrapulmonary (EP) sites. In South Africa, which has the highest incidence of TB in the world of 981/100,000 population, 15.5 percent of all new TB cases in 2010 were EPTB. One of the most debilitating forms of EPTB is spinal TB (Pott's Disease). The tissue composition and microenvironment of the skeletal system varies greatly from that of the lung. In the spine, Mtb infection is contained in the form of a "cold" epidural abscess, associated with bone and cartilage destruction, which may cause collapse of the spinal column, deformity and neurological complications. There is limited understanding of EPTB disease pathogenesis, which hinders control of the epidemic. I will determine the specific mechanisms by which Mtb infection of the spine drives excessive inflammation and inappropriate bone and cartilage homeostasis.
Specific Aim 1 will define the pathways and molecular networks that underlie Mtb-induced bone and cartilage destruction by utilizing microarray, histological and mass spectrometry analysis.
Specific Aim 2 will test the hypothesis that a combinatorial signature of markers of bone/cartilage turnover and Mtb-driven immunity will be detectable in the circulation of patients with Pott's disease. TB is a major opportunistic infection in HIV and HIV is known to affect bone health.
In Specific Aim 3, I will therefore investigate the impact of HIV co-infection n 1) the mechanisms causing tissue-specific pathology in Spinal TB and 2) the expression of candidate biomarkers, in the circulation. All studies will be conducted on excised, granulomatous tissue and bloods from adult patients from Durban, South Africa whose course of treatment for spinal TB necessitates surgery. This study will address an outstanding question in TB research, namely a molecular definition of the immunopathogenesis of Spinal TB. Ultimately, the results of this project can contribute towards improved diagnostic tools, monitoring strategies and therapeutic approaches in TB patients.

Public Health Relevance

Tuberculosis (TB) is responsible for over 1.5 million deaths annually and is the most common cause of death for people with HIV in sub-Saharan Africa. HIV co-infection is one reason for more complex manifestations of the disease, such as extrapulmonary TB (EPTB), but there is a striking lack of understanding on how the immune system combats extrapulmonary infection. The results from the proposed project will address this outstanding question, contributing to the improved diagnosis and management of patients with EPTB.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32AI102566-01A1
Application #
8526886
Study Section
Special Emphasis Panel (ZRG1-F13-C (20))
Program Officer
Jacobs, Gail G
Project Start
2013-03-15
Project End
2013-06-30
Budget Start
2013-03-15
Budget End
2013-06-30
Support Year
1
Fiscal Year
2013
Total Cost
$12,751
Indirect Cost
Name
University of Medicine & Dentistry of NJ
Department
None
Type
Schools of Medicine
DUNS #
623946217
City
Newark
State
NJ
Country
United States
Zip Code
07107