# Clinical Core

> **NIH NIH U19** · WEILL MEDICAL COLL OF CORNELL UNIV · 2024 · $490,792

## Abstract

Abstract: The goal of the Clinical Core is to recruit and characterize patient cohorts in Haiti, and to collect and
ship clinical samples for studies of tuberculosis (TB) persistence in Projects 1- 3. Core activities will be performed
by the Groupe Haitien d'Etude du Sarcome de Kaposi et des Infections Opportunistes (GHESKIO) in Port au
Prince, Haiti. GHESKIO is a Haitian non-profit organization which was founded in 1982 and is dedicated to
research, service, and training in HIV and tuberculosis. It has conducted NIH supported clinical research for 38
years and has all the essential core components for the conduct of the proposed TBRU studies, including:
experienced research staff, out-patient clinics, access to large TB patient populations, a BSL-3 TB laboratory, a
data management center, and an institutional review board. In 2019, GHESKIO diagnosed and treated 1,456
patients with culture confirmed TB including 225 re-treatment patients with a second episode of TB, 15 families
with multiple siblings with TB, and 321 HIV-negative patients with pulmonary cavity disease and high sputum
bacillary load who are at high risk of recurrence after completion of TB treatment. A major focus of this Tri-I
TBRU is on post-treatment persistent infection (PTPI) and TB recurrence. Given that more than 1 million of the
world’s 10 million cases of TB diagnosed in 2018 were recurrent TB cases, understanding genetic, immunologic
and pharmacokinetic correlates for TB persistence and recurrence is critical.
The Specific Objectives of the Tri-I TBRU Clinical Core are:
1) Conduct a cross-sectional study of 250 HIV-negative patients with recurrent TB, 250 HIV-negative
 controls with a single episode of TB, and 50 families with active TB in multiple siblings. Controls with
 a single episode of TB and post-treatment follow-up will be matched to recurrent cases by age, sex, and time
 since completion of first TB regimen. There will be a single study visit. Clinical samples including whole
 blood for host DNA and RNA, serum, PBMCs, urine, and stool will be shipped to New York.
2) Conduct a longitudinal cohort study of 500 HIV-negative drug-sensitive TB patients with pulmonary
 cavities on chest radiograph, high sputum bacillary load and high risk for recurrent TB. Participants
 will be enrolled at initiation of anti-tuberculosis therapy (2HRZE/4HR) and followed for 24 months after
 completion of therapy (30 months total). We estimate that 40 - 50 participants will develop recurrent TB (4-
 5 recurrences/100 patient years). M. tuberculosis isolates will be genotyped to determine if recurrence is
 from relapse of prior infection (estimated 85% of cases) or reinfection with new strain (15%). We will quantify
 M. tuberculosis in sputum at weeks 1, 2, 3, 4, 8 and 24 weeks during therapy using BACTEC time-to-
 positivity. We will collect samples including blood, PBMCs, urine, and stool at enrollment, week 2, 4, 8, at the
 completion of therapy and 3 and 6 months after therapy for ...

## Key facts

- **NIH application ID:** 10830987
- **Project number:** 5U19AI162568-04
- **Recipient organization:** WEILL MEDICAL COLL OF CORNELL UNIV
- **Principal Investigator:** Daniel W Fitzgerald
- **Activity code:** U19 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $490,792
- **Award type:** 5
- **Project period:** 2021-07-01 → 2026-04-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10830987

## Citation

> US National Institutes of Health, RePORTER application 10830987, Clinical Core (5U19AI162568-04). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10830987. Licensed CC0.

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