4.5 Article

Cascade Immune Mechanisms of Protection against Mycobacterium tuberculosis (IMPAc-TB): study protocol for the Household Contact Study in the Western Cape, South Africa

期刊

BMC INFECTIOUS DISEASES
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12879-022-07349-8

关键词

Tuberculosis; Immune response; Bronchoalveolar lavage; PET-CT imaging; Household contacts; SARS-CoV-2; Interferon-gamma release assay

资金

  1. National Institute of Allergy and Infectious Diseases (NIAID)
  2. NIH [75N93019C0070]
  3. South African Tuberculosis Bioinformatics Initiative
  4. Strategic Health Innovation Partnership grant from the South African Medical Research Council (SAMRC)
  5. South African Department of Science and Innovation (SA-DSI)
  6. European Union [TMA2016CDF1576]
  7. South African National Research Foundation
  8. SARChI TB Biomarkers [86535]
  9. Faculty of Medicine and Health Sciences (FMHS)
  10. Stellenbosch University (SU), South Africa - Bill and Melinda Gates Foundation (BMGF)
  11. SAMRC
  12. EDCTP
  13. SANRF

向作者/读者索取更多资源

This study aims to analyze the protective pathways of natural and vaccine-induced immunity against Mycobacterium tuberculosis by collecting data and samples from participants, including lung imaging and laboratory tests.
Background Natural immunity against Mycobacterium tuberculosis exists, and > 90% of those infected remain disease-free. Innate and adaptive immune responses required to mediate such protection against tuberculosis (TB) are, however, poorly understood. Methods This is an analytical study exploring protective and non-protective pathways of immunity against Mycobacterium tuberculosis. Adults without HIV infection are recruited at community healthcare clinics in high TB incidence areas of the Western Cape Province, South Africa. Data regarding participants' medical, social and medication usage will be collected, and clinical examinations and point-of-care tests documented. Reference tests for TB (chest radiographs and sputum tests for GeneXpert MTB/RIF Ultra (R), Auramine smear and liquid cultures) and investigations to classify infection states [interferon-gamma release assay (IGRA) and SARS-CoV-2 polymerase chain reaction (PCR) nasopharyngeal swab and IgG], are done on all participants who meet the inclusion criteria. 18F-Fluorodeoxyglucose positron emission tomography combined with computerized tomography will be done on all close contacts (contacts) and healthy control (controls) participants. Participants are divided into 12 study groups representing a spectrum of TB clinical phenotypes and prior SARS-CoV-2 infection based on their TB status, exposure history, results of IGRA test at baseline and 3 months, SARS-CoV-2 serology, and PCR results, and for contacts and controls, PET-CT imaging findings indicative of sub-clinical TB lesions. Samples for experimental assays include whole blood for isolation of peripheral blood mononuclear cells and blood in PAXgene (R) tubes for RNA isolation. All SARS-CoV-2 PCR negative study participants undergo bronchoscopy for collecting bronchoalveolar lavage samples. Discussion The paired blood and BAL samples will be used for comprehensive analyses of the tissue-specific and systemic immunity that will include e.g., cytometry by time-of-flight analyses, RNA-sequencing, multiplex immunoassays, epigenetic analysis, and mechanistic studies of control of infection by Mycobacterium tuberculosis. Results will be integrated with those from mice and non-human primate studies to provide a comprehensive analysis of protective pathways in natural and vaccine-induced immunity against Mycobacterium tuberculosis.

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