Author:
Nakiboneka Ritah,Margaritella Nicolò,Nyirenda Tonney,Chaima David,Walbaum Natasha,Musisi Emmanuel,Tionge Sikwese,Msosa Takondwa,Nliwasa Marriott,Msefula Chisomo L.,Sloan Derek,Sabiiti Wilber
Abstract
AbstractThe World Health Organization End TB strategy aims for a 90% reduction of tuberculosis (TB) incidence by 2035. Systematic testing and treatment of latent TB infection (LTBI) among contacts of active TB patients is recommended as one of the ways to curtail TB incidence. However, there is a shortage of tools to accurately diagnose LTBI. We assessed the appropriateness of whole blood host transcriptomic markers (TM) to diagnose LTBI among household contacts of bacteriologically confirmed index cases compared to HIV negative healthy controls (HC). QuantiFERON-TB Gold Plus Interferon gamma release assay (IGRA) and reverse-transcriptase quantitative PCR were used to determine LTBI and quantify TM expression respectively. Association between TM expression and LTBI was evaluated by logistic regression modelling. A total of 100 participants, 49 TB exposed (TBEx) household contacts and 51 HC, were enrolled. Twenty-five (51%) TBEx individuals tested positive by IGRA, and were denoted as LTBI individuals, and 37 (72.5%) HC were IGRA-negative. Expression of 11 evaluated TM was significantly suppressed among LTBI compared to HC. Out of the 11 TM, ZNF296 and KLF2 expression were strongly associated with LTBI and successfully differentiated LTBI from HC. Paradoxically, 21 (49%) TBEx participants who tested IGRA negative exhibited the same pattern of suppressed TM expression as IGRA positive (LTBI-confirmed individuals). Results suggest that suppression of gene expression underlies LTBI and may be a more sensitive diagnostic biomarker than standard-of-care IGRA.
Funder
Wellcome Trust Institutional Strategic Support fund of the University of St Andrews
Helse Nord Tuberculosis Initiative (HNTI), Pathology Department, Kamuzu University of Health Sciences
Africa Centre for Public Health and Herbal Medicines (ACEPHEM), Kamuzu University of Health Sciences
School of Medicine, University of St Andrews, UK
Uganda Virus Research Institute, Entebbe, Uganda
School of Mathematics and Statistics, University of St Andrews, UK
Department of Pathology, Kamuzu University of Health Sciences
Adroit Biomedical and Bioentrepreneurship Research Service
Publisher
Springer Science and Business Media LLC
Reference43 articles.
1. Mack, U. et al. LTBI Latent tuberculosis infection or lasting immune responses to M. tuberculosis? A TBNET consensus statement. Eur. Respir. J. 33, 956–973 (2009).
2. Comstock, G. W., Livesay, V. T. & Woolpert, S. F. The prognosis of a positive tuberculin reaction in childhood and adolescence. Am. J. Epidemiol. 99, 131–138 (1974).
3. Li, M. et al. Global, regional, and national prevalence of diabetes mellitus in patients with pulmonary tuberculosis: A systematic review and meta-analysis. Diabetol. Metab. Syndr. 13, 1–8 (2021).
4. Louie, L. G. et al. Mycobacterium tuberculosis/HIV-1 coinfection and disease: Role of human leukocyte antigen variation. J. Infect. Dis. 189, 1084–1090 (2004).
5. Batten, J. C. & Mccune, R. M. The influence of corticotrophin and cortisone with antituberculous drugs on population of Mycobacterium tuberculosis in tissues of mice. Br. J. Exp. Pathol. 38, 424–437 (1957).