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Mycobacterium tuberculosis antigen-specific T-cell responses in smear-negative pulmonary tuberculosis patients.
Esmael, Ahmed; Abebe, Tamrat; Mihret, Adane; Mussa, Daniel; Neway, Sebsib; Ernst, Joel; Rengarajan, Jyothi; Wassie, Liya; Howe, Rawleigh.
Affiliation
  • Esmael A; Department of Medical Laboratory Science, College of Health Sciences, Debre Markos University, Debre Markos, Amhara Regional State, Ethiopia.
  • Abebe T; Department of Microbiology, Immunology and Parasitology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
  • Mihret A; Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
  • Mussa D; Department of Microbiology, Immunology and Parasitology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
  • Neway S; Department of Microbiology, Immunology and Parasitology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
  • Ernst J; Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
  • Rengarajan J; Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
  • Wassie L; Armauer Hansen Research Institute, Addis Ababa, Ethiopia.
  • Howe R; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, USA.
Clin Exp Immunol ; 209(1): 99-108, 2022 07 22.
Article in En | MEDLINE | ID: mdl-35552657
ABSTRACT
Despite recent improvements in microbial detection, smear-negative TB remains a diagnostic challenge. In this study, we investigated the potential discriminatory role of polychromatic flow cytometry of M. tuberculosis antigen-specific T cells to discriminate smear-negative TB from health controls with or without latent TB infection, and non-TB respiratory illnesses in an endemic setting. A cross-sectional study was conducted on HIV negative, newly diagnosed smear-positive PTB (n = 34), smear-negative/GeneXpert negative PTB (n = 29) patients, non-TB patients with respiratory illness (n = 33) and apparently healthy latent TB infected (n = 30) or non-infected (n = 23) individuals. The expression of activation (HLA-DR, CD-38), proliferation (Ki-67), and functional (IFN-γ, TNF-α) T-cell markers using polychromatic flow cytometry was defined after stimulation with PPD antigens. Sputum samples were collected and processed from all patients for Mtb detection using a concentrated microscopy, LJ/MGIT culture, and RD9 typing by PCR. Our study showed CD4 T cells specific for PPD co-expressed activation/proliferation markers together with induced cytokines IFN-γ or TNF-α were present at substantially higher levels among patients with smear-positive and smear-negative pulmonary TB than among healthy controls and to a lesser extent among patients with non-TB illness. Our study conclude that smear-negative TB can be distinguished from non-TB respiratory illness and healthy controls with a flow cytometric assay for PPD-specific T cells co-expressing activation/proliferation markers and cytokines.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis, Pulmonary / Latent Tuberculosis / Mycobacterium tuberculosis Type of study: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Humans Language: En Journal: Clin Exp Immunol Year: 2022 Type: Article Affiliation country: Ethiopia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tuberculosis, Pulmonary / Latent Tuberculosis / Mycobacterium tuberculosis Type of study: Diagnostic_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Humans Language: En Journal: Clin Exp Immunol Year: 2022 Type: Article Affiliation country: Ethiopia