T cell activation, apoptosis and cytokine dysregulation in the (co)pathogenesis of HIV and pulmonary tuberculosis (TB)

Author:

Hertoghe T12,Wajja A3,Ntambi L1,Okwera A3,Aziz M A4,Hirsch C5,Johnson J5,Toossi Z5,Mugerwa R3,Mugyenyi P6,Colebunders R7,Ellner J5,Vanham G1

Affiliation:

1. Institute of Tropical Medicine, Department of Microbiology, Antwerp and

2. Department of Physiology and Pathology, Free University of Brussels (VUB), Brussels, Belgium

3. Uganda–Case Western Reserve University (CWRU) Research Collaboration, Tuberculosis Project Clinic, Mulago Hospital and

4. National Tuberculosis and Leprosy Program, German Leprosy Relief Association, Ministry of Health, Kampala, Uganda

5. Tuberculosis Research Unit, Case Western Reserve University, Cleveland, OH, USA

6. Joint Clinical Research Center (JCRC), Kampala, Uganda

7. Institute of Tropical Medicine, Department of Clinical Sciences, Antwerp, Belgium

Abstract

SUMMARY Immune parameters were compared in four groups of Ugandan subjects: HIV−and HIV+ adult patients with active pulmonary TB (HIV− PTB n = 38; HIV+ PTB n = 28), patients with HIV infection only (n = 26) and PPD+ healthy controls (n = 25). Compared with healthy controls, CD4 and CD8 T cells from patients with HIV and/or PTB expressed more activation markers (HLA-DR, CD38); their CD8 T cells expressed more CD95 (pre-apoptosis) and less CD28 (co-stimulatory receptor). Peripheral blood mononuclear cells (PBMC) of patients with either HIV or PTB were impaired in interferon-gamma (IFN-γ) production upon antigenic stimulation. PTB (with or without HIV) was characterized by monocytosis, granulocytosis, increased transforming growth factor-beta 1 production and PPD-induced apoptosis. In vivo CD4 T cell depletion, in vitro increased spontaneous CD4 T cell apoptosis and defects in IFN-γ responses upon mitogenic stimulation were restricted to HIV+ subjects (with or without PTB). Overlapping and distinctive immune alterations, associated with PTB and HIV, might explain mutual unfavourable influences of both diseases.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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