Changes in leucocyte and lymphocyte subsets during tuberculosis treatment; prominence of CD3dimCD56+ natural killer T cells in fast treatment responders

Author:

Veenstra H1,Baumann R1,Carroll N M1,Lukey P T2,Kidd M3,Beyers N4,Bolliger C T5,Van Helden P D1,Walzl G1

Affiliation:

1. Division of Molecular Biology and Genetics and MRC Centre for Molecular and Cellular Biology, University of Stellenbosch, South Africa

2. GlaxoSmithKline R&D, Stevenage, UK

3. Centre for Statistical Consultation, University of Stellenbosch, South Africa

4. Desmond Tutu TB Centre, Department of Paediatrics and Child Health, University of Stellenbosch, South Africa

5. Lung Unit, Internal Medicine, University of Stellenbosch, South Africa

Abstract

Summary The immune responses against pulmonary tuberculosis are still poorly defined. This study describes changes in leucocyte and lymphocyte subsets during treatment to find reliable immunological markers for the disease and treatment response. Flow cytometric peripheral blood immune phenotyping, routine haematology and sputum microbiology were performed on 21 HIV-negative adult tuberculosis (TB) patients with positive sputum cultures during therapy in comparison with 14 healthy purified protein derivative (PPD)-positive volunteers. Patients at diagnosis showed high absolute neutrophil and monocyte counts which fell during treatment but low lymphocyte subset counts which increased [except natural killer (NK) and NK T cells]. High counts of a population of CD3dim/CD56+ NK T cells at diagnosis correlated significantly with negative sputum culture after 8 weeks of treatment. A multivariate classification technique showed improved correlation when NK cells were taken into account. In conclusion, peripheral blood white cell counts change significantly during treatment and counts at diagnosis, especially CD3dim/CD56+ NK T cells, hold promise in predictive models of TB treatment response.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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