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DOI 10.4314/ahs.v17i4.2

Медицинская библиотека · African health sciences · 2017

The effect of interrupted anti-retroviral treatment on the reconstitution of memory and naive T cells during tuberculosis treatment in HIV patients with active pulmonary tuberculosis.

Nalukwago Sophie, Lancioni Christina L, Oketcho Joy Baseke, Canaday Dave H E, Boom W Henry, Ojok Lonzy, Mayanja-Kizza Harriet

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Аннотация

BACKGROUND

The reconstitution of cellular immune components contributes to clinical outcome of HIV and Mycobacterium tuberculosis (MTB) infection. Interruption of anti-retroviral therapy (ART) could lead to perturbations in reconstitution of T cells in HIV/ tuberculosis (TB) patients.

OBJECTIVES

To ascertain the effect of interrupted ART on reconstitution of CD4+ and CD8+ T sub-sets in TB patients.

METHODS

Participants with HIV (CD4>350 cells/µL) and TB were recruited under a larger phase 3 open label randomised controlled clinical trial. The CD45RO and CD62L markers were measured on CD4+ and CD8+ cells by flow cytometry. Samples were analysed at baseline, 3, 6, 12 months.

RESULTS

There was a significant increase of naive CD8+ cells (p = 0.003) and a decrease in effector CD8+ cells (p = 0.004) among participants in ART/TB treatment arm during the first 6 months. Withdrawing ART led to naive CD8+ cells reduction (p=0.02) to values close to baseline. An increase of naive CD8+ cells after 6 months of TB treatment in TB alone treatment arm (p=0.01) was observed. A trend towards increment of naive CD4+ sub sets in either treatment arms was observed.

CONCLUSION

Interrupting ART alters CD8+ but not CD4+ sub-sets in patients with less advanced HIV infection and TB.

Для цитирования: Nalukwago Sophie, Lancioni Christina L, Oketcho Joy Baseke, Canaday Dave H E, Boom W Henry, Ojok Lonzy, Mayanja-Kizza Harriet. The effect of interrupted anti-retroviral treatment on the reconstitution of memory and naive T cells during tuberculosis treatment in HIV patients with active pulmonary tuberculosis.. African health sciences. 2017. DOI: 10.4314/ahs.v17i4.2.

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