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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
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: T...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Makerere Medical School
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870287/ https://www.ncbi.nlm.nih.gov/pubmed/29937865 http://dx.doi.org/10.4314/ahs.v17i4.2 |
Sumario: | 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. |
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