Abstract

BackgroundWhile the risk of TB is elevated in HIV-positive subjects with low CD4 cell counts, TB may in itself be associated with CD4 lymphocytopenia. We investigated markers of immune activation (neopterin) and inflammation (CRP) in TB patients with and without HIV coinfection and their association with CD4 cell levels, and determined their predictive capacity as alternative markers of advanced immunosuppression.MethodsParticipants selected from a cohort of adults with TB at Ethiopian health centers (195 HIV+/TB+, 170 HIV-/TB+) and 31 controls were tested for plasma levels of neopterin and CRP. Baseline levels of neopterin and CRP were correlated to CD4 cell count before and after anti-TB treatment (ATT). The performance to predict CD4 cell strata for both markers were investigated using receiver operating curves.ResultsLevels of both biomarkers were elevated in TB patients (neopterin: HIV+/TB+ 54 nmol/l, HIV-/TB+ 23 nmol/l, controls 3.8 nmol/l; CRP: HIV+/TB+ 36 μg/ml, HIV-/TB+ 33 μg/ml, controls 0.5 μg/ml). Neopterin levels were inversely correlated (-0.53, p<0.001) to CD4 cell count, whereas this correlation was weaker for CRP (-0.25, p<0.001). Neither of the markers had adequate predictive value for identification of subjects with CD4 cell count <100 cells/mm3 (area under the curve [AUC] 0.64 for neopterin, AUC 0.59 for CRP).ConclusionNeopterin levels were high in adults with TB, both with and without HIV coinfection, with inverse correlation to CD4 cell count. This suggests that immune activation may be involved in TB-related CD4 lymphocytopenia. However, neither neopterin nor CRP showed promise as alternative tests for immunosuppression in patients coinfected with HIV and TB.

Highlights

  • TB is the most common opportunistic infection (OI) and cause of death in people living with HIV (PLHIV) globally, with the highest case burden in sub-Saharan Africa [1]

  • Neopterin levels were inversely correlated (-0.53, p

  • Neopterin levels were high in adults with TB, both with and without HIV coinfection, with inverse correlation to CD4 cell count

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Summary

Introduction

TB is the most common opportunistic infection (OI) and cause of death in people living with HIV (PLHIV) globally, with the highest case burden in sub-Saharan Africa [1]. CD4 cell depletion is characteristic of HIV disease, subnormal CD4 cell levels can occur in other conditions [3], which may coexist in PLHIV. This includes active TB [4,5,6]; the mechanisms involved in TB-related CD4 lymphocytopenia are unclear. In HIV infection, the main cause of CD4 cell depletion and disease progression is chronic immune activation [7,8]. While the risk of TB is elevated in HIV-positive subjects with low CD4 cell counts, TB may in itself be associated with CD4 lymphocytopenia. We investigated markers of immune activation (neopterin) and inflammation (CRP) in TB patients with and without HIV coinfection and their association with CD4 cell levels, and determined their predictive capacity as alternative markers of advanced immunosuppression

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