Open AccessLack of elevated pre-ART elastase-ANCA levels in patients developing TB-IRIS
Author(s) -
Odin Goovaerts,
Marguerite Massinga-Loembé,
Pascale Ondoa,
Ann Ceulemans,
William Worodria,
Harriet MayanjaKizza,
Robert Colebunders,
Luc Kestens
Publication year - 2020
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0244800
Subject(s) - medicine , immune reconstitution inflammatory syndrome , elastase , proteinase 3 , lactoferrin , immunology , tuberculosis , neutrophil elastase , antibody , myeloperoxidase , gastroenterology , human immunodeficiency virus (hiv) , autoantibody , antiretroviral therapy , viral load , inflammation , pathology , enzyme , biology , biochemistry , genetics
Background Tuberculosis-associated immune reconstitution inflammatory syndrome (TB-IRIS) in HIV-TB co-infected patients receiving antiretroviral therapy (ART) has been linked to neutrophil activation. Anti-neutrophil cytoplasmic antibodies (ANCAs) are also associated with neutrophil activation. Since ANCAs are reportedly skewed in TB and HIV infections, we investigated plasma levels of 7 ANCAs in TB-IRIS patients. Methods We retrospectively compared 17 HIV-TB patients who developed TB-IRIS with controls of similar CD4 count, age and gender who did not (HIV + TB + n = 17), HIV-infected patients without TB (HIV + TB - , n = 17) and 10 HIV-negative (HIV - TB - ) controls. Frozen plasma was collected before ART, at 3 and 9 months of ART, and examined by ELISA for levels of 7 ANCAs directed against; Proteinase 3 (PR3), Myeloperoxidase (MPO), Permeability-increasing protein (BPI), Elastase, Cathepsin, Lysozyme, and Lactoferrin. Results Compared to HIV + TB + controls, pre-ART anti-elastase levels were lower in TB-IRIS patients (p = 0.026) and HIV - TB - controls (p = 0.044), whereas other ANCAs did not show significant differences between groups at any time point. A significant decrease over time could be observed in TB-IRIS patients during ART for anti -PR3 (p = 0.027), -lysozyme (p = 0.011), and -lactoferrin (p = 0.019). Conversely, HIV + TB + controls showed a significant decrease over time for anti -MPO (p = 0.002), -lyzosyme (p = 0.002) and -elastase (p < 0.001). Conclusion The lack of elevated anti-elastase levels in TB-IRIS patients as opposed to HIV + TB + controls correspond to previous findings of lowered immune capacity in patients that will develop TB-IRIS. This may suggest a specific role for anti-elastase, elastase or even matrix-metalloproteinases in TB-IRIS. The precise dynamics of neutrophil activation in HIV-TB merits further investigation and could provide more insight in the early mechanisms leading up to TB-IRIS.