HIV-1 transcription inhibitor 1E7-03 restores LPS-induced alteration of lung leukocytes’ infiltration dynamics and resolves inflammation in HIV transgenic mice
Document Type
Article
Publication Date
1-1-2020
Abstract
Human immunodeficiency virus (HIV)-infected individuals treated with anti-retroviral therapy often develop chronic non-infectious lung disease. To determine the mechanism of HIV-1-associated lung disease we evaluated the dynamics of lung leukocytes in HIV-1 transgenic (Tg) mice with integrated HIV-1 provirus. In HIV-Tg mice, lipopolysacharide (LPS) induced significantly higher levels of neutrophil infiltration in the lungs compared to wild-type (WT) mice. In WT mice, the initial neutrophil infiltration was followed by macrophage infiltration and fast resolution of leukocytes infiltration. In HIV-Tg mice, resolution of lung infiltration by both neutrophils and macrophages was significantly delayed, with macrophages accumulating in the lumen of lung capillaries resulting in a 45% higher rate of mortality. Trans-endothelial migration of HIV-Tg macrophages was significantly reduced in vitro and this reduction correlated with lower HIV-1 gene expression. HIV-1 transcription inhibitor, 1E7-03, enhanced trans-endothelial migration of HIV-Tg macrophages in vitro, decreased lung neutrophil infiltration in vivo, and increased lung macrophage levels in HIV-Tg mice. Moreover, 1E7-03 reduced levels of inflammatory IL-6 cytokine, improved bleeding score and decreased lung injury. Together this indicates that inhibitors of HIV-1 transcription can correct abnormal dynamics of leukocyte infiltration in HIV-Tg, pointing to the utility of transcription inhibition in the treatment of HIV-1 associated chronic lung disease.
Recommended Citation
Jerebtsova, Marina; Ahmad, Asrar; Niu, Xiaomei; Rutagarama, Ornela; and Nekhai, Sergei, "HIV-1 transcription inhibitor 1E7-03 restores LPS-induced alteration of lung leukocytes’ infiltration dynamics and resolves inflammation in HIV transgenic mice" (2020). The Center For Sickle Cell Disease Faculty Publications. 16.
https://dh.howard.edu/sicklecell_fac/16