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Cigarette smoke and HIV synergistically affect lung pathology in cynomolgus macaques
Hitendra S. Chand, … , Shilpa Buch, Mohan Sopori
Hitendra S. Chand, … , Shilpa Buch, Mohan Sopori
Published October 2, 2018
Citation Information: J Clin Invest. 2018;128(12):5428-5433. https://doi.org/10.1172/JCI121935.
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Concise Communication AIDS/HIV Pulmonology

Cigarette smoke and HIV synergistically affect lung pathology in cynomolgus macaques

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Abstract

In the era of combined antiretroviral therapy (cART), lung diseases such as chronic bronchitis (CB) and chronic obstructive pulmonary disease (COPD) are common among persons living with HIV (PLWH), particularly smokers. Although smoking is highly prevalent among PLWH, HIV may be an independent risk factor for lung diseases; however, the role of HIV and cigarette smoke (CS) and their potential interaction in the development of chronic lung diseases among PLWH has not been delineated. To investigate this interaction, cynomolgus macaques were exposed to CS and/or simian-adapted human immunodeficiency virus (SHIV) and treated with cART. The development of CB and the lung functions were evaluated following CS±SHIV treatment. The results showed that in the lung, SHIV was a strong independent risk factor for goblet cell metaplasia/hyperplasia and mucus formation, MUC5AC synthesis, loss of tight junction proteins, and increased expression of Th2 cytokines/transcription factors. In addition, SHIV and CS synergistically reduced lung function and increased extrathoracic tracheal ring thickness. Interestingly, SHIV infection generated significant numbers of HIV-gp120+ epithelial cells (HGECs) in small airways and alveoli, and their numbers doubled in CS+SHIV-infected lungs. We conclude that even with cART, SHIV independently induces CB and pro-COPD changes in the lung, and the effects are exacerbated by CS.

Authors

Hitendra S. Chand, Rodrigo Vazquez-Guillamet, Christopher Royer, Karin Rudolph, Neerad Mishra, Shashi P. Singh, Shah S. Hussain, Edward Barrett, Shannon Callen, Siddappa N. Byrareddy, Maria Cristina Vazquez Guillamet, Jawad Abukhalaf, Aryaz Sheybani, Vernat Exil, Veena Raizada, Hemant Agarwal, Madhavan Nair, Francois Villinger, Shilpa Buch, Mohan Sopori

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Figure 1

CS increases the number of gp120-immunopositive lung epithelial cells in SHIV-infected and cART-treated cynomolgus macaques.

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CS increases the number of gp120-immunopositive lung epithelial cells in...
Formalin-fixed and paraffin-embedded (FFPE) lung tissue sections (5 μm) from each group were immunostained for the epithelial cell marker pan-cytokeratin (pCK) and for HIV-gp120. (A) Representative micrographs of bronchial airway epithelial cells (AECs) showing pCK (green) and HIV-gp120 (red) immunopositivity along with the DAPI-stained nuclei (blue) from each group. Scale bars: 5 μm. Percentages of gp120+ AECs were quantified. (B) Micrographs of alveolar region showing pCK (green) and HIV-gp120 (red) immunopositivity from each group. The percentage of gp120+ alveolar epithelial cells were quantified. Scale bars: 10 μm. Data for A and B are mean ± SEM, n = 7/group; *P ≤ 0.05 by Student’s t test. (C) Viral titers in the plasma and in the plasma and bronchoalveolar lavage (BAL) of SHIV and CS+SHIV-exposed animals at weeks 2 and 16 postinfection, respectively. (D) Body weights of macaques at the baseline and at indicated times during the experiment. Data are mean ± SEM, n = 4–7/group.

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