TY - JOUR
T1 - Short-term Treatment With Interferon Alfa Diminishes Expression of HIV-1 and Reduces CD4 + T-Cell Activation in Patients Coinfected With HIV and Hepatitis C Virus and Receiving Antiretroviral Therapy
AU - Morón-López, Sara
AU - Gómez-Mora, Elisabet
AU - Salgado, Maria
AU - Ouchi, Dan
AU - Puertas, Maria C.
AU - Urrea, Víctor
AU - Navarro, Jordi
AU - Jou, Antoni
AU - Pérez, Mercedes
AU - Tural, Cristina
AU - Clotet, Bonaventura
AU - Montaner, Luis J.
AU - Blanco, Julià
AU - Crespo, Manuel
AU - Martinez-Picado, Javier
PY - 2016/3/15
Y1 - 2016/3/15
N2 - © 2015 The Author. All rights reserved. Long-term treatment with interferon (IFN) alfa plus ribavirin decreases the proviral human immunodeficiency virus type 1 (HIV) DNA level. However, the short-term impact of IFN alfa on persistent HIV and its effects on immune activation after antiretroviral therapy remain unknown. Our study showed that the cell-associated HIV RNA level and CD4 + T-cell activation decreased in the IFN group (n = 10). No changes were detected in levels of residual plasma viremia, replication-competent reservoirs, proviral DNA, or 2-long-terminal repeat circles, although APOBEC3G, TRIM5α, BST2, and TRIM22 were upregulated in the IFN group. These data suggest that short-term treatment with IFN alfa combined with RBV decreases HIV expression, in part through inhibition of HIV transcription by TRIM22 and decrease in T-cell activation.
AB - © 2015 The Author. All rights reserved. Long-term treatment with interferon (IFN) alfa plus ribavirin decreases the proviral human immunodeficiency virus type 1 (HIV) DNA level. However, the short-term impact of IFN alfa on persistent HIV and its effects on immune activation after antiretroviral therapy remain unknown. Our study showed that the cell-associated HIV RNA level and CD4 + T-cell activation decreased in the IFN group (n = 10). No changes were detected in levels of residual plasma viremia, replication-competent reservoirs, proviral DNA, or 2-long-terminal repeat circles, although APOBEC3G, TRIM5α, BST2, and TRIM22 were upregulated in the IFN group. These data suggest that short-term treatment with IFN alfa combined with RBV decreases HIV expression, in part through inhibition of HIV transcription by TRIM22 and decrease in T-cell activation.
KW - CD4 T-cell subpopulations +
KW - HIV persistence
KW - HIV RNA expression
KW - HIV/HCV coinfection
KW - IFN alfa
KW - immune activation
KW - Siglec-1
KW - TRIM22
U2 - 10.1093/infdis/jiv521
DO - 10.1093/infdis/jiv521
M3 - Article
SN - 0022-1899
VL - 213
SP - 1008
EP - 1012
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 6
ER -