APOBEC3G/3A Expression in Human Immunodeficiency Virus Type 1-Infected Individuals Following Initiation of Antiretroviral Therapy Containing Cenicriviroc or Efavirenz

被引:9
作者
Covino, Daniela A. [1 ]
Purificato, Cristina [1 ]
Catapano, Laura [1 ]
Galluzzo, Clementina M. [1 ]
Gauzzi, Maria Cristina [1 ]
Vella, Stefano [1 ]
Lefebvre, Eric [2 ]
Seyedkazemi, Star [2 ]
Andreotti, Mauro [1 ]
Fantuzzi, Laura [1 ]
机构
[1] Ist Super Sanita, Natl Ctr Global Hlth, Rome, Italy
[2] Allergan Plc, San Francisco, CA USA
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
关键词
APOBEC3A; APOBEC3G; antiretroviral therapy; cenicriviroc; chronic inflammation; disease progression; MESSENGER-RNA LEVELS; IMMUNE ACTIVATION; HIV-1; INFECTION; MACROPHAGES; HYPERMUTATION; RESTRICTION; PATHOGENESIS; REPLICATION; LYMPHOCYTES; MONOCYTES;
D O I
10.3389/fimmu.2018.01839
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Apolipoprotein B mRNA editing enzyme catalytic polypeptide-like 3 (APOBEC3) family members are cytidine deaminases that play crucial roles in innate responses to retrovirus infection. The mechanisms by which some of these enzymes restrict human immunodeficiency virus type 1 (HIV-1) replication have been extensively investigated in vitro. However, little is known regarding how APOBEC3 proteins affect the pathogenesis of HIV-1 infection in vivo and how antiretroviral therapy influences their expression. In this work, a longitudinal analysis was performed to evaluate APOBEC3G/3A expression in peripheral blood mononuclear cells of antiretroviral-naive HIV-1-infected individuals treated with cenicriviroc (CVC) or efavirenz (EFV) at baseline and 4, 12, 24, and 48 weeks post-treatment follow-up. While APOBEC3G expression was unaffected by therapy, APOBEC3A levels increased in CVC but not EFV arm at week 48 of treatment. APOBEC3G expression correlated directly with CD4(+) cell count and CD4(+)/CD8(+) cell ratio, whereas APOBEC3A levels inversely correlated with plasma soluble CD14. These findings suggest that higher APOBEC3G/3A levels may be associated with protective effects against HIV-1 disease progression and chronic inflammation and warrant further studies.
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页数:8
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