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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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