CXCR4-Using HIV Type 1 Variants Are More Commonly Found in Peripheral Blood Mononuclear Cell DNA Than in Plasma RNA

被引:46
作者
Verhofstede, Chris [1 ]
Vandekerckhove, Linos [2 ]
Van Eygen, Veerle [3 ]
Demecheleer, Els [1 ]
Vandenbroucke, Ina [3 ]
Winters, Bart [3 ]
Plum, Jean [1 ]
Vogelaers, Dirk [2 ]
Stuyver, Lieven [3 ]
机构
[1] Univ Ghent, Aids Reference Lab, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Aids Reference Ctr, B-9000 Ghent, Belgium
[3] Virco, Mechelen, Belgium
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; CORECEPTOR USAGE; REPLICATIVE CAPACITY; BIOINFORMATIC TOOLS; DISEASE PROGRESSION; VIRAL ENTRY; V3; REGION; PHENOTYPE; ZIDOVUDINE; POPULATION;
D O I
10.1097/QAI.0b013e31819118fa
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To compare the distribution of R5-like and X4-like HIV-1 envelope sequences in plasma and peripheral blood mononuclear cell (PBMC). Methods: Clonal sequencing of the HIV-1 glycoprotein 120 region was performed on PBMC DNA and plasma RNA of 11 HIV-1 subtype B-infected patients with high probability of carrying X4 virus. Coreceptor use was predicted using the position-specific scoring matrix (PSSM). Results: A total of 330 and 427 clonal envelope sequences were obtained from PBMC and plasma, respectively. PSSM interpretation revealed the presence of a mixture of predicted X4 and R5 sequences in 10 patients and pure R5 sequences in 1. The X4 sequences were significantly more represented in PBMC (with an average of 52.2% of the clonal proviral sequences scored X4) compared with plasma (19.7% X4 sequences) (P < 0.0001). At the single patient level, the higher representation of X4 sequences in PBMC reached statistical significance (P < 0.002) in 6 individuals. Conclusions: Mixtures of X4 and R5 sequences with highly divergent PSSM scores are present in both plasma and PBMC, but a shift toward a more abundant representation of X4-like PSSM scores in PBMC-derived DNA was apparent. Additional studies are needed to evaluate the clinical importance of these findings with regard to tropism prediction and the use of CCR5 anatagonists.
引用
收藏
页码:126 / 136
页数:11
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