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Genetic variation in CCR2 and CXCL12 genes impacts on CD4 restoration in patients initiating cART with advanced immunesupression.

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2019-03-28

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Restrepo, Clara
Gutierrez-Rivas, Mónica
Pacheco, Yolanda M
García, Marcial
Blanco, Julià
Medrano, Luz M
Navarrete-Muñoz, María A
Gutiérrez, Félix
Miralles, Pilar
Dalmau, David

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We investigated the association of genetic polymorphisms in chemokine and chemokine receptor genes with poor immunological recovery in HIV patients starting combined antiretroviral therapy (cART) with low CD4 T-cell counts. A case-control study was conducted in 412 HIV-infected patients starting cART with CD4 T-cell count Thirty two percent (134/412) of patients were classified as INR. After adjusting by age, route of HIV infection, length of infection before cART and viral hepatitis coinfection, CCR2 rs1799864-AG genotype was significantly associated with INR status (OR [95% CI]: 1.80 [1.04-3.11]; p = 0.04), and CXCL12 rs1801157-TT genotype showed a trend (OR [95% CI]: 2.47 [0.96-6.35]; p = 0.06). CCR2 rs1799864-AG or CXCL12 rs1801157-TT genotypes influence on the probability of poor CD4 recovery in the population of HIV patients starting cART with low CD4 counts. Genotyping of these polymorphisms could be used to estimate the risk of poor CD4 restoration, mainly in patients who are diagnosed late in the course of infection.

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Adult
Antiretroviral Therapy, Highly Active
CD4 Lymphocyte Count
Chemokine CXCL12
Female
HIV Infections
Humans
Immune Tolerance
Male
Middle Aged
Polymorphism, Genetic
Receptors, CCR2
Retrospective Studies
Treatment Outcome
Virus Replication

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