CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individuals

The 32-bp deletion in the HIV-1 co-receptor CCR5 confers a high degree of resistance to HIV-1 infection in homozygous individuals for the deleted allele and partial protection against HIV-1 during disease progression in heterozygotes. Natural ligands for CCR5, MIP-1alpha, MIP-1ß and RANTES, have bee...

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Main Authors: Mikawa A.Y., Tagliavini S.A., Costa P.I.
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2002-01-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2002001100011
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author Mikawa A.Y.
Tagliavini S.A.
Costa P.I.
author_facet Mikawa A.Y.
Tagliavini S.A.
Costa P.I.
author_sort Mikawa A.Y.
collection DOAJ
description The 32-bp deletion in the HIV-1 co-receptor CCR5 confers a high degree of resistance to HIV-1 infection in homozygous individuals for the deleted allele and partial protection against HIV-1 during disease progression in heterozygotes. Natural ligands for CCR5, MIP-1alpha, MIP-1ß and RANTES, have been shown to inhibit HIV replication in CD4+ T cells. In the present study, we examined the CCR5 genotype by PCR and the plasma levels of RANTES and MIP-1alpha by ELISA among blood donors (N = 26) and among HIV-1-infected individuals (N = 129). The control group consisted of healthy adult volunteers and HIV-1-infected subjects were an asymptomatic and heterogeneous group of individuals with regard to immunologic and virologic markers of HIV-1 disease. The frequency of the CCR5 mutant allele (delta32ccr5) in this population was 0.032; however, no delta32ccr5 homozygote was detected. These results could be related to the intense ethnic admixture of the Brazilian population. There was no correlation between circulating ß-chemokines (MIP-1alpha, RANTES) and viral load in HIV-infected individuals. RANTES concentrations in plasma samples from HIV+ patients carrying the homozygous CCR5 allele (CCR5/CCR5) (28.23 ng/ml) were higher than in the control samples (16.07 ng/ml; P<0.05); however, this HIV+ patient group (mean 26.23 pg/ml) had significantly lower concentrations of MIP-1alpha than those observed in control samples (mean 31.20 pg/ml; P<0.05). Both HIV-1-infected and uninfected individuals heterozygous for the delta32ccr5 allele had significantly lower concentrations of circulating RANTES (mean 16.07 and 6.11 ng/ml, respectively) than CCR5/CCR5 individuals (mean 28.23 and 16.07 ng/ml, respectively; P<0.05). These findings suggest that the CCR5 allele and ß-chemokine production may affect the immunopathogenesis of HIV-1.
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spelling doaj.art-33bbaccf5f064e11bc4c24a29d8c20042022-12-22T00:09:44ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X0034-73102002-01-01351113331337CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individualsMikawa A.Y.Tagliavini S.A.Costa P.I.The 32-bp deletion in the HIV-1 co-receptor CCR5 confers a high degree of resistance to HIV-1 infection in homozygous individuals for the deleted allele and partial protection against HIV-1 during disease progression in heterozygotes. Natural ligands for CCR5, MIP-1alpha, MIP-1ß and RANTES, have been shown to inhibit HIV replication in CD4+ T cells. In the present study, we examined the CCR5 genotype by PCR and the plasma levels of RANTES and MIP-1alpha by ELISA among blood donors (N = 26) and among HIV-1-infected individuals (N = 129). The control group consisted of healthy adult volunteers and HIV-1-infected subjects were an asymptomatic and heterogeneous group of individuals with regard to immunologic and virologic markers of HIV-1 disease. The frequency of the CCR5 mutant allele (delta32ccr5) in this population was 0.032; however, no delta32ccr5 homozygote was detected. These results could be related to the intense ethnic admixture of the Brazilian population. There was no correlation between circulating ß-chemokines (MIP-1alpha, RANTES) and viral load in HIV-infected individuals. RANTES concentrations in plasma samples from HIV+ patients carrying the homozygous CCR5 allele (CCR5/CCR5) (28.23 ng/ml) were higher than in the control samples (16.07 ng/ml; P<0.05); however, this HIV+ patient group (mean 26.23 pg/ml) had significantly lower concentrations of MIP-1alpha than those observed in control samples (mean 31.20 pg/ml; P<0.05). Both HIV-1-infected and uninfected individuals heterozygous for the delta32ccr5 allele had significantly lower concentrations of circulating RANTES (mean 16.07 and 6.11 ng/ml, respectively) than CCR5/CCR5 individuals (mean 28.23 and 16.07 ng/ml, respectively; P<0.05). These findings suggest that the CCR5 allele and ß-chemokine production may affect the immunopathogenesis of HIV-1.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2002001100011HIV-1CC chemokine receptor 5delta32ccr5 Frequency alleleChemokines
spellingShingle Mikawa A.Y.
Tagliavini S.A.
Costa P.I.
CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individuals
Brazilian Journal of Medical and Biological Research
HIV-1
CC chemokine receptor 5
delta32ccr5 Frequency allele
Chemokines
title CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individuals
title_full CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individuals
title_fullStr CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individuals
title_full_unstemmed CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individuals
title_short CCR5 genotype and plasma ß-chemokine concentration of Brazilian HIV-infected individuals
title_sort ccr5 genotype and plasma ss chemokine concentration of brazilian hiv infected individuals
topic HIV-1
CC chemokine receptor 5
delta32ccr5 Frequency allele
Chemokines
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2002001100011
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