Prognostic Value of the Stromal Cell–Derived Factor 1 3′A Mutation in Pediatric Human Immunodeficiency Virus Type 1 Infection
Author(s) -
Eleonora Tresoldi,
Maria Luisa Romiti,
Michele Boniotto,
Sérgio Crovella,
Francesca Salvatori,
Elvia Palomba,
Angela Pastore,
Caterina Cancrini,
Maurizio de Martino,
A Plebani,
Guido Castelli Gattinara,
Paolo Rossi,
PierAngelo Tovo,
Antonio Amoroso,
Gabriella Scarlatti
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/339004
Subject(s) - loss of heterozygosity , immunology , biology , virus , viral disease , allele , virology , sida , stromal cell , disease , transmission (telecommunications) , risk factor , immunopathology , medicine , gene , genetics , cancer research , electrical engineering , engineering
A mutation of the stromal cell-derived factor 1 gene (SDF-1 3'A) was shown to protect adults exposed to human immunodeficiency virus type 1 (HIV-1) from infection and to affect HIV disease progression in adults. The presence of this mutation in HIV-1-infected Kenyan children did not predict mother-to-child virus transmission. The SDF-1 3'A polymorphism was studied in 256 HIV-1-infected, 118 HIV-1-exposed but uninfected, and 170 unexposed and uninfected children of Italian origin, and the frequency of SDF-1 3'A heterozygosity and homozygosity in each of the 3 groups was similar. Of the 256 HIV-1-infected children, 194 were regularly followed up and were assigned to groups according to disease progression. The frequency of the SDF-1 3'A allele was substantially lower among children with long-term nonprogression than among children with rapid (P =.0329) or delayed (P =.0375) progression. We show that the presence of the SDF-1 3'A gene correlates with accelerated disease progression in HIV-1-infected children born to seropositive mothers but does not protect against mother-to-child HIV-1 transmission.
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