Abstract

The link between HLA types and HIV disease progression has been well established with alleles and residues associated to progression or non-progression to AIDS. Vertical transmission rate of HIV in Cameroon is still very high (10%). The aim of this study was to describe the diversity of HLA class I in infants born to HIV infected mothers and to determine the influence of HLA genotype in mother to child HIV transmission in Cameroon. Thirty four HIV infected infants and 28 HIV exposed but non infected infants born to HIV-positive mothers were enrolled in this study. HLA-A, HLA-B, group allele frequencies were determined by low-resolution polymerase chain reaction using sequencespecific primers. Nineteen HLA-A, 20 HLA-B allelic groups were identified in the study population. Among all the allelic variants identified, only HLA-B*44 allelic frequency resulted significantly increased in exposed non infected children (12.5% in exposed non infected versus 2.9% in exposed HIV-infected children, p=0.04). HLA-B*44 may be associated with the resistance to HIV infection upon mother to child exposure.

Highlights

  • human leukocyte antigen (HLA), the most genetically diverse loci in the human genome [1], play a crucial role in host-pathogen interaction by mediating innate and adaptive cellular immune responses [2]

  • We describe the diversity of HLA class I in infants born to HIV infected mothers and to determine the influence of HLA genotype in perinatal HIV transmission in Cameroon

  • HLA-B*44 resulted with an increase allelic frequency in exposed non infected (12.5% in HIV-exposed uninfected (HIVe) versus 2.9% in HIV infected (HIVi), p=0.04)

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Summary

Introduction

HLA, the most genetically diverse loci in the human genome [1], play a crucial role in host-pathogen interaction by mediating innate and adaptive cellular immune responses [2]. For a vast number of infectious diseases various HLA alleles have been associated with disease outcome. Limited information is available about HLA in Central Africa where diseases such as HIV/AIDS, Hepatitis, malaria, tuberculosis and dengue fever are largely diffused. The genetic make-up of a person's HLA affects the rate of HIV disease progression [3]. It has been shown that HLA class I alleles B*27 and B*57 are associated with better disease prognosis, while others (such as B*35) are associated with worse outcome. The protection is not entirely explained by a confounding effect of a few highly protective HLA-B types such as B*57, B*58, B*27, B*51, and B*81 [4,5]

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