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Coregulation of HIV-1 dependency factors in individuals heterozygous to the CCR5-delta32 deletion
Authors:Email author" target="_blank">Gero?HütterEmail author  Christian?Blüthgen  Martin?Neumann  Mark?Reinwald  Daniel?Nowak  Harald?Klüter
Institution:1.Institute of Transfusion Medicine and Immunology, Medical Faculty Mannheim,Heidelberg University, German Red Cross Blood Service Baden-Württemberg- Hessen,Mannheim,Germany;2.Cellex GmbH,Dresden,Germany;3.Medical Department III (Hematology, Oncology),Charité Campus Benjamin Franklin,Berlin,Germany;4.Medical Department III (Hematology, Oncology),University Medical Centre Mannheim, Heidelberg University,Heidelberg,Germany
Abstract:

Background

CCR5-delta32 heterozygous individuals are susceptible to HIV-1. However, it is not clear if there is a relevant protective effect against transmission and a beneficial effect in terms of HIV progression which cannot be attributed to CCR5 surface density alone. Therefore we investigated HIV-1 dependency factors (HDF) which might be differently regulated in CCR5 wild type (WT) and CCR5-delta32 heterozygous individuals.

Methods

We examined CD34+ hematopoietic progenitor cells derived from bone marrow samples from 19 healthy volunteers, 12 individuals with CCR5 WT and 7 with heterozygous CCR5-delta32 deletion. Samples were analyzed using a global gene expression oligonucleotide microarray (HG-U133plus 2.0, Affymetrix Inc.).

Results

A total of 205 genes were found with altered expression (3fold difference, present call rate of 75%, p?<?0.05) and 7 of these had a connection to HIV-1 pathogenesis. In 4 genes: TOP1, CXCR2, SREBF2, and TAP we found a different regulation which was consistent with a supposed beneficial effect for CCR5-delta32 heterozygotes.

Conclusion

The CCR5-delta32 deletion is associated with other HDFs in HIV-1 pathogenesis as a possible explanation for beneficial effects regarding the deletion leading to a variant expression profile in heterozygous carriers of this mutation.
Keywords:
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