Please use this identifier to cite or link to this item:
|Title:||No Evidence for Association of β-Defensin Genomic Copy Number with HIV Susceptibility, HIV Load during Clinical Latency, or Progression to AIDS|
IAVI Africa HIV prevention Partnership
Swiss HIV Cohort Study
|Publisher:||Wiley for University College London|
|Citation:||Annals of Human Genetics, 2017, 81, pp. 27–34.|
|Abstract:||Common single nucleotide variation in the host accounts for 25% of the variability in the plasma levels of HIV during the clinical latency stage (viral load setpoint). However, the role of rare variants and copy number variants remains relatively unexplored. Previous work has suggested copy number variation of a cluster of β-defensin genes affects HIV load in treatment-naïve sub-Saharan Africans and rate of response to anti-retroviral treatment. Here we analyse a total of 1827 individuals from two cohorts of HIV-infected individuals from Europe and sub-Saharan Africa to investigate the role of β-defensin copy number variation on HIV load at setpoint. We find no evidence of for association of copy number with viral load. We also compare distribution of β-defensin copy number between European cases and controls and find no differences, arguing against a role of β-defensin copy number in HIV acquisition. Taken together, our data argues against an effect of copy number variation of the β-defensin region in the spontaneous control of HIV infection.|
|Rights:||Copyright © 2017, Wiley for University College London. Deposited with reference to the publisher’s open access archiving policy.|
|Description:||Author confirms PDF is post-print.|
The file associated with this record is under embargo until 12 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.
|Appears in Collections:||Published Articles, Dept. of Genetics|
Files in This Item:
|s1-ln25138710-2128546017-1939656818Hwf-995315869IdV-38491003025138710PDF_HI0001.pdf||Post-review (final submitted author manuscript)||727.94 kB||Adobe PDF||View/Open|
Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.