| Literature DB >> 22693228 |
Jiangmei Yin1, Maryanne T Vahey, Anlan Dai, Mark G Lewis, Tatiana Arango, Jake Yalley-Ogunro, Jack Greenhouse, Karla Mendoza, Amir Khan, Niranjan Y Sardesai, Walter Weiss, Jack Komisar, Jean D Boyer.
Abstract
Human immunodeficiency virus type 1 and malaria are co-endemic in many areas. We evaluated the effects of Plasmodium inui infection on the performance of a simian immunodeficiency virus (SIV) DNA vaccine. Rhesus macaques were infected with P. inui by transfusion of whole blood from a persistently infected animal. Animals with and animals without P. inui infection were then vaccinated 4 times with an SIV DNA vaccine encoding SIVgag, SIVpol, and SIVenv. Animals were subsequently challenged with thirty 50% rhesus monkey infectious doses of SIVmac251 6 weeks after the last vaccination. P. inui-infected immunized animals showed a significantly higher viral load than animals without P. inui infection (P = .010, by the Wilcoxon rank sum test). The higher viral loads in the P. inui-infected animals were durable and were observed at all sampling time points across the study (P = .00245, by the Wilcoxon rank test). The P. inui-infected animals also had correspondingly lower CD4(+) cell counts. There were fewer vaccine-specific CD4(+) and CD8(+) cells in the P. inui-infected animals, compared with uninfected animals. Of importance, P. inui infection seemed to decrease the number of CD8(+) cells that could proliferate or secrete interferon γ, although the number of CD8(+) cells capable of secreting tumor necrosis factor α following in vitro stimulation was increased. This study demonstrated that P. inui infection had an influence on the immune response to an SIV DNA vaccine and decreased the vaccine's efficacy.Entities:
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Year: 2012 PMID: 22693228 PMCID: PMC3491732 DOI: 10.1093/infdis/jis404
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226