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Increased Mucosal CD4 + T Cell Activation in Rhesus Macaques following Vaccination with an Adenoviral Vector
Author(s) -
Irene Bukh,
Roberto Calcedo,
Soumitra Roy,
Diane G. Carnathan,
Rebecca Grant,
Qiuyue Qin,
Surina Boyd,
Sarah J. Ratcliffe,
Christin L Veeder,
Scarlett L. Bellamy,
Michael R. Betts,
James M. Wilson
Publication year - 2014
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.03850-13
Subject(s) - rhesus macaque , vaccination , simian immunodeficiency virus , macaque , viral vector , biology , virology , immunology , t cell , vector (molecular biology) , adenoviridae , virus , immune system , genetic enhancement , recombinant dna , paleontology , gene , biochemistry
The possibility that vaccination with adenovirus (AdV) vectors increased mucosal T cell activation remains a central hypothesis to explain the potential enhancement of HIV acquisition within the Step trial. Modeling this within rhesus macaques is complicated because human adenoviruses, including human adenovirus type 5 (HAdV-5), are not endogenous to macaques. Here, we tested whether vaccination with a rhesus macaque-derived adenoviral vector (simian adenovirus 7 [SAdV-7]) enhances mucosal T cell activation within rhesus macaques. Following intramuscular SAdV-7 vaccination, we observed a pronounced increase in SAdV-7-specific CD4(+) T cell responses in peripheral blood and, more dramatically, in rectal mucosa tissue. Vaccination also induced a significant increase in the frequency of activated memory CD4(+) T cells in SAdV-7- and HAdV-5-vaccinated animals in the rectal mucosa but not in peripheral blood. These fluctuations within the rectal mucosa were also associated with a pronounced decrease in the relative frequency of naive resting CD4(+) T cells. Together, these results indicate that peripheral vaccination with an AdV vector can increase the activation of mucosal CD4(+) T cells, potentially providing an experimental model to further evaluate the role of host-vector interactions in increased HIV acquisition after AdV vector vaccination.

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