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DNA-based HIV vaccines do not induce generalized activation in mucosal tissue T cells
Journal article   Open access   Peer reviewed

DNA-based HIV vaccines do not induce generalized activation in mucosal tissue T cells

Morgan A Reuter, Sally Yuan, Preston A Marx, Michele A Kutzler, David B Weiner and Michael R Betts
Human vaccines & immunotherapeutics, v 8(11), pp 1648-1653
01 Nov 2012
PMID: 23111167
url
https://doi.org/10.4161/hv.22247View
Published, Version of Record (VoR) Open

Abstract

DNA vaccine Research Paper HIV mucosal tissue activation T cell
HIV preferentially infects activated T cells, and activated mucosal CD4 + T cells are the primary sites of viral replication. One potential explanation for increased HIV acquisition rates in the STEP study is that vaccination with adenoviral (Ad) vectors increased CD4 + T cell activation levels at the site of infection, a concept that others and we continue to explore. 1 , 2 Whether vaccination with HIV vaccine platforms increases the activation state of CD4 + T cells within peripheral tissues, such as the gastro-intestinal (GI) mucosa, is exceptionally important to determine as a vaccine safety measure, given the susceptibility of activated CD4 + T cells to HIV infection.   In this study we examined whether vaccination with DNA plasmids and chemokine adjuvants alter the activation state of T cells within the GI mucosa, inguinal LN, and peripheral blood. T cell activation state was measured by expression of CD25, CD69, and HLA-DR over the course of the prime/boost study. DNA plasmid vaccination did not increase expression of any of these markers in the 3 tissues studied. Addition of the gut-homing chemokine TECK during DNA plasmid vaccination did not alter activation levels of CD4 + T cells at any of these sites. These findings indicate that DNA vaccines do not elicit generalized mucosal T cell activation. Thus, DNA platforms may be especially suitable for HIV vaccine development, where bystander activation could promote increased HIV transmission.

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Collaboration types
Domestic collaboration
Web of Science research areas
Biotechnology & Applied Microbiology
Immunology
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