Altered Response Hierarchy and Increased T-Cell Breadth upon HIV-1 Conserved Element DNA Vaccination in Macaques
Author(s) -
Viraj Kulkarni,
Antonio Valentin,
Margherita Rosati,
Candido Alicea,
Ashish Kumar Singh,
Rashmi Jalah,
Kate E. Broderick,
Niranjan Y. Sardesai,
Sylvie Le Gall,
Beatriz Mothe,
Christian Brander,
Morgane Rolland,
James I. Mullins,
George N. Pavlakis,
Barbara K. Felber
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0086254
Subject(s) - immunogen , epitope , dna vaccination , biology , virology , vaccination , conserved sequence , immunity , aids vaccines , hiv vaccine , macaque , immune system , dna , genetics , computational biology , antibody , vaccine trial , immunization , monoclonal antibody , base sequence , paleontology
HIV sequence diversity and potential decoy epitopes are hurdles in the development of an effective AIDS vaccine. A DNA vaccine candidate comprising of highly conserved p24 gag elements (CE) induced robust immunity in all 10 vaccinated macaques, whereas full-length gag DNA vaccination elicited responses to these conserved elements in only 5 of 11 animals, targeting fewer CE per animal. Importantly, boosting CE-primed macaques with DNA expressing full-length p55 gag increased both magnitude of CE responses and breadth of Gag immunity, demonstrating alteration of the hierarchy of epitope recognition in the presence of pre-existing CE-specific responses. Inclusion of a conserved element immunogen provides a novel and effective strategy to broaden responses against highly diverse pathogens by avoiding decoy epitopes, while focusing responses to critical viral elements for which few escape pathways exist.
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