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Induction of HIV-1–Specific Mucosal Immune Responses Following Intramuscular Recombinant Adenovirus Serotype 26 HIV-1 Vaccination of Humans
- Baden, Lindsey R;
- Liu, Jinyan;
- Li, Hualin;
- Johnson, Jennifer A;
- Walsh, Stephen R;
- Kleinjan, Jane A;
- Engelson, Brian A;
- Peter, Lauren;
- Abbink, Peter;
- Milner, Danny A;
- Golden, Kevin L;
- Viani, Kyle L;
- Stachler, Matthew D;
- Chen, Benjamin J;
- Pau, Maria G;
- Weijtens, Mo;
- Carey, Brittany R;
- Miller, Caroline A;
- Swann, Edith M;
- Wolff, Mark;
- Loblein, Hayley;
- Seaman, Michael S;
- Dolin, Raphael;
- Barouch, Dan H
- et al.
Published Web Location
https://doi.org/10.1093/infdis/jiu485Abstract
Background
Defining mucosal immune responses and inflammation to candidate human immunodeficiency virus type 1 (HIV-1) vaccines represents a current research priority for the HIV-1 vaccine field. In particular, it is unclear whether intramuscular immunization can elicit immune responses at mucosal surfaces in humans.Methods
In this double-blind, randomized, placebo-controlled clinical trial, we evaluated systemic and mucosal immune responses to a candidate adenovirus serotype 26 (Ad26) vectored HIV-1 envelop (Env) vaccine in baseline Ad26-seronegative and Ad26-seropositive healthy volunteers. Systematic mucosal sampling with rectal Weck-Cel sponges and rectal biopsies were performed.Results
Intramuscular immunization elicited both systemic and mucosal Env-specific humoral and cellular immune responses in the majority of subjects. Individuals with preexisting Ad26-specific neutralizing antibodies had vaccine-elicited immune responses comparable to those of subjects who were Ad26 seronegative. We also observed no increase in activated total or vector-specific mucosal CD4+ T lymphocytes following vaccination by either histopathology or flow cytometry.Conclusions
These data demonstrate that a single intramuscular administration of this Ad26-vectored HIV-1 Env vaccine elicited both systemic and mucosal immune responses in humans. Induction of antigen-specific humoral and cellular mucosal immunity was not accompanied by a detectable increase in mucosal inflammation.Clinical trials registration
NCT01103687.Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.
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