Induction of HIV-1-Specific Mucosal Immune Responses Following Intramuscular Recombinant Adenovirus Serotype 26 HIV-1 Vaccination of Humans
02/2015
Journal Article
Authors:
Baden, L.;
Liu, J.;
Li, H.;
Johnson, J.;
Walsh, S.;
Kleinjan, J.;
Engelson, B.;
Peter, L.;
Abbink, P.;
, ;
Golden, K.;
Viani, K.;
Stachler, M.;
Chen, B.;
, ;
Wolff, M.;
Loblein, H.;
Seaman, M.;
Dolin, R.;
Barouch, D.
Secondary:
J Infect Dis
Volume:
211
Pagination:
518-528
URL:
http://www.ncbi.nlm.nih.gov/pubmed/25165165
Keywords:
adenovirus; HIV; mucosal immunity; vaccine
Abstract:
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.
