Induction of HIV-1-specific mucosal immune responses following intramuscular recombinant adenovirus serotype 26 HIV-1 vaccination of humans.

نویسندگان

  • Lindsey R Baden
  • Jinyan Liu
  • Hualin Li
  • Jennifer A Johnson
  • Stephen R Walsh
  • Jane A Kleinjan
  • Brian A Engelson
  • Lauren Peter
  • Peter Abbink
  • Danny A Milner
  • Kevin L Golden
  • Kyle L Viani
  • Matthew D Stachler
  • Benjamin J Chen
  • Maria G Pau
  • Mo Weijtens
  • Brittany R Carey
  • Caroline A Miller
  • Edith M Swann
  • Mark Wolff
  • Hayley Loblein
  • Michael S Seaman
  • Raphael Dolin
  • Dan H Barouch
چکیده

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.

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عنوان ژورنال:
  • The Journal of infectious diseases

دوره 211 4  شماره 

صفحات  -

تاریخ انتشار 2015