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Characterization of B-cell and T-cell responses to a tetravalent dengue purified inactivated vaccine in healthy adults.
Friberg, Heather; Gargulak, Morgan; Kong, Amanda; Lin, Leyi; Martinez, Luis J; Schmidt, Alexander C; Paris, Robert M; Jarman, Richard G; Diaz, Clemente; Thomas, Stephen J; Moris, Philippe; Currier, Jeffrey R.
Afiliación
  • Friberg H; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA. heather.l.friberg-robertson.civ@health.mil.
  • Gargulak M; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Kong A; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Lin L; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Martinez LJ; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Schmidt AC; GSK, Rockville, MD, USA.
  • Paris RM; GSK, Rockville, MD, USA.
  • Jarman RG; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Diaz C; University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
  • Thomas SJ; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
  • Moris P; GSK, Rixensart, Belgium.
  • Currier JR; Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, MD, USA.
NPJ Vaccines ; 7(1): 132, 2022 Oct 31.
Article en En | MEDLINE | ID: mdl-36316335
ABSTRACT
The increasing global impact of dengue underscores the need for a dengue virus (DENV) vaccine. We assessed B-cell and T-cell responses following vaccination with four formulations of a tetravalent dengue purified inactivated vaccine (DPIV) in dengue-primed and dengue-naive adults from two studies (NCT01666652, NCT01702857). Frequencies of DPIV-induced memory B cells specific to each DENV serotype remained high up to 12 months post-vaccination, and were higher in the dengue-primed than dengue-naive adults. A subsequent DPIV booster dose induced strong anamnestic B-cell responses. Multifunctional CD4+ T cells (predominantly expressing IL-2) were induced by DPIV, with higher frequencies in dengue-primed adults. DPIV-induced CD4+ T cells also demonstrated in vitro proliferative capacity and antigen-specific production of GM-CSF, IFN-γ, and IL-13. CD8+ T-cell responses were undetectable in dengue-naive adults and low in dengue-primed individuals. B- and T-cell responses persisted up to 12 months post-vaccination in both dengue-primed and dengue-naive adults.