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Meeting report VLPNPV: Session 3: Immune responses

Trudy G Morrison1

  • 1a Department of Microbiology and Physiological Systems ; University of Massachusetts Medical School ; Worcester , MA USA.

Human Vaccines & Immunotherapeutics
|December 23, 2014
PubMed
Summary

Virus-like particles (VLPs) and nanoparticles (NPs) show promise as vaccines for diseases. Research is advancing VLP and NP development, characterization, production, and immune responses for future applications.

Keywords:
BLys, B lymphocyte stimulatorELISpot, enzyme-linked immunoSpotF, fusionG, glycoproteinHIV, human immunodeficiency virusHN, hemagglutinin-neuraminidaseLLPC, long-lived plasma cellsM, membraneMHC, major histocompatibility complexNDV, Newcastle disease virusNOD, nucleotide-binding oligomerization domainsNP, nanoparticles or nucleocapsid proteinPBL, peripheral blood lymphocytesRHDV, rabbit hemorrhagic disease virusRSV, respiratory syncytial virusT cell responsesTLR, toll-like receptorTMV, tobacco mosaic virusTrV, triatoma virusVLPs, virus-like particlesVirus-like particlesadjuvantsanti-glycan immunityhuman humoral immune responsesmemory responsesmucosal immunity

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