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Merck
  • Route of Vaccine Administration Alters Antigen Trafficking but Not Innate or Adaptive Immunity.

Route of Vaccine Administration Alters Antigen Trafficking but Not Innate or Adaptive Immunity.

Cell reports (2020-03-27)
Sebastian Ols, Lifei Yang, Elizabeth A Thompson, Pradeepa Pushparaj, Karen Tran, Frank Liang, Ang Lin, Bengt Eriksson, Gunilla B Karlsson Hedestam, Richard T Wyatt, Karin Loré
摘要

Although intramuscular (i.m.) administration is the most commonly used route for licensed vaccines, subcutaneous (s.c.) delivery is being explored for several new vaccines under development. Here, we use rhesus macaques, physiologically relevant to humans, to identify the anatomical compartments and early immune processes engaged in the response to immunization via the two routes. Administration of fluorescently labeled HIV-1 envelope glycoprotein trimers displayed on liposomes enables visualization of targeted cells and tissues. Both s.c. and i.m. routes induce efficient immune cell infiltration, activation, and antigen uptake, functions that are tightly restricted to the skin and muscle, respectively. Antigen is also transported to different lymph nodes depending on route. However, these early differences do not translate into significant differences in the magnitude or quality of antigen-specific cellular and humoral responses over time. Thus, although some distinct immunological differences are noted, the choice of route may instead be motivated by clinical practicality.

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Sigma-Aldrich
胆固醇, powder, BioReagent, suitable for cell culture, ≥99%
Sigma-Aldrich
来自美洲商陆(商陆)的凝集素, lyophilized powder, BioReagent, suitable for cell culture
Millipore
Multiscreen® 96孔板,疏水性PVDF膜, pore size 0.45 μm, sterile
Sigma-Aldrich
Biotin-XX-tyramide, ≥95% (HPLC)
Sigma-Aldrich
N-乙酰-D-乳糖胺, ≥98% (TLC)
Avanti
16:0 PE MCC, 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N-[4-(p-maleimidomethyl)cyclohexane-carboxamide] (sodium salt), chloroform