Clearance of depot vaccine SPIO-labeled antigen and substrate visualized using MRI

被引:20
作者
Brewer, Kimberly D. [1 ,2 ]
Lake, Kerry [3 ]
Pelot, Nicole [3 ]
Stanford, Marianne M. [1 ,4 ]
DeBay, Drew R. [3 ]
Penwell, Andrea [1 ]
Weir, Genevieve M. [1 ,4 ]
Karkada, Mohan [1 ,4 ]
Mansour, Marc [1 ]
Bowen, Chris V. [2 ,3 ,5 ,6 ]
机构
[1] Immunovaccine Inc, Halifax, NS, Canada
[2] Dalhousie Univ, Sch Biomed Engn, Halifax, NS, Canada
[3] Biomed Translat Imaging Ctr BIOTIC, Halifax, NS B3H 3A7, Canada
[4] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS, Canada
[5] Dalhousie Univ, Dept Radiol, Halifax, NS, Canada
[6] Dalhousie Univ, Dept Phys, Halifax, NS B3H 3J5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Cancer; Vaccines; Superparamagnetic iron oxide (SPIO); MRI; HPV-16; LYMPH-NODES; PEPTIDE; TUMORS; VACCIMAX(R); CAPACITY; PLATFORM; THERAPY;
D O I
10.1016/j.vaccine.2014.10.058
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunotherapies, including peptide-based vaccines, are a growing area of cancer research, and understanding their mechanism of action is crucial for their continued development and clinical application. Exploring the biodistribution of vaccine components may be key to understanding this action. This work used magnetic resonance imaging (MRI) to characterize the in vivo biodistribution of the antigen and oil substrate of the vaccine delivery system known as DepoVax (TM). DepoVax uses a novel adjuvanted lipid-in-oil based formulation to solubilise antigens and promote a depot effect. In this study, antigen or oil were tagged with superparamagnetic iron oxide (SPIO), making them visible on MR images. This enables tracking of individual vaccine components to determine changes in biodistribution. Mice were injected with SPIO-labeled antigen or SPIO-labeled oil, and imaged to examine clearance of labeled components from the vaccine site. The SPIO-antigen was steadily cleared, with nearly half cleared within two months post-vaccination. In contrast, the SPIO-oil remained relatively unchanged. The biodistribution of the SPIO-antigen component within the vaccine site was heterogeneous, indicating the presence of active clearance mechanisms, rather than passive diffusion or drainage. Mice injected with SPIO-antigen also showed MRI contrast for several weeks post-vaccination in the draining inguinal lymph node. These results indicate that MRI can visualize the in vivo longitudinal biodistribution of vaccine components. The sustained clearance is consistent with antigen up-take and trafficking by immune cells, leading to accumulation in the draining lymph node, which corresponds to the sustained immune responses and reduced tumor burden observed in vaccinated mice. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6956 / 6962
页数:7
相关论文
共 23 条
  • [1] Cancer therapy and vaccination
    Aly, Hamdy A. A.
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 2012, 382 (1-2) : 1 - 23
  • [2] In vivo magnetic resonance imaging of dendritic cell migration into the draining lymph nodes of mice
    Baumjohann, Dirk
    Hess, Andreas
    Budinsky, Lubos
    Brune, Kay
    Schuler, Gerold
    Lutz, Manfred B.
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 2006, 36 (09) : 2544 - 2555
  • [3] First-in-man application of a novel therapeutic cancer vaccine formulation with the capacity to induce multi-functional T cell responses in ovarian, breast and prostate cancer patients
    Berinstein, Neil L.
    Karkada, Mohan
    Morse, Michael A.
    Nemunaitis, John J.
    Chatta, Gurkamal
    Kaufman, Howard
    Odunsi, Kunle
    Nigam, Rita
    Sammatur, Leeladhar
    MacDonald, Lisa D.
    Weir, Genevieve M.
    Stanford, Marianne M.
    Mansour, Marc
    [J]. JOURNAL OF TRANSLATIONAL MEDICINE, 2012, 10
  • [4] Application of the static dephasing regime theory to superparamagnetic iron-oxide loaded cells
    Bowen, CV
    Zhang, XW
    Saab, G
    Gareau, PJ
    Rutt, BK
    [J]. MAGNETIC RESONANCE IN MEDICINE, 2002, 48 (01) : 52 - 61
  • [5] Vaccine adjuvants alum and MF59 induce rapid recruitment of neutrophils and monocytes that participate in antigen transport to draining lymph nodes
    Calabro, Samuele
    Tortoli, Marco
    Baudner, Barbara C.
    Pacitto, Alessandra
    Cortese, Mario
    O'Hagan, Derek T.
    De Gregorio, Ennio
    Seubert, Anja
    Wack, Andreas
    [J]. VACCINE, 2011, 29 (09) : 1812 - 1823
  • [6] A cationic vaccine adjuvant based on a saturated quaternary ammonium lipid have different in vivo distribution kinetics and display a distinct CD4 T cell-inducing capacity compared to its unsaturated analog
    Christensen, Dennis
    Henriksen-Lacey, Malou
    Kamath, Arun T.
    Lindenstrom, Thomas
    Korsholm, Karen S.
    Christensen, Jan P.
    Rochat, Anne-Francoise
    Lambert, Paul-Henri
    Andersen, Peter
    Siegrist, Claire-Anne
    Perrie, Yvonne
    Agger, Else Marie
    [J]. JOURNAL OF CONTROLLED RELEASE, 2012, 160 (03) : 468 - 476
  • [7] Da Costa Martins R, 2012, J CONTROL RELEASE, V162, P533
  • [8] Eradication of established HPV 16-expressing tumors by a single administration of a vaccine composed of a liposome-encapsulated CTL-T helper fusion peptide in a water-in-oil emulsion
    Daftarian, Pirouz
    Mansour, Marc
    Benoit, Anita C.
    Pohajdak, Bill
    Hoskin, David W.
    Brown, Robert G.
    Kast, W. Martin
    [J]. VACCINE, 2006, 24 (24) : 5235 - 5244
  • [9] Rejection of large HPV-16 expressing tumors in aged mice by a single immunization of VacciMax® encapsulated CTL/T helper peptides
    Daftarian, Pirouz M.
    Mansour, Marc
    Pohajdak, Bill
    Fuentes-Ortega, Antar
    Korets-Smith, Ella
    MacDonald, Lisa
    Weir, Genevieve
    Brown, Robert G.
    Kast, W. Martin
    [J]. JOURNAL OF TRANSLATIONAL MEDICINE, 2007, 5 (1)
  • [10] DeBay D, P 19 ANN ISMRM