Cancer nanomedicine and the complement system activation paradigm: Anaphylaxis and tumour growth

被引:71
作者
Moghimi, S. M. [1 ,2 ]
机构
[1] Univ Copenhagen, Dept Pharm, Nanomed Res Grp, DK-2100 Copenhagen O, Denmark
[2] Univ Copenhagen, Dept Pharm, Ctr Pharmaceut Nanotechnol & Nanotoxicol, DK-2100 Copenhagen O, Denmark
关键词
Cancer; Cardiopulmonary distress; Complement activation; Polystyrene nanoparticles; Poloxamine; 908; Tumour growth; IMMUNE-RESPONSE; SERUM; PROPERDIN; PHARMACOKINETICS; NANOTECHNOLOGY; CLEARANCE; PATHWAYS; VACCINE; INNATE; CELLS;
D O I
10.1016/j.jconrel.2014.03.051
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A wide variety of nanocarriers and particularly cancer nanomedicines activate the complement system, which is the first line of the innate immune defence mechanism. Complement activation may induce inflammatory responses, but such responses arising from uncontrolled complement activation could be life threatening. Accordingly, the role of complement in initiation of adverse reactions to particulate and polymer therapeutics is receiving increasing attention. Furthermore, the involvement of complement-activation products in promoting tumour growth has also been indicated. This could be of serious concern for development of cancer nanomedicines and cancer nanotechnology initiatives. These concepts are reviewed with preliminary evidence that intra-tumoural accumulation of model long circulating nanoparticles could promote tumour growth. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:556 / 562
页数:7
相关论文
共 42 条
  • [1] Single-Walled Carbon Nanotube Surface Control of Complement Recognition and Activation
    Andersen, Alina J.
    Robinson, Joshua T.
    Dai, Hongjie
    Hunter, A. Christy
    Andresen, Thomas L.
    Moghimi, S. Moein
    [J]. ACS NANO, 2013, 7 (02) : 1108 - 1119
  • [2] [Anonymous], 2009, DELIVERY TECHNOLOGIE
  • [3] C3d of complement as a molecular adjuvant: Bridging innate and acquired immunity
    Dempsey, PW
    Allison, MED
    Akkaraju, S
    Goodnow, CC
    Fearon, DT
    [J]. SCIENCE, 1996, 271 (5247) : 348 - 350
  • [4] Low-molecular-weight peptidic and cyclic antagonists of the receptor for the complement factor C5a
    Finch, AM
    Wong, AK
    Paczkowski, NJ
    Wadi, SK
    Craik, DJ
    Fairlie, DP
    Taylor, SM
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (11) : 1965 - 1974
  • [5] Pharmacokinetics of pegylated liposomal doxorubicin - Review of animal and human studies
    Gabizon, A
    Shmeeda, H
    Barenholz, Y
    [J]. CLINICAL PHARMACOKINETICS, 2003, 42 (05) : 419 - 436
  • [6] Complement monitoring of Pluronic 127 gel and micelles: Suppression of copolymer-mediated complement activation by elevated serum levels of HDL, LDL, and apolipoproteins AI and B-100
    Hamad, Islam
    Hunter, A. Christy
    Moghimi, S. Moein
    [J]. JOURNAL OF CONTROLLED RELEASE, 2013, 170 (02) : 167 - 174
  • [7] Distinct Polymer Architecture Mediates Switching of Complement Activation Pathways at the Nanosphere-Serum Interface: Implications for Stealth Nanoparticle Engineering
    Hamad, Islam
    Al-Hanbali, Othman
    Hunter, A. Christy
    Rutt, Kenneth J.
    Andresen, Thomas L.
    Moghimi, S. Moein
    [J]. ACS NANO, 2010, 4 (11) : 6629 - 6638
  • [8] Poly(ethylene glycol)s generate complement activation products in human serum through increased alternative pathway turnover and a MASP-2-dependent process
    Hamada, I.
    Hunter, A. C.
    Szebeni, J.
    Moghimi, S. M.
    [J]. MOLECULAR IMMUNOLOGY, 2008, 46 (02) : 225 - 232
  • [9] Regulation of transport pathways in tumor vessels: Role of tumor type and microenvironment
    Hobbs, SK
    Monsky, WL
    Yuan, F
    Roberts, WG
    Griffith, L
    Torchilin, VP
    Jain, RK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (08) : 4607 - 4612
  • [10] Delivering nanomedicine to solid tumors
    Jain, Rakesh K.
    Stylianopoulos, Triantafyllos
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2010, 7 (11) : 653 - 664