Adjuvanticity and toxicity of cobalt oxide nanoparticles as an alternative vaccine adjuvant

Author:

Cho Wan-Seob12,Dart Kenneth13,Nowakowska Dominika J3,Zheng Xiaozhong3,Donaldson Ken1,Howie Sarah EM4

Affiliation:

1. ELEGI/Colt Laboratory, Center for Inflammation Research, University of Edinburgh, Edinburgh, EH16 4TJ, UK

2. Department of Medicinal Biotechnology, College of Natural Resources and Life Science, Dong-A University, Busan 604–714, South Korea

3. Immunity and Chronic Inflammation Group, Center for Inflammation Research, University of Edinburgh, Edinburgh, EH16 4TJ, UK

4. ELEGI/Colt Laboratory, Center for Inflammation Research, University of Edinburgh, Edinburgh, EH16 4TJ, UK.

Abstract

Aim: There are very few adjuvants licensed for use in human vaccination, and alum-based adjuvants are the most widely used. Alum adjuvants predominantly boost Th2 immune responses and there is a need for new adjuvants that also stimulate Th1 immunity. We recently reported that cobalt oxide nanoparticles (Co3O4NPs) stimulate Th1-type immune responses in vivo. Here, we exploited this property to examine whether Co3O4NP could act as an adjuvant using the model antigen ovalbumin. Materials & methods: Female C57BL/6 mice were immunized subcutaneously twice with ovalbumin plus adjuvant (Co3O4NPs or Imject® Alum) followed by intraperitoneal stimulation with soluble ovalbumin. Results: Co3O4NPs induced a more balanced Th1- and Th2-type response, triggering higher specific Th1-dependent IgG2c production in addition to Th2-dependent IgG1 and less ‘allergic’ IgE production, and induced less inflammation at both the subcutaneous and intraperitoneal injection sites. Discussion: Co3O4NPs could be a very useful adjuvant where both Th1 and Th2 responses are needed to clear pathogens. Original submitted 22 August 2011; Revised submitted 28 February 2012; Published online 20 July 2012

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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