Modulating the adjuvanticity of alum by co-administration of muramyl di-peptide (MDP) or Quil-A.

Moschos, Sterghios, Bramwell, Vincent, Somavarapu, Satyanarayna and Alpar, H. Oya (2006) Modulating the adjuvanticity of alum by co-administration of muramyl di-peptide (MDP) or Quil-A. Vaccine, 24 (8). pp. 1081-1086. ISSN 0264-410X

Full text not available from this repository. (Request a copy)
Official URL: http://dx.doi.org/10.1016/j.vaccine.2005.09.007

Abstract

The characterization of the immunological cascades of the innate immune system activated by pathogen associated molecular patterns (PAMP) recognized by pattern recognition receptors (PRR) have allowed the elucidation of the mechanisms underlying the immunomodulatory properties of adjuvants. Thus, the combinatorial use of adjuvants with specific, complementary functions is investigated to achieve tailored immune responses to subunit vaccines. We have previously shown how combinatorial administration of chitosan and cholera toxin B or muramyl-di-peptide (MDP) intranasally, but not intramuscularly, can allow small doses of MDP which, when administered alone cannot adjuvantise Helicobacter pylori urease (rUre), achieve an immunomodulatory effect through the specific physiological effect of chitosan. The aim of this study was to investigate if in the context of rUre the adjuvantising effect of MDP could be realized via the intramuscular route by combination with aluminium hydroxide, as compared with the routinely used veterinary adjuvant combination of alum and Quil-A. Serum IgG kinetics were comparable between the two adjuvant combination groups. However, the alum + MDP combination afforded higher antigen-specific recall responses in splenocyte cultures, associated with elevated release of the type I immune response cytokines IFN-gamma and IL-2. This data suggests that the adjuvanticity of MDP can be modulated in the context of alum in a manner dissimilar to that of Quil-A, achieving a balancing effect on the responses elicited by alum adjuvantisation.

Item Type: Article
Uncontrolled Keywords: Muramyl di-peptide, Alum, Quil-A, adjuvant synergy, BALB/c, Urease
Subjects: A300 Clinical Medicine
B200 Pharmacology, Toxicology and Pharmacy
C700 Molecular Biology, Biophysics and Biochemistry
Department: Faculties > Health and Life Sciences > Applied Sciences
Depositing User: Sterghios Moschos
Date Deposited: 24 Oct 2016 09:33
Last Modified: 12 Oct 2019 17:30
URI: http://nrl.northumbria.ac.uk/id/eprint/28150

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics