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Cysteine proteinase type I, encapsulated in solid lipid nanoparticles induces substantial protection against Leishmania major infection in C57BL/6 mice.

Abstract
Appropriate adjuvant, proper antigen(s) and a suitable formulation are required to develop stable, safe and immunogenic vaccines. Leishmanial cysteine proteinase type I (CPB) is a promising vaccine candidate; nevertheless, it requires a delivery system to induce a potent immune response. Herein, solid lipid nanoparticles (SLN) have been applied for CPB [with and without C-terminal extension (CTE)] formulation to utilize as a vaccine against Leishmania major infection in C57BL/6 mice. Therefore, SLN-CPB and SLN-CPB(-CTE) formulations were prepared from cetyl palmitate and cholesterol, using melt emulsification method. After intraperitoneal vaccination and subsequent L. major challenge, a strong antigen-specific T-helper type 1 (Th1) immune response was induced compared to control groups. Lymph node cells from immunized mice displayed lower parasite burden, higher IFN-γ, IgG2a and lower IL-4 production, indicating that robust Th1 immune response had been induced. Our results revealed that CTE is not necessary for inducing protective responses against L. major infection as the IFN-γ/IL-4 ratio was significantly higher, whereas IgG1 responses were lower in the SLN-CPB(-CTE) vaccinated group, post-challenge. Thus, SLN-CPB(-CTE) was shown to induce specific Th1 immune responses to control L. major infection, through effective antigen delivery to the peritoneal antigen presenting cells.
AuthorsD Doroud, F Zahedifard, A Vatanara, A R Najafabadi, S Rafati
JournalParasite immunology (Parasite Immunol) Vol. 33 Issue 6 Pg. 335-48 (Jun 2011) ISSN: 1365-3024 [Electronic] England
PMID21410716 (Publication Type: Journal Article)
Copyright© 2011 Blackwell Publishing Ltd.
Chemical References
  • Adjuvants, Immunologic
  • Drug Carriers
  • Immunoglobulin G
  • Liposomes
  • Protozoan Vaccines
  • Interleukin-4
  • Interferon-gamma
  • Cysteine Proteases
Topics
  • Adjuvants, Immunologic (administration & dosage, chemistry)
  • Animals
  • Cysteine Proteases (administration & dosage, immunology)
  • Drug Carriers (administration & dosage, chemistry)
  • Female
  • Immunoglobulin G (immunology)
  • Interferon-gamma (metabolism)
  • Interleukin-4 (metabolism)
  • Leishmania major (immunology)
  • Leishmaniasis, Cutaneous (prevention & control)
  • Leukocytes, Mononuclear (immunology)
  • Liposomes (administration & dosage, chemistry)
  • Lymph Nodes (immunology)
  • Mice
  • Mice, Inbred C57BL
  • Nanoparticles (administration & dosage, chemistry)
  • Protozoan Vaccines (administration & dosage, immunology)

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