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Clinical and Vaccine Immunology, April 2008, p. 668-674, Vol. 15, No. 4
1071-412X/08/$08.00+0     doi:10.1128/CVI.00413-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Coencapsulation of CpG Oligodeoxynucleotides with Recombinant Leishmania major Stress-Inducible Protein 1 in Liposome Enhances Immune Response and Protection against Leishmaniasis in Immunized BALB/c Mice{triangledown}

Ali Badiee,1,2 Mahmoud R. Jaafari,1 Afshin Samiei,1 Dina Soroush,1 and Ali Khamesipour2*

School of Pharmacy, Biotechnology Research Center and Pharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran,1 Center for Research and Training in Skin Diseases and Leprosy, Medical Sciences/University of Tehran, Tehran, Iran2

Received 9 October 2007/ Returned for modification 14 December 2007/ Accepted 21 January 2008

CpG oligodeoxynucleotides (CpG ODN) have been shown to have potent adjuvant activity for a wide range of antigens. The purpose of this study was to determine the potential benefit of using liposomes as a delivery vehicle to enhance the adjuvant activity of CpG ODN with Leishmania major stress-inducible protein 1 (LmSTI1) antigen in induction of the Th1 response in a murine model of leishmaniasis. BALB/c mice were immunized subcutaneously three times in 3-week intervals with liposomal recombinant LmSTI1 (Lip-rLmSTI1), rLmSTI1 coencapsulated with CpG ODN in a liposome (Lip-rLmSTI1-CpG ODN), rLmSTI1 plus CpG ODN in phosphate-buffered saline (PBS), rLmSTI1 plus non-CpG ODN in PBS, rLmSTI1 in PBS, empty liposome, or PBS. The intensity of infection induced by L. major promastigote challenge was measured by footpad swelling. A significant (P < 0.001) inhibition of infection in mice immunized with Lip-rLmSTI1-CpG ODN was shown compared to the other groups, and no parasite was detected in the spleens of this group 14 weeks after challenge. The highest immunoglobulin G2a (IgG2a) titer and the highest IgG2a/IgG1 ratio were also shown in the sera of mice immunized with Lip-rLmSTI1-CpG ODN before and 14 weeks after challenge. The results indicated the superiority of CpG ODN in its liposomal form over its soluble form to induce the Th1 response when used in association with rLmSTI1 antigen. It seems that using a liposome delivery system carrying CpG ODN as an adjuvant coencapsulated with Leishmania antigen plays an important role in vaccine development strategies against leishmaniasis.


* Corresponding author. Mailing address: Center for Research and Training in Skin Diseases and Leprosy, Medical Sciences/University of Tehran, P.O. Box 14155-6383, Tehran 14166, Iran. Phone: (98-21) 8897 0657. Fax: (98-21) 8897 0658. E-mail: khamesipour_ali{at}yahoo.com

{triangledown} Published ahead of print on 30 January 2008.


Clinical and Vaccine Immunology, April 2008, p. 668-674, Vol. 15, No. 4
1071-412X/08/$08.00+0     doi:10.1128/CVI.00413-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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