- Open Access
Evaluation of the humoral immune response and cross reactivity against Mycobacterium tuberculosis of mice immunized with liposomes containing glycolipids of Mycobacterium smegmatis
© Borrero et al; licensee BioMed Central Ltd. 2013
- Published: 25 February 2013
Mycobacterium smegmati s (Ms) is a nonpathogenic mycobacteria of rapid growth, which shares many characteristics with Mycobacterium tuberculosis (MTB), the major causative agent of tuberculosis. MTB has several cell wall glycolipids in common with Ms, which play an important role in the pathogenesis of tuberculosis and the induction of a protective immune response against MTB infection in some animal models. In this study, the humoral immune response and cross reactivity against MTB, of liposomes containing a mixture of cell wall glycolipids of Ms and commercial lipids was evaluated, in order to study its possible use as a component of a vaccine candidate against tuberculosis. Liposomes containing total lipids extracted from Ms, distearoyl phosphatidyl choline and cholesterol were prepared by the dehydration-rehydration technique. Balb/c mice were immunized with the liposomes obtained and the antibody response and cross reactivity against MTB were tested by ELISA. Total lipids extract from Ms showed the presence of several polar glycolipids in common with MTB, such as phosphatidylinositol mannosides. Liposomes that contained glycolipids of Ms were capable of inducing a specific IgG antibody response that allowed the recognition of surface antigens of MTB. The results of this study demonstrated the presence of immunogenic glycolipids in Ms, which could be included to enhance the protective effects of subunit vaccine formulations against tuberculosis.
- Total Lipid
- Humoral Immune Response
- Cross Reactivity
- Vaccine Candidate
- Mycobacterium Smegmatis
Tuberculosis (TB) is still one of the most lethal infectious diseases worldwide . The only TB vaccine available for human use is the bacille Calmette-Guerin (BCG), an attenuated strain of Mycobacterium bovis . However, this vaccine protects only against the most severe forms of the disease during childhood and their effectiveness has failed in the adult population. In recent years various glycolipids of the mycobacterial cell wall have become attractive candidates for a vaccine against TB because they constitute important virulence factors for initiating the establishment of infection by MTB . These glycolipids have been demonstrated to be capable of stimulating T lymphocytes through the presentation by CD1 molecules . In addition, mycobacterium lipids have been shown to induce protection in certain experimental animal models against infection by MTB [5, 6]. Some of these glycolipids are present in the cell wall of Mycobacterium smegmatis (Ms), a non-pathogenic mycobacteria of rapid growth, which has been used as a study model for TB. Liposomes prepared from glycolipids of Ms have also been reported to possess immunoadjuvant capacity . Hence, it is interesting to evaluate the use of cell wall glycolipids of Ms as potential vaccine candidates against TB. Therefore, this study aims to assess the humoral immune response and cross reactivity induced by immunization of mice with liposomes containing a mixture of Ms total lipids and commercial lipids against MTB cell wall antigens.
Total lipids from Ms mc2 155 were extracted according to the methodology proposed by Rosenkrands et al . Briefly, 30 mL of chloroform: methanol (2:1) was added to 10 g wet weight of biomass and mixed in a shaker overnight at room temperature. The chloroform phase and the extracted lipids were analyzed by one dimensional TLC. Liposomes were prepared according to the technical procedure of dehydration-rehydration . Lipid composition of liposomes was basically distearoyl phosphatidyl choline (Sigma) and cholesterol (Sigma) at a molar ratio 1:1. Ten mg of Ms total lipids was then added to this mixture. Balb/c mice between 8 to 12 weeks were used in this study. Mice were divided into 4 groups of 10 animals each and were immunized subcutaneously with the appropriate preparation obtained as described below. Two control groups were used: the negative control group received 0.1 mL of PBS and the positive control group recieved 5 x 106 CFU of M. bovis BCG Danish strain. Another group received 0.1 mL of a liposomal preparation formulated with commercial lipids (LipE) and a third group was inoculated with 0.1 mL of a liposomal preparation containing 1 mg of Ms total lipids and commercial lipids (LipMs). Groups inoculated with the liposome preparation (LipE and LipMs) received 3 doses administered 21 days apart from each other. The humoral immune response and cross reactivity against MTB was evaluated by indirect ELISA using Ms total lipid and subcellular fraction of MTB cell wall (CW), respectively.
In this study, we demonstrated that total lipids of Ms included in liposomes are able to induce humoral immune response in mice and posses cross-reactivity to MTB. These results support the strategy of employing Ms as a possible source of lipid antigens to be part of a vaccine candidate against TB.
This work was supported by the Ministry of Science, Technology and Innovation, Malaysia (10-01-05-MEB002) the Ministry of Higher Education, Malaysia LRGS Grant (203.PSK.6722001) and Ministry of Science and Technology, Cuba.
This article has been published as part of BMC Immunology Volume 14 Supplement 1, 2013: Proceedings from Delivery Systems and Current strategies to drug design. The full contents of the supplement are available online at http://0-www.biomedcentral.com.brum.beds.ac.uk/bmcimmunol/supplements/14/S1.
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