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1.
Vaccine ; 20(27-28): 3304-9, 2002 Sep 10.
Artigo em Inglês | MEDLINE | ID: mdl-12213400

RESUMO

Non-pathogenic lactic acid bacteria (LAB) are attractive as live carriers to deliver protective antigens to the mucosal immune system. Both persisting and non-persisting strains of lactic acid bacteria have been evaluated and seem to work equally well by the systemic and nasal routes of administration. However, it is not known if persistence and viability of the strain play a critical role when immunizing by the oral route. To address this question, recombinant LAB strains, able to persist (Lactobacillus plantarum NCIMB8826/pMEC127) or not (Lactococcus lactis MG1363/pMEC46) in the gastro-intestinal tract of mice and producing equivalent amounts of the tetanus toxin fragment C (TTFC) were compared to each other. A very strong ELISA TTFC-specific and protective humoral response was elicited by either live or UV-inactivated recombinant Lb. plantarum strains. In a similar protocol, recombinant Lc. lactis seemed to be somewhat less efficient than the former host. It is thus tempting to propose that the difference in the capacity of the bacterial vector to persist in the gastro-intestinal tract impacts on its immunogenicity and on the level of protection it may induce. Protection was slightly superior after administration of live strains.


Assuntos
Lactobacillus/genética , Lactobacillus/imunologia , Lactococcus lactis/genética , Lactococcus lactis/imunologia , Toxina Tetânica/imunologia , Toxina Tetânica/toxicidade , Toxoide Tetânico/administração & dosagem , Administração Oral , Animais , Anticorpos Antibacterianos/biossíntese , Antígenos de Bactérias/biossíntese , Antígenos de Bactérias/genética , Clostridium tetani/genética , Clostridium tetani/imunologia , Clostridium tetani/patogenicidade , Feminino , Imunidade nas Mucosas , Camundongos , Camundongos Endogâmicos C57BL , Fragmentos de Peptídeos/genética , Fragmentos de Peptídeos/imunologia , Tétano/imunologia , Tétano/prevenção & controle , Toxina Tetânica/genética , Toxoide Tetânico/genética , Toxoide Tetânico/imunologia , Vacinas Sintéticas/administração & dosagem , Vacinas Sintéticas/genética , Vacinas Sintéticas/imunologia
2.
Infect Immun ; 72(5): 2731-7, 2004 May.
Artigo em Inglês | MEDLINE | ID: mdl-15102782

RESUMO

The potential of recombinant lactic acid bacteria (LAB) to deliver heterologous antigens to the immune system and to induce protective immunity has been best demonstrated by using the C subunit of tetanus toxin (TTFC) as a model antigen. Two types of LAB carriers have mainly been used, Lactobacillus plantarum and Lactococcus lactis, which differ substantially in their abilities to resist passage through the stomach and to persist in the mouse gastrointestinal tract. Here we analyzed the effect of a deficiency in alanine racemase, an enzyme that participates in cell wall synthesis, in each of these bacterial carriers. Recombinant wild-type and mutant strains of L. plantarum NCIMB8826 and L. lactis MG1363 producing TTFC intracellularly were constructed and used in mouse immunization experiments. Remarkably, we observed that the two cell wall mutant strains were far more immunogenic than their wild-type counterparts when the intragastric route was used. However, intestinal TTFC-specific immunoglobulin A was induced only after immunization with the recombinant L. plantarum mutant strain. Moreover, the alanine racemase mutant of either LAB strain allowed induction of a much stronger serum TTFC-specific immune response after immunization via the vagina, which is a quite different ecosystem than the gastrointestinal tract. The design and use of these mutants thus resulted in a major improvement in the mucosal delivery of antigens exhibiting vaccine properties.


Assuntos
Antígenos/administração & dosagem , Lactobacillus/genética , Lactobacillus/imunologia , Lactococcus lactis/genética , Lactococcus lactis/imunologia , Administração Intravaginal , Animais , Anticorpos Antibacterianos/sangue , Antígenos/genética , Parede Celular/genética , Parede Celular/imunologia , Feminino , Mucosa Gástrica/imunologia , Imunidade nas Mucosas , Imunização , Camundongos , Camundongos Endogâmicos C57BL , Fragmentos de Peptídeos/administração & dosagem , Fragmentos de Peptídeos/genética , Fragmentos de Peptídeos/imunologia , Proteínas Recombinantes/administração & dosagem , Proteínas Recombinantes/genética , Proteínas Recombinantes/imunologia , Recombinação Genética , Toxina Tetânica/administração & dosagem , Toxina Tetânica/genética , Toxina Tetânica/imunologia
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