immunology of infectious and parasitic diseases - XXXVII Congress ...
immunology of infectious and parasitic diseases - XXXVII Congress ...
immunology of infectious and parasitic diseases - XXXVII Congress ...
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SMTEG IMMUNIZATION WITHOUT AJUVANTS INDUCES A MODULATORY<br />
IMMUNE RESPONSE IN MICE.<br />
CLARICE CARVALHO ALVES 1 ; JULIANO MICHEL ARAUJO 1 ; TATIANE<br />
TEIXEIRA DE MELO 1 ; ISABELA CAMPOS DE SENA 1 ; NEUSA ARAUJO 1 ;<br />
FERNANDA DO VALLE DURÃES 2 ; DEBORAH LARANJEIRA FERREIRA<br />
PIMENTA 1 ; SERGIO COSTA OLIVEIRA 2 ; CRISTINA TOSCANO FONSECA 1,3 .<br />
1 Centro de Pesquisas René Rachou, Fiocruz-MG, Belo Horizonte, Minas<br />
Gerais, Brazil; 2 Departamento de Bioquímica e imunologia, Instituto de Ciências<br />
Biológicas, Univesidade Federal de Minas Gerais, Belo Horizonte, Minas<br />
Gerais, Brazil; 3 Instituto Nacional de Ciências e Tecnologia em Doenças<br />
Tropicais (INCT-DT), Brazil.<br />
Introduction: Vaccine development is essential to control schistosomiasis<br />
since chemotherapy does not prevent reinfections. The S. mansoni<br />
schistosomula tegument (Smteg) is an interesting parasite structure to be used<br />
in a vaccine formulation against schistosomiasis, since it is a dynamic hostinteractive<br />
layer. We have recently demonstrated that Smteg is able to activate<br />
innate immune response <strong>and</strong> to induce protective immunity reducing parasite<br />
burden, egg elimination <strong>and</strong> disease morbidity in a vaccine formulation with<br />
Freunds adjuvant. In this work, we evaluated the immunological response<br />
trigged by Smteg immunization in the absence <strong>of</strong> adjuvant <strong>and</strong> its ability to elicit<br />
protection against S. mansoni challenge infection. Methods <strong>and</strong> Results:<br />
Female C57BL/6 mice were immunized subcutaneously with three doses <strong>of</strong><br />
Smteg (25µg) or saline (control group) in a 15 day-interval regimen. Thirty days<br />
after the last boost, mice were challenged through percutaneous exposure <strong>of</strong><br />
abdominal skin. Fifty days after challenge, adult worms were perfused from the<br />
portal system <strong>and</strong> the protection level was calculated. Unexpectedly,<br />
immunization failed to induce protection in mice. To evaluate humoral immune<br />
response, blood samples were collected from retro orbital sinus <strong>of</strong> each mouse<br />
with an interval <strong>of</strong> 15 days beginning 15 days after the first immunization for<br />
measurement <strong>of</strong> specific anti-Smteg antibodies. Immunization with Smteg lead<br />
to production <strong>of</strong> specific IgG antibodies indicating that immunization was able to<br />
activate immune response. Cytokines production (IL-4, IL-10, TNF-a, IFN-g)<br />
was assessed by splenocytes culture <strong>and</strong> intracellular staining ten days after<br />
the last immunization. An increased percentage <strong>of</strong> CD4+IFN-g+ (p