ICMI 2015

T.99 Aedes aegypti Salivary Gland Extract as Important Novel Therapeutic Option for Experimental Colitis

Thursday, July 16, 2015
Grand Hall and Gallery, Ground Floor & 1st Floor (Maritim Hotel)
Helioswilton Campos , University of Sao Paulo, Uberaba, MG, Brazil
Paulo José Basso , School of Medicine of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
Giuliano Bonfa, PhD , Department of Biochemistry and Immunology School of Medicine of Ribeirão Preto, Ribeirao Preto, Brazil
Viviani Nardini , School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
Anderson Daniel Ramos, PhD , Departamento de Bioquímica e Imunologia - Universidade de São Paulo, São Paulo, São Paulo, Brazil – USP, Sao Paulo, Brazil
Anderson Sá-Nunes, PhD , Departamento de Bioquímica e Imunologia - Universidade de São Paulo, São Paulo, São Paulo, Brazil – USP, Sao Paulo, Brazil
Cristina Cardoso, PhD , School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
Current therapies for inflammatory bowel disease (IBD) are not totally effective, resulting in continued disease burden for many patients.  Mosquito saliva contains immunomodulatory molecules and therein could represent a novel therapy for IBD. To investigate the impact of Aedes aegypti salivary gland extract (SGE) on an experimental model of IBD, C57BL/6 male mice were exposed to 3% DSS in drinking water for 6 days and concurrently treated with SGE or PBS. On the 6th day, spleens and mesenteric lymph nodes (MLN) were harvested. Cytokine production and leukocytes profiles were assessed using flow cytometry. SGE treatment resulted in improved clinical disease outcome and postmortem scores. Within both the spleen and MLN, frequency of CD3-CD49b+ cells was reduced. In the MLN, frequency of CD4+CD25+ cells was increased. Cultured CD4+ cells from spleen and MLN of SGE-treated mice produced lower levels of IFN-γ, IL17, and IL4, when compared to CD4+ cells from PBS-treated mice (Fig. 3). These results indicate that SGE could be a source of immunomodulatory molecules with promising therapeutic activity for IBD.