CIBICI   14215
CENTRO DE INVESTIGACION EN BIOQUIMICA CLINICA E INMUNOLOGIA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
ANALYSIS OF CELLS INVOLVED IN GERMINAL CENTER REACTION DURING Trypanosoma cruzi INFECTION.
Autor/es:
ALMADA L; GRUPPI A; MONTES CL; GAZZONI Y; ACOSTA RODRIGUEZ EV
Lugar:
Tucuman
Reunión:
Congreso; LXVII reunión anual de la Sociedad Argentina de Inmunología.; 2019
Institución organizadora:
Sociedad Argentina de Inmunología
Resumen:
ANALYSIS OF CELLS INVOLVED IN GERMINAL CENTER REACTION DURING Trypanosoma cruzi INFECTIONYamila Gazzoni1, Laura Almada1, Carolina L Montes1, Eva V Acosta-Rodriguez1, Adriana Gruppi1.1 Centro de Investigaciones en Bioquímica Clínica e Inmunología (CIBICI)-CONICET, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, X5000HUA, Córdoba, Argentina.Germinal Centers (GCs) are micro-anatomical structures that emerge within secondary lymphoid organs in response to T cell-dependent antigens. Within GCs, B cells can differentiate into antibody-secreting cells (ASC) and memory B cells. Follicular helper T cells (Tfh) are instrumental in supporting Antibody (Ab) affinity maturation and humoral memory. Other GC protagonists are follicular cytotoxic T cells (Tfc) whose function is not well established. We aimed to study the response of the different cell subsets involved in GC reaction during T. cruzi infection. For that, C57BL/6 mice were intraperitoneally infected with 5.000 trypomastigotes (Tulahuén strain); and the frequency and number of the different populations in the spleen and lymph nodes were evaluated by flow cytometry at different days post infection. Mice injected with PBS were evaluated as controls. We observed that the peak of Tfh (CD4+CD8-B220-CXCR5+ICOS+PD-1+), Tfc (CD8+CD4-B220-CXCR5+PD-1+ICOS+) and ASC (B220loCD138+) response preceded the peak of GCs-B cells (B220+FAS+GL-7+Bcl-6+). Additionally, considering that IL-17A is a regulator of B cell trafficking in the GC and its biological effect is mediated by IL-17RA we also evaluated the expression of this receptor on CG-B cells, Tfh and Tfc. We observed that IL-17RA expression was higher in CG-B cells than in other B cell subsets (naïve, follicular and ASC) (p