INVESTIGADORES
MORON Victor Gabriel
congresos y reuniones científicas
Título:
NEUTROPHILS RECRUITMENT IMPACT ON T CELL RESPONSE IN LYMPH NODES
Autor/es:
SOFÍA CASTELL; FLORENCIA HARMAN; CAROLINA GORLINO; G MORON; BELKYS A. MALETTO; MARÍA C. PISTORESI-PALENCIA
Lugar:
Mar del Plata
Reunión:
Congreso; LXII Reunión de la Sociedad Argentina de Inmunología. Mar del Plata; 2014
Institución organizadora:
Sociedad Argentina de Inmunología
Resumen:
Previously we demonstrated that when mice
were immunized with OVA emulsified in Freund?s complete adjuvant (OVA/CFA) at
days 0, 15, 30, and ten days after the last immunization were injected with OVA-FITC
in the footpad, the main OVA-FITC+ cells recruited in draining popliteal lymph
nodes were neutrophils, this influx was dependent on an antigen-specific
response (Maletto et al, Blood, 2006; Gorlino et al, Journal of Immunology,
2014). In order to reduce CFA potentially harmful effects, in the present study
we performed only two immunizations, for this, mice were immunized with OVA/CFA
and 15 days after boosted with OVA/IFA; IFA is Freund?s adjuvant incomplete form
that lacks the mycobacterial components. Ten days after the last immunization,
mice were injected with OVA-FITC in the footpad and we still found neutrophils
migration in draining popliteal lymph nodes (p<0.05). Next we evaluated
whether neutrophils recruitment impact in T cell response. We analyzed CD25 and
CD69 molecules in T lymphocytes of draining popliteal lymph nodes compared with
the not draining. Interestingly, we observed that in presence of neutrophils, T
cells upregulate those activation markers (p<0,001). Cytokines levels were measured in culture
supernatants of popliteal lymph nodes cells after 72h of OVA stimulation.
Importantly, higher levels of IL-17 were found in draining popliteal lymph
nodes compared to not draining (p<0.05). In conclusion, these results
suggest that in the less harmful model of immunization we also found neutrophil
recruitment in draining popliteal lymph nodes and these cells could be modulating the T cell response.