TY - JOUR
T1 - Galactomannan from Caesalpinia spinosa induces phenotypic and functional maturation of human dendritic cells
AU - Santander, S. P.
AU - Aoki, M.
AU - Hernandez, J. F.
AU - Pombo, M.
AU - Moins-Teisserenc, H.
AU - Mooney, N.
AU - Fiorentino, S.
N1 - Funding Information:
Financial support was provided by the Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnología “Francisco Jose de Caldas” (COLCIENCIAS) Bogotá, Colombia . Grant number 324-2007 Cod 1203408204 (S. Fiorentino). M.A. was a postdoctoral fellow funded by Fondation de France . S.P.S. and J.F.H. are PhD student funded by COLCIENCIAS.
PY - 2011/6
Y1 - 2011/6
N2 - Plant polysaccharides present an interesting potential as immunomodulators, particularly in the induction of antitumoral responses, principally because of their molecular complexity and low in vivo toxicity. Activation of dendritic cells (DCs) could improve antitumoral responses usually diminished in cancer patients, and natural adjuvants provide a possibility of inducing this activation. Herein, we investigated the immunomodulatory activity of a neutral plant polysaccharide Galactomannan on human monocyte-derived DCs (MDDC). MDDCs were stimulated with Galactomannan (GLM) from Caesalpinia spinosa and both phenotypic and functional activities were assessed by flow cytometry and real-time PCR. The phagocytic ability of MDDCs was determined by using E-coli pHrodo particles and induction of T-lymphocyte allostimulation was determined after T-cell staining with carboxyfluorescein succinimidyl ester (CFSE). In MDDCs, purified Galactomannan induced phenotypic maturation revealed by increased expression of CD83, CD86, CD206, and HLA-DR. Functional experiments showed the loss of particulate antigen uptake in Galactomannan-stimulated DCs and increased alloantigen presentation capacity. Finally, Galactomannan increased protein and mRNA levels of pro-inflammatory cytokines including IL-1β, IL-6, IL-8, IL-12p70, and TNF-α. These data reveal that Galactomannan obtained from Caesalpinia spinosa promotes effective activation of MDDCs. This adjuvant-like activity may have therapeutic applications in clinical settings where immune responses need boosting.
AB - Plant polysaccharides present an interesting potential as immunomodulators, particularly in the induction of antitumoral responses, principally because of their molecular complexity and low in vivo toxicity. Activation of dendritic cells (DCs) could improve antitumoral responses usually diminished in cancer patients, and natural adjuvants provide a possibility of inducing this activation. Herein, we investigated the immunomodulatory activity of a neutral plant polysaccharide Galactomannan on human monocyte-derived DCs (MDDC). MDDCs were stimulated with Galactomannan (GLM) from Caesalpinia spinosa and both phenotypic and functional activities were assessed by flow cytometry and real-time PCR. The phagocytic ability of MDDCs was determined by using E-coli pHrodo particles and induction of T-lymphocyte allostimulation was determined after T-cell staining with carboxyfluorescein succinimidyl ester (CFSE). In MDDCs, purified Galactomannan induced phenotypic maturation revealed by increased expression of CD83, CD86, CD206, and HLA-DR. Functional experiments showed the loss of particulate antigen uptake in Galactomannan-stimulated DCs and increased alloantigen presentation capacity. Finally, Galactomannan increased protein and mRNA levels of pro-inflammatory cytokines including IL-1β, IL-6, IL-8, IL-12p70, and TNF-α. These data reveal that Galactomannan obtained from Caesalpinia spinosa promotes effective activation of MDDCs. This adjuvant-like activity may have therapeutic applications in clinical settings where immune responses need boosting.
KW - Caesalpinia spinosa
KW - Dendritic cells
KW - Galactomannan
KW - Gene expression
KW - Immunomodulation
KW - Polysaccharide
UR - http://www.scopus.com/inward/record.url?scp=79955793026&partnerID=8YFLogxK
U2 - 10.1016/j.intimp.2011.01.006
DO - 10.1016/j.intimp.2011.01.006
M3 - Article
C2 - 21255695
AN - SCOPUS:79955793026
SN - 1567-5769
VL - 11
SP - 652
EP - 660
JO - International Immunopharmacology
JF - International Immunopharmacology
IS - 6
ER -