TY - JOUR
T1 - Early Induction of Human Regulatory Dermal Antigen Presenting Cells by Skin-Penetrating Schistosoma Mansoni Cercariae
AU - Winkel, Béatrice M F
AU - Dalenberg, Mirjam R
AU - de Korne, Clarize M
AU - Feijt, Carola
AU - Langenberg, Marijke C C
AU - Pelgrom, Leonard
AU - Ganesh, Munisha S
AU - Yazdanbakhsh, Maria
AU - Smits, Hermelijn Helene
AU - de Jong, Esther C
AU - Everts, Bart
AU - van Leeuwen, Fijs W B
AU - Hokke, Cornelis H
AU - Roestenberg, Meta
N1 - Publisher Copyright:
© 2018 Frontiers Media S.A. All rights reserved.
PY - 2018
Y1 - 2018
N2 - Following initial invasion of Schistosoma mansoni cercariae, schistosomula reside in the skin for several days during which they can interact with the dermal immune system. While murine experiments have indicated that exposure to radiation-attenuated (RA) cercariae can generate protective immunity which is initiated in the skin stage, contrasting non-attenuated cercariae, such data is missing for the human model. Since murine skin does not form a reliable marker for immune responses in human skin, we used human skin explants to study the interaction with non-attenuated and RA cercariae with dermal innate antigen presenting cells (APCs) and the subsequent immunological responses.We exposed human skin explants to cercariae and visualized their invasion in real time (initial 30min) using novel imaging technologies. Subsequently, we studied dermal immune responses and found an enhanced production of regulatory cytokine interleukin (IL)-10, pro-inflammatory cytokine IL-6 and macrophage inflammatory protein (MIP)-1a within 3 days of exposure. Analysis of dermal dendritic cells (DDCs) for their phenotype revealed an increased expression of immune modulators programmed death ligand (PD-L) 1 and 2, and increased IL-10 production. Ex vivo primed DDCs suppress Th1 polarization of naïve T-cells and increase T-cell IL-10 production, indicating their regulatory potential. These immune responses were absent or decreased after exposure to RA parasites. Using transwells, we show that direct contact between APCs and cercariae is required to induce their regulatory phenotype. To the best of our knowledge this is the first study that attempts to provide insight in the human dermal S. mansoni cercariae invasion and subsequent immune responses comparing non-attenuated with RA parasites. We reveal that cercariae induce a predominantly regulatory immune response whereas RA cercariae fail to achieve this. This initial understanding of the dermal immune suppressive capacity of S. mansoni cercariae in humans provides a first step toward the development of an effective schistosome vaccine.
AB - Following initial invasion of Schistosoma mansoni cercariae, schistosomula reside in the skin for several days during which they can interact with the dermal immune system. While murine experiments have indicated that exposure to radiation-attenuated (RA) cercariae can generate protective immunity which is initiated in the skin stage, contrasting non-attenuated cercariae, such data is missing for the human model. Since murine skin does not form a reliable marker for immune responses in human skin, we used human skin explants to study the interaction with non-attenuated and RA cercariae with dermal innate antigen presenting cells (APCs) and the subsequent immunological responses.We exposed human skin explants to cercariae and visualized their invasion in real time (initial 30min) using novel imaging technologies. Subsequently, we studied dermal immune responses and found an enhanced production of regulatory cytokine interleukin (IL)-10, pro-inflammatory cytokine IL-6 and macrophage inflammatory protein (MIP)-1a within 3 days of exposure. Analysis of dermal dendritic cells (DDCs) for their phenotype revealed an increased expression of immune modulators programmed death ligand (PD-L) 1 and 2, and increased IL-10 production. Ex vivo primed DDCs suppress Th1 polarization of naïve T-cells and increase T-cell IL-10 production, indicating their regulatory potential. These immune responses were absent or decreased after exposure to RA parasites. Using transwells, we show that direct contact between APCs and cercariae is required to induce their regulatory phenotype. To the best of our knowledge this is the first study that attempts to provide insight in the human dermal S. mansoni cercariae invasion and subsequent immune responses comparing non-attenuated with RA parasites. We reveal that cercariae induce a predominantly regulatory immune response whereas RA cercariae fail to achieve this. This initial understanding of the dermal immune suppressive capacity of S. mansoni cercariae in humans provides a first step toward the development of an effective schistosome vaccine.
KW - Animals
KW - Antigen-Presenting Cells/immunology
KW - Apoptosis Regulatory Proteins/immunology
KW - Cell Line
KW - Cercaria/immunology
KW - Coculture Techniques/methods
KW - Humans
KW - Interleukin-10/immunology
KW - Interleukin-6/immunology
KW - Macrophage Inflammatory Proteins/immunology
KW - Schistosoma mansoni/immunology
KW - Schistosomiasis mansoni/immunology
KW - Skin/immunology
U2 - 10.3389/fimmu.2018.02510
DO - 10.3389/fimmu.2018.02510
M3 - Article
C2 - 30429854
SN - 1664-3224
VL - 9
SP - 2510
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 2510
ER -