• No results found

Molecular interplay between dendritic cells and schistosomes : consequences for immune polarization Everts, B.

N/A
N/A
Protected

Academic year: 2021

Share "Molecular interplay between dendritic cells and schistosomes : consequences for immune polarization Everts, B."

Copied!
9
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

Molecular interplay between dendritic cells and

schistosomes : consequences for immune polarization

Everts, B.

Citation

Everts, B. (2010, April 13). Molecular interplay between dendritic cells and schistosomes : consequences for immune polarization. Retrieved from https://hdl.handle.net/1887/15222

Version: Corrected Publisher’s Version

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden

Downloaded from: https://hdl.handle.net/1887/15222

Note: To cite this publication please use the final published version (if

applicable).

(2)

Molecular interplay between dendritic cells and schistosomes:

consequences for immune polarization

(3)
(4)

Molecular interplay between dendritic cells and schistosomes:

consequences for immune polarization

Proefschrift

ter verkrijging van de graad Doctor aan de Universiteit Leiden, op gezag van de Rector Magnificus Prof. Mr. P.F. van der Heijden,

volgens besluit van het College voor Promoties te verdedigen op dinsdag 13 april 2010

klokke 16.15 uur door

Bart Everts

geboren te Naarden in 1981

(5)

Promotiecommissie

Promotor: Prof. Dr. M. Yazdanbakhsh

Copromotores: Dr. C.H. Hokke Dr. H.H. Smits

Overige Leden: Prof. Dr. T.B.H. Geijtenbeek (AMC, Amsterdam) Dr. H. Haas (Research Center Borstel, Duitsland) Dr. E.C. de Jong (AMC, Amsterdam)

Prof. Dr. F. Koning Prof. Dr. C. van Kooten

Dr. E.J. Pearce (Trudeau Institute, VS)

Cover: scanning electronmicroscopy photos of paired adult male and female S. mansoni worms (in red on front cover), a dendritic cell (in lilac/blue on front and back cover) and T lymphocytes (in lilac/blue on back cover). Design by B. Everts

Financial support for the publication of this thesis was kindly provided by the Jurriaanse Stichting

Corning BD Biosciences

Printed by Ipskamp Drukkers ISBN: 978-90-9025206-3

2010 B. Everts

(6)

‘I have no special talent.

I am only passionately curious’

Albert Einstein

(7)
(8)

Content

Chapter 1 General Introduction 9

Chapter 2 Functional impairment of human myeloid dendritic cells 39 during Schistosoma haematobium infection

Chapter 3 Combined TLR2 and TLR4 ligation in the context of bacterial 59 or helminth extracts in human monocyte-derived dendritic cells:

molecular correlates for Th1/Th2 polarization

Chapter 4 Omega-1, a glycoprotein secreted by Schistosoma mansoni 79 eggs, drives Th2 responses.

Chapter 5 The molecular mechanisms underlying Th2 polarisation by 99 schistosome egg-derived omega-1: the mannose receptor

and protein synthesis inhibition

Chapter 6 General discussion 131

Nederlandse samenvatting voor niet ingewijden 143

Dankwoord 149

Curriculum vitae 153

Publication list 157

(9)

Referenties

GERELATEERDE DOCUMENTEN

While helminth infections are the most potent natural inducers of Th2 responses in which host-derived inflammatory mediators, as described above, can play a role, they are also

We found that plasmacytoid (pDCs) and myeloid DC (mDCs) from infected subjects were present at lower frequencies in peripheral blood and that mDCs displayed lower expression levels

To study the molecular characteristics of DCs exposed to compounds that engage TLR2 and 4, yet lead to differential skewing of immune responses in terms of Th1 and Th2

In order to improve efficiency and increase complexity, in Chapter 6 an enhanced HTS platform system combined with the orthogonal double gradient surface was developed to

Adequate picscntation and ccll suiiacc cxpiession of foieign minoi histocompatibility antigens (mHag) to allogcneie Τ cells tan lead to gialt veisus host disease (GvHD) aftei HI

To analyze whether the conjugates SLP-Pam and MDP-SLP have retained their ability to trigger TLR2 and NOD2, respectively, HEK293 cells transfected with either human TLR2 ( Figure 3

FIGURE 4 Tryptophan fluorescence measurements on (a) wild-type, (b) W64F mutant, and (c) W104F mutant of the AppA BLUF domain at 280 nm excitation in dark (solid lines) and

The discussion in Section 7.1 shows that it appears possible to develop an abstract concept such as energy conservation while embedding the learning process