• No results found

Immunotherapy of melanoma : toward clinical application Jorritsma-Smit, A.

N/A
N/A
Protected

Academic year: 2021

Share "Immunotherapy of melanoma : toward clinical application Jorritsma-Smit, A."

Copied!
9
0
0

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

Hele tekst

(1)

Citation

Jorritsma-Smit, A. (2008, September 4). Immunotherapy of melanoma : toward clinical application. Retrieved from https://hdl.handle.net/1887/13085

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/1887/13085

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

(2)

Immunotherapy of melanoma:

towards clinical application

(3)
(4)

Immunotherapy of melanoma:

towards clinical application

Proefschrift

ter verkrijging van

de graad van Doctor aan de Universiteit Leiden,

op gezag van Rector Magnificus prof.mr. P.F. van der Heijden,

volgens besluit van het College voor Promoties

te verdedigen op donderdag 4 september 2008

klokke 13.45 uur

door

Annelies Jorritsma-Smit

geboren te Groningen

in 1977

(5)

Referent: Prof. Dr. M. Theobald (Universiteit van Utrecht)

Overige leden: Prof. E.A.J.M. Goulmy

Prof. C. Melief

Prof. W.E. Fibbe

Dr. B. Nuijen (NKI-AvL/Slotervaart Ziekenhuis)

(6)

Voor mijn ouders, voor Rutger & Doeke

(7)

The studies described in this thesis were performed at the Department of Immunology at the Netherlands Cancer Institute (NKI), Amsterdam.

This study was financially supported by the Dutch Cancer Society (KWF grant 2001-2417) and by ZonMW grant 4310005 .

The printing of this thesis was financially supported by the J.E. Jurriaanse Stichting and the Dutch Cancer Society.

The cover photo was taken at the National Pharmaceutical Museum in Gouda, the Netherlands, by Rutger Smit.

(8)

Contents

Chapter 1: Introduction 9

Chapter 2: A rapid and potent DNA vaccination strategy defined by in vivo 19 monitoring of antigen expression.

Nature Med. 2005;11(8):899-904

Chapter 3: Skewing the T-cell repertoire by combined DNA vaccination, 27 host conditioning, and adoptive transfer.

Cancer Res. 2008;68:2455-2462

Chapter 4: Human telomerase reverse transcriptase-transduced human 37 cytotoxic T cells suppress the growth of human melanoma in

immunodeficient mice.

Cancer Res. 2004 Mar 15;64(6):2153-61.

Chapter 5: Requirements for effective anti-tumor responses of TCR 49

transduced T cells

Submitted for publication

Chapter 6: Selecting highly affine and well-expressed TCRs for gene 69

therapy of melanoma.

Blood 2007;110:3564-3572

Chapter 7: Discussion 81

Summary 99

Nederlandse samenvatting 101

Curriculum Vitae 105

List of publications 107

(9)

Referenties

GERELATEERDE DOCUMENTEN

Peripheral blood cells were stained with HLA-A2.1 tetramers containing the tyrosinase368–376 peptide followed by staining with a panel of lineage antibodies, as described in

Blades and blade fragments seem to have been especially used for longitudinal motions, mainly on plant material (7/12). Flake and flake fragments are used in different motions on

This shape also occurs in the combination artefacts (see below). The shape is the result of intensive use in a repetitive abrasive motion, carried out from different angles. In

Since expression of Serpins may facilitate the immune escape of HLA positive tumors, we next analysed the effect of Serpin expression on survival in cases with normal/partial

Adoptive T cell therapy using antigen-specific CD8+ T cell clones for the treatment of patients with metastatic melanoma: in vivo persistence, migration, and antitumor effect

De behandeling van patiënten met genetisch gemodificeerde T-cellen heeft bovendien de meeste kans van slagen wanneer een TCR gebruikt wordt met een sterke herkenning van

Deze cellen zijn echter niet in staat gedurende langere tijd aanwezig te blijven, waardoor ook het antitumoreffect transient van aard is.. Een lage transductie-efficiëntie zal

Detection of amyloid plaques in mouse models of Alzheimer’s disease by magnetic resonance imaging.. Apostolova