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Featured researches published by Nicole Cillien.


European Journal of Obstetrics & Gynecology and Reproductive Biology | 1993

The relationship between urinary Tamm-Horsfall glycoprotein excretion and urinary activity of glycosidases in normal pregnancy and pre-eclampsia

Thomas Nesselhut; W. Rath; Elke Grunow; Gesa Kaufholz; Ursula Ostermai; Nicole Cillien; W. Kuhn

Electrophoretic analyses of the urinary proteins of pre-eclamptic patients revealed a decrease in the staining intensity of the protein band representing the Tamm-Horsfall glycoprotein (THP). In the present study the quantitative analysis of the THP excretion rate and the urinary activity of THP oligosaccharide metabolizing glycosidases were investigated. The median THP excretion rate of non-pregnant women (n = 24) was 20 mg/g creatinine (crea.). An increase in the THP excretion rate was seen in pregnancy to a level between 43 mg/g crea. (II. trimester) and 32 mg/g crea. (III. trimester) (n = 29). Hypertension in pregnancy was associated with a decrease in the THP excretion rate to 9 mg/g crea. (n = 85). Post partum, a transient elevated THP excretion rate up to 109 mg/g crea was recorded in the group of hypertensive patients. The urinary activities of the lysosomal beta-mannosidase, alpha-fucosidase, alpha-mannosidase (pH 4.5) and beta-galactosidase increased in normal pregnancy. This effect was most pronounced in the beta-galactosidase activity which increased from 50 U/mg crea. before pregnancy to 280 U/mg crea. at term. Hypertension in pregnancy was associated with a further increase in the activities of the lysosomal glycosidases. In the case of the beta-galactosidase a significant rise from 68 to 310 U/mg crea. was found. The urinary activity of the alpha-mannosidase (pH 5.5) originating from the Golgi apparatus was only elevated in patients with severe pre-eclampsia. Casuistic post partum recordings demonstrated that an elevation of the lysosomal glycosidases activities was followed by a transient increase in the THP excretion rate.


Journal of Clinical Oncology | 2010

Immunotherapy with dendritic cells as a second-line therapy in advanced pleural mesothelioma.

Jan Nesselhut; D. Marx; Raymond Y. Chang; D. Lorenzen; Nicole Cillien; W. Goebel; F. Fändrich; Thomas Nesselhut

e13063 Background: Malignant pleural mesothelioma (MPM) is an aggressive disease with an unfavorable prognosis. The current front-line treatment for nonoperable stages is cisplatinum in combination with pemetrexed chemotherapy. The reported median overall survival times are less than 15 months. After failure of first-line therapy there is currently no proven effective therapy, whereas potential side effects from further treatments may impair quality of life. In those cases, we report that immunotherapy with monocyte-derived dendritic cells (MoDC) can be effective without significant impact on life quality. Methods: After isolating monocytes from peripheral blood of n=14 patients with stage 4 MPM who failed first-line chemotherapy, MoDC were generated using standard protocols. The MoDC were primed on day 5 with tumor-lysate and co-cultured with toll-like receptor ligands to induce a TH1-polarization of the MoDC. In one case, an allogeneic cell line lysed by the oncolytic Newcastle disease virus (NDV) was u...


Journal of Clinical Oncology | 2016

Systemic treatment with anti-PD-1 antibody nivolumab in combination with vaccine therapy in advanced pancreatic cancer.

Jan Nesselhut; D. Marx; Hans Lange; Gonçalo Regalo; Nicole Cillien; Raymond Y. Chang; Thomas Nesselhut


Journal of Clinical Oncology | 2004

Cancer therapy with unloaded monocyte-derived dendritic cells in patients with inoperable pancreatic and gall bladder cancer

Thomas Nesselhut; Raymond Y. Chang; C. Matthes; D. Marx; D. Lorenzen; Nicole Cillien; Michael Gary Martin; R. Gorter; J. H. Peters


Journal of Clinical Oncology | 2005

Cancer therapy with immature monocyte-derived dendritic cells in patients with advanced breast cancer

Thomas Nesselhut; C. Matthes; D. Marx; Raymond Y. Chang; J. Nesselhut; Nicole Cillien; D. Lorenzen; R. Gorter; W. Stucker; J. H. Peters


Journal of Clinical Oncology | 2011

Improvement of dendritic cell therapy in glioblastoma multiforme WHO 4 by Newcastle disease virus.

Jan Nesselhut; D. Marx; D. Lorenzen; Nicole Cillien; W. Goebel; Raymond Y. Chang; W. Brockmann; J. H. Peters; K. Nesselhut; F. Fändrich; Thomas Nesselhut


Journal of Clinical Oncology | 2017

Comparison of early versus late onset of cellular immunotherapy in glioblastoma multiforme WHO IV.

Jan Nesselhut; D. Marx; Nicole Cillien; Raymond Y. Chang; Wulf-Peter Brockmann; Michael Gary Martin; Thomas Nesselhut


Journal of Clinical Oncology | 2017

γδ T cells in combination with Newcastle disease virus and dendritic cell therapy as a novel immunotherapeutic approach in treating of advanced lung cancer.

Jan Nesselhut; D. Marx; Michael Herrmann; Nicole Cillien; Raymond Y. Chang; Thomas Nesselhut


Journal of Clinical Oncology | 2017

Dendritic cells generated with PDL-1 checkpoint blockade for treatment of advanced pancreatic cancer.

Jan Nesselhut; D. Marx; Nicole Cillien; Hans Lange; Gonçalo Regalo; Michael Herrmann; Timo Hupfeld; Raymond Y. Chang; Thomas Nesselhut


Journal of Clinical Oncology | 2013

NfP2X7, a novel target for immune therapeutic approaches in cancer treatment.

Jan Nesselhut; Julian Barden; D. Marx; Nicole Cillien; Wiebke Goebel; Michael Herrmann; Raymond Y. Chang; Thomas Nesselhut

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Elke Grunow

University of Göttingen

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Gesa Kaufholz

University of Göttingen

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W. Kuhn

University of Göttingen

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W. Rath

University of Göttingen

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