Literature DB >> 20467733

Pharmacokinetics of natural mistletoe lectins after subcutaneous injection.

Roman Huber1, Jürgen Eisenbraun, Barbara Miletzki, Michael Adler, Rainer Scheer, Reinhild Klein, Christoph H Gleiter.   

Abstract

PURPOSE: Knowledge of natural mistletoe lectins (nML) pharmacokinetics can be regarded as essential for further rational studies with mistletoe preparations. Studies with intravenous application of a recombinant type II ribosome inactivating protein (rML) analogous to nML revealed a short half-life of about 13 min in cancer patients. This open-label, phase I, monocenter clinical trial was performed in order to describe the pharmacokinetics of nML.
METHODS: In 15 healthy male volunteers aged 18-42 years, nML were detected with a modified sandwich immuno-polymerase chain reaction (PCR) technique (Imperacer, Chimera Biotec) after single subcutaneous injection of a mistletoe extract (abnobaVISCUM(R) Fraxini 20 mg) with marketing authorization containing about 20 microg nML/ml. Secondary objectives were safety and the number of activated natural killer cells (CD54(+)/CD94(+)).
RESULTS: In none of the volunteers were nML detectable before the injection, and in all volunteers, nML were detected in serum samples after injection. Individual variability, however, was large. Mean and median peak concentrations were reached 1 and 2 h after injection, respectively. In some volunteers, nML were still detectable at the final investigation 2 weeks after injection. The injection resulted in fever and flu-like symptoms in all volunteers, but no serious adverse events occurred. All symptoms and local reactions at the injection site completely disappeared within a range of 4-95 days. The number of activated natural killer (NK) cells did not change.
CONCLUSIONS: Natural ML from abnobaVISCUM Fraxini 20 mg are detectable in serum after a single subcutaneous injection. Detectability is considerably longer compared with intravenously administered rML. The subcutaneous injection of this preparation without usual pretreatment with lower doses results in short-lasting fever and other flu-like symptoms.

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Year:  2010        PMID: 20467733     DOI: 10.1007/s00228-010-0830-5

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  17 in total

1.  Biological effects of natural and recombinant mistletoe lectin and an aqueous mistletoe extract on human monocytes and lymphocytes in vitro.

Authors:  U Elsässer-Beile; M Voss; R Schühle; U Wetterauer
Journal:  J Clin Lab Anal       Date:  2000       Impact factor: 2.352

2.  In vivo-induction of antibodies to mistletoe lectin-1 and viscotoxin by exposure to aqueous mistletoe extracts: a randomised double-blinded placebo controlled phase I study in healthy individuals.

Authors:  R Klein; K Classen; P A Berg; R Lüdtke; M Werner; R Huber
Journal:  Eur J Med Res       Date:  2002-04-30       Impact factor: 2.175

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Review 4.  Ribosome-inactivating proteins from plants: present status and future prospects.

Authors:  F Stirpe; L Barbieri; M G Battelli; M Soria; D A Lappi
Journal:  Biotechnology (N Y)       Date:  1992-04

5.  Anticancer activity of a lectin-rich mistletoe extract injected intratumorally into human pancreatic cancer xenografts.

Authors:  M Rostock; R Huber; T Greiner; P Fritz; R Scheer; J Schueler; H H Fiebig
Journal:  Anticancer Res       Date:  2005 May-Jun       Impact factor: 2.480

6.  Mistletoe treatment induces GM-CSF- and IL-5 production by PBMC and increases blood granulocyte- and eosinophil counts: a placebo controlled randomized study in healthy subjects.

Authors:  Roman Huber; M Rostock; R Goedl; R Lüdtke; K Urech; S Buck; R Klein
Journal:  Eur J Med Res       Date:  2005-10-18       Impact factor: 2.175

7.  Characterization of recombinant and plant-derived mistletoe lectin and their B-chains.

Authors:  J Eck; M Langer; B Möckel; K Witthohn; H Zinke; H Lentzen
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8.  [Ingredients of mistletoe (Viscum album L.) as potential drugs].

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10.  Phase II study of viscum fraxini-2 in patients with advanced hepatocellular carcinoma.

Authors:  M Mabed; L El-Helw; S Shamaa
Journal:  Br J Cancer       Date:  2004-01-12       Impact factor: 7.640

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5.  Quality of life, immunomodulation and safety of adjuvant mistletoe treatment in patients with gastric carcinoma - a randomized, controlled pilot study.

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Journal:  BMC Complement Altern Med       Date:  2012-10-03       Impact factor: 3.659

6.  NCCAM/NCI Phase 1 Study of Mistletoe Extract and Gemcitabine in Patients with Advanced Solid Tumors.

Authors:  Patrick J Mansky; Dawn B Wallerstedt; Timothy S Sannes; Jamie Stagl; Laura Lee Johnson; Marc R Blackman; Jean L Grem; Sandra M Swain; Brian P Monahan
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8.  Fever Therapy With Intravenously Applied Mistletoe Extracts for Cancer Patients: A Retrospective Study.

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9.  Adjuvant Therapy Using Mistletoe Containing Drugs Boosts the T-Cell-Mediated Killing of Glioma Cells and Prolongs the Survival of Glioma Bearing Mice.

Authors:  Sonja Schötterl; Stephan M Huber; Hans Lentzen; Michel Mittelbronn; Ulrike Naumann
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10.  European Mistletoe (Viscum album) Extract Is Cytotoxic to Canine High-Grade Astrocytoma Cells In Vitro and Has Additive Effects with Mebendazole.

Authors:  Anna Wright; Rie Watanabe; Jey W Koehler
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  10 in total

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