Volume 79, Issue 4 pp. 281-286

Mesothelin, a possible target for immunotherapy, is expressed in primary AML cells

Daniel Steinbach

Daniel Steinbach

University Children’s Hospital Jena, Germany

University Children’s Hospital Ulm, Germany

Search for more papers by this author
Masanori Onda

Masanori Onda

Laboratory of Molecular Biology, National Cancer Institute, Bethesda, MD, USA

Search for more papers by this author
Astrid Voigt

Astrid Voigt

University Children’s Hospital Jena, Germany

Search for more papers by this author
Kristin Dawczynski

Kristin Dawczynski

University Children’s Hospital Jena, Germany

Search for more papers by this author
Susan Wittig

Susan Wittig

University Children’s Hospital Jena, Germany

Search for more papers by this author
Raffit Hassan

Raffit Hassan

Laboratory of Molecular Biology, National Cancer Institute, Bethesda, MD, USA

Search for more papers by this author
Bernd Gruhn

Bernd Gruhn

University Children’s Hospital Jena, Germany

Search for more papers by this author
Ira Pastan

Ira Pastan

Laboratory of Molecular Biology, National Cancer Institute, Bethesda, MD, USA

Search for more papers by this author
First published: 21 July 2007
Citations: 28
Daniel Steinbach, MD, University Children’s Hospital Ulm, Eythstrasse 24, 89075 Ulm, Germany. Tel: +49 (0) 731 50057126; Fax: +49 (0) 731 50026682; e-mail: [email protected]

Abstract

Background: Mesothelin is a promising candidate for tumor-specific therapy because of its limited expression in normal tissues and high expression in several cancers. The expression of the protein mesothelin in hematological malignancies has not yet been analyzed. SS1(dsFv)PE38 is a recombinant anti-mesothelin immunotoxin which is undergoing clinical evaluation in patients with mesothelin-expressing tumors.

Methods and Results: In this study we show that the mesothelin protein is expressed in leukemic cells from children with acute myeloid leukemia (AML). This finding was confirmed by western blot, immunocytochemistry and real time polymerase chain reaction (PCR). Despite the expression of mesothelin, the patient samples were not sensitive to immunotoxin SS1(dsFv)PE38 in MTT assays.

Conclusions: Primary AML cells express mesothelin but SS1(dsFv)PE38 is not active in killing these cells. Other approaches that utilize mesothelin as a target might be more effective and should be tested against AML cells.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.