NYAS Conferences
New York Academy of Sciences
left end
Search
divider divider feedback right end
Annals of the New York Academy of Sciences Annals of the New York Academy of Sciences login

Main

Browse Volumes

Forthcoming Volumes

Annals PrePrints

Annals Extra

E-mail Alerts

Subscriptions & Orders

New Proposals

Author Guidelines

About Annals

Help

Get free Annals volume as a NYAS member: http://www.nyas.org/annalsreaderhw
Issue 938 coverHEMATOPOIETIC STEM CELLS 2000: BASIC AND CLINICAL SCIENCES: Third International Conference Copyright © 2001 by the New York Academy of Sciences
description

This Volume
Table of Contents
Description
This Article
Full Text
Full Text (PDF)
Services
Similar articles in this journal
Similar articles in PubMed
Alert me to new issues of the journal
Download to citation manager
Citing Articles
Citing Articles via Google Scholar
Google Scholar
Articles by BRUGGER, W.
Articles by BROSSART, P.
Search for Related Content
PubMed
PubMed Citation
Articles by BRUGGER, W.
Articles by BROSSART, P.
Annals of the New York Academy of Sciences 938:359-363 (2001)
© 2001 New York Academy of Sciences

Dendritic Cell-Based Vaccines in Patients with Hematological Malignancies

WOLFRAM BRUGGER, ANYA SCHNEIDER, THEODORA SCHAMMANN, PATRICIA DILL, FRANK GRÜNEBACH, HANS-JÖRG BÜHRING, LOTHAR KANZ AND PETER BROSSART

University of Tübingen, Medical Center II, Department of Hematology, Oncology, Immunology, and Rheumatology, 72076 Tübingen, Germany

Address for correspondence: Wolfram Brugger, M.D., University of Tübingen, Medical Center, Dept. of Hematology, Oncology, Immunology, and Rheumatology, Otfried-Müller Str. 10, 72076 Tübingen, Germany. Voice: +49-7071-29-83698; fax: +49-7071-29-5591.
wolfram.brugger{at}med.uni-tuebingen.de

The epithelial mucin MUC1 is overexpressed on many epithelial malignancies as well as on some B-cell lymphomas and multiple myelomas. In the present study, we describe MUC1 expression also on primary AML blasts. To analyze the presentation of MUC1-derived HLA-A2 restricted peptides by primary AML blasts, we induced MUC1-specific cytotoxic T-lymphocytes (CTLs) in vitro using peptide pulsed dendritic cells from HLA-A2+ healthy donors as antigen-presenting cells. These CTLs efficiently lysed primary AML blasts that constitutively expressed both MUC1 and HLA-A2. The specificity of the CTLs was confirmed in a cold target inhibition assay. Our data demonstrate that MUC1-derived peptides are tumor antigens in AML which could potentially be used for immunotherapeutic approaches.

Key Words: MUC1 • AML • T-cell epitopes • Dendritic cells • Immunotherapy • Leukemia






footerLeft footerRight