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Published in: Cancer Immunology, Immunotherapy 3/2008

01-03-2008 | Original Article

Phase I study of α-galactosylceramide-pulsed antigen presenting cells administration to the nasal submucosa in unresectable or recurrent head and neck cancer

Authors: Tetsuro Uchida, Shigetoshi Horiguchi, Yuriko Tanaka, Heizaburo Yamamoto, Naoki Kunii, Shinichiro Motohashi, Masaru Taniguchi, Toshinori Nakayama, Yoshitaka Okamoto

Published in: Cancer Immunology, Immunotherapy | Issue 3/2008

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Abstract

Background

Human Vα24 natural killer T (NKT) cells are activated by the specific ligand, α-galactosylceramide (α-GalCer), in a CD1d-dependent manner. Potent anti-tumor activity of activated NKT cells has been previously demonstrated.

Methods

We conducted a phase I study with α-GalCer-pulsed antigen presenting cells (APCs) administered in the nasal submucosa of patients with head and neck cancer, and evaluated the safety and feasibility of such a treatment. Nine patients with unresectable or recurrent head and neck cancer received two treatments 1 week apart, of 1 × 108 of α-GalCer-pulsed autologous APCs into the nasal submucosa.

Results

During the clinical study period, no serious adverse events (Common Terminology Criteria for Adverse Events version 3.0 greater than grade 3) were observed. After the first and the second administration of α-GalCer-pulsed APCs, an increased number of NKT cells was observed in four patients and enhanced natural killer activity was detected in the peripheral blood of eight patients.

Conclusion

The administration of α-GalCer-pulsed APCs into the nasal submucosa was found to be safe and induce anti-tumor activity in some patients.
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Metadata
Title
Phase I study of α-galactosylceramide-pulsed antigen presenting cells administration to the nasal submucosa in unresectable or recurrent head and neck cancer
Authors
Tetsuro Uchida
Shigetoshi Horiguchi
Yuriko Tanaka
Heizaburo Yamamoto
Naoki Kunii
Shinichiro Motohashi
Masaru Taniguchi
Toshinori Nakayama
Yoshitaka Okamoto
Publication date
01-03-2008
Publisher
Springer-Verlag
Published in
Cancer Immunology, Immunotherapy / Issue 3/2008
Print ISSN: 0340-7004
Electronic ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-007-0373-5

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