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Neurosci Lett ; 327(3): 189-92, 2002 Jul 26.
Article in English | MEDLINE | ID: mdl-12113909

ABSTRACT

Oligodeoxynucleotides containing CpG motifs (CpG-ODN) are powerful immunostimulating agents that are currently entering clinical trials in various human diseases. Concerns exist about potential auto-immune diseases triggered by such treatment. We thus investigated whether tumor rejection induced by CpG-ODN treatment could lead to a harmful auto-immune reaction against the nervous system (neurological paraneoplastic disease) at the time of acute tumor rejection, or in long-term surviving animals. Mice bearing established neuroblastomas were treated with intra-tumoral injections of CpG-ODN, resulting in tumor inhibition and tumor rejection in one-third of the animals. Immunocytochemistry and Western blot studies revealed no specific anti-neuronal antibodies. None of the animals developed neurological disabilities and histological studies of the nervous system were normal. CpG-ODN can therefore trigger neuroblastoma rejection without inducing neurological paraneoplastic disease.


Subject(s)
Adjuvants, Immunologic/adverse effects , Neuroblastoma/drug therapy , Oligodeoxyribonucleotides/adverse effects , Paraneoplastic Polyneuropathy/chemically induced , Paraneoplastic Polyneuropathy/immunology , Animals , Autoimmunity , Blotting, Western , Immunohistochemistry , Mice , Time Factors
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