Abstract |
Most patients with paraneoplastic encephalomyelitis/sensory neuronopathy PEM/SN have small-cell lung cancer (SCLC) and develop antibodies against neuronal-specific Hu proteins, which are abnormally expressed in the tumor. Anti-Hu reactivity is present in ~16% of SCLC patients without PEM/SN. Here we test the hypothesis that engineered SCLC-prone mice may exhibit anti-Hu reactivity. We show that tumors from SCLC-prone mice misexpress Hu proteins, and 14% of mice harbor anti-Hu antibodies. Mice appear to show reactivity prior to clinical diagnosis of SCLC. This mouse model system will be useful to study SCLC-associated autoimmunity, its diagnostic value, and the potential protective role of oncoantigen-directed autoantibodies.
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Authors | Meleeneh Kazarian, Joaquim Calbo, Natalie Proost, Catherine L Carpenter, Anton Berns, Ite A Laird-Offringa |
Journal | Journal of neuroimmunology
(J Neuroimmunol)
Vol. 217
Issue 1-2
Pg. 38-45
(Dec 10 2009)
ISSN: 1872-8421 [Electronic] Netherlands |
PMID | 19765830
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies
- Autoantibodies
- ELAV Proteins
- RNA, Messenger
- Vaccines, DNA
- Luciferases
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Topics |
- Animals
- Antibodies
(blood)
- Autoantibodies
(immunology, metabolism)
- Disease Models, Animal
- ELAV Proteins
(genetics, immunology)
- Humans
- Luciferases
(genetics)
- Lung Neoplasms
(blood, immunology, mortality)
- Magnetic Resonance Imaging
- Mice
- Neoplasm Transplantation
(immunology)
- RNA, Messenger
(metabolism)
- Small Cell Lung Carcinoma
(blood, immunology, mortality)
- Survival Analysis
- Time Factors
- Vaccines, DNA
(immunology)
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