CpG oligodeoxynucleotides are effective in therapy of minimal residual tumour disease after chemotherapy or surgery in a murine model of MHC class I-deficient, HPV16-associated tumours
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F07%3A00092894" target="_blank" >RIV/68378050:_____/07:00092894 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
CpG oligodeoxynucleotides are effective in therapy of minimal residual tumour disease after chemotherapy or surgery in a murine model of MHC class I-deficient, HPV16-associated tumours
Original language description
Oligodeoxynucleotides containing guanine-cytidine dimers (CpG ODN) are potent inducers of anti-tumour immune responses. In this study, we analyzed the capacity of CpG ODN to inhibit the growth of both MHC class I-positive and -deficient tumours after debulking the tumour mass by chemotherapy or surgery. We employed an animal model resembling human papillomavirus (HPV) 16-associated tumours. Tumour cell lines with distinct cell surface expression of the MHC class I molecules were injected into syngeneicC57BL/6 mice, and the growing tumours were either subjected to cytoreductive chemotherapy with ifosfamide derivative, CBM-4A, or surgically removed. Subsequent treatment with synthetic CpG ODN significantly blocked the growth of the recurrent tumours. Our results indicate that the therapy with CpG ODN can be effective for the treatment of minimal residual tumour disease of the tumours that have escaped from the immune surveillance by downmodulating the MHC class I expression.
Czech name
CpG oligonukleotidy jsou účinné při terapii minimální zbytkové nádorové choroby MHC I negativních myších nádorů asociovaných s HPV16 po chemoterapii nebo jejich chirurgickém dstranění
Czech description
Byla analyzována účinnost CpG oligonukleotidů obsahujících dimery guanin-cytidin inhibovat růst rekurencí MHC I negativních myších nádorů asociovaných s HPV16 po chemoterapii nebo po jejich chirugickém odstranění. Podání CpG oligonukleotidů signifikantněinhibovalo růst rekurencí nádorů a lze je proto použít pro terapii nádorů jak MHC I pozitivních, tak i jejich MHC I negativních variant vzniklých v průběhu růstu nádorů vlivem imunoselekčního prostředí.
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EB - Genetics and molecular biology
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2007
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
International Journal of Oncology
ISSN
1019-6439
e-ISSN
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Volume of the periodical
30
Issue of the periodical within the volume
5
Country of publishing house
GR - GREECE
Number of pages
5
Pages from-to
1247-1251
UT code for WoS article
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EID of the result in the Scopus database
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