Cell-mediated immunity in cervical cancer evolution
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19337890
DOI
10.1080/15368370802708868
PII: 910061278
Knihovny.cz E-zdroje
- MeSH
- antigeny nádorové metabolismus MeSH
- buněčná adheze MeSH
- buněčná imunita * MeSH
- L-laktátdehydrogenasa metabolismus MeSH
- LDH virus metabolismus MeSH
- leukocyty cytologie MeSH
- lidé MeSH
- mitochondrie metabolismus MeSH
- nádory děložního čípku genetika imunologie patologie MeSH
- prekancerózy MeSH
- T-lymfocyty patologie virologie MeSH
- vysokoúčinná kapalinová chromatografie MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny nádorové MeSH
- L-laktátdehydrogenasa MeSH
Cell-mediated immunity (CMI) response to different antigens was examined in healthy women, in patients with cervical precancerous lesions, and in patients with cervical cancer. Cervical lesions were diagnosed by cytological (PAP) smears, from examination by colposcopy, and from "punch" biopsy material by histology. CMI response is related to specific processes in healthy and cancer cells. CMI was investigated by leukocyte adherence inhibition (LAI) assay using specific antigen (prepared from cervical carcinoma tissue) and non specific antigen (prepared from blood of mice infected by LDH--lactate dehydrogenase--virus). The CMI responses of healthy women and cancer patients to the antigens used are different: the majority of T lymphocytes display adherence and non adherence, respectively (but the CMI responses elicited by the antigens are not equal and small quantitative differences are observed). Regardless of the CIN (cervical intraepithelial neoplasia) grades, CMI responses correspond either to healthy women or to cervical carcinoma patients (at about similar ratio of cases in all the CIN groups). Effect of non specific antigen suggests that cervical carcinoma transformation may be connected with reduction of mitochondrial activity similar to processes in LDH virus infection.
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