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1.
Rev. invest. clín ; 72(4): 188-197, Jul.-Aug. 2020. tab, graf
Article in English | LILACS | ID: biblio-1251856

ABSTRACT

ABSTRACT Optimal function of the immune system allows the recognition and elimination of infected and tumor cells. However, these cells can develop mechanisms to evade the cellular immune response. In human papillomavirus (HPV) infection, dysregulation of major histocompatibility complex Class I molecules and other components of the innate immune system promote the survival of infected cells by allowing the infection to persist which, in turn, favors the development of cancer. Further, tumor cells possess inherent mechanisms designed to block the recognition and activation of cytotoxic lymphocytes: particularly, HPV proteins such as E1 and E2 and oncoproteins E5, E6, and E7 that inhibit immune mechanisms and/or stimulate the expression of immunosuppressive cytokines. These mechanisms include a decrease in receptor activation and costimulating molecules on the surface of immune cells, as well as the constitutive expression of molecules that inhibit their function, which allow HPV persistence and tumor progression. Immunotherapy-based therapeutic options are positioned as excellent candidates for the treatment of cervical cancer.


Subject(s)
Humans , Female , Histocompatibility Antigens Class I , Uterine Cervical Neoplasms/immunology , Oncogene Proteins, Viral , Papillomavirus Infections/complications , Papillomavirus Infections/therapy , Uterine Cervical Neoplasms/virology , Papillomavirus E7 Proteins , Immunotherapy
2.
Rev. invest. clín ; 72(4): 198-212, Jul.-Aug. 2020. tab, graf
Article in English | LILACS | ID: biblio-1251857

ABSTRACT

ABSTRACT Infection with high-risk human papillomavirus (HPV) increases the likelihood of developing cervical cancer (CC). A plethora of cellular processes is required to produce pre-malignant lesions, which in turn may become malignant if left untreated. Those changes are induced by viral oncoproteins, which represent an ideal target to identify the viral presence, or by some particularities of the host that ultimately promote the establishment of CC. This article describes the different methods used for HPV detection and quantification, as well as the current trend of secondary screening approaches to detect premalignant lesions and CC. In addition, we analyzed validated biomarkers and those under clinical investigation for the classification (triage) of women at risk of developing CC after an initial positive HPV test and that could be used as prognostic biomarkers for CC. The use of molecular biomarkers, together with the detection of HPV DNA sequences, provides a high impact diagnostic and prognostic tool in the detection of patients at increased risk of developing CC and also may guide their clinical management. In addition, some of those biomarkers could represent pharmacological targets for the future design of therapeutic approaches to CC treatment.


Subject(s)
Humans , Female , Uterine Cervical Neoplasms/diagnosis , Papillomavirus Infections/complications , Papillomavirus Infections/diagnosis , Alphapapillomavirus , Biomarkers , Triage
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