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Immunology of cervical cancer
Manzo-Merino, Joaquín; Toro-Arreola, Susana del; Rocha-Zavaleta, Leticia; Peralta-Zaragoza, Óscar; Jiménez-Lima, Roberto; Madrid-Marina, Vicente.
  • Manzo-Merino, Joaquín; Instituto Nacional de Cancerología. Department of Basic Research. Mexico City. MX
  • Toro-Arreola, Susana del; Universidad de Guadalajara. University Center for Health Sciences. Department of Physiology. Guadalajara. MX
  • Rocha-Zavaleta, Leticia; Universidad Nacional Autónoma de México. Instituto de Investigaciones Biomédicas. Department of Molecular Biology and Biotechnology. Mexico City. MX
  • Peralta-Zaragoza, Óscar; Instituto Nacional de Salud Pública. Infectious Diseases Research Center. Cuernavaca. MX
  • Jiménez-Lima, Roberto; Instituto Nacional de Cancerología. Department of Clinical Research. Mexico City. MX
  • Madrid-Marina, Vicente; Instituto Nacional de Salud Pública. Infectious Diseases Research Center. Cuernavaca. MX
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)


Full text: Available Index: LILACS (Americas) Main subject: Histocompatibility Antigens Class I / Uterine Cervical Neoplasms / Oncogene Proteins, Viral / Papillomavirus Infections Limits: Female / Humans Language: English Journal: Rev. invest. clín Journal subject: Medicine Year: 2020 Type: Article Affiliation country: Denmark / Mexico Institution/Affiliation country: Instituto Nacional de Cancerología/MX / Instituto Nacional de Salud Pública/MX / Universidad Nacional Autónoma de México/MX / Universidad de Guadalajara/MX

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Full text: Available Index: LILACS (Americas) Main subject: Histocompatibility Antigens Class I / Uterine Cervical Neoplasms / Oncogene Proteins, Viral / Papillomavirus Infections Limits: Female / Humans Language: English Journal: Rev. invest. clín Journal subject: Medicine Year: 2020 Type: Article Affiliation country: Denmark / Mexico Institution/Affiliation country: Instituto Nacional de Cancerología/MX / Instituto Nacional de Salud Pública/MX / Universidad Nacional Autónoma de México/MX / Universidad de Guadalajara/MX