Cervical Cancer Clinical Trial
Official title:
Screening and Identification of Novel Diagnostic and Prognosis Biomarkers on Cervical Cancers
Cervical cancer the most frequent neoplasm and the fifth mortality rate of malignancies of
the women in the world. It results in about 1,000 women in Taiwan and about 200,000 women
worldwide dying of cervical cancer each year. Human papilloma viruses (HPV) have been
consistently implicated in causing cervical cancer especially those high-risk types (HPV
16,18,31,45) have been strongly associated with cervical cancer. Around 50-80 % of women are
infected by HPV within their whole lives. However, only 1% of HPV-infected women have
cervical cancer eventually. Seventy and 91% of HPV infection could be cleaned up by host
immune responses within 1 and 2 years later. It shows that host immunity plays an important
role in the progression, persistence, or regression of HPV infection.
There are two main defense lines in the host immunity including innate immunity and adoptive
immunity. Adoptive immunity plays more important roles in the defense of HPV infections than
innate immunity. The adoptive immunity could be further divided into humoral immunity and
cell-mediated immunity. Humoral immunity regulated by Th2 helper T lymphocytes to generate
memory B cells to produce antibody which provide the protective function to HPV infection.
Cell-mediated immunity regulated by Th1 helper T lymphocytes to induce antigen-specific
cytotoxic T cells which could kill the HPV-infected cells. Although there are many
researches focused on the immunity to HPV infection, there is no conclusion about the
relationship between humoral and cell-mediated immunities on HPV infection and roles of
humoral and cell-mediated immunities in the prognosis of HPV-infected population and
cervical cancer patients.
Our research team has focused on the establishment of platforms on cell-mediated immunity to
HPV infection and on the correlation of cell-mediated immunity and prognosis of HPV-infected
population and cervical cancer patients for years. In order to survey the host immunity to
HPV infection more comprehensively, we propose this 3-year proposal. First, we would like to
set up the platforms to survey the humoral immunity to HPV infection in normal population
and patients with CIN lesion or cervical cancer. Second, we would to elucidate the
correlation between humoral immunity and status and clinico-pathologic items of HPV-infected
populations. Third, we would like to survey if the humoral immunity correlate with the
prognosis of patients with cervical lesions. Fourth, we would like to elucidate the
correlation betweenHLA haplotype and humoral immunity in HPV-infected populations. Our
research results will have a more comprehensive overview in the host immunity to HPV
infection and its related diseases. It could provide more information in the prevention and
treatment of HPV infection in the future.
n/a
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
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