cancer HPV-induced malignancies
Conditions
Interventions
None listed
Sponsors
Leids Universitair Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: HPV-related infection or HPV-related anogenital and/or cervical premalignant lesion, or HPV-related carcinoma
Exclusion criteria
Exclusion criteria: Younger than 18 years Non-HPV related disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The presence, number, phenotype and function of both circulating (blood) and locally present (lesion/tumor/lymph node) HPV-specific immune cells under several conditions will be measured by the use of ELISPOT, proliferation, cytokine production by bead array, CFSE based suppression assays, cytotoxicity assays, multi-parameter flow cytometry and ELISA. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objectives of this study are to assess: - The linkage between immunity-related genetic variation and disease susceptibility. - Clinical responsiveness and HPV-specific immunity. - Influence of therapy on HPV-specific immunity and vice verse. - Factors influencing tissue-infiltration by different populations of (HPV-specific) immune cells. - The possibility to specifically expand defined populations of HPV-specific immune cells. | — |
Countries
Netherlands
Outcome results
None listed