Safety and Clinical Efficacy Evaluation of Intralesional Administration of Tolerogenic Dendritic Cells in Patients With Refractory Crohn's Disease
Safety and Clinical Efficacy Evaluation of Intralesional Administration of Tolerogenic Dendritic Cells in Patients With Refractory Crohn's Disease
Intralesional Tolerogenic Dendritic Cells in Crohn's Disease Treatment.
The main objective is to evaluate the safety and clinical response of intralesional injection of Autologous peripheral blood differentiated adult dendritic cells expanded tolerogenic in patients with refractory Crohn's disease treatment.
Inclusion Criteria:
Exclusion Criteria:
No injuries in pre-screening resonance
Pregnancy, lactation or women of childbearing age not taking appropriate contraceptive measures
Patients HIV + and Hepatitis C Virus + Hepatitis B Virus +
Serious concomitant disease:
Symptoms attributable to fibrotic strictures in Crohn's disease at the discretion of the investigators
Diarrhea attributable to " short bowel syndrome"
Active infection , including tuberculosis
Participation in research studies of new drugs in the 3 months prior to inclusion.
Vaccination with live/attenuated germs in the previous 3 months
Personal history of cancer (active or complete remission) or known family history of hereditary cancer.
Patients in whom , after observation of the state of their veins , these are considered inaccessible and impossible to perform apheresis