Study Evaluating the Efficacy and Safety With CAR-T for Recurrent or Refractory Diffuse Large B Cell Lymphoma

Inclusion Criteria: 1. Confirmed by pathological biopsy in patients with diffuse large B cell lymphoma by standard solution treatment is invalid or recurrence of refractory, and by flow cytometry or pathological immunohistochemical examination, confirmed the tumor cell surface expression positive intervention molecular targets, mainly for the CD19 (+) and/or CD20 (+). 2. Age 3 to 75 years old, both male and female; 3. Is expected to survive more than 3 months; 4. Physical condition is good: 0-2 score ECOG score; 5. In group of four weeks before Canon imaging examination evaluation body tumor load, recommend line PET - CT examination. 6. General requirements peripheral blood as basic, normal blood T lymphocytes in peripheral blood count must \>= 0.2 x10\^9 / L; 7. No obvious abnormal heart, liver, kidney, no large wounds that haven't healed on the body; 8. Into groups to participate in voluntarily, good adherence, can cooperate test observation, childbearing age women must be 7 days before starting treatment expert pregnancy test and the results were negative, and signed a written informed consent form. Exclusion Criteria: 1. The recurrent or refractory patients with diffuse large B cell lymphoma. 2. Organ failure, such as heart: Class III and IV; liver: to Child grading of liver function grade C; kidney: kidney failure and uremia stage; lung: symptoms of severe respiratory failure; brain: disorder of consciousness; 3. Existing serious acute infection, uncontrollable, or have fester sex and chronic infection, wound in delay no more; 4. Patients with significant graft versus host disease (GVHD) after organ transplant history or allogeneic hematopoietic stem cell transplantation; 5. Systemic autoimmune diseases or immunodeficiency disease, patients with allergic constitution; 6. Coagulation abnormalities and severe thrombosis; 7. Pregnancy and lactation women; 8. Any other chronic disease patients who have been treated with immune agents or hormone therapy; 9. Patients who have participated in other clinical trials or other clinical trials in the past 30 days; 10. The Investigator believe the patients should not participate in this experiment.