Methods for expansion or depletion of t-regulatory cells
The invention features methods of producing compositions enriched in Tregs and methods for treating immunological disorders using these compositions. The invention also features methods for producing compositions enriched in lymphocytes and depleted of Tregs and the use of these compositions in the treatment of proliferative disorders.
1. A method of treating a proliferative disorder or an infectious disease in a subject comprising administering to said subject an isolated human, humanized, or chimeric antibody, or antigen-binding fragment thereof, that selectively binds to an epitope of TNFR 2 that is bound by antibody clone MAB726 or by antibody clone M1.
2. The method of claim 1 , wherein said proliferative disorder is a cancer selected from the group consisting of Acute Lymphoblastic Leukemia, Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, Adrenocortical Carcinoma, AIDS-Related Lymphoma, AIDS-Related Malignancies, Anal Cancer, Astrocytoma, Bile Duct Cancer, Bladder Cancer, Bone Cancer, Osteosarcoma/Malignant Fibrous Histiocytoma, Brain Stem Glioma, Visual Pathway and Hypothalamic Glioma, Breast Cancer, Bronchial Adenomas/Carcinoids, Chronic Lymphocytic Leukemia, Chronic Myelogenous Leukemia, Chronic Myeloproliferative Disorders, Clear Cell Sarcoma of Tendon Sheaths, Colon Cancer, Colorectal Cancer, Cutaneous T-Cell Lymphoma, Endometrial Cancer, Epithelial Cancer, Esophageal Cancer, Ewing's Family of Tumors, Extracranial Germ Cell Tumor, Extragonadal Germ Cell Tumor, Extrahepatic Bile Duct Cancer, Eye Cancer, Intraocular Melanoma, Retinoblastoma, Gallbladder Cancer, Gastric (Stomach) Cancer, Hairy Cell Leukemia, Head and Neck Cancer, Hepatocellular (Liver) Cancer, Hodgkin's Lymphoma, Hypopharyngeal Cancer, Kaposi's Sarcoma, Kidney Cancer, Laryngeal Cancer, Pituitary Cancer, Plasma Cell Neoplasm/Multiple Myeloma, Pleuropulmonary Blastoma, Skin Cancer, Small Cell Lung Cancer, Small Intestine Cancer, Soft Tissue Sarcoma, Squamous Neck Cancer, Testicular Cancer, Thyroid Cancer, Urethral Cancer, Uterine Sarcoma, and Vaginal Cancer, or wherein said proliferative disorder is a solid tumor of the brain, lung, breast, lymphoid, gastrointestinal tract, genitourinary tract, pharynx, prostate, or ovary.
3. The method of claim 1 , wherein said infectious disease is selected from the group consisting of a bacterial infection, a viral infection, a fungal infection, and a parasitic infection.
4. The method of claim 1 , wherein said epitope comprises amino acids 135-147 of SEQ ID NO: 1.
5. The method of claim 1 , wherein said proliferative disorder is a cancer selected from the group consisting of breast cancer, T-cell lymphoma, endometrial cancer, esophageal cancer, gastric cancer, hepatocellular cancer, Hodgkin's lymphoma, kidney cancer, multiple myeloma, skin cancer, lung cancer, and ovarian cancer.
6. The method of claim 1 , wherein said subject is a mammal.
7. The method of claim 6 , wherein said mammal is a human.
8. The method of claim 1 , wherein said method comprises treating the proliferative disorder.
9. The method of claim 1 , wherein said proliferative disorder is a cancer.
10. The method of claim 1 , wherein said method comprises treating the infectious disease.