26
Views
4
CrossRef citations to date
0
Altmetric
Original Article

Modulation of Costimulatory Molecules on Follicular Lymphoma Cells by TNF and CD40

, , , , , & show all
Pages 331-341 | Published online: 01 Jul 2009

References

  • Liu Y. J., Banchereau J. Regulation of B‐cell commitment to plasma cells or to memory B cells. Seminars in Immunology 1997; 9: 235–240
  • Bazzoni F., Beutler B. The Tumor Necrosis Factor Ligand and Receptor Family. New England Journal of Medicine 1996; 334: 1717–1725
  • Beutler B. Tumor Necrosis Factors: The Molecules and Their Emerging Role in Medicine. Raven Press, Ltd., New‐York, NY 1992
  • Warzocha K., Bienvenu J., Coiffier B., Salles G. Mechanisms of Action of the Tumor Necrosis Factor and Lymphotoxin Ligand‐Receptor System. European Cytokine Network 1994; 5: 83–96
  • Aggarwal B., Natarajan K. Tumor Necrosis Factors: Developments During the Last Decade. European Cytokine Network 1996; 7: 93–124
  • Pasparakis M., Alexopoulo L., Episkopoulo V., Kollias G. Immune and Inflammatory Responses in TNFα‐deficient Mice: A Critical Requirement for TNFα in the Formation of Primary B Cell Follicules, Follicular Dendritic Cell Networks and Germinal Centers, and in the Maturation of the Humoral Immune Response. Journal of Experimental Medicine 1996; 184: 1397–1411
  • Matsumoto M., Mariathasan S., Nahm M. H., Baranyay E., Peschon J. J., Chaplin D. D. Role of Lymphotoxin and Type I TNF Receptor in the Formation of Germinal Centers. Science 1996; 271: 1289–1291
  • Liu Y. ‐J., Banchereau J. Mutant Mice Without B Lymphocytes Follicles. Journal of Experimental Medicine 1996; 184: 1207–1211
  • Harris N. L., Jaffe E. S., Stein H., Banks P. M., Chan J. C. K., Cleary M. L., Delsol G., de Wolf‐Peeters C., Falini B., Gat‐ter K. C., Grogan T. M., Isaacson P. G., Knowles D. M., Mason D. Y., Muller‐Hermelink H. ‐K., Pileri S. A., Piris M. A., Ralfkiaer E., Warlike R. A. A Revised European‐American Classification of Lymphoid Neoplasms: A proposal From the International Lymphoma Study Group. Blood 1994; 84: 1361–1392
  • Yang E., Korsmeyer S. Molecular thanatopsis: a discourse on the BCL2 family and cell death. Blood 1996; 88: 386–401
  • Townsend S. E., Allison J. P. Tumor Rejection After Direct Costimulation of CD8+ T Cells by B7‐Trans‐fected Melanoma Cells. Science 1993; 259: 368–370
  • Lenschow D. J., Walunas T. L., Bluestone J. A. CD28/B7 System of T Cell Costimulation. Annual Review in Immunology 1996; 14: 233–258
  • Salles G., Bienvenu J., Bastion Y., Barbier Y., Doche C., Warzocha C., Gutowski M. ‐C., Rieux C., Coiffier B. Elevated Circulating Levels of TNFot and its P55 Receptor are Associated with an Adverse Prognosis in Lymphoma Patients. British Journal of Haematology 1996; 93: 352–359
  • Warzocha K., Salles G., Bienvenu J., Bastion Y., Dumon‐tet C., Renard N., Neidhardt E. ‐M., Coiffier B. Tumor Necrosis Factor Ligand‐Receptor System Can Predict Treatment Outcome in Lymphoma Patients. Journal of Clinical Oncology 1997; 15: 499–508
  • Ryffel B., Brockhaus M., Durmuller U., Gudat F. Tumor necrosis factor receptors in lymphoid tissues and lymphomas. Source and site of action of tumor necrosis factor alpha. American Journal of Pathology 1991; 139: 7–15
  • Sappino A. ‐P., Seelentag W., Pelte M. ‐F., Alberto P., Vassali P. Tumor Necrosis Factor/Cachectin and Lymphotoxin Gene Expression in Lymph Nodes Lymphoma Patients. Blood 1990; 75: 958–962
  • Gruss H. ‐J., Dower S. Tumor Necrosis Factor Ligand Superfamily: Involvement in the pathology of malignant lymphomas. Blood 1995; 85: 3378–3404
  • Trentin L., Zambello R., Agostini C., Siviero F., Adami R., Marcolongo R., Raimondi R., Chisesi T., Pizzolo G., Semenzato G. Expression and functional role of tumor necrosis factor receptors on leukemic cells from patients with type B chronic rymphoproliferative disorders. Blood 1993; 81: 752–758
  • Ranheim E. A., Kipps T. J. Tumor necrosis factor‐alpha facilitates induction of CD80 (B7–1) and CD54 on human B cells by activated T cells: complex regulation by IL‐4, IL‐10, and CD40L. Cellular Immunology 1995; 161: 226–235
  • Garrone P., Neidhardt E. ‐M., Garcia E., Galibert L., van Kooten C., Banchereau J. Fas Ligation Induces Apoptosis of CD40‐Activated Human B lymphocytes. Journal of Experimental Medicine 1996; 182: 1265–1273
  • Vallé A., Garrone P., Yssel H., Bonnefoy J. ‐Y., Freedman A. S., Nadler L. M. mAb 104, a New Monoclonal Antibody, recognizes the B7 Antigen that is Expressed on Activated B Cells and HTLV‐1‐Transformed T Cells. Immunology 1990; 69: 531–535
  • Azuma M., Ito D., Yagita H., Okumura K., Philipps J. H., Lanier L. L., Somoza C. B70 Antigen is a Second Ligand for CTLA‐4 and CD28. Nature 1993; 366: 76–79
  • Stack R. M., Lenshow D. J., Gray G. S., Bluestone J. A., Fitch F. W. IL‐4 Treatment of Small Splenic B Cells Induces Costimulatory Molecules B7.1 and B7.2. Journal of Immunology 1994; 152: 5723–5733
  • Roy M., Aruffo A., Ledbetter J., Kerhy M., Noelle R. Studies on the Interdependence of gp39 and B7 Expression and Function During Antigen‐specific Immune Response. European Journal of Immunology 1995; 25: 596–603
  • Yang Y., Wilson J. M. CD40 Ligand‐Dependent T cell Activation: Requirement of B7‐CD28 Signaling through CD40. Science 1996; 273: 1862–1864
  • Ranheim E. A., Cantwell M. J., Kipps T. J. Expression of CD27 and its ligand, CD70, on chronic lymphocytic leukemia B cells. Blood 1995; 85: 3556–3565
  • Lens S. M., de Jong R., Hooibrink B., Koopman G., Pals S. T., van Oers M. H., van Lier R. A. Phenotype and function of human B cells expressing CD70 (CD27 ligand). European Journal of Immunology 1996; 26: 2964–2971
  • Adami R., Guarini A., Pini M., Siviero R., Sancetta R., Massiai M., Trentin L., Foa R., Semenzato G. Serum levels of tumor necrosis factor‐alpha in patients with B‐cell chronic lymphocytic leukaemia. European Journal of Cancer 1994; 30A: 1259–1263
  • Macia J., Gomez X., Perez B. Prognostic Value of Tumor Necrosis Factor in Plasma of Patients with Chronic Lymphocytic Leukemia. Blood 1994; 84: 989–991
  • Schultze J. L., Cardoso A. A., Freeman G. R., Seamon M. J., Daley J., Pinkus G. S., Gribben J. G., Nadler L. M. Follicular Lymphomas Can be Induced to Present Alloantigen Efficiently: A Conceptual Model to Improve Their Tumor Immunogenicity. Proceedings of the National Academy of Sciences (USA) 1995; 92: 8200–8204
  • Plumas J., Chaperot L., Jacob M. ‐C., Molens J. P., Giroux C., Sotto J. ‐J., Bensa J. ‐C. Malignant B Lymphocytes From Non‐Hodgkin's Lymphoma Induce Allogeneic Proliferative and Cytotoxic T Cell Responses in Primary Mixed Lymphocyte Cultures: an Important Role of Costimulatory Molecules CD80 (B7.1)and CD86 (B7.2) in Stimulation by Tumor Cells. European Journal of Immunology 1995; 25: 3332–3341
  • Shamash J., Davies D. C., Salam A., Rohatiner A. Z., Young B. D., Lister T. A. Induction of CD80 expression in low‐grade B cell lymphoma—a potential immunotherapeutic target. Leukemia 1995; 9: 1349–1352
  • Jeanin P., Delneste Y., Lecoanet‐Henchoz S., Gauchat J. ‐R., Ellis J., Bonnefoy J. ‐Y. CD86 (B7.2) on Human B cells. Journal of Biological Chemistry 1997; 272: 15613–15619
  • Ranheim E. A., Kipps T. J. Activated T cells induce expression of B7/BB1 on normal or leukemic B cells through a CD40‐dependent signal. Journal of Experimental Medicine 1993; 177: 925–935
  • Vallé A., Aubry J. ‐P., Durand I., Bancherau J. IL‐4 and IL‐2 Upregulate the Expression of the Antigen B7, the B Cell counterstructure to T Cell CD28: an Amplification Mechanism for T‐B cell Interactions. International Immunology 1991; 3: 229–235
  • Lahvis G. P., Cerny J. Induction of Germinal Center B Cell Markers In Vitro by activated CD4+ T Lymphocytes. The Role of CD40 Ligand, Soluble Factors, and B Ceil Antigen Receptor Cross‐Linking. Journal of Immunology 1997; 159: 1783–1793
  • van Oers M. H., Pals S. T., Evers L. M., van der Schoot C. E., Koopman G., Bonfrer J. M., Hintzen R. Q., von dem Borne A. E., van Lier R. A. Expression and release of CD27 in human B‐cell malignancies. Blood 1993; 82: 3430–3436
  • Lens S. M., de Jong R., Hintzen R. Q., Koopman G., van Lier R. A., van Oers R. H. CD27‐CD70 interaction: unraveling its implication in normal and neoplastic B‐cell growth. Leukemia and Lymphoma 1995; 18: 51–59
  • Maurer D., Holter W., Majdic O., Fischer G. F., Knapp W. CD27 Expression by a Distinct Subpopulation of Human B Lymphocytes. European Journal of Immunology 1990; 20: 2679–2684
  • Lens S. M., Keehnen R. M., van Oers M. H., van Lier R. A., Pals S. T., Koopman G. Identification of a novel subpopulation of germinal center B cells characterized by expression of IgD and CD70. European Journal of Immunology 1996; 26: 1007–1011
  • Agematsu K., Nagumo H., Oguchi Y., Nakazawa T., Fuku‐shima K., Yasui K., Ito S., Kobata T., Morimoto C., Komiyama A. Generation of Plasma Cells From Peripheral Blood Memory B Cells: Synergistic Effect of Interleukin‐10 and CD27/CD70 Interaction. Blood 1998; 91: 173–180
  • Digel W., Stefanic M., Schoniger W., Buck C., Raghava‐char A., Frickhofen N., Heimpel H., Porzsolt F. Tumor necrosis factor induces proliferation of neoplastic B‐Cells from chronic lymphocytic leukemia. Blood 1989; 73: 1242–1246
  • Brown G. R., Meek K., Nishioka Y., Thiele D. L. CD27‐CD27 ligand/CD70 interactions enhance alloantigen‐induced proliferation and cytolytic activity in CD8+ T lymphocytes. Journal of Immunology 1995; 154: 3686–3695
  • Ramarathinam L., Castle M., Wu Y., Liu Y. T cell Costimulation by B7/BB1 Induces CD8 T Cell‐dependent Tumor Rejection: An Important.Role of B7/BB in the Induction, Recruitment, and Effector Function of Antitumor T Cells. Journal of Experimental Medicine 1994; 179: 1205–1214
  • Chen L., Ashe S., Brady W., Hellström I., Hellström K. E., Ledbetter J. A., McGowan P., Linsley P. S. Costimulation of Antitumor Immunity by the B7 Counter‐receptor for the T Lymphocyte Molecules CD28 and CTLA‐4. Cell 1992; 71: 1093–1102
  • Chen L., McGowan P., Ashe S., Johnston J., Li Y., Hellström I., Hellström K. E. Tumor Immunogenicity Determines the Effect of B7 Costimulation on T Cell‐mediated Tumor Immunity. Journal of Experimental Medicine 1994; 179: 523–532
  • Viola A., Lanzavecchia A. T Cell Activation Determined by T cell Receptor Number and Tunable Thresholds. Science 1996; 273: 104–106

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.