17
Views
13
CrossRef citations to date
0
Altmetric
Original Article

Effects of Anti-Fas Antibodies on Lymphocytes and Other Organs: Preparation of Original and New Monoclonal Antibodies and Amelioration of Systemic Autoimmune Disease

Pages 329-345 | Published online: 10 Jul 2009

References

  • Yonehara S., Ishii A., Yonehara M. A cell-killing monoclonal antibody (anti-Fas) to a cell surface antigen co-downregulated with the receptor of tumor necrosis factor. J. Exp. Med. 1989; 169: 747–1756
  • Itoh N., Yonehara S., Ishii A., Yonehara M., Mizushima S., Sameshima M., Hase A., Seto Y., Nagata S. The polypeptide encoded by the cDNA for human cell surface antigen Fas can mediate apoptosis. Cell 1991; 66: 233–243
  • Trauth B. C., Klas C., Peters A. M. J., Matzku S., Moller P., Falk W. K., Debatin M., Krammer P. H. Monoclonal antibody-mediated tumor regression by induction of apoptosis. Science 1989; 245: 301–305
  • Oehm A., Behrmann I., Falk W., Pawlita M., Maier G., Klas C., Li W. M., Richards S., Dhein J., Trauth B. C., Ponsting H., Krammer P. H. Purification and molecular cloning of the APO-1 cell surface antigen, a member of the tumor necrosis factor receptor superfamily: Sequence identity with the Fas antigen. J. Biol. Chem. 1992; 267: 10709–10715
  • Suda T., Takahashi T., Golstein P., Nagata S. Molecular cloning and expression of the Fas ligand, a novel member of the tumor necrosis factor family. Cell 1993; 75: 1169–1178
  • Watanabe R., FukunagaBrannan C. I., Copeland N. G., Jenkins N. A., Nagata S. Lymphoproliferation disorder in mice explained by defects in Fas that mediates apoptosis. Nature 1992; 356: 314–317
  • Takahashi T., Tanaka M., Brannan C. I., Jenkins N. A., Copeland N. G., Suda T., Nagata S. Generalized lymphoproliferative disease in mice caused by a point mutation in the Fas ligand. Cell 1994; 76: 969–976
  • Andrews B. S., Eisenberg R. A., Theofilopoulos A. N., Izui S., Wilson C. B., Mc P. J., ConahMurphy E. D., Roths J. B., Dixon F. J. Spontaneous murine lupus-like syndromes. Clinical and immunopathologic manifestations in several strains. J. Exp. Med. 1978; 148: 1198–1215
  • Cohen P. L., Eisenberg R. A. Lpr and gld. Single gene models of systemic autoimmunity and lymphoproliferative disease. Annu. Rev. Immunol. 1991; 9: 243–269
  • Murphy E. D., Roths J. B. Autoimmunity and lymphoproliferation. Induction by mutant gene lpr, and acceleration by a male-associated factor in strain BXSB mice. Genetic Control of Autoimmune Disease, N. R. Rose, P. E. Bigazzi, N. L. Werner. Elsevier North Holland Inc., NY 1979; 207–221
  • Nose M., Nishimura M., Kyogoku M. Analysis of granulomatous arthritis in MRL/Mp autoimmune disease mice bearing lymphoproliferative genes. Am. J. Pathol. 1989; 135: 271–280
  • Matsumoto K., Yoshikai Y., Asano T., Himeno K., Iwasaki A., Nomoto K. Defect in negative selection in lpr donor-derived T cells differentiating in non-lpr host thymus. J. Exp. Med. 1991; 173: 127–132
  • Zhou T., Bluethmann H., Eldridge J., Brockhaus M., Berry K., Mountz J. D. Abnormal thymocyte development and production of autoreactive T cells in T cell receptor transgenic autoimmune mice. J. Immunol. 1991; 147: 466
  • Taniguchi Y., Ito M. R., Yonehara S., Nose M. Role of macrophages in the development of arteritis in MRL strains of mice with a deficit in Fas-mediated apoptosis. Clin. Exp. Immunol. 1996; 106: 26–34
  • Russell J. H., Rush B., Weaver C., Wang R. Mature T cells of autoimmune lpr/lpr mice have a defect in antigen-stimulated suicide. Proc. Natl. Acad. Sci. USA 1993; 90: 4409–4413
  • Singer G. G., Abbas A. K. The Fas antigen is involved in peripheral but not thymic deletion of T lymphocytes in T cell receptor transgenic mice. Immunity 1994; 1: 365–371
  • Hanabuchi S., Koyanagi M., Kawasaki A., Shinohara N., Matsuzawa A., Nishimura Y., Kobayashi Y., Yonehara S., Yagita H., Okumura K. Fas and its ligand in general mechanism of T-cell-mediated cytotoxicity. Proc. Natl. Acad. Sci. USA 1994; 91: 4930–4934
  • Rouvier E. M., Luciani F., Golstein P. Fas involvement in Ca2+-independent T cell-mediated cytotoxicity. J. Exp. Med. 1993; 177: 195–200
  • Nagata S. Apoptosis by death factor. Cell 1997; 88: 355–365
  • Giordano C., Stasse G., De Maria R., Todaro M., Richiusa P., Papoff G., Ruberti G., Bagnasco M., Testi R., Galluzzo A. Potential involvement of Fas and its ligand in the pathogenesis of Hashimoto's thyroiditis. Science 1997; 275: 960–963
  • Nishio A., Katakai T., Oshima C., Kasakura S., Sakai M., Yonehara S., Suda T., Nagata S., Masuda T. A possible involvement of Fas-Fas ligand signaling in the pathogenesis of murine autoimmune gastritis. Gastroenterology 1996; 111: 959–967
  • Chervonsky A. V., Wang Y., Wong F. S., Visintin I., Flavell R. A., Matis L. A. The role of Fas in autoimmune diabetes. Cell 1997; 99: 17–24
  • Sabelko K. A., Kelly K. A., Nahm M. H., Cross A. H., Russell J. H. Fas and Fas ligand enhance the pathogenesis of experimental allergic encephalomyelitis, but are not essential for immune privilege in the central nervous system. J. Immunol. 1997; 159: 3096–3099
  • Ogasawara J., Watanabe F. R., Adachi M., Matsuzawa A., Kasugai T., Kitamura Y., Itoh N., Suda T., Nagata S. Lethal effect of the anti-Fas antibody in mice. Nature 1993; 364: 806–809
  • Nishimura Y., Ishii A., Kobayashi Y., Yamasaki Y., Yonehara S. Expression and function of mouse Fas on immature and mature T cells. J. Immunol. 1995; 154: 4395–4403
  • Nishimura Y., Hirabayashi Y., Matsuzaki Y., Musette P., Ishii A., Nakauchi H., Inoue T., Yonehara S. In vivo analysis of Fas antigen-mediated apoptosis. Effects of agonistic anti-mouse Fas monoclonal antibody on thymus, spleen and liver. Int. Immunol. 1997; 9: 307–316
  • Nishimura Y., MoritaNose M., Inoue T., Yonehara S. Amelioration of systemic autoimmune disease by the stimulation of apoptosis-promoting receptor Fas with anti-Fas mAb. Int. Immunol. 1997; 9: 1793–1799
  • Tanaka M., Suda T., Yatomi T., Nakamura N., Nagata S. Lethal effect of recombinant human Fas ligand in mice pretreated with. Propionibacterium acnes. J. Immunol. 1997; 158: 2303–2309
  • Boldin M. P., Varfolomeev E. E., Pancer Z., Mett I. L., Camonis J. H., Wallach D. A novel protein that interacts with the death domain of Fas/APOl contains a sequence motif related to the death domain. J. Biol. Chem. 1995; 270: 7795–7798
  • Chinnaiyan A. M., O'Rourke K., Tewari M., Dixit V. M. FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis. Cell 1995; 81: 505–512
  • Yang X., Khosravi R., FarChang H. Y., Baltimore D. Daxx, a novel Fas-binding protein that activates INK and apoptosis. Cell 1997; 99: 1067–1076
  • Dhein J., Walczak H., Baumler C. K., Debatin M., Krammer P. H. Autocrine T-cell suicide mediated by APO-l/(Fas/CD95). Nature 1995; 373: 438–441
  • Brunner T., Mogil R. J., La D., FaceYoo N. J., Mahboubi A., Echeverri F., Force S. J., Force W. R., Lynch D. H., Ware C. F., Green D. R. Cell-autonomous Fas (CD95)/Fas-ligand interaction mediates activation-induced apoptosis in T-cell hybridomas. Nature 1995; 373: 441–444
  • Sju T., Panka D. J., Cui H., Ettinger R., El M., KhatibSherr D. H., Stanger B. Z., Marshak Rothstein A. Fas (CD95)/FasL interactions required for programmed cell death after T-cell activation. Nature 1995; 373: 444–448

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.