Abstract
Our present knowledge of how T cells eliminate cancer is mainly based on memory immune responses investigated with vaccinated mice1,2. In-vivo depletion studies with anti-CD4 monoclonal antibodies (mAb) have revealed that the antitumor immunity conferred by prophylactic vaccination is usually CD4+ T cell dependent. CD4+ T cells were required for vaccination-induced immunity against the B16 melanoma3–5, against the Mc51.9 fibrosarcoma6, against the J558 plasmacytoma7, and against the A20 lymphoma7.
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8. References
L. Gross. Intradermal immunization of C3H mice against a sarcoma that originated in an animal of the same line. Cancer Res 3:326–333 (1943).
R.G. Lynch, R.J. Graff, S. Sirisinha, E.S. Simms and H.N. Eisen. Myeloma proteins as tumor-specific transplantation antigens. Proc Natl Acad Sci USA 69:1540–1544 (1972).
G. Dranoff, E. Jaffee, A. Lazenby, P. Golumbek, H. Levitsky, K. Brose, V. Jackson, H. Hamada, D. Pardoll and R.C. Mulligan. Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity. Proc Natl Acad Sci USA 90:3539–3543 (1993).
H.I. Levitsky, A. Lazenby, R.J. Hayashi and D.M. Pardoll. In vivo priming of two distinct antitumor effector populations: the role of MHC class I expression. J Exp Med 179:1215–1224 (1994).
K. Hung, R. Hayashi, A. Lafond-Walker, C. Lowenstein, D. Pardoll and H. Levitsky. The central role of CD4(+) T cells in the antitumor immune response. J Exp Med 188:2357–2368 (1998).
Z. Qin and T. Blankenstei. CD4+ T cell-mediated tumor rejection involves inhibition of angiogenesis that is dependent on IFN gamma receptor expression by non-hematopoietic cells. Immunity 12:677–686 (2000).
K. Liu, J. Idoyaga, A. Charalambous, S. Fujii, A. Bonito, J. Mordoh, R. Wainstok, X.F. Bai, Y. Liu and R.M. Steinman. Innate NKT lymphocytes confer superior adaptive immunity via tumor-capturing dendritic cells. J Exp Med 202:1507–1516 (2005).
H. Fujiwara, M. Fukuzawa, T. Yoshioka, H. Nakajima and T. Hamaoka. The role of tumor-specific Lyt-1+2-T cells in eradicating tumor cells in vivo, I: lyt-1+2-T cells do not necessarily require recruitment of host’s cytotoxic T cell precursors for implementation of in vivo immunity. J Immunol 133:1671–1676 (1984).
B. Bogen, L. Munthe, A. Sollien, P. Hofgaard, H. Omholt, F. Dagnaes, Z. Dembic and G.F. Lauritzsen. Naive CD4+ T cells confer idiotype-specific tumor resistance in the absence of antibodies. Eur J Immunol 25:3079–3086 (1995).
D. Mumberg, P.A. Monach, S. Wanderling, M. Philip, A.Y. Toledano, R.D. Schreiber and H. Schreiber. CD4(+) T cells eliminate MHC class II-negative cancer cells in vivo by indirect effects of IFN-gamma. Proc Natl Acad Sci USA 96:8633–8638 (1999).
F. Fallarino, U. Grohmann, R. Bianchi, C. Vacca, M.C. Fioretti and P. Puccetti. Th1 and Th2 cell clones to a poorly immunogenic tumor antigen initiate CD8+ T cell-dependent tumor eradication in vivo. J Immunol 165:5495–5501 (2000).
Z. Dembic, K. Schenck and B. Bogen. Dendritic cells purified from myeloma are primed with tumor-specific antigen (idiotype) and activate CD4+ T cells. Proc Natl Acad Sci USA 97:2697–2702 (2000).
Z. Dembic, J.A. Rottingen, J. Dellacasagrande, K. Schenck and B. Bogen. Phagocytic dendritic cells from myelomas activate tumor-specific T cells at a single cell level. Blood 97:2808–2814 (2001).
F. Ossendorp, E. Mengede, M. Camps, R. Filius and C.J. Melief. Specific T helper cell requirement for optimal induction of cytotoxic T lymphocytes against major histocompatibility complex class II negative tumors. J Exp Med 187:693–702 (1998).
D.R. Surman, M.E. Dudley, W.W. Overwijk and N.P. Restifo. Cutting edge: CD4+ T cell control of CD8+ T cell reactivity to a model tumor antigen. J Immunol 164:562–565 (2000).
F.G. Gao, V. Khammanivong, W.J. Liu, G.R. Leggatt, I.H. Frazer and G.J. Fernando. Antigen-specific CD4+ T-cell help is required to activate a memory CD8+ T cell to a fully functional tumor killer cell. Cancer Res 62:6438–6441 (2002).
P.D. Greenberg, D.E. Kern and M.A. Cheever. Therapy of disseminated murine leukemia with cyclophosphamide and immune Lyt-1+,2-T cells: tumor eradication does not require participation of cytotoxic T cells. J Exp Med 161:1122–1134 (1985).
C.M. Coughlin, K.E. Salhany, M.S. Gee, D.C. LaTemple, S. Kotenko, X. Ma, G. Gri, M. Wysocka, J.E. Kim, L. Liu, F. Liao, J.M. Farber, S. Pestka, G. Trinchieri and W.M. Lee. Tumor cell responses to IFNgamma affect tumorigenicity and response to IL-12 therapy and antiangiogenesis. Immunity 9:25–34 (1998).
P.D. Greenberg, M.A. Cheever and A. Fefer. Eradication of disseminated murine leukemia by chemoimmunotherapy with cyclophosphamide and adoptively transferred immune syngeneic Lyt-1+2-lymphocytes. J Exp Med 154:952–963 (1981).
M. Kahn, H. Sugawara, P. McGowan, K. Okuno, S. Nagoya, K.E. Hellstrom, I. Hellstrom and P. Greenberg. CD4+ T cell clones specific for the human p97 melanoma-associated antigen can eradicate pulmonary metastases from a murine tumor expressing the p97 antigen. J Immunol 146:3235–3241 (1991).
T. Nishimura, K. Iwakabe, M. Sekimoto, Y. Ohmi, T. Yahata, M. Nakui, T. Sato, S. Habu, H. Tashiro, M. Sato and A. Ohta. Distinct role of antigen-specific T helper type 1 (Th1) and Th2 cells in tumor eradication in vivo. J Exp Med 190:617–627 (1999).
K.U. Lundin, P.O. Hofgaard, H. Omholt, L.A. Munthe, A. Corthay and B. Bogen. Therapeutic effect of idiotype-specific CD4+ T cells against B-cell lymphoma in the absence of anti-idiotypic antibodies. Blood 102:605–612 (2003).
F.M. Burnet. The concept of immunological surveillance. Prog Exp Tumor Res 13:1–27 (1970).
D.H. Kaplan, V. Shankaran, A.S. Dighe, E. Stockert, M. Aguet, L.J. Old and R.D. Schreiber. Demonstration of an interferon gamma-dependent tumor surveillance system in immunocompetent mice. Proc Natl Acad Sci USA 95:7556–7561 (1998).
M.J. Smyth, K.Y. Thia, S.E. Street, E. Cretney, J.A. Trapani, M. Taniguchi, T. Kawano, S.B. Pelikan, N.Y. Crowe and D.I. Godfrey. Differential tumor surveillance by natural killer (NK) and NKT cells. J Exp Med 191:661–668 (2000).
M.J. Smyth, K.Y. Thia, S.E. Street, D. MacGregor, D.I. Godfrey and J.A. Trapani. Perforin-mediated cytotoxicity is critical for surveillance of spontaneous lymphoma. J Exp Med 192:755–760 (2000).
V. Shankaran, H. Ikeda, A.T. Bruce, J.M. White, P.E. Swanson, L.J. Old and R.D. Schreiber. IFNgamma and lymphocytes prevent primary tumour development and shape tumour immunogenicity. Nature 410:1107–1111 (2001).
M. Girardi, D.E. Oppenheim, C.R. Steele, J.M. Lewis, E. Glusac, R. Filler, P. Hobby, B. Sutton, R.E. Tigelaar and A.C. Hayday. Regulation of cutaneous malignancy by gammadelta T cells. Science 294:605–609 (2001).
S.E. Street, J.A. Trapani, D. MacGregor and M.J. Smyth. Suppression of lymphoma and epithelial malignancies effected by interferon gamma. J Exp Med 196:129–134 (2002).
K. Takeda, M.J. Smyth, E. Cretney, Y. Hayakawa, N. Kayagaki, H. Yagita and K. Okumura. Critical role for tumor necrosis factor-related apoptosis-inducing ligand in immune surveillance against tumor development. J Exp Med 195:161–169 (2002).
R.A. Gatti and R.A. Good. Occurrence of malignancy in immunodeficiency diseases: a literature review. Cancer 28:89–98 (1971).
S.A. Birkeland, H.H. Storm, L.U. Lamm, L. Barlow, I. Blohme, B. Forsberg, B. Eklund, O. Fjeldborg, M. Friedberg and L. Frodin. Cancer risk after renal transplantation in the Nordic countries, 1964–1986. Int J Cancer 60:183–189 (1995).
A. Corthay, D.K. Skovseth, K.U. Lundin, E. Rosjo, H. Omholt, P.O. Hofgaard, G. Haraldsen and B. Bogen. Primary antitumor immune response mediated by CD4+ T cells. Immunity 22:371–383 (2005).
G.F. Lauritzsen, S. Weiss, Z. Dembic and B. Bogen. Naive idiotype-specific CD4+ T cells and immunosurveillance of B-cell tumors. Proc Natl Acad Sci USA 91:5700–5704 (1994).
Z. Dembic, P.O. Hofgaard, H. Omholt and B. Bogen. Anti-class II antibodies, but not cytotoxic T-lymphocyte antigen 4-immunoglobulin hybrid molecules, prevent rejection of major histocompatibility complex class II-negative myeloma in T-cell receptor-transgenic mice. Scand J Immunol 60:143–152 (2004).
H.K. Kleinman, M.L. McGarvey, J.R. Hassell, V.L. Star, F.B. Cannon, G.W. Laurie and G.R. Martin. Basement membrane complexes with biological activity. Biochemistry 25:312–318 (1986).
B. Bottazzi, N. Polentarutti, R. Acero, A. Balsari, D. Boraschi, P. Ghezzi, M. Salmona and A. Mantovani. Regulation of the macrophage content of neoplasms by chemoattractants. Science 220:210–212 (1983).
R.D. Schreiber, J.L. Pace, S.W. Russell, A. Altman and D.H. Katz. Macrophage-activating factor produced by a T cell hybridoma: physiochemical and biosynthetic resemblance to gamma-interferon. J Immunol 131:826–832 (1983).
A. Mantovani, et al. A. Sica, S. Sozzani, P. Allavena, A. Vecchi and M. Locati. The chemokine system in diverse forms of macrophage activation and polarization. Trends Immunol 25:677–686 (2004).
R. Evans and P. Alexander. Cooperation of immune lymphoid cells with macrophages in tumour immunity. Nature 228:620–622 (1970).
R. Evans and P. Alexander. Mechanism of immunologically specific killing of tumour cells by macrophages. Nature 236:168–170 (1972).
L. Bingle, N.J. Brown and C.E. Lewis. The role of tumour-associated macrophages in tumour progression: implications for new anticancer therapies. J Pathol 196:254–265 (2002).
J.W. Pollard. Tumour-educated macrophages promote tumour progression and metastasis. Nat Rev Cancer 4:71–78 (2004).
K. Tsung, J.P. Dolan, Y.L. Tsung and J.A. Norton. Macrophages as effector cells in interleukin 12-induced T cell-dependent tumor rejection. Cancer Res 62:5069–5075 (2002).
C. Guiducci, A.P. Vicari, S. Sangaletti, G. Trinchieri and M.P. Colombo. Redirecting in vivo elicited tumor infiltrating macrophages and dendritic cells towards tumor rejection. Cancer Res 65:3437–3446 (2005).
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Corthay, A. (2007). CD4+ T Cells Cooperate With Macrophages for Specific Elimination of MHC Class II-Negative Cancer Cells. In: Katsikis, P.D., Schoenberger, S.P., Pulendran, B. (eds) Crossroads between Innate and Adaptive Immunity. Advances in Experimental Medicine and Biology, vol 590. Springer, Boston, MA. https://doi.org/10.1007/978-0-387-34814-8_14
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DOI: https://doi.org/10.1007/978-0-387-34814-8_14
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