Han-zhong LI, Yu-shi ZHANG, Guo-yang ZHENG. Commentary on and Expectation of Tumor Immunotherapy[J]. Medical Journal of Peking Union Medical College Hospital, 2018, 9(4): 289-294. doi: 10.3969/j.issn.1674-9081.2018.04.001
Citation: Han-zhong LI, Yu-shi ZHANG, Guo-yang ZHENG. Commentary on and Expectation of Tumor Immunotherapy[J]. Medical Journal of Peking Union Medical College Hospital, 2018, 9(4): 289-294. doi: 10.3969/j.issn.1674-9081.2018.04.001

Commentary on and Expectation of Tumor Immunotherapy

doi: 10.3969/j.issn.1674-9081.2018.04.001
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  • Corresponding author: 李汉忠 电话:010-69152510, E-mail:hzlipumch@163.com LI Han-zhong Tel:010-69152510, E-mail:hzlipumch@163.com
  • Received Date: 2018-04-11
  • Publish Date: 2018-07-30
  • With the rapid development of tumor immunology, immunotherapy for malignant tumors is becoming a research focus, offering an effective opportunity for the treatment of patients with advanced tumors. Immune checkpoint inhibitors, such as programmed cell death 1 receptor/programmed cell death 1 ligand 1 antibody and CTLA-4 antibody, are an important research hotspot of immunotherapy for advanced cancers. FDA has approved some immune checkpoint antibodies for the treatment of advanced metastatic melanoma, non-small cell lung cancer, renal cell carcinoma, uroepithelium carcinoma, and non-Hodgkin's lymphoma, and the efficacy and safety for above tumors has been confirmed. In addition, chemiric antigen receptor T-cell therapy treatment showed a strong and persistent therapeutic effect for hematologic malignancy, as another successful case of immunotherapy. Cancer vaccine such as Simpuleucel-T was also another milestone in the development of tumor immunotherapy. Currently, immunotherapy for malignant tumors is presenting a promising future.
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  • [1] Panaccio M, Zalcberg JR, Thompson CH, et al. Heteroge-neity of the human transferrin receptor and use of anti-transferrin receptor antibodies to detect tumours in vivo[J]. Immunol Cell Biol, 1987, 65:461-472. doi:  10.1038/icb.1987.55
    [2] Burnet FM. The concept of immunological surveillance[J]. Prog Exp Tumor Res, 1970, 13:1-27. doi:  10.1159/000386035
    [3] Traversari C, van der Bruggen P, Luescher IF, et al. A nonapeptide encoded by human gene MAGE-1 is recognized on HLA-A1 by cytolytic T lymphocytes directed against tumor antigen MZ2-E[J]. J Exp Med, 1992, 176:1453-1457. doi:  10.1084/jem.176.5.1453
    [4] Jensen PE. Recent advances in antigen processing and presentation[J]. Nat Immunol, 2007, 8:1041-1048. doi:  10.1038/ni1516
    [5] Topalian SL, Drake CG, Pardoll DM. Targeting the PD-1/B7-H1(PD-L1) pathway to activate anti-tumor immunity[J]. Curr Opin Immunol, 2012, 24:207-212. doi:  10.1016/j.coi.2011.12.009
    [6] Ishida Y, Agata Y, Shibahara K, et al. Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death[J]. EMBO J, 1992, 11: 3887-3895. doi:  10.1002/j.1460-2075.1992.tb05481.x
    [7] Keir ME, Butte MJ, Freeman GJ, et al. PD-1 and its ligands in tolerance and immunity[J]. Annu Rev Immunol, 2008, 26:677-704. doi:  10.1146/annurev.immunol.26.021607.090331
    [8] Dong H, Zhu G, Tamada K, et al. B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion[J]. Nat Med, 1999, 5:1365-1369. doi:  10.1038/70932
    [9] Latchman Y, Wood CR, Chernova T, et al. PD-L2 is a second ligand for PD-1 and inhibits T cell activation[J]. Nat Immunol, 2001, 2:261-268. doi:  10.1038/85330
    [10] Buchbinder EI, Desai A. CTLA-4 and PD-1 Pathways: Similarities, Differences, and Implications of Their Inhibition[J]. Am J Clin Oncol, 2016, 39:98-106. doi:  10.1097/COC.0000000000000239
    [11] Fife BT, Pauken KE, Eagar TN, et al. Interactions between PD-1 and PD-L1 promote tolerance by blocking the TCR-induced stop signal[J]. Nat Immunol, 2009, 10:1185-1192. doi:  10.1038/ni.1790
    [12] Keir ME, Liang SC, Guleria I, et al. Tissue expression of PD-L1 mediates peripheral T cell tolerance[J]. J Exp Med, 2006, 203:883-895. doi:  10.1084/jem.20051776
    [13] Chemnitz JM, Parry RV, Nichols KE, et al. SHP-1 and SHP-2 associate with immunoreceptor tyrosine-based switch motif of programmed death 1 upon primary human T cell stimulation, but only receptor ligation prevents T cell activation[J]. J Immunol, 2004, 173:945-954. doi:  10.4049/jimmunol.173.2.945
    [14] Parry RV, Chemnitz JM, Frauwirth KA, et al. CTLA-4 and PD-1 receptors inhibit T-cell activation by distinct mech-anisms[J]. Mol Cell Biol, 2005, 25:9543-9553. doi:  10.1128/MCB.25.21.9543-9553.2005
    [15] Homet Moreno B, Ribas A. Anti-programmed cell death protein-1/ligand-1 therapy in different cancers[J]. Br J Cancer, 2015, 112:1421-1427. doi:  10.1038/bjc.2015.124
    [16] Motzer RJ, Rini BI, McDermott DF, et al. Nivolumab for metastatic renal cell carcinoma: results of a randomized phase Ⅱ trial[J]. J Clin Oncol, 2015, 33:1430-1437. doi:  10.1200/JCO.2014.59.0703
    [17] Topalian SL, Hodi FS, Brahmer JR, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer[J]. N Engl J Med, 2012, 366:2443-2454. doi:  10.1056/NEJMoa1200690
    [18] Motzer RJ, Escudier B, McDermott DF, et al. Nivolumab versus Everolimus in Advanced Renal-Cell Carcinoma[J]. N Engl J Med, 2015, 373:1803-1813. doi:  10.1056/NEJMoa1510665
    [19] Rosenberg JE, Hoffman-Censits J, Powles T, et al. Atezolizumab in patients with locally advanced and metastatic urothelial carcinoma who have progressed following treatment with platinum-based chemotherapy: a single arm, phase 2 trial[J]. Lancet, 2016, 387:1909-1920. doi:  10.1016/S0140-6736(16)00561-4
    [20] Gandini S, Massi D, Mandalà M. PD-L1 expression in cancer patients receiving anti PD-1/PD-L1 antibodies: A systematic review and meta-analysis[J]. Crit Rev Oncol Hematol, 2016, 100:88-98. doi:  10.1016/j.critrevonc.2016.02.001
    [21] McDermott DF, Sosman JA, Sznol M, et al. Atezolizumab, an Anti-Programmed Death-Ligand 1 Antibody, in Metastatic Renal Cell Carcinoma: Long-Term Safety, Clinical Activity, and Immune Correlates from a Phase Ia Study[J]. J Clin Oncol, 2016, 34:833-842. doi:  10.1200/JCO.2015.63.7421
    [22] Robert C, Long GV, Brady B, et al. Nivolumab in previously untreated melanoma without BRAF mutation[J]. N Engl J Med, 2015, 372:320-330. doi:  10.1056/NEJMoa1412082
    [23] Brahmer J, Reckamp KL, Baas P, et al. Nivolumab versus docetaxel in advanced squamous-cell non-small-cell lung cancer[J]. N Engl J Med, 2015, 373:123-135. doi:  10.1056/NEJMoa1504627
    [24] Hammers HJ, Plimack ER, Infante JR, et al. Safety and Efficacy of Nivolumab in Combination with Ipilimumab in Metastatic Renal Cell Carcinoma: The CheckMate 016 Study[J]. J Clin Oncol, 2017, 35:3851-3858. doi:  10.1200/JCO.2016.72.1985
    [25] Weinstock M, McDermott D. Targeting PD-1/PD-L1 in the treatment of metastatic renal cell carcinoma[J]. Ther Adv Urol, 2015, 7:365-377. doi:  10.1177/1756287215597647
    [26] Anassi E, Ndefo UA. Sipuleucel-T (provenge) injection: the first immunotherapy agent (vaccine) for hormone-refractory prostate cancer[J]. P T, 2011, 36:197-202.
    [27] Cheever MA, Higano CS. PROVENGE (Sipuleucel-T) in prostate cancer: the first FDA-approved therapeutic cancer vaccine[J]. Clin Caner Res, 2011, 17:3520-3526. doi:  10.1158/1078-0432.CCR-10-3126
    [28] Small EJ, Schellhammer PF, Higano CS, et al. Placebo-controlled phase Ⅲ trial of immunologic therapy with sipuleucel-T (APC8015) in patients with metastatic, asymptomatic hormone refractory prostate cancer[J]. J Clin Oncol, 2006, 24:3089-3094. doi:  10.1200/JCO.2005.04.5252
    [29] Kantoff PW, Higano CS, Shore ND, et al. Sipuleucel-T immunotherapy for castration-resistant prostate cancer[J]. N Engl Med, 2010, 363:411-422. doi:  10.1056/NEJMoa1001294
    [30] Gross G, Waks T, Eshhar Z. Expression of immunoglobulin-T-cell receptor chimeric molecules as functional receptors with antibody-type specificity[J]. Proc Natl Acad Sci U S A, 1989, 86: 10024-10028. doi:  10.1073/pnas.86.24.10024
    [31] Porter DL, Levine BL, Kalos M, et al. Chimeric antigen receptor-modified T cells in chronic lymphoid leukemia[J]. N Engl J Med, 2011, 365:725-733. doi:  10.1056/NEJMoa1103849
    [32] Cheadle EJ, Gornall H, Baldan V, et al. CAR-T cells: Driving the road from the laboratory to the clinic[J]. Immunol Rev, 2014, 257:91-106. doi:  10.1111/imr.12126
    [33] Sadelain M, Rivière I, Riddell S. Therapeutic T cell engineering[J]. Nature, 2017, 545:423-431. doi:  10.1038/nature22395
    [34] Bukowski RM. Natural history and therapy of metastatic renal cell carcinoma: the role of interleukin-2[J]. Cancer, 1997, 80:1198-1220. doi:  10.1002/(SICI)1097-0142(19971001)80:7<1198::AID-CNCR3>3.0.CO;2-H
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