ARTYKUŁ PRZEGLĄDOWY
Wartości odsetkowe komórek iNKT na tle innych komórek układu odpornościowego w różnych stadiach zaawansowana raka krtani
Janusz Klatka 1 , Ewelina Grywalska 2 , Magdalena Wasiak 1 , Justyna Markowicz 3 , Piotr Trojanowski 1 , Witold Olszański 1 , Jacek Roliński1. Department of Otolaryngology and Laryngeal Oncology, Medical University of Lublin, Lublin, Poland
2. epartment of Clinical Immunology and Immunotherapy, Medical University of Lublin, Lublin, Poland
3. Department of Clinical Immunology and Immunotherapy, Medical University of Lublin, Lublin, Poland
Opublikowany: 2016-04-28
DOI: 10.5604/17322693.1200688
GICID: 01.3001.0009.6820
Dostępne wersje językowe: pl en
Wydanie: Postepy Hig Med Dosw 2016; 70 : 392-399
Abstrakt
Przypisy
- 1. Aragane Y., Maeda A., Cui C.Y., Tezuka T., Kaneda Y., Schwarz T.:Inhibition of growth of melanoma cells by CD95 (Fas/APO-1) genetransfer in vivo. J. Invest. Dermatol., 2000; 115: 1008-1014
Google Scholar - 2. Bendelac A., Savage P.B., Teyton L.: The biology of NKT cells.Annu. Rev. Immunol., 2007; 25: 297-336
Google Scholar - 3. Bojarska-Junak A., Tabarkiewicz J., Roliński J.: NKT cells: theirdevelopment, mechanisms and effects of action. Postepy Hig. Med.Dośw., 2013; 67: 65-78
Google Scholar - 4. Chen B., Zhang D., Zhou J., Li Q., Zhou L., Li S.M., Zhu L., Chou K.Y.,Zhou L., Tao L., Lu L.M.: High CCR6/CCR7 expression and Foxp3+ Tregcell number are positively related to the progression of laryngealsquamous cell carcinoma. Oncol. Rep., 2013; 30: 1380-1390
Google Scholar - 5. De Santo C., Salio M., Masri S.H., Lee L.Y., Dong T., Speak A.O.,Porubsky S., Booth S., Veerapen N., Besra G.S., Gröne H.J., Platt F.M.,Zambon M., Cerundolo V.: Invariant NKT cells reduce the immunosuppressiveactivity of influenza A virus-induced myeloid-derived suppressor cells in mice and humans. J. Clin. Invest., 2008;118: 4036-4048
Google Scholar - 6. Klatka J., Grywalska E., Klatka M., Rahnama M., Polak A., RolinskiJ.: Expression of CD200 and CD200R regulatory molecules on theCD83+ monocyte-derived dendritic cells generated from patientswith laryngeal cancer. Folia Histochem. Cytobiol., 2013; 51: 59-65
Google Scholar - 7. Marschner A., Rothenfusser S., Hornung V., Prell D., Krug A., KerkmannM., Wellisch D., Poeck H., Greinacher A., Giese T., Endres S.,Hartmann G.: CpG ODN enhance antigen-specific NKT cell activationvia plasmacytoid dendritic cells. Eur. J. Immunol., 2005; 35: 2347-2357
Google Scholar - 8. Matsuda J.L., Mallevaey T., Scott-Browne J., Gapin L.: CD1d-restrictediNKT cells, the ‘Swiss-Army knife’ of the immune system.Curr. Opin. Immunol., 2008; 20: 358-368
Google Scholar - 9. Molling J.W., Langius J.A., Langendijk J.A., Leemans C.R., BontkesH.J., van der Vliet H.J., von Blomberg B.M., Scheper R.J., van den EertweghA.J.: Low levels of circulating invariant natural killer T cellspredict poor clinical outcome in patients with head and neck squamouscell carcinoma. J. Clin. Oncol., 2007; 25: 862-868
Google Scholar - 10. Molling J.W., Moreno M., van der Vliet H.J., van den EertweghA.J., Scheper R.J., von Blomberg B.M., Bontkes H.J.: Invariant naturalkiller T cells and immunotherapy of cancer. Clin. Immunol., 2008;129: 182-194
Google Scholar - 11. Motohashi S., Ishikawa A., Ishikawa E., Otsuji M., Iizasa T., HanaokaH., Shimizu N., Horiguchi S., Okamoto Y., Fujii S., Taniguchi M.,Fujisawa T., Nakayama T.: A phase I study of in vitro expanded naturalkiller T cells in patients with advanced and recurrent non-smallcell lung cancer. Clin. Cancer Res., 2006; 12: 6079-6086
Google Scholar - 12. Motohashi S., Kobayashi S., Ito T., Magara K.K., Mikuni O., KamadaN., Iizasa T., Nakayama T., Fujisawa T., Taniguchi M.: PreservedIFN-α production of circulating Vα24 NKT cells in primary lung cancerpatients. Int. J. Cancer, 2002; 102: 159-165
Google Scholar - 13. Motohashi S., Okamoto Y., Yoshino I., Nakayama T.: Anti-tumorimmune responses induced by iNKT cell-based immunotherapyfor lung cancer and head and neck cancer. Clin. Immunol., 2011;140: 167-176
Google Scholar - 14. Nelke K.H., Pawlak W., Leszczyszyn J., Gerber H.: Photodynamictherapy in head and neck cancer. Postępy Hig. Med. Dośw., 2014;68: 119-128
Google Scholar - 15. Pantel M., Guntinas-Lichius O.: Laryngeal carcinoma: epidemiology,risk factors and survival. HNO, 2012; 60: 32-40
Google Scholar - 16. Ren J., Zhu D., Liu M., Sun Y., Tian L.: Downregulation of miR- 21 modulates Ras expression to promote apoptosis and suppressinvasion of laryngeal squamous cell carcinoma. Eur. J. Cancer, 2010;46: 3409-3416
Google Scholar - 17. Ritoe S.C., de Vegt F., Scheike I.M., Krabbe P.F., Kaanders J.H., vanden Hoogen F.J., Verbeek A.L., Marres H.A.: Effect of routine followupafter treatment for laryngeal cancer on life expectancy and mortality:results of a Markov model analysis. Cancer, 2007; 109: 239-247
Google Scholar - 18. Sakuishi K., Oki S., Araki M., Porcelli S.A., Miyake S., YamamuraT.: Invariant NKT cells biased for IL-5 production act as crucial regulatorsof inflammation. J. Immunol., 2007; 179: 3452-3462
Google Scholar - 19. Song L., Asgharzadeh S., Salo J., Engell K., Wu H.W., SpostoR., Ara T., Silverman A.M., DeClerck Y.A., Seeger R.C., MetelitsaL.S.: Vα24-invariant NKT cells mediate antitumor activity viakilling of tumor-associated macrophages. J. Clin. Invest., 2009;119: 1524-1536
Google Scholar - 20. Starska K., Głowacka E., Kulig A., Lewy-Trenda I., Bryś M., LewkowiczP.: The role of tumor cells in the modification of T lymphocytesactivity–the expression of the early CD69+, CD71+ and the late CD25+,CD26+, HLA/DR+ activation markers on T CD4+ and CD8+ cells in squamouscell laryngeal carcinoma. Part I. Folia Histochem. Cytobiol.,2011; 49: 579-592
Google Scholar - 21. Starska K., Głowacka E., Kulig A., Lewy-Trenda I., Bryś M., LewkowiczP.: Prognostic value of the immunological phenomena andrelationship with clinicopathological characteristics of the tumor- the expression of the early CD69+, CD71+ and the late CD25+, CD26+,HLA/DR+ activation markers on T CD4+ and CD8+ lymphocytes insquamous cell laryngeal carcinoma. Part II. Folia Histochem. Cytobiol.,2011; 49: 593-603
Google Scholar - 22. Sun W., Li W.J., Wu C.Y., Zhong H., Wen W.P.: CD45RA-Foxp3highbut not CD45RA+Foxp3low suppressive T regulatory cells increased inthe peripheral circulation of patients with head and neck squamouscell carcinoma and correlated with tumor progression. J. Exp. Clin.Cancer Res., 2014: 25: 33: 35
Google Scholar - 23. Tagawa T., Wu L., Anraku M., Yun Z., Rey-McIntyre K., de PerrotM.: Antitumor impact of interferon-γ producing CD1d-restrictedNKT cells in murine malignant mesothelioma. J. Immunother.,2013; 36: 391-399
Google Scholar - 24. Tahir S.M., Cheng O., Shaulov A., Koezuka Y., Bubley G.J., WilsonS.B., Balk S.P., Exley M.A.: Loss of IFN-γ production by invariant NK Tcells in advanced cancer. J. Immunol., 2001; 167: 4046-4050
Google Scholar - 25. Terabe M., Berzofsky J.A.: The role of NKT cells in tumor immunity.Adv. Cancer Res., 2008; 101: 277-348
Google Scholar - 26. van der Vliet H.J., Molling J.W., von Blomberg B.M., Kölgen W.,Stam A.G., de Gruijl T.D., Mulder C.J., Janssen H.L., Nishi N., vanden Eertwegh A.J., Scheper R.J., van Nieuwkerk C.J.: CirculatingVα24+Vβ11+ NKT cell numbers and dendritic cell CD1d expression inhepatitis C virus infected patients. Clin. Immunol., 2005; 114: 183-189
Google Scholar - 27. Wu L., Gabriel C.L., Parekh V.V., Van Kaer L.: Invariant naturalkiller T cells: innate-like T cells with potent immunomodulatoryactivities. Tissue Antigens, 2009; 73: 535-545
Google Scholar - 28. Yanagisawa K., Seino K., Ishikawa Y., Nozue M., Todoroki T.,Fukao K.: Impaired proliferative response of Vα 24 NKT cells fromcancer patients against α-galactosylceramide. J. Immunol., 2002;168: 6494-6499
Google Scholar - 29. Ziolkowska E., Wolowiec D., Cebula-Obrzut B., Blonski J.Z.,Smolewski P., Robak T., Korycka-Wolowiec A.: Cytotoxic and apoptosis-inducing effects of bendamustine used alone and in combinationwith rituximab on chronic lymphocytic leukemia cells in vitro.Postępy Hig. Med. Dośw., 2014; 68: 1433-1443
Google Scholar