Number of purchasers: 2, views: 1538
Readers community rating: votes 0
1. Fridman W.-H., Dieu-Nosjean M.-C., Pagès F., Cremer I., Damotte D., Sautès-Fridman C., Galon J. The immune microenvironment of human tumors: general signifi cance and clinical impact. Cancer Microenviron. 2013. 6 (2), 117–122.
2. Fridman W. H., Pagès F., Sautès-Fridman C., Galon J. The immune contexture in human tumours: impact on clinical outcome. Nat. Rev. Cancer 2012, 12 (4), 298–306.
3. Hadrup S., Donia M., Thor Straten P. Eff ector CD4 and CD8 T cells and their role in the tumor microenvironment. Cancer Microenviron. 2013, 6 (2), 123–133.
4. Gu-Trantien C., Loi S., Garaud S., Equeter C., Libin M., de Wind A., Ravoet M., Le Buanec H., Sibille C., Manfouo-Foutsop G., Veys I., Haibe-Kains B., Singhal S. K., Michiels S., Rothé F., Salgado R., Duvillier H., Ignatiadis M., Desmedt C., Bron D., Larsimont D., Piccart M., Sotiriou C., Willard-Gallo K., Perou C., Sorlie T., Sotiriou C., Pusztai L., Sotiriou C., Ascierto M., Teschendorff A., Miremadi A., Pinder S., Ellis I., Caldas C., Alexe G., Desmedt C., Schmidt M., Rody A., Yau C., Esserman L., Moore D., Waldman F., Sninsky J., Benz C., Ascierto M., Rody A., Rahir G., Moser M., Mahmoud S., Mahmoud S., Lee A., Ellis I., Green A., Bos R., Marquardt K., Cheung J., Sherman L., Bos R., Sherman L., Ruff ell B., DeNardo D., Aff ara N., Coussens L., Zamarron B., Chen W., Gobert M., Wilke C., Ye J., Livergood R., Peng G., deLeeuw R., Kost S., Kakal J., Nelson B., Chaisemartin L. de, Dieu-Nosjean M., Coppola D., Vinuesa C., Cyster J., Ruff ell B., Au A., Rugo H., Esserman L., Hwang E., Coussens L., Chtanova T, Miyara M., Lee M., Hanspers K., Barker C., Korn A., McCune J., Ravoet M., Zaunders J., Baniyash M., Fazilleau N., Mark L., McHeyzer-Williams L., McHeyzer-Williams M., Balkwill F., Razis E., Panse J., Link A., Crotty S., Viegas M., Crotty S., Ignatiadis M., Grange C., Hayden M., Ghosh S., Kim T., Chang M., Yu K., Kwon H., Norman D., Vig E., Goebl M., Harrington M., Macian F., Lopez-Rodriguez C., Rao A., Xiao G., Deng A., Liu H., Ge G., Liu X., Ghebeh H., Good-Jacobson K., Szumilas C., Chen L., Sharpe A., Tomayko M., Shlomchik M., Mihalj M., Kellermayer Z., Balogh P., Inozume T., O’Shea J., Paul W., Galon J., Yoon H., Orrock J., Foster N., Sargent D., Smyrk T., Sinicrope F., Shankaran V., Curtis N., Primrose J., Thomas G., Mirnezami A., Ottensmeier C., Haabeth O., Braumuller H., Ji Y., Zhang W., Kryczek I., Curiel T., Ladoire S., Kim M., Watanabe M., Oda J., Amarante M., Voltarelli J. C., Bates G., West N., Breitfeld D., Schaerli P., Willimann K., Lang A., Lipp M., Loetscher P., Moser B., McHeyzer-Williams M., Okitsu S., Wang N., McHeyzer-Williams L., Ramiscal R., Vinuesa C., Nelson B., Lohr M., Mahmoud S., Lee A., Paish E., Macmillan R., Ellis I., Green A., Nielsen J., Ladanyi A., Maletzki C., Jahnke A., Ostwald C., Klar E., Prall F., Linnebacher M., Coronella J., Coronella-Wood J., Hersh E., Bianchini G., Foo S., Phipps S., Martinet L., Muller G., Hopken U., Lipp M., Wang C., Hillsamer P., Kim C., Denkert C., Haibe-Kains B. CD4+ follicular helper T cell infi ltration predicts breast cancer survival. J. Clin. Invest. 2013, 123 (7), 2873–2892.
5. Bronkhorst I. H. G., Vu T. H. K., Jordanova E. S., Luyten G. P. M., Burg S. H. van der, Jager M. J. Diff erent Subsets of Tumor-Infi ltrating Lymphocytes Correlate with Macrophage Infl ux and Monosomy 3 in Uveal Melanoma. Investig. Opthalmology Vis. Sci. 2012, 53 (9), 5370.
6. Chaudhary B., Elkord E. Regulatory T Cells in the Tumor Microenvironment and Cancer Progression: Role and Therapeutic Targeting. Vaccines 2016, 4 (3), 28.
7. Sakuishi K., Apetoh L., Sullivan J. M., Blazar B. R., Kuchroo V. K., Anderson A. C. Targeting Tim-3 and PD-1 pathways to reverse T cell exhaustion and restore anti-tumor immunity. J. Exp. Med. 2010, 207 (10), 2187–2194.
8. Park H.J., Kusnadi A., Lee E.-J., Kim W. W., Cho B. C., Lee I. J., Seong J., Ha S.-J. Tumor-infi ltrating regulatory T cells delineated by upregulation of PD-1 and inhibitory receptors. Cell. Immunol. 2012, 278 (1–2), 76–83.
9. Schmidt A., Oberle N., Krammer P. H. Molecular mechanisms of treg-mediated T cell suppression. Front. Immunol. 2012, 3, 51.
10. Dieu-Nosjean M.-C., Antoine M., Danel C., Heudes D., Wislez M., Poulot V., Rabbe N., Laurans L., Tartour E., de Chaisemartin L., Lebecque S., Fridman W.-H., Cadranel J. Long-term survival for patients with non-smallcell lung cancer with intratumoral lymphoid structures. J. Clin. Oncol. 2008, 26 (27), 4410–4417.
11. Dieu-Nosjean M.-C., Giraldo N. A., Kaplon H., Germain C., Fridman W. H., Sautès-Fridman C. Tertiary lymphoid structures, drivers of the anti-tumor responses in human cancers. Immunol. Rev. 2016, 271 (1), 260–275.
12. Castan J., Tenner-Racz K., Racz P., Fleischer B., Bröker B. M. Accumulation of CTLA-4 expressing T lymphocytes in the germinal centres of human lymphoid tissues. Immunology 1997, 90 (2), 265–271.
13. Wang C. J., Heuts F., Ovcinnikovs V., Wardzinski L., Bowers C., Schmidt E. M., Kogimtzis A., Kenefeck R., Sansom D. M., Walker L. S. K. CTLA-4 controls follicular helper T-cell diff erentiation by regulating the strength of CD28 engagement. Proc. Natl. Acad. Sci. U. S. A. 2015, 112 (2), 524–529.
14. Sage P. T., Paterson A. M., Lovitch S. B., Sharpe A. H. The coinhibitory receptor CTLA-4 controls B cell responses by modulating T follicular helper, T follicular regulatory, and T regulatory cells. Immunity 2014, 41 (6), 1026–1039.
15. Sage P. T., Francisco L. M., Carman C. V, Sharpe A. H. The receptor PD-1 controls follicular regulatory T cells in the lymph nodes and blood. Nat. Immunol. 2013, 14 (2), 152–161.
16. Solinas C., Garaud S., De Silva P., Boisson A., Van den Eynden G., de Wind A., Risso P., Rodrigues Vitória J., Richard F., Migliori E., Noël G., Duvillier H., Craciun L., Veys I., Awada A., Detours V., Larsimont D., Piccart-Gebhart M., Willard-Gallo K. Immune Checkpoint Molecules on Tumor-Infi ltrating Lymphocytes and Their Association with Tertiary Lymphoid Structures in Human Breast Cancer. Front. Immunol. 2017, 8, 1412.
17. Apel R. L., Asa S. L., LiVolsi V. A. Papillary Hürthle cell carcinoma with lymphocytic stroma. «Warthin-like tumor» of the thyroid. Am. J. Surg. Pathol. 1995, 19 (7), 810–814.
18. D’Antonio A., De Chiara A., Santoro M., Chiappetta G., Losito N. S. Warthin-like tumour of the thyroid gland: RET/PTC expression indicates it is a variant of papillary carcinoma. Histopathology 2000, 36 (6), 493–498.
19. Urano M., Abe M., Kuroda M., Mizoguchi Y., Horibe Y., Kasahara M., Tanaka K., Sudo K., Hirasawa Y. Warthin-like tumor variant of papillary thyroid carcinoma: case report and literature review. Pathol. Int. 2001, 51 (9), 707–712.
20. Vera-Sempere F. J., Prieto M., Camañas A. Warthinlike Tumor of the Thyroid: A Papillary Carcinoma with Mitochondrion-rich Cells and Abundant Lymphoid Stroma. A Case Report. Pathol. – Res. Pract. 1998, 194 (5), 341–347.
21. Lam K. Y., Lo C. Y., Wei W. I. Warthin tumor-like variant of papillary thyroid carcinoma: a case with dedifferentiation (anaplastic changes) and aggressive biological behavior. Endocr. Pathol. 2005, 16 (1), 83–89.
22. Amico P., Lanzafame S., Li Destri G., Greco P., Caltabiano R., Vecchio G. M., Magro G. Warthin tumor-like papillary thyroid carcinoma with a minor dediff erentiated component: report of a case with clinicopathologic considerations. Case Rep. Med. 2010, 495281.
23. Shi J., Hou S., Fang Q., Liu X., Liu X., Qi H. PD-1 Controls Follicular T Helper Cell Positioning and Function. Immunity 2018, 49 (2), 264–274.e4.
24. Joshi N. S., Akama-Garren E. H., Lu Y., Lee D.-Y., Chang G. P., Li A., DuPage M., Tammela T., Kerper N. R., Farago A. F., Robbins R., Crowley D. M., Bronson R. T., Jacks T. Regulatory T Cells in Tumor-Associated Tertiary Lymphoid Structures Suppress Anti-tumor T Cell Responses. Immunity 2015, 43 (3), 579–590.