Tertiary Lymphoid Structures and Cancer Prognosis (Brief Review)
https://doi.org/10.24060/2076-3093-2019-9-4-293-296
Abstract
It should be emphasized that the clinical significance of tertiary lymphoid structures ranges from a destructive to protective impact, which indicates the need for an improved understanding of the structure and case-specific function of these organs before conducting clinical targeting.
Keywords
About the Authors
R. A. RustamkhanovRussian Federation
Rustamkhanov Rasul Aydarovich — Assistant lecturer of the Department of Oncology with Oncology and Anatomical Pathology courses in the Institute of Additional Professional Education
3 Lenin str., Ufa, 450008
K. Sh. Gantsev
Russian Federation
Gantsev Kamil Shamilevich — Doctor of Medical Sciences, Professor of the Department of Oncology, Oncologist at the Department of Urology No. 7
3 Lenin str., Ufa, 450008;
73/1 Oktyabrya ave., Ufa, 450054
D. S. Tursumetov
Russian Federation
Tursumetov Davlat Saytmuratovich — Candidate of Medical Sciences, Associate Professor of the Department of Oncology with Oncology and Anatomical Pathology courses in the Institute of Additional Professional Education
References
1. Fridman W.H., Zitvogel L., Sautès-Fridman C., Kroemer G. The immune contexture in cancer prognosis and treatment. Nat Rev Clin Oncol. 2017;14(12):717–34. DOI: 10.1038/nrclinonc.2017.101
2. Sautès-Fridman C., Lawand M., Giraldo N.A., Kaplon H., Germain C., Fridman W.H., et al. Tertiary lymphoid structures in cancers: prognostic value, regulation, and manipulation for therapeutic intervention. Front Immunol. 2016;7:407. DOI: 10.3389/fi mmu.2016.00407
3. Guo J., Qian J., Zhang R. The pathological features of ectopic lymphoid neogenesis in idiopathic dacryoadenitis. BMC Ophthalmol. 2016;16:66. DOI: 10.1186/s12886-016-0250-0
4. Dieu-Nosjean M.C., Antoine M., Danel C., Heudes D., Wislez M., Poulot V., et al. Long-term survival for patients with non-small-cell lung cancer with intratumoral lymphoid structures. J Clin Oncol. 2008;26(27):4410–7. DOI: 10.1200/ JCO.2007.15.0284
5. Ladányi A., Kiss J., Somlai B., Gilde K., Fejos Z., Mohos A., et al. Density of DC-LAMP(+) mature dendritic cells in combination with activated T lymphocytes infiltrating primary cutaneous melanoma is a strong independent prognostic factor. Cancer Immunol Immunother. 2007;56(9):1459–69. DOI: 10.1007/s00262-007-0286-3
6. 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):260–75. DOI: 10.1111/imr.12405
7. Dieu-Nosjean M.C., Goc J., Giraldo N.A., Sautès-Fridman C., Fridman W.H. Tertiary lymphoid structures in cancer and beyond. Trends Immunol. 2014;35(11):571–80. DOI: 10.1016/j.it.2014.09.006
8. Germain C., Gnjatic S., Tamzalit F., Knockaert S., Remark R., Goc J., et al. Presence of B cells in tertiary lymphoid structures is associated with a protective immunity in patients with lung cancer. Am J Respir Crit Care Med. 2014;189(7):832–44. DOI: 10.1164/rccm.201309-1611OC
9. Goc J., Germain C., Vo-Bourgais T.K., Lupo A., Klein C., Knockaert S., et al. Dendritic cells in tumor-associated tertiary lymphoid structures signal a Th1 cytotoxic immune contexture and license the positive prognostic value of infiltrating CD8 + T cells. Cancer Res. 2014;74(3):705–15. DOI: 10.1158/0008-5472.CAN-13-1342
10. Giraldo N.A., Becht E., Pagès F., Skliris G., Verkarre V., Vano Y., et al. Orchestration and prognostic significance of immune checkpoints in the microenvironment of primary and metastatic renal cell cancer. Clin Cancer Res. 2015;21(13):3031–40. DOI: 10.1158/1078-0432.CCR-14-2926
11. Martinet L., Filleron T., Le Guellec S., Rochaix P., Garrido I., Girard J.P. High endothelial venule blood vessels for tumor-infiltrating lymphocytes are associated with lymphotoxin β-producing dendritic cells in human breast cancer. J Immunol. 2013;191(4):2001–8. DOI: 10.4049/jimmunol.1300872
12. Remark R., Alifano M., Cremer I., Lupo A., Dieu-Nosjean M.C., Riquet M., et al. Characteristics and clinical impacts of the immune environments in colorectal and renal cell carcinoma lung metastases: influence of tumor origin. Clin Cancer Res. 2013;19(15):4079–91. DOI: 10.1158/1078-0432.CCR- 12-3847
13. Messina J.L., Fenstermacher D.A., Eschrich S., Qu X., Berglund A.E., Lloyd M.C., et al. 12-chemokine gene signature identifies lymph node-like structures in melanoma: potential for patient selection for immunotherapy? Sci Rep. 2012;2:765. DOI: 10.1038/srep00765
14. Coppola D., Nebozhyn M., Khalil F., Dai H., Yeatman T., Loboda A., et al. Unique ectopic lymph node-like structures present in human primary colorectal carcinoma are identified by immune gene array profiling. Am J Pathol. 2011;179(1):37–45. DOI: 10.1016/j.ajpath.2011.03.007
15. Bindea G., Mlecnik B., Tosolini M., Kirilovsky A., Waldner M., Obenauf A.C., et al. Spatiotemporal dynamics of intratumoral immune cells reveal the immune landscape in human cancer. Immunity. 2013;39(4):782–95. DOI: 10.1016/j. immuni.2013.10.003
16. Hennequin A., Derangère V., Boidot R., Apetoh L., Vincent J., Orry D., et al. Tumor infiltration by Tbet + effector T cells and CD20 + B cells is associated with survival in gastric cancer patients. Oncoimmunology. 2016;5(2):e1054598. DOI: 10.1080/2162402X.2015.1054598
17. Finkin S., Yuan D., Stein I., Taniguchi K., Weber A., Unger K., et al. Ectopic lymphoid structures function as microniches for tumor progenitor cells in hepatocellular carcinoma. Nat Immunol. 2015;16(12):1235–44. DOI: 10.1038/ ni.3290
18. Sautès-Fridman C., Fridman W.H. TLS in tumors: what lies within. Trends Immunol. 2016;37(1):1–2. DOI: 10.1016/j.it.2015.12.001
19. Meshcheryakova A., Tamandl D., Bajna E., Stift J., Mittlboeck M., Svoboda M., et al. B cells and ectopic follicular structures: novel players in anti-tumor programming with prognostic power for patients with metastatic colorectal cancer. PLoS One. 2014;9(6):e99008. DOI: 10.1371/journal.pone.0099008
20. Wirsing A.M., Rikardsen O.G., Steigen S.E., Uhlin-Hansen L., HadlerOlsen E. Characterisation and prognostic value of tertiary lymphoid structures in oral squamous cell carcinoma. BMC Clin Pathol. 2014;14:38. DOI: 10.1186/1472-6890-14-38
21. Hosmalin A., Sautès-Fridman C., Fougereau M., Yssel H., Fischer A. 50(th) Anniversary of the French Society for Immunology (SFI). Eur J Immunol. 2016;46(7):1545–7. DOI: 10.1002/eji.201670073
22. Maldonado L., Teague J.E., Morrow M.P., Jotova I., Wu T.C., Wang C., et al. Intramuscular therapeutic vaccination targeting HPV16 induces T cell responses that localize in mucosal lesions. Sci Transl Med. 2014;6(221):221ra13. DOI: 10.1126/scitranslmed.3007323
23. Lutz E.R., Wu A.A., Bigelow E., Sharma R., Mo G., Soares K., et al. Immunotherapy converts non-immunogenic pancreatic tumors into immunogenic foci of immune regulation. Cancer Immunol Res. 2014;2(7):616–31. DOI: 10.1158/2326-6066.CIR-14-0027
Review
For citations:
Rustamkhanov R.A., Gantsev K.Sh., Tursumetov D.S. Tertiary Lymphoid Structures and Cancer Prognosis (Brief Review). Creative surgery and oncology. 2019;9(4):293-296. (In Russ.) https://doi.org/10.24060/2076-3093-2019-9-4-293-296