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Analysis of the lymphoid tumor microenvironment (TILs) in breast cancer by flow cytometry

https://doi.org/10.15789/1563-0625-AOT-16855

Abstract

Despite the success in early diagnosis and drug treatment of breast cancer patients, long-term treatment results are still unsatisfactory, and in this regard, the role of research aimed at studying various mechanisms of development of this disease is increasing. It has been established that the degree of tumor infiltration by immune cells and their composition are directly related to the development of the disease and the response to therapy. Multiparameter flow cytometry (PC) allows studies of the subpopulation composition of TILs. The aim of the work was to study the features of the lymphoid microenvironment (TILs) of tumors in patients with primary operable and locally advanced breast cancer by PC. The study included patients with primary operable breast cancer (group 1, n = 121) and locally advanced (group 2, n = 80) receiving treatment at the N. N. Blokhin NMRCO. The TILs of a tumor obtained intraoperatively or by a core-biopsy were examined. The patients were divided into 3 subgroups: 1 subgroup – the degree of infiltration up to 1%, 2 subgroup – the degree of infiltration from 1 to 10%, and 3 subgroup – the degree of infiltration over 10%. Patients of group 1 were characterized by high functional activity and concentration of effector cells with a low degree of tumor infiltration, and as the number of lymphocytes in the tumor increased, an increase in the pool of CD4+ cells and CD4 Treg was noted simultaneously with a decrease in the number and functional activity of effector TILs. In group 2 were no significant differences in the cellular composition of TILs in subgroups with a weak and moderate degree of infiltration, and a variant with infiltration of more than 10% was recorded in only one patient. The lack of association of the TILs subpopulation structure in subgroups with varying degrees of tumor infiltration indicates a similar nature of the local immune response in locally advanced breast cancer.

Thus, unlike patients with locally advanced breast cancer, patients with primary operable breast cancer show a change in the type of local immune response from effector to regulatory. A high degree of tumor infiltration is characterized by depletion of effector cell function.

About the Authors

T. N. Zabotina
N. Blokhin National Medical Research Center of Oncology
Russian Federation

Tatiana N. Zabotina - PhD, MD (Biology), Head, Laboratory of Clinical Immunology and Innovative Technologies,

24 Kashirskoe Highway, Moscow 115522



A. A. Borunova
N. Blokhin National Medical Research Center of Oncology
Russian Federation

PhD (Medicine), Senior Research Associate, Laboratory of Clinical Immunology and Innovative Technologies, 

24 Kashirskoe Highway, Moscow 115522



A. I. Сhertkova
N. Blokhin National Medical Research Center of Oncology
Russian Federation

PhD (Medicine), Senior Research Associate, Laboratory of Clinical Immunology and Innovative Technologies, 

24 Kashirskoe Highway, Moscow 115522



I. B. Shoua
N. Blokhin National Medical Research Center of Oncology
Russian Federation

PhD (Biology), Doctor of Clinical Laboratory Diagnostics, Laboratory of Clinical Immunology and Innovative Technologies,

24 Kashirskoe Highway, Moscow 115522



Z. G. Kadagidze
N. Blokhin National Medical Research Center of Oncology
Russian Federation

PhD, MD (Medicine), Professor, Senior Research Associate, Laboratory of Clinical Immunology and Innovative Technologies,

24 Kashirskoe Highway, Moscow 115522



References

1. The state of oncological care for the population of Russia in 2022. Edited by A.D. Kaprin, V.V. Starinsky, A.O. Shakhzadova. Moscow: P. Herzen Moscow State Medical Research Institute – branch of the Federal State Budgetary Institution “NMIC of Radiology” Ministry of Health of Russia, 2022. 239 p.

2. Blok E.J., Engels C.C., Dekker-Ensink G. Exploration of tumour-infiltrating lymphocytes as a predictive biomarker for adjuvant endocrine therapy in early breast cancer. Breast Cancer Res. Treat., 2018, Vol. 171, pp. 65-74.

3. Goff S.L., Danforth D.N. The role of immune cells in breast tissue and immunotherapy for the treatment of breast cancer. Clin. Breast Cancer, 2021, Vol. 21, no. 1, pp. e63-e73.

4. Lan H.R., Du W.L., Liu Y., Mao C.S., Jin K.T., Yang X. Role of immune regulatory cells in breast cancer: Foe or friend? Int. Immunopharmacol., 2021, Vol. 96, 107627. doi: 10.1016/j.intimp.2021.107627.

5. Levy E.M., Roberti M.P., Mordoh J. Natural killer cells in human cancer: from biological functions to clinical applications. J. Biomed. Biotechnol., 2011, Vol. 2011, 676198. doi: 10.1155/2011/676198.

6. Lundgren C., Bendahl P.O., Ekholm M. Tumour-infiltrating lymphocytes as a prognostic and tamoxifen predictive marker in premenopausal breast cancer: data from a randomised trial with long-term follow-up. Breast Cancer Res., 2020, Vol. 22, 140. doi: 10.1186/s13058-020-01364-w.

7. Usman A.N., Ahmad M., Sinrang A.W., Natsir S., Takko A.B., Ariyandy A., Ilhamuddin I., Eragradini A.R., Hasan I.I., Hasyim S. Regulatory T cells on prognosis of breast cancer. Breast Dis., 2023, Vol. 42, no. 1, pp. 213-218. doi: 10.3233/BD-239002.

8. Virassamy B., Caramia F., Savas P., Sant S., Wang J., Christo S.N., Byrne A., Clarke K., Brown E., Teo Z.L., von Scheidt B., Freestone D., Gandolfo L.C., Weber K., Teply-Szymanski J., Li R., Luen S.J., Denkert C., Loibl S., Lucas O., Swanton C., Speed T.P., Darcy P.K., Neeson P.J., Mackay L.K., Loi S. Intratumoral CD8(+) T cells with a tissue-resident memory phenotype mediate local immunity and immune checkpoint responses in breast cancer. Cancer Cell, 2023, Vol. 41, no. 3, pp. 585-601.


Review

For citations:


Zabotina T.N., Borunova A.A., Сhertkova A.I., Shoua I.B., Kadagidze Z.G. Analysis of the lymphoid tumor microenvironment (TILs) in breast cancer by flow cytometry. Medical Immunology (Russia). 2024;26(4):819-826. (In Russ.) https://doi.org/10.15789/1563-0625-AOT-16855

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ISSN 1563-0625 (Print)
ISSN 2313-741X (Online)