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PHENOTYPIC CHARACTERISATION OF PERIPHERAL BLOOD CYTOTOXIC T LYMPHOCYTES: REGULATORY AND EFFECTOR MOLECULES

https://doi.org/10.15789/1563-0625-2018-2-227-240

Abstract

Cytotoxic T lymphocytes (CD3+CD8+, Tcyt) play a major role in protective immunity against intracellular pathogens and can eradicate malignant cells. As based on CD45RA and CD62L expression, the peripheral CD3+CD8+ blood lymphocytes were divided into "na ve" (N) cells, central memory (CM) and effector memory (EM), as well as "terminally-differentiated" CD45RA-positive effector cells (TEMRA). Using multicolor flow cytometry, a co-expression of effector (perforin, granzyme B and CD57) and regulatory (CD27, CD28, CD244 (2B4), CD279 (PD-1) and KLRG1) molecules was studied on all these subsets. CD57 was expressed in 2.39±0.31% “na ve” and 5.45±0.91% of central memory Tcyt. Meanwhile, within EM and TEMRA Tcyt subset, its expression was identified on the cell membranes of 26.53±2.20% and 51.43±2.55% of cells, respectively. Cytolytic effector molecules (granzyme B and perforin) were detected in cytoplasmic granules of 4.22±0.36% and 5.30±0.43% of na ve Tcyt, respectively. For CM cells, these values were 10.09±1.17% and 24.90±3.10%, respectively. Dramatic increases of granzyme B and perforin expression were observed in the “EM → TEMRA” cell lineage, when the relative number of granzyme B-positive cells increased to 41.05±2.63% and 66.73±3.29%, respectively, while perforin was detected in 59.33±4.26% and 75.08±3.12% of cells, respectively. For regulatory molecules, CD244 and KLRG1, the similar dynamics were observed, their expression increased from “na ve” to late maturation stages, while the expression of two main costimulatory molecules – CD27 and CD28, decreased in the lineage N → CM → EM → TEMRA cells. The highest level of CD279 was observed in EM cells. It was shown that CD57-positive cells contain perforin and granzyme B in their cytoplasmic granules and lack CD28 expression. Furthermore, CD57 can be used as a surrogate marker for multicolor immunophenotyping to identify most mature effector cells containing cytolytic enzymes. Our results on the co-expression of all the beforementioned molecules suggest that the most mature CD45RA+CD62L– effector peripheral blood cytotoxic T cells express CD244 and CD57, lack costimulation molecules CD27 and of CD28, as well as inhibitory receptors KLRG1 and CD279.

About the Authors

I. V. Kudryavtsev
Institute of Experimental Medicine; First St. Petersburg State I. Pavlov Medical University
Russian Federation

PhD (Biology), Senior Research Associate, Department of Immunology

Assistant Professor, Department of Immunology



A. G. Borisov
Research Institute of Medical Problems of the North, Krasnoyarsk Science Center, Siberian Branch of Russian Academy of Sciences; Krasnoyarsk State V.F. Voino-Yasenetsky Medical University
Russian Federation

PhD (Medicine), Leading Research Associate, Laboratory of Cellular and Molecular Physiology and Pathology

Associate Professor, Department of Infectious Diseases



E. V. Vasilyeva
St. Petersburg Pasteur Institute
Russian Federation
PhD (Biology), Junior Research Associate, Laboratory of Biopreparations


I. I. Krobinets
Russian Research Institute of Hematology and Transfusiology
Russian Federation
PhD (Biology), Senior Research Associate, Laboratory of Isoserology


A. A. Savchenko
Research Institute of Medical Problems of the North, Krasnoyarsk Science Center, Siberian Branch of Russian Academy of Sciences; Krasnoyarsk State V.F. Voino-Yasenetsky Medical University
Russian Federation

PhD, MD (Medicine), Professor, Head, Laboratory of Cellular and Molecular Physiology and Pathology

Head, Physiology Department



M. K. Serebriakova
Institute of Experimental Medicine
Russian Federation
Research Associate, Department of Immunology


A. Totolian Areg
First St. Petersburg State I. Pavlov Medical University; St. Petersburg Pasteur Institute
Russian Federation
PhD, MD (Medicine), Professor, Full Member, Russian Academy of Sciences, Director, St. Petersburg Pasteur Institute; Head, Department of Immunology


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Kudryavtsev I.V., Borisov A.G., Vasilyeva E.V., Krobinets I.I., Savchenko A.A., Serebriakova M.K., Totolian Areg A. PHENOTYPIC CHARACTERISATION OF PERIPHERAL BLOOD CYTOTOXIC T LYMPHOCYTES: REGULATORY AND EFFECTOR MOLECULES. Medical Immunology (Russia). 2018;20(2):227-240. (In Russ.) https://doi.org/10.15789/1563-0625-2018-2-227-240

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