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Manufacturing and characterization of autologous CD19-specific CAR T-cell products for patients with autoimmune rheumatic diseases. / Беловежец, Татьяна Николаевна; Омельченко, Виталий Олегович; Рыбакова, Анна Дмитриевна et al.

In: Cellular Therapy and Transplantation, Vol. 14, No. 3, 5, 30.09.2025, p. 59-65.

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Беловежец ТН, Омельченко ВО, Рыбакова АД, Королев МА, Горчаков АА, Кулемзин СВ. Manufacturing and characterization of autologous CD19-specific CAR T-cell products for patients with autoimmune rheumatic diseases. Cellular Therapy and Transplantation. 2025 Sept 30;14(3):59-65. 5. doi: 10.18620/ctt-1866-8836-2025-14-3-59-65

Author

Беловежец, Татьяна Николаевна ; Омельченко, Виталий Олегович ; Рыбакова, Анна Дмитриевна et al. / Manufacturing and characterization of autologous CD19-specific CAR T-cell products for patients with autoimmune rheumatic diseases. In: Cellular Therapy and Transplantation. 2025 ; Vol. 14, No. 3. pp. 59-65.

BibTeX

@article{e84b2294755041bea2d285019f87f3d1,
title = "Manufacturing and characterization of autologous CD19-specific CAR T-cell products for patients with autoimmune rheumatic diseases",
abstract = "CAR T-cell therapy of patients with autoimmune diseases is an emerging approach to selectively deplete B cells, thereby reducing the need for lifelong use of immunosuppressive drugs. In theory, all autoimmune diseases in which B cells are known to be key pathogenic effectors could respond well to B-cell targeting CAR T-cell therapy. In practice, however, successful manufacturing of autologous CAR T-cell products critically depends on the quality of the patient{\textquoteright}s T cells as a starting material, and may require early discontinuation of immunosuppressive therapy prior to apheresis. Additionally, many autoimmune diseases are characterized by abnormal levels of proinflammatory cytokines, which shift T-cell subpopulations toward less functional phenotypes. In this study, we demonstrate the feasibility of generating CD19-specific CAR T-cell products from several patients with different autoimmune diseases, including systemic lupus erythematosus, rheumatoid arthritis, and systemic sclerosis. For five out of six patients, CAR T-cell products displaying pronounced cytotoxicity against B-cell targets were successfully manufactured and compared side by side with CAR T-cell products derived from healthy donors.",
keywords = "CAR T терапия, CD19, В-клетки, аутоиммунные заболевания, CAR T THERAPY, B CELLS, CD19, AUTOIMMUNE DISEASES",
author = "Беловежец, {Татьяна Николаевна} and Омельченко, {Виталий Олегович} and Рыбакова, {Анна Дмитриевна} and Королев, {Максим Александрович} and Горчаков, {Андрей Александрович} and Кулемзин, {Сергей Викторович}",
note = "Manufacturing and characterization of autologous CD19-specific CAR T-cell products for patients with autoimmune rheumatic diseases / T. N. Belovezhets, V. O. Omelchenko, A. D. Rybakova [et al.] // Cellular Therapy and Transplantation. – 2025. – Vol. 14. - No. 3. – P. 59-65. – DOI 10.18620/ctt-1866-8836-2025-14-3-59-65. – EDN KFIOGW. The work was performed by agreement No. 075-15-2025-580 from June 25, 2025 between the Ministry of Science and Higher Education of the Russian Federation, and the Institute of Cytology and Genetics SB RAS.",
year = "2025",
month = sep,
day = "30",
doi = "10.18620/ctt-1866-8836-2025-14-3-59-65",
language = "English",
volume = "14",
pages = "59--65",
journal = "Cellular Therapy and Transplantation",
issn = "1867-416X",
publisher = "Universitatsklinikum Hamburg - Eppendorf",
number = "3",

}

RIS

TY - JOUR

T1 - Manufacturing and characterization of autologous CD19-specific CAR T-cell products for patients with autoimmune rheumatic diseases

AU - Беловежец, Татьяна Николаевна

AU - Омельченко, Виталий Олегович

AU - Рыбакова, Анна Дмитриевна

AU - Королев, Максим Александрович

AU - Горчаков, Андрей Александрович

AU - Кулемзин, Сергей Викторович

N1 - Manufacturing and characterization of autologous CD19-specific CAR T-cell products for patients with autoimmune rheumatic diseases / T. N. Belovezhets, V. O. Omelchenko, A. D. Rybakova [et al.] // Cellular Therapy and Transplantation. – 2025. – Vol. 14. - No. 3. – P. 59-65. – DOI 10.18620/ctt-1866-8836-2025-14-3-59-65. – EDN KFIOGW. The work was performed by agreement No. 075-15-2025-580 from June 25, 2025 between the Ministry of Science and Higher Education of the Russian Federation, and the Institute of Cytology and Genetics SB RAS.

PY - 2025/9/30

Y1 - 2025/9/30

N2 - CAR T-cell therapy of patients with autoimmune diseases is an emerging approach to selectively deplete B cells, thereby reducing the need for lifelong use of immunosuppressive drugs. In theory, all autoimmune diseases in which B cells are known to be key pathogenic effectors could respond well to B-cell targeting CAR T-cell therapy. In practice, however, successful manufacturing of autologous CAR T-cell products critically depends on the quality of the patient’s T cells as a starting material, and may require early discontinuation of immunosuppressive therapy prior to apheresis. Additionally, many autoimmune diseases are characterized by abnormal levels of proinflammatory cytokines, which shift T-cell subpopulations toward less functional phenotypes. In this study, we demonstrate the feasibility of generating CD19-specific CAR T-cell products from several patients with different autoimmune diseases, including systemic lupus erythematosus, rheumatoid arthritis, and systemic sclerosis. For five out of six patients, CAR T-cell products displaying pronounced cytotoxicity against B-cell targets were successfully manufactured and compared side by side with CAR T-cell products derived from healthy donors.

AB - CAR T-cell therapy of patients with autoimmune diseases is an emerging approach to selectively deplete B cells, thereby reducing the need for lifelong use of immunosuppressive drugs. In theory, all autoimmune diseases in which B cells are known to be key pathogenic effectors could respond well to B-cell targeting CAR T-cell therapy. In practice, however, successful manufacturing of autologous CAR T-cell products critically depends on the quality of the patient’s T cells as a starting material, and may require early discontinuation of immunosuppressive therapy prior to apheresis. Additionally, many autoimmune diseases are characterized by abnormal levels of proinflammatory cytokines, which shift T-cell subpopulations toward less functional phenotypes. In this study, we demonstrate the feasibility of generating CD19-specific CAR T-cell products from several patients with different autoimmune diseases, including systemic lupus erythematosus, rheumatoid arthritis, and systemic sclerosis. For five out of six patients, CAR T-cell products displaying pronounced cytotoxicity against B-cell targets were successfully manufactured and compared side by side with CAR T-cell products derived from healthy donors.

KW - CAR T терапия

KW - CD19

KW - В-клетки

KW - аутоиммунные заболевания

KW - CAR T THERAPY

KW - B CELLS

KW - CD19

KW - AUTOIMMUNE DISEASES

UR - https://www.scopus.com/pages/publications/105024120397

UR - https://elibrary.ru/item.asp?id=83202444

UR - https://www.mendeley.com/catalogue/13b63426-1878-3b0a-8afd-dda4ada3db52/

U2 - 10.18620/ctt-1866-8836-2025-14-3-59-65

DO - 10.18620/ctt-1866-8836-2025-14-3-59-65

M3 - Article

VL - 14

SP - 59

EP - 65

JO - Cellular Therapy and Transplantation

JF - Cellular Therapy and Transplantation

SN - 1867-416X

IS - 3

M1 - 5

ER -

ID: 72576058