Preview

Medical Immunology (Russia)

Advanced search

INFLUENCE OF DEXAMETHASONE-MODIFIED DENDRITIC CELLS GENERATED WITH IFNα UPON AUTOLOGOUS T LYMPHOCYTE FUNCTIONS IN THE PATIENTS WITH RHEUMATOID ARTHRITIS

https://doi.org/10.15789/1563-0625-2019-5-835-846

Abstract

Dendritic cells (DCs) play a key role in maintaining the peripheral tolerance of lymphocytes to autoantigens. Recovery of immunological tolerance in autoimmune diseases, particularly, in rheumatoid arthritis (RA) is considered a new therapeutic strategy. The aim of this work was to study the effect of dexamethasone-modified DCs generated from monocytes of RA patients in the presence of IFNα (DCsDex), upon autologous T lymphocytes in mixed leukocyte culture (auto-MLC), and to investigate possible mechanisms of the DCsdex tolerogenic effect upon autoreactive T cells. We have shown, that DCsDex from RA patients induce T cell hyporeactivity in auto-MLC. Hyporeactivity of T cells is associated with cell cycle blockage in CD4+T lymphocytes and decreased IFNγ, IL-17, IL-4 and IL-13 production, which indicates the induction of CD4+T cell anergy. In this case, inhibition of Th1/Th17 has been more pronounced than the suppression of Th2 cells producing IL-4 and IL-13. Along with T cell anergy, the decrease of proliferative response in auto-MLC is associated with increased CD3+T lymphocyte apoptosis. In addition, the DCsDex of RA patients suppresses the proliferation of autologous T cells stimulated by unmodified DCs. This effect is associated with enhancement of IL-10-producing CD4+T cells in the auto-MLC, thus being indicative for an ability of DCsDex to induce conversion of CD4+T lymphocytes into regulatory T cells (Tr1). The data obtained characterize a new type of tolerogenic DCs, generated from blood monocytes of RA patients in the presence of IFNα and modified by dexamethasone, thus revealing a mechanism for tolerogenic effect of DCsDex upon T cells that recognize self-antigens in auto-MLC.

About the Authors

Yu. D. Kurochkina
Institute of Fundamental and Clinical Immunology
Russian Federation

Kurochkina Yuliya D., Postgraduate Student, Laboratory of Cellular Immunotherapy, Rheumatologist, Clinic of Immunopathology

630099, Russian Federation, Novosibirsk, Yadrintsevskaya str., 14.

Phone: 7 (383) 228-21-01. Fax: 7 (383) 222-70-28.



T. V. Tyrinova
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Medicine), Research Associate, Laboratory of Cellular Immunotherapy

Novosibirsk


O. Yu. Leplina
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD, MD (Medicine), Leading Research Associate, Laboratory of Cellular Immunotherapy

Novosibirsk


M. A. Tikhonova
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Biology), Senior Research Associate, Laboratory of Cellular Immunotherapy,

Novosibirsk


A. E. Sizikov
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Medicine), Head, Rheumatology Department, Clinic of Immunopathology

Novosibirsk


A. E. Sulutian
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Medicine), Rheumatologist, Rheumatology Department, Clinic of Immunopathology

Novosibirsk


O. A. Chumasova
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Medicine), Rheumatologist, Rheumatology Department, Clinic of Immunopathology

Novosibirsk


A. A. Ostanin
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD, MD (Medicine), Professor, Main Research Associate, Laboratory of Cellular Immunotherapy

Novosibirsk


E. R. Chernykh
Institute of Fundamental and Clinical Immunology
Russian Federation

PhD, MD (Medicine), Professor, Corresponding Member, Russian Academy of Sciences, Head, Laboratory of Cellular Immunotherapy

Novosibirsk



References

1. Kurochkina Yu.D., Leplina O.Yu., Tikhonova M.A., Tyrinova T.V., Batorov E.V., Sizikov A.E., Ostanin A.A., Chernykh E.R. Effect of dexamethasone on interferon-α-induced differentiation of monocytes to dendritic cells. Meditsinskaya immunologiya = Medical Immunology (Russia), 2016, Vol. 18, no. 4, pp. 347-356. (In Russ.) doi: 10.15789/1563-0625-2016-4-347-356.

2. Tyrinova T.V., Leplina O.Yu., Tikhonova M.A., Sakhno L.V., Ostanin A.A., Chernykh E.R. Characteristics of signaling pathways mediating a cytotoxic effect of dendritic cells upon activated т lymphocytes and NK cells. Meditsinskaya immunologiya = Medical Immunology (Russia), 2012, Vol. 14, no. 1-2, pp. 43-50. (In Russ.) doi: 10.15789/1563-0625-2012-1-2-43-50.

3. AmelKashipaz M.R., Huggins M.L., Powell R.J., Todd I. Human autologous mixed lymphocyte reaction as an in vitro model for autoreactivity to apoptotic antigens. Immunology, 2002, Vol. 107, no. 3, pp. 358-365.

4. Bosma B.M., Metselaar H.J., Nagtzaam N.M., de Haan R., Mancham S., van der Laan L.J., Kuipers E.J., Kwekkeboom J. Dexamethasone transforms lipopolysaccharide-stimulated human blood myeloid dendritic cells into myeloid dendritic cells that prime interleukin-10 production in T cells. Immunology, 2008, Vol. 125, no. 1, pp. 91-100.

5. Calmette J., Ellouze M., Tran T., Karaki S., Ronin E., Capel F., Pallardy M., Bachelerie F., Krzysiek R., Emilie D., Schlecht-Louf G., Godot V. Glucocorticoidinduced leucine zipper enhanced expression in dendritic cells is sufficient to drive regulatory T cells expansion in vivo. J. Immunol., 2014, Vol. 193, no. 12, pp. 5863-5872.

6. Castaneda-Delgado J.E., Bastian-Hernandez Y., Macias-Segura N., Santiago-Algarra D., Castillo-Ortiz J.D., Aleman-Navarro A.L., Martinez-Tejada P., Enciso-Moreno L., Garcia-De Lira Y., Olguin-Calderon D., Trouw L.A., Ramos-Remus C., Enciso-Moreno J.A. Type I interferon gene response is increased in early and established rheumatoid arthritis and correlates with autoantibody production. Front. Immunol., 2017, Vol. 8, 285. doi: 10.3389/fimmu.2017.00285.

7. Chamorro S., García-Vallejo J.J., Unger W.W., Fernandes R.J., Bruijns S.C., Laban S., Roep B.O., Hart B.A., van Kooyk Y. TLR triggering on tolerogenic dendritic cells results in TLR2 up-regulation and a reduced proinflammatory immune program. J. Immunol., 2009, Vol. 183, no. 5, pp. 2984-2994.

8. Choy E.H., Kavanaugh A.F., Jones S.A. The problem of choice: current biologic agents and future prospects in RA. Nat. Rev. Rheumatol., 2013, Vol. 9, no. 3, pp. 154-163.

9. Dai S., Jia R., Zhang X., Fang Q., Huang L. The PD-1/PD-Ls pathway and autoimmune diseases. Cell. Immunol., 2014, Vol. 290, no. 1, pp. 72-79.

10. Domogalla M.P., Rostan P.V., Raker V.K., Steinbrink K. Tolerance through education: how tolerogenic dendritic cells shape immunity. Front. Immunol., 2017, Vol. 8, 1764. doi: 10.3389/fimmu.2017.01764.

11. Garcia-Gonzalez P.A., Schinnerling K., Sepulveda-Gutierrez A., Maggi J., Hoyos L., Morales R.A., Mehdi A.M., Nel H.J., Soto L., Pesce B., Molina M.C., Cuchacovich M., Larrondo M.L., Neira O., Catalan D.F., Hilkens C.M., Thomas R., Verdugo R.A., Aguillon J.C. Treatment with dexamethasone and monophosphoryl lipid A removes disease-associated transcriptional signatures in monocyte-derived dendritic cells from rheumatoid arthritis patients and confers tolerogenic features. Front. Immunol., 2016, Vol. 7, 458. doi: 10.3389/fimmu.2016.00458.

12. Ge Q., Palliser D., Eisen H.N., Chen J. Homeostatic T cell proliferation in a T cell-dendritic cell coculture system. Proc. Natl. Acad. Sci. USA, 2002, Vol. 99, no. 5, pp. 2983-2988.

13. Gessani S., Conti L., Del Cornò M., Belardelli F. Type I interferons as regulators of human antigen presenting cell functions. Toxins (Basel), 2014, Vol. 6, no. 6, pp. 1696-1723.

14. Guo Q., Wang Y., Xu D., Nossent J., Pavlos N.J., Xu J. Rheumatoid arthritis: pathological mechanisms and modern pharmacologic therapies. Bone Res., 2018, Vol. 6, p. 15.

15. Harry R.A., Anderson A.E., Isaacs J.D., Hilkens C.M. Generation and characterization of therapeutic tolerogenic dendritic cells for rheumatoid arthritis. Ann. Rheum. Dis., 2010, Vol. 69, no. 11, pp. 2042-2050.

16. Hilkens C.M., Isaacs J.D. Tolerogenic dendritic cell therapy for rheumatoid arthritis: where are we now? Clin. Exp. Immunol., 2013, Vol. 172, no. 2, pp. 148-157.

17. Kimura S., Fujimoto N., Okada H. Impaired autologous mixed-lymphocyte reaction of peripheral blood lymphocytes in adult periodontitis. Infect. Immun.,1991, Vol. 59, no. 12, pp. 4418-4424.

18. Kondo T., Cortese I., Markovic-Plese S., Wandinger K.P., Carter C., Brown M., Leitman S., Martin R. Dendritic cells signal T cells in the absence of exogenous antigen. Nat. Immunol., 2001, Vol. 2, no. 10, pp. 932-938.

19. Leplina O.Y., Tyrinova T.V., Tikhonova M.A., Ostanin A.A., Chernykh E.R. Interferon alpha induces generation of semi-mature dendritic cells with high pro-inflammatory and cytotoxic potential. Cytokine, 2015, Vol. 71, no. 1, pp. 1-7.

20. Manoharan I., Hong Y., Suryawanshi A., Angus-Hill M.L., Sun Z., Mellor A.L., Munn D.H., Manicassamy S. TLR2-dependent activation of β-catenin pathway in dendritic cells induces regulatory responses and attenuates autoimmune inflammation. J. Immunol., 2014, Vol. 193, no. 8, pp. 4203-4213.

21. Naranjo-Gómez M., Raich-Regue D., Onate C., Grau-Lopez L., Ramo-Tello C., Pujol-Borrell R., MartinezCaceres E., Borras F.E.. Comparative study of clinical grade human tolerogenic dendritic cells. J. Transl. Med., 2011, Vol. 9, p. 89.

22. Netea M.G., Sutmuller R., Hermann C., van der Graaf C.A., van der Meer J.W., van Krieken J.H., Hartung T., Adema G., Kullberg B.J. Toll-like receptor 2 suppresses immunity against Candida albicans through induction of IL-10 and regulatory T cells. J. Immunol., 2004, Vol. 172, no. 6, pp. 3712-3718.

23. Osorio F., Fuentes C., Lуpez M.N., Salazar-Onfray F., Gonzalez F.E. Role of dendritic cells in the induction of lymphocyte tolerance. Front. Immunol., 2015, Vol. 6, 535. doi: 10.3389/fimmu.2015.00535.

24. Piemonti L., Monti P., Allavena P., Sironi M., Soldini L., Leone B.E., Socci C., di Carlo V. Glucocorticoids affect human dendritic cell differentiation and maturation. J. Immunol., 1999, Vol. 162, no. 11, pp. 6473-6481.

25. Romain P.L., Schlossman S.F., Reinherz E.L. Surface molecules involved in self-recognition and T cell activation in the autologous mixed lymphocyte reaction. J. Immunol., 1984, Vol. 133, no. 3, pp. 1093-1100.

26. Sakhno L.V., Tikhonova M.A., Tyrinova T.V., Leplina O.Yu., Shevela E.Ya., Nikonov S.D., Zhdanov O.A., Ostanin A.A., Chernykh E.R. Cytotoxic activity of dendritic cells as a possible mechanism of negative regulation of T lymphocytes in pulmonary tuberculosis. Clin. Dev. Immunol., 2012, Vol. 2012, 628635. doi: 10.1155/2012/628635.

27. Selim A., Yong-Soo B. Dendritic cell-based immunotherapy for rheumatoid arthritis: from bench to bedside. Immune Network, 2016, Vol. 16, no. 1, pp. 44-51.

28. Stoop J.N., Robinson J.H., Hilkens C.M. Developing tolerogenic dendritic cell therapy for rheumatoid arthritis: what can we learn from mouse models? Ann. Rheum. Dis., 2011, Vol. 70, no. 9, pp. 1526-1533.

29. Surh C.D., Sprent J.. Homeostatic T cell proliferation: how far can T cells be activated to self-ligands? J. Exp. Med., 2000, Vol. 192, no. 4, pp. 9-14.

30. Unger W.W., Laban S., Kleijwegt F.S., van der Slik A.R., Roep B.O. Induction of Treg by monocyte-derived DC modulated by vitamin D3 or dexamethasone: differential role for PD-L1. Eur. J. Immunol., 2009, Vol. 39, no. 11, pp. 3147-3159.

31. Vakkila J., Hurme M. Both dendritic cells and monocytes induce autologous and allogeneic T cells receptive to interleukin 2. Scand. J. Immunol., 1990, Vol. 31, no. 1, pp. 75-83.

32. van Duivenvoorde L.M., Han W.G.H., Bakker A.M., Louis-Plence P., Charbonnier L.-M., Apparailly F., van der Voort E.I.H., Jorgensen C., Huizinga T.W.J., Toes R.E.M. Immunomodulatory dendritic cells inhibit Th1 responses and arthritis via different mechanisms. J. Immunol, 2007, Vol. 179, no. 3, pp. 1506-1515.

33. Wagner U., Pierer M., Wahle M., Moritz F., Kaltenhäuser S., Häntzschel H. Ex vivo homeostatic proliferation of CD4 + T cells in rheumatoid arthritis is dysregulated and driven by membrane-anchored TNF-alpha. J. Immunol., 2004, Vol. 173, no. 4, pp. 2825-2833.

34. Wampler M.T, Vashisht P., Dorschner J.M., Jensen M.A., Chrabot B.S., Kern M., Curtis J.R., Danila M.I., Cofield S.S., Shadick N., Nigrovic P.A., St Clair E.W., Bingham C.O., Furie R., Robinson W., Genovese M.0, Striebich C.C., O’Dell J.R., Thiele G.M., Moreland L.W., Levesque M., Bridges S.L. Jr, Gregersen P.K., Niewold  T.B. Increased pretreatment serum IFN-β/α ratio predicts non-response to tumor necrosis factor α inhibition in rheumatoid arthritis. Ann. Rheum. Dis., 2016, Vol. 75, no. 10, pp. 1757-1762.

35. Woltman A.M., van der Kooij S.W., de Fijter J.W., van Kooten C. Maturationresistant dendritic cells induce hyporesponsiveness in alloreactive CD45RA + and CD45RO + T-cell populations. Am. J. Transplant., 2006, Vol. 6, no. 11, pp. 2580-2591.

36. Xia C.Q., Peng R., Beato F., Clare-Salzler M.J. Dexamethasone induces IL-10-producing monocyte-derived dendritic cells with durable immaturity. Scand. J. Immunol., 2005, Vol. 62, no. 1, pp. 45-54.


Supplementary files

1. Метаданные
Subject
Type Исследовательские инструменты
Download (48KB)    
Indexing metadata ▾
2. Подписи авторов
Subject
Type Исследовательские инструменты
Download (240KB)    
Indexing metadata ▾
3. Титульный лист
Subject
Type Исследовательские инструменты
Download (68KB)    
Indexing metadata ▾
4. Резюме
Subject
Type Исследовательские инструменты
Download (66KB)    
Indexing metadata ▾
5. Рисунок 1
Subject
Type Исследовательские инструменты
Download (23MB)    
Indexing metadata ▾
6. Рисунок 2
Subject
Type Исследовательские инструменты
Download (10MB)    
Indexing metadata ▾
7. Подписи к рисункам
Subject
Type Исследовательские инструменты
Download (54KB)    
Indexing metadata ▾
8. Таблица 1
Subject
Type Исследовательские инструменты
Download (95KB)    
Indexing metadata ▾
9. Таблица 2
Subject
Type Исследовательские инструменты
Download (76KB)    
Indexing metadata ▾
10. Таблица 3
Subject
Type Исследовательские инструменты
Download (73KB)    
Indexing metadata ▾
11. Литература таблица
Subject
Type Исследовательские инструменты
Download (369KB)    
Indexing metadata ▾

Review

For citations:


Kurochkina Yu.D., Tyrinova T.V., Leplina O.Yu., Tikhonova M.A., Sizikov A.E., Sulutian A.E., Chumasova O.A., Ostanin A.A., Chernykh E.R. INFLUENCE OF DEXAMETHASONE-MODIFIED DENDRITIC CELLS GENERATED WITH IFNα UPON AUTOLOGOUS T LYMPHOCYTE FUNCTIONS IN THE PATIENTS WITH RHEUMATOID ARTHRITIS. Medical Immunology (Russia). 2019;21(5):835-846. (In Russ.) https://doi.org/10.15789/1563-0625-2019-5-835-846

Views: 1201


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


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