MUTHU RAJA, Karthick Raja, Lucie ŘÍHOVÁ, Lenka ZAHRADOVÁ, Mária KLINCOVÁ, Miroslav PENKA and Roman HÁJEK. Increased T regulatory cells are associated with adverse clinical features and predict progression in multiple myeloma. PLOS ONE. San Francisco: Public Library of Science, 2012, vol. 7, No 10, p. 1-11. ISSN 1932-6203. Available from: https://dx.doi.org/10.1371/journal.pone.0047077.
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Basic information
Original name Increased T regulatory cells are associated with adverse clinical features and predict progression in multiple myeloma.
Authors MUTHU RAJA, Karthick Raja (356 India, belonging to the institution), Lucie ŘÍHOVÁ (203 Czech Republic, belonging to the institution), Lenka ZAHRADOVÁ (203 Czech Republic), Mária KLINCOVÁ (703 Slovakia), Miroslav PENKA (203 Czech Republic) and Roman HÁJEK (203 Czech Republic, guarantor, belonging to the institution).
Edition PLOS ONE, San Francisco, Public Library of Science, 2012, 1932-6203.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW Full Text
Impact factor Impact factor: 3.730
RIV identification code RIV/00216224:14110/12:00057825
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1371/journal.pone.0047077
UT WoS 000312385200077
Keywords in English Regulatory T cells; multiple myeloma; dexamethasone; immune system
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 17/12/2019 15:39.
Abstract
Background: Regulatory T (Treg) cells play an important role in the maintenance of immune system homeostasis. Multiple myeloma (MM) is a plasma cell disorder frequently associated with impaired immune cell numbers and functions. Methods: We analyzed Treg cells in peripheral blood (n = 207) and bone marrow (n = 202) of pre-malignant and malignant MM patients using flow cytometry. Treg cells and their subsets from MM patients and healthy volunteers were functionally evaluated for their suppressive property. A cohort of 25 patients was analyzed for lymphocytes, CD4 T cells and Treg cells before and after treatment with cyclophosphamide, thalidomide plus dexamethasone (CTD). Results: We found elevated frequencies of Treg cells in newly diagnosed (P<0.01) and relapsed MM patients (P<0.0001) compared to healthy volunteers. Also, Treg subsets including naive (P = 0.015) and activated (P = 0.036) Treg cells were significantly increased in MM patients compared to healthy volunteers. Functional studies showed that Treg cells and their subsets from both MM and healthy volunteers were similar in their inhibitory function. Significantly increased frequencies of Treg cells were found in MM patients with adverse clinical features such as hypercalcemia (.10 mg/dL), decreased normal plasma cell (<5%) count and IgA myeloma subtype. We also showed that MM patients with >5% of Treg cells had inferior time to progression (TTP) (13 months vs. median not reached; P = 0.013). Furthermore, we demonstrated the prognostic value of Treg cells in prediction of TTP by Cox regression analysis (P = 0.045). CTD treatment significantly reduced frequencies of CD4 T cells (P = 0.001) and Treg cells (P = 0.018) but not Treg cells/CD4 T cells ratio compared to pretreatment. Conclusions: Our study showed immune deregulation in MM patients which is evidenced by elevated level of functionally active Treg cells and patients with increased Treg cells have higher risk of progression.
Links
GAP304/10/1395, research and development projectName: Analýza klonálních progenitorů plazmatických buněk u monoklonálních gamapatií
Investor: Czech Science Foundation
MSM0021622434, plan (intention)Name: Od klasických prognostických markerů ke klinicky aplikovatelným farmakogenomickým a farmakoproteomickým projektům u mnohočetného myelomu a monoklonálních gamapatií
Investor: Ministry of Education, Youth and Sports of the CR, From classic prognostic markers to clinical applications in selected pharmacogenomic and pharmacoproteomic projects in multiple myeloma and monoclonal gammapathies
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  • a concrete person Mgr. Karthick Raja Muthu Raja, Ph.D., učo 106209
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  • a concrete person MUDr. Lenka Zahradová, Ph.D., učo 22118
  • a concrete person prof. MUDr. Roman Hájek, CSc., učo 33302
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  • a concrete person Mgr. Karthick Raja Muthu Raja, Ph.D., učo 106209
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  • a concrete person Mgr. Lucie Říhová, Ph.D., učo 20214
  • a concrete person MUDr. Lenka Zahradová, Ph.D., učo 22118
  • a concrete person prof. MUDr. Roman Hájek, CSc., učo 33302
  • a concrete person MUDr. Mária Klincová, učo 363482
  • a concrete person Mgr. Marie Šípková, DiS., učo 437722
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