Functional regulatory T-cells in rheumatoid arthritis bone marrow are modulated by IL-15 and strong antigenic stimulation
PBN-AR
Instytucja
Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji im. prof. dr hab. med. Eleonory Reicher
Informacje podstawowe
Główny język publikacji
angielski
Czasopismo
ANNALS OF THE RHEUMATIC DISEASES
ISSN
0003-4967
EISSN
1468-2060
Wydawca
B M J PUBLISHING GROUP
DOI
URL
Rok publikacji
2016
Numer zeszytu
supl 1
Strony od-do
A17
Numer tomu
75
Link do pełnego tekstu
Liczba arkuszy
0,5
Konferencja
Indeksowana w Scopus
nie
Indeksowana w Web of Science Core Collection
tak
Liczba cytowań z Web of Science Core Collection
Nazwa konferencji (skrócona)
EWRR
Nazwa konferencji
36th European Workshop for Rheumatology Research
Początek konferencji
2016-02-25
Koniec konferencji
2016-02-27
Lokalizacja konferencji
Londyn
Kraj konferencji
GB
Lista innych baz czasopism i abstraktów w których była indeksowana
Streszczenia
Język
angielski
Treść
Background and objectives Role of CD4+Foxp3+ regulatory T cells in control of autoimmune processes, including rheumatoid arthritis (RA) is well proved, however knowledge about Tregs functions in bone marrow (BM) is sparse. As concept of BM active participation in pathogenesis of RA is still developing, in the present work we compared the phenotype of Tregs in paired samples of bone marrow and peripheral blood from patients with RA and osteoarthritis (OA). Impact of IL-15, overexpressed in RA BM, on functional activity of BM Tregs was also investigated. Materials and methods Samples of BM and peripheral blood were obtained from RA and OA patients during hip replacement surgery. Tregs phenotype was assessed by FACS analysis and immunohistochemical staining. Bone marrow mononuclear cells were cultured with or without IL-15 before functional assays were done (measurement of cells proliferation and cytokines production). Data are shown as mean ± SEM. Results Treg cells isolated from BM and peripheral blood shared phenotype of memory CD45RO+ cells, with significantly higher proportion of activated CD4+Foxp3+CD127+ cells and lower proportion of CXCR4+ Tregs in RA BM. Tregs from OA and RA BM as well as from blood of healthy blood donors were functional and suppressed proliferation and cytokines production in coculture with effector T cells. Stronger signal mediated by anti-CD3/CD28 Abs sustained functionality only in RA Treg. After IL-15 treatment, suppression of proliferation by Tregs from OA BM was broken by stronger TCR signal. In contrast, RA Tregs functionality was maintained only when additionally stimulation by anti-CD3/CD28 Abs was supplied (63.3%±6.6%; p = 0.028 and 54.0%±6.1%; p = 0.067 respectively). Despite active suppression RA Tregs pre-stimulated by IL-15 and cultured in presence of anti-CD3/CD28 Abs produced significantly more TNF then Treg from blood of healthy blood donors (42.6 ± 7.4 vs 17.1 ± 5.7; p = 0.028) and OA BM (42.6 ± 7.4 vs 21.0 ± 8.6; ns). Pre-stimulation of the culture by IL-15 did not increase proportion of CD4+Foxp3+CXCR4+ in any patients groups. Conclusions Phenotype and activation status of Tregs present in RA BM are influenced by locally overexpressed IL-15 that finally may contribute to RA pathogenesis, especially in context of TNF production and poor retention of Treg in BM compartment.
Cechy publikacji
abstrakt
Inne
System-identifier
PX-58b02ce3d5dec03e45d2ef81
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