Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model

Collagen-induced arthritis in DBA/1 mice is a model of rheumatoid arthritis with marked synovitis and erosions. The disease can be adoptively transferred to SCID mice with arthritogenic splenocytes from DBA/1 mice injected with bovine collagen type II. However, infection of arthritogenic splenocytes...

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Autores principales: Chernajovsky, Y., Adams, G., Triantaphyllopoulos, K., Ledda, M.F., Podhajcer, O.L.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_09697128_v4_n6_p553_Chernajovsky
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spelling todo:paper_09697128_v4_n6_p553_Chernajovsky2023-10-03T15:55:27Z Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model Chernajovsky, Y. Adams, G. Triantaphyllopoulos, K. Ledda, M.F. Podhajcer, O.L. Cytokine receptors Cytokines Rheumatoid arthritis T lymphocytes TGF β1 retrovirus collagen collagen antibody gelatinase transforming growth factor beta1 animal cell animal experiment animal model animal tissue antiinflammatory activity article enzyme activity gene transfer lymphoid cell male mouse nonhuman paw edema priority journal protein expression Retrovirus rheumatoid arthritis spleen cell synovitis T lymphocyte Animalia Bovinae unidentified retrovirus Collagen-induced arthritis in DBA/1 mice is a model of rheumatoid arthritis with marked synovitis and erosions. The disease can be adoptively transferred to SCID mice with arthritogenic splenocytes from DBA/1 mice injected with bovine collagen type II. However, infection of arthritogenic splenocytes with a retrovirus expressing TGF β1 inhibits development of arthritis in SCID mice. When DBA/1 mice, at onset of arthritis have additional arthritgenic splenocytes transferred, exacerbation occurs, reflected in a rapid increase in the number of arthritic joints, increased paw swelling and higher levels of anti-collagen antibody. By infecting arthritogenic splenocytes ex vivo with TGF β1 retrovirus, this exacerbation was inhibited. TGF β1 was effective in lowering inflammation of joints with already established arthritis and inhibiting the spreading of the disease to other joints. Transient reduction on anti-collagen antibody levels could also be obtained using purified T cells infected woth TGF β1 retrovirus. In addition, expression of TGF β1 in lymphocytes reduced the levels of gelatinase (MMP2) activity in inflamed joints. Fil:Ledda, M.F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Podhajcer, O.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_09697128_v4_n6_p553_Chernajovsky
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Cytokine receptors
Cytokines
Rheumatoid arthritis
T lymphocytes
TGF β1 retrovirus
collagen
collagen antibody
gelatinase
transforming growth factor beta1
animal cell
animal experiment
animal model
animal tissue
antiinflammatory activity
article
enzyme activity
gene transfer
lymphoid cell
male
mouse
nonhuman
paw edema
priority journal
protein expression
Retrovirus
rheumatoid arthritis
spleen cell
synovitis
T lymphocyte
Animalia
Bovinae
unidentified retrovirus
spellingShingle Cytokine receptors
Cytokines
Rheumatoid arthritis
T lymphocytes
TGF β1 retrovirus
collagen
collagen antibody
gelatinase
transforming growth factor beta1
animal cell
animal experiment
animal model
animal tissue
antiinflammatory activity
article
enzyme activity
gene transfer
lymphoid cell
male
mouse
nonhuman
paw edema
priority journal
protein expression
Retrovirus
rheumatoid arthritis
spleen cell
synovitis
T lymphocyte
Animalia
Bovinae
unidentified retrovirus
Chernajovsky, Y.
Adams, G.
Triantaphyllopoulos, K.
Ledda, M.F.
Podhajcer, O.L.
Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model
topic_facet Cytokine receptors
Cytokines
Rheumatoid arthritis
T lymphocytes
TGF β1 retrovirus
collagen
collagen antibody
gelatinase
transforming growth factor beta1
animal cell
animal experiment
animal model
animal tissue
antiinflammatory activity
article
enzyme activity
gene transfer
lymphoid cell
male
mouse
nonhuman
paw edema
priority journal
protein expression
Retrovirus
rheumatoid arthritis
spleen cell
synovitis
T lymphocyte
Animalia
Bovinae
unidentified retrovirus
description Collagen-induced arthritis in DBA/1 mice is a model of rheumatoid arthritis with marked synovitis and erosions. The disease can be adoptively transferred to SCID mice with arthritogenic splenocytes from DBA/1 mice injected with bovine collagen type II. However, infection of arthritogenic splenocytes with a retrovirus expressing TGF β1 inhibits development of arthritis in SCID mice. When DBA/1 mice, at onset of arthritis have additional arthritgenic splenocytes transferred, exacerbation occurs, reflected in a rapid increase in the number of arthritic joints, increased paw swelling and higher levels of anti-collagen antibody. By infecting arthritogenic splenocytes ex vivo with TGF β1 retrovirus, this exacerbation was inhibited. TGF β1 was effective in lowering inflammation of joints with already established arthritis and inhibiting the spreading of the disease to other joints. Transient reduction on anti-collagen antibody levels could also be obtained using purified T cells infected woth TGF β1 retrovirus. In addition, expression of TGF β1 in lymphocytes reduced the levels of gelatinase (MMP2) activity in inflamed joints.
format JOUR
author Chernajovsky, Y.
Adams, G.
Triantaphyllopoulos, K.
Ledda, M.F.
Podhajcer, O.L.
author_facet Chernajovsky, Y.
Adams, G.
Triantaphyllopoulos, K.
Ledda, M.F.
Podhajcer, O.L.
author_sort Chernajovsky, Y.
title Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model
title_short Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model
title_full Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model
title_fullStr Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model
title_full_unstemmed Pathogenic lymphoid cells engineered to express TGF β1 ameliorate disease in a collagen-induced arthritic model
title_sort pathogenic lymphoid cells engineered to express tgf β1 ameliorate disease in a collagen-induced arthritic model
url http://hdl.handle.net/20.500.12110/paper_09697128_v4_n6_p553_Chernajovsky
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AT triantaphyllopoulosk pathogeniclymphoidcellsengineeredtoexpresstgfb1amelioratediseaseinacollageninducedarthriticmodel
AT leddamf pathogeniclymphoidcellsengineeredtoexpresstgfb1amelioratediseaseinacollageninducedarthriticmodel
AT podhajcerol pathogeniclymphoidcellsengineeredtoexpresstgfb1amelioratediseaseinacollageninducedarthriticmodel
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