Abstract
Integrin αvβ3 is important for cell survival, signaling and migration, particularly during angiogenesis and tumorigenesis, where it has been proposed as a therapeutic target. αvβ3 is up-regulated following transplantation and β3 polymorphisms are associated with increased acute kidney rejection, suggesting that αvβ3 may also play a role in transplant rejection. Here, using a model of allogeneic heart transplantation, we show that allograft survival is prolonged in β3 integrin-deficient (β3-/-) mice. This is associated with Th2-type immune responses and reduced T-cell infiltration into grafts and T cells from β3-/- mice show impaired adhesion and migration, consistent with a role for αvβ3 in transmigration. These studies provide evidence that targeting β3 integrins impairs recruitment of effector cells and alters cytokine production, so prolonging graft survival. We also show that low doses of blocking antibodies against leukocyte function associated antigen-1 (LFA-1)/αLβ2 and very late antigen-4 (VLA-4)/α4β1, when combined with deletion of β3, lead to long-term survival of allografts with no evidence of chronic rejection. Hence we provide strong mechanistic evidence supporting previous genetic studies, demonstrate the involvement of β3 integrins in both acute and chronic rejection and identify β3 as a new target for immunosuppressive therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 1080-1090 |
| Number of pages | 11 |
| Journal | American Journal of Transplantation |
| Volume | 7 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - May 2007 |
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Keywords
- Acute rejection
- Chronic rejection
- Extracellular matrix
- Integrin
- Migration
ASJC Scopus subject areas
- Immunology
Cite this
β3 integrins regulate lymphocyte migration and cytokine responses in heart transplant rejection. / Lacy-Hulbert, A.; Ueno, T.; Ito, T.; Jurewicz, M.; Izawa, A.; Smith, R. N.; Chase, C. M.; Tanaka, K.; Fiorina, P.; Russell, P. S.; Auchincloss, H.; Sayegh, M. H.; Hynes, R. O.; Abdi, R.
In: American Journal of Transplantation, Vol. 7, No. 5, 05.2007, p. 1080-1090.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - β3 integrins regulate lymphocyte migration and cytokine responses in heart transplant rejection
AU - Lacy-Hulbert, A.
AU - Ueno, T.
AU - Ito, T.
AU - Jurewicz, M.
AU - Izawa, A.
AU - Smith, R. N.
AU - Chase, C. M.
AU - Tanaka, K.
AU - Fiorina, P.
AU - Russell, P. S.
AU - Auchincloss, H.
AU - Sayegh, M. H.
AU - Hynes, R. O.
AU - Abdi, R.
PY - 2007/5
Y1 - 2007/5
N2 - Integrin αvβ3 is important for cell survival, signaling and migration, particularly during angiogenesis and tumorigenesis, where it has been proposed as a therapeutic target. αvβ3 is up-regulated following transplantation and β3 polymorphisms are associated with increased acute kidney rejection, suggesting that αvβ3 may also play a role in transplant rejection. Here, using a model of allogeneic heart transplantation, we show that allograft survival is prolonged in β3 integrin-deficient (β3-/-) mice. This is associated with Th2-type immune responses and reduced T-cell infiltration into grafts and T cells from β3-/- mice show impaired adhesion and migration, consistent with a role for αvβ3 in transmigration. These studies provide evidence that targeting β3 integrins impairs recruitment of effector cells and alters cytokine production, so prolonging graft survival. We also show that low doses of blocking antibodies against leukocyte function associated antigen-1 (LFA-1)/αLβ2 and very late antigen-4 (VLA-4)/α4β1, when combined with deletion of β3, lead to long-term survival of allografts with no evidence of chronic rejection. Hence we provide strong mechanistic evidence supporting previous genetic studies, demonstrate the involvement of β3 integrins in both acute and chronic rejection and identify β3 as a new target for immunosuppressive therapy.
AB - Integrin αvβ3 is important for cell survival, signaling and migration, particularly during angiogenesis and tumorigenesis, where it has been proposed as a therapeutic target. αvβ3 is up-regulated following transplantation and β3 polymorphisms are associated with increased acute kidney rejection, suggesting that αvβ3 may also play a role in transplant rejection. Here, using a model of allogeneic heart transplantation, we show that allograft survival is prolonged in β3 integrin-deficient (β3-/-) mice. This is associated with Th2-type immune responses and reduced T-cell infiltration into grafts and T cells from β3-/- mice show impaired adhesion and migration, consistent with a role for αvβ3 in transmigration. These studies provide evidence that targeting β3 integrins impairs recruitment of effector cells and alters cytokine production, so prolonging graft survival. We also show that low doses of blocking antibodies against leukocyte function associated antigen-1 (LFA-1)/αLβ2 and very late antigen-4 (VLA-4)/α4β1, when combined with deletion of β3, lead to long-term survival of allografts with no evidence of chronic rejection. Hence we provide strong mechanistic evidence supporting previous genetic studies, demonstrate the involvement of β3 integrins in both acute and chronic rejection and identify β3 as a new target for immunosuppressive therapy.
KW - Acute rejection
KW - Chronic rejection
KW - Extracellular matrix
KW - Integrin
KW - Migration
UR - http://www.scopus.com/inward/record.url?scp=34247525543&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34247525543&partnerID=8YFLogxK
U2 - 10.1111/j.1600-6143.2007.01757.x
DO - 10.1111/j.1600-6143.2007.01757.x
M3 - Article
C2 - 17359504
AN - SCOPUS:34247525543
VL - 7
SP - 1080
EP - 1090
JO - American Journal of Transplantation
JF - American Journal of Transplantation
SN - 1600-6135
IS - 5
ER -