Combination therapy with anti-ICOS and cyclosporine enhances cardiac but not islet allograft survival.

Abstract:

:The blockade of costimulatory signals is a powerful strategy to prevent allograft rejection and facilitate transplantation tolerance. In recent years, a series of novel costimulatory molecules have been identified, including an inducible costimulatory molecule (ICOS). To date, little has been uncovered regarding the therapeutic potential of blocking ICOS signaling in the setting of transplantation. In a fully MHC-mismatched mouse model, we studied the effect of blocking ICOS signaling using a specific monoclonal antibody (anti-ICOS mAb) in combination with cyclosporine on cardiac and islet allograft survival. We demonstrated that combined treatment with anti-ICOS mAb and cyclosporine can induce long-term graft acceptance in cardiac but not islet allografts, suggesting that the type of transplanted tissue significantly influences the immunologic patterns of graft acceptance or rejection in this model.

journal_name

Transplant Proc

authors

Nanji SA,Hancock WW,Anderson CC,Zhu LF,Kneteman NM,Shapiro AM

doi

10.1016/j.transproceed.2003.08.029

subject

Has Abstract

pub_date

2003-11-01 00:00:00

pages

2477-8

issue

7

eissn

0041-1345

issn

1873-2623

pii

S0041134503008911

journal_volume

35

pub_type

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