After an allograft placement, the body faces an intricate task of mounting a balanced immune response to foreign antigens. The ideal response entails maintaining enough immunity to prevent infections and cancer yet not endangering the ability to achieve and maintain organ tolerance. Programmed death-1 and its ligands expressed on non-professional antigen-presenting cells such as the renal tubular epithelium function to downregulate allogenic T-cell responses and thus play an important role in achieving this balance
Increased circulating follicular helper T cells with decreased programmed death-1 in chronic renal a...
To avoid immune rejection, allograft recipients require drug-based immunosuppression, which has sign...
Interferon-γ-treated renal tubular epithelial cells induce allospecific tolerance. Following organ t...
Renal proximal tubular epithelial cells, a target of infiltrating T cells during renal allograft rej...
After an allograft placement, the body faces an intricate task of mounting a balanced immune respons...
The control of alloimmunity is essential to the success of organ transplantation. Upon alloantigen e...
Balancing enough immunosuppression to prevent allograft rejection and yet maintaining an intact immu...
Multidrug immunosuppressive protocols have increased short-term patient and graft survival rates fro...
AbstractThe alloimmune response can be divided into specific junctures where critical decisions betw...
Background. The interaction of the T-cell molecule PD-1 (programmed death-1) with its ligands PD-L1 ...
Although transplantation tolerance cannot be yet reliably achieved in humans, there is evidence that...
Acute rejection (AR) is responsible for up to 12% of graft loss with the highest risk generally occu...
AbstractSecondary, so-called costimulatory, signals are critically required for the process of T cel...
Peripheral mechanisms of self-tolerance often depend on the quiescent state of the immune system. To...
Background. The interaction of the T-cell molecule PD-1 (programmed death-1) with its ligands PD-L1 ...
Increased circulating follicular helper T cells with decreased programmed death-1 in chronic renal a...
To avoid immune rejection, allograft recipients require drug-based immunosuppression, which has sign...
Interferon-γ-treated renal tubular epithelial cells induce allospecific tolerance. Following organ t...
Renal proximal tubular epithelial cells, a target of infiltrating T cells during renal allograft rej...
After an allograft placement, the body faces an intricate task of mounting a balanced immune respons...
The control of alloimmunity is essential to the success of organ transplantation. Upon alloantigen e...
Balancing enough immunosuppression to prevent allograft rejection and yet maintaining an intact immu...
Multidrug immunosuppressive protocols have increased short-term patient and graft survival rates fro...
AbstractThe alloimmune response can be divided into specific junctures where critical decisions betw...
Background. The interaction of the T-cell molecule PD-1 (programmed death-1) with its ligands PD-L1 ...
Although transplantation tolerance cannot be yet reliably achieved in humans, there is evidence that...
Acute rejection (AR) is responsible for up to 12% of graft loss with the highest risk generally occu...
AbstractSecondary, so-called costimulatory, signals are critically required for the process of T cel...
Peripheral mechanisms of self-tolerance often depend on the quiescent state of the immune system. To...
Background. The interaction of the T-cell molecule PD-1 (programmed death-1) with its ligands PD-L1 ...
Increased circulating follicular helper T cells with decreased programmed death-1 in chronic renal a...
To avoid immune rejection, allograft recipients require drug-based immunosuppression, which has sign...
Interferon-γ-treated renal tubular epithelial cells induce allospecific tolerance. Following organ t...