Andere Kunden interessierten sich auch für
![Autophagy in Immune Response: Impact on Cancer Immunotherapy]( "Autophagy in Immune Response: Impact on Cancer Immunotherapy")
Autophagy in Immune Response: Impact on Cancer Immunotherapy114,99 €![Skin and Arthropod Vectors]( "Skin and Arthropod Vectors")
Skin and Arthropod Vectors65,99 €![The compounds of Monopterus albus skin mucus using LC-QTOF-MS and GCMS]( "The compounds of Monopterus albus skin mucus using LC-QTOF-MS and GCMS")
The compounds of Monopterus albus skin mucus using LC-QTOF-MS and GCMS26,99 €![The therapeutic activity of skin mucus from Monopterus albus in-vivo]( "The therapeutic activity of skin mucus from Monopterus albus in-vivo")
The therapeutic activity of skin mucus from Monopterus albus in-vivo26,99 €![The biological activities of skin mucus from Monopterus albus in-vitro]( "The biological activities of skin mucus from Monopterus albus in-vitro")
The biological activities of skin mucus from Monopterus albus in-vitro26,99 €![Development of a novel hydrogel for skin regeneration]( "Development of a novel hydrogel for skin regeneration")
Development of a novel hydrogel for skin regeneration26,99 €![Effect of buckling on the rejection power of plantain]( "Effect of buckling on the rejection power of plantain")
Effect of buckling on the rejection power of plantain29,99 €
In this book it has been clearly explained about the role of immune cells in allograft rejection. Both antigen specific and non-specific mechanisms of tissue destruction characterize rejection responses to skin allografts, although it is the antigen-specific action of Tc cells that primarily determines survival or rejection of the engrafted skin. Skin allograft rejection responses are initiated in vivo by activation of antigen-reactive TH cells by donor Langerhans cells resident in the graft. It appears possible to promote allograft acceptance by selective inactivation of either antigen-reactive TH cells or Tc cells by several different experimental protocol. TH cells can be inactivated by exposure to alloantigen in the absence of TH cells or their products. Self-tolerance can be induced by using many of the monoclonal antibodies, dendritic cells, HLA-G molecules. Even mixed chimerism and antisense technology are being extensively used for tolerance development and wide verities of drugs are commonly used to suppress the immune system, which may be specific or nonspecific.