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10.1016/j.addr.2017.04.005

http://scihub22266oqcxt.onion/10.1016/j.addr.2017.04.005
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C5582017!5582017!28414079
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suck abstract from ncbi


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pmid28414079      Adv+Drug+Deliv+Rev 2017 ; 114 (ä): 240-55
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  • In vivo reprogramming of immune cells: Technologies for induction of antigen-specific tolerance #MMPMID28414079
  • Pearson RM; Casey LM; Hughes KR; Miller SD; Shea LD
  • Adv Drug Deliv Rev 2017[May]; 114 (ä): 240-55 PMID28414079show ga
  • Technologies that induce antigen-specific immune tolerance by mimicking naturally occurring mechanisms have the potential to revolutionize the treatment of many immune-mediated pathologies such as autoimmunity, allograft rejection, and allergy. The immune system intrinsically has central and peripheral tolerance pathways for eliminating or modulating antigen-specific responses, which are being exploited through emerging technologies. Antigen-specific tolerogenic responses have been achieved through the functional reprogramming of antigen-presenting cells or lymphocytes. Alternatively, immune privileged sites have been mimicked using biomaterial scaffolds to locally suppress immune responses and promote long-term allograft survival. This review describes natural mechanisms of peripheral tolerance induction and the various technologies being developed to achieve antigen-specific immune tolerance in vivo. As currently approved therapies are non-specific and carry significant associated risks, these therapies offer significant progress towards replacing systemic immune suppression with antigen-specific therapies to curb aberrant immune responses.
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