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10.1073/pnas.1619386114

http://scihub22266oqcxt.onion/10.1073/pnas.1619386114
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suck abstract from ncbi


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pmid28416698      Proc+Natl+Acad+Sci+U+S+A 2017 ; 114 (18): E3689-98
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  • Selective in vivo removal of pathogenic anti-MAG autoantibodies, an antigen-specific treatment option for anti-MAG neuropathy #MMPMID28416698
  • Herrendorff R; Hänggi P; Pfister H; Yang F; Demeestere D; Hunziker F; Frey S; Schaeren-Wiemers N; Steck AJ; Ernst B
  • Proc Natl Acad Sci U S A 2017[May]; 114 (18): E3689-98 PMID28416698show ga
  • Anti-MAG (myelin-associated glycoprotein) neuropathy is a rare but disabling autoimmune disorder affecting the peripheral nervous system. The pathogenicity of anti-MAG IgM autoantibodies that target the HNK-1 glycoepitope is well established. Current therapies are mostly immunosuppressive but so far are neither approved nor sufficiently effective. Therefore we designed a glycopolymer that acts as an autoantibody scavenger by mimicking the natural HNK-1 glycoepitope and demonstrated that the glycopolymer neutralizes disease-causing antibodies in patient sera. Moreover, pathogenic antibodies were removed efficiently in an immunological mouse model of anti-MAG neuropathy. Because clinical improvement of patients? neuropathic symptoms correlates with reduced serum levels of anti-MAG antibodies, the glycopolymer represents a promising antigen-specific therapeutic option for the treatment of this neuropathy.
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