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10.1371/journal.pone.0161826

http://scihub22266oqcxt.onion/10.1371/journal.pone.0161826
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C4999199!4999199!27561008
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suck abstract from ncbi


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pmid27561008      PLoS+One 2016 ; 11 (8): ä
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  • Effect of IVIG Formulation on IgG Binding to Self- and Exo- Antigens In Vitro and In Vivo #MMPMID27561008
  • Cattepoel S; Gaida A; Kropf A; Nolte MW; Bolli R; Miescher SM
  • PLoS One 2016[]; 11 (8): ä PMID27561008show ga
  • In relation to the recent trials of Intravenous Immunoglobulin (IVIG) in Alzheimer?s Disease (AD) it was demonstrated that different IgG preparations contain varying amounts of natural anti-amyloid ? (A?) antibodies as measured by ELISA. We therefore investigated the relevance of ELISA data for measuring low-affinity antibodies, such as anti-A?. We analysed the binding of different commercial Immunoglobulin G (IgG) preparations to A?, actin and tetanus toxoid in different binding assays to further investigate the possible cause for observed differences in binding to A? and actin between different IgG preparations. We show that the differences of commercial IgG preparations in binding to A? and actin in ELISA assays are artefactual and only evident in in vitro binding assays. In functional assays and in vivo animal studies the different IVIG preparations exhibited very similar potency. ELISA data alone are not appropriate to analyse and rank the binding capacity of low-affinity antibodies to A? or other endogenous self-antigens contained in IgG preparations. Additional analytical methods should be adopted to complement ELISA data.
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