作者: Ronald E. Esser , Stephen A. Stimpson , William J. Cromartie , John H. Schwab
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摘要: Joint inflammation initially induced by intraarticular injection of an aqueous suspension peptidoglycan-polysaccharide (PG-PS) fragments isolated from Streptococcus pyogenes was reactivated systemic a normally subarthropathic dose homologous or heterologous cell wall polymers, including muramyl dipeptide and lipopolysaccharide. Reactivation not correlated with the severity initial inflammatory reaction. Results studies utilizing 125I-labeled PG-PS suggested that reactivation associated increased localization in joint following reinjection. These results indicate injury S increases susceptibility to subsequent injury. Furthermore, once reaction is initiated, it can be perpetuated variety ubiquitous polymers derived normal flora as well pathogenic bacteria.