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Institut für Medizinische Mikrobiologie, Johannes-Gutenberg-Universität, Mainz, Germany
Abstract
Dinitrophenyl-human serum albumin (DNP-HSA) preparations activate C3 via the alternate pathway of the complement system depending on the grade of DNP substitution. This potency seems to be due to the polyanionic character of DNP-HSA and thus resembles in its behavior other polyanions.
Footnotes
1 This work was supported by grants of the Sonderforschungsbereich 107 (Immunology) at Mainz.
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