Abstract
Summary
The ingestion of soluble ferritin-antiferritin complexes was studied by parallel immunofluorescent, electron microscopic and isotope trace labeled antigen methods. The complexes were ingested by guinea pig spleen cells or mouse peritoneal macrophages. The degree of cellular activity demonstrated by these techniques was dependent on the degree of antigen excess used in preparation of the complexes, the source of antisera and the particular methodology applied.
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