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From the Department of Microbiology, Lobund Laboratory, University of Notre Dame, Notre Dame, Indiana 46556
Abstract
The biosynthetic potential of IgM and IgG plaque-forming cells in the spleens of mice during the first 8 days after immunization with sheep erythrocytes was examined. The double immunofluorescence technique was used to detect cells synthesizing both IgM and IgG hemolysins simultaneously. A total of 5944 plaque-forming cells (PFC) were examined: 2329 were IgG hemolysin producers, 3585 were IgM hemolysin producers, and only 30 could be classified as double (IgM-IgG) antibody producers. The proportion of double producers never exceeded 1.2% and it was usually below 1%.
It is concluded that the single antibody-producing cell is phenotypically restricted to the synthesis of one immunoglobulin antibody class at a time. The percentage (0.79%) of double IgM-IgG producers that was found at the time when IgM PFC were decreasing and IgG PFC were increasing in number is too low to suggest that the rapid rise of IgG PFC was due to the majority of the IgM PFC switching to the production of IgG hemolysin.
Footnotes
This study was supported by United States Public Health Service Grant AI-07659.
2 Submitted to the Graduate School of the University of Notre Dame in partial fulfillment of the requirements for the degree of Doctor of Philosophy.
3 Supported by Marion County Cancer Society.
4 Recipient of National Institutes of Health Career Development Award 1K 3-AI-37562.
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