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From the Laboratory of Microbial Immunity, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20014
Abstract
Treatment with several preparations of anti-lymphocyte or anti-thymocyte serum (ALS or ATS)1 has been shown to cause a significant increase (10- to 20-fold) in the magnitude of the plaque-forming cell (PFC) and serum antibody response to Type III pneumococcal polysaccharide (SSS-III) in different strains of mice (14); such enhancement is evident with respect to both PFC/106 nucleated spleen cells and PFC/spleen, indicating that it is not due simply to splenomegaly (3). These observations have been confirmed using preparations of ALS and SSS-III, made independently by different methods (5). In all of these studies, sheep erythrocytes, sensitized with purified SSS-III by the CrCl3 coupling method (6), were used as indicator cells for the detection of PFC making antibody specific for SSS-III. Despite these reproducible findings and their independent confirmation, some investigators have reported that treatment with ALS produces either no change, or a significant reduction in the number of PFC found after immunization with this antigen (79); here, sheep erythrocytes, sensitized with uncharacterized filtrates from broth cultures of pneumococci (10), were used as indicator cells in assays for PFC.
Footnotes
1 Abbreviations used in this paper: ALS, anti-lymphocyte serum; ATS, anti-thymocyte serum; PFC, plaque-forming cell; SSS-III, type III pneumococcal polysaccharide.
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