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The Journal of Immunology, 1975, 115: 891-892.
Copyright © 1975 by The American Association of Immunologists, Inc.

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The Basis for Conflicting Results Obtained in Studies on the Plaque-Forming Cell Response to Type III Pneumococcal Polysaccharide

Phillip J. Baker and Benjamin Prescott

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 (1–4); 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 (7–9); 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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