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Pneumococcal cell wall phosphorylcholine elicits polyclonal antibody secretion in mice
European Journal of Immunology
|July 1, 1984
Summary
Immunizing mice with Staphylococcus pneumoniae bacteria containing phosphorylcholine (PC) triggers both a specific immune response to PC and a broad, polyclonal increase in antibody-producing cells. This suggests bacterial PC acts as both a specific antigen and a polyclonal activator.
Area of Science:
- Immunology
- Microbial Pathogenesis
- B Cell Activation
Background:
- * Staphylococcus pneumoniae possesses phosphorylcholine (PC) on its surface.
- * PC-bearing bacteria can elicit specific antibody responses.
- * The impact of bacterial PC on broader immune responses is not fully understood.
Purpose of the Study:
- * To investigate the dual role of bacterial phosphorylcholine (PC) as both a specific antigen and a polyclonal activator.
- * To determine the mechanisms underlying PC-induced specific and polyclonal immune responses.
- * To assess the influence of host immune status on these responses.
Main Methods:
- * Immunization of mice with phosphorylcholine (PC)-bearing Staphylococcus pneumoniae R36a.
- * Measurement of PC-specific and polyclonal splenic plaque-forming cells.
- * Enzyme-linked immunosorbent assay (ELISA) to quantify bacterial surface PC.
- * Use of immunodeficient mouse models (X-linked immune defect, athymic nude mice).
Main Results:
- * R36a immunization induced both PC-specific and polyclonal increases in plaque-forming cells.
- * The polyclonal response was present even in mice with undetectable anti-PC responses.
- * Polyclonal response magnitude correlated with bacterial surface PC levels.
- * Athymic nude mice showed a PC-specific response but lacked a significant polyclonal response.
Conclusions:
- * Phosphorylcholine on the bacterial cell wall functions as both a specific antigen and a polyclonal activator.
- * Distinct mechanisms likely mediate the specific and polyclonal activation by bacterial PC.
- * T-cell independent mechanisms may be involved in the polyclonal activation by bacterial PC.