Abstract
In mice, pneumococcal polysaccharide (PPS) vaccines generate antigen-specific immunoglobulin M (IgM) and immunoglobulins G1, G2, and G3. Antibody and complement-dependent opsonophagocytosis correlates with the protection induced by PPS vaccines in vivo. Since IgM is a very efficient immunoglobulin isotype in activating the complement system, we evaluated whether anti-PPS IgM alone is sufficient to confer protective immunity to Streptococcus pneumoniae. We found that immunization of wild-type and activation-induced cytidine deaminase–deficient mice capable of producing only IgM with Pneumovax 23 generated comparable anti-PPS IgM and resistance to lethal systemic challenge with S pneumoniae. These data suggest that an IgM response to PPS vaccines is sufficient for conferring immunity.
| Original language | English |
|---|---|
| Pages (from-to) | 1852-1856 |
| Number of pages | 5 |
| Journal | Journal of Infectious Diseases |
| Volume | 226 |
| Issue number | 10 |
| DOIs | |
| State | Published - 15 Nov 2022 |
Keywords
- AID
- B cells
- IgM
- Streptococcus pneumoniae
- pneumococcal polysaccharide vaccine
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