The Effect of a 13-Valent Conjugate Pneumococcal Vaccine on Circulating Antibodies Against Oxidized LDL and Phosphorylcholine in Man, A Randomized Placebo-Controlled Clinical Trial.
Hendrika W GrievinkPim GalMaria Ozsvar KozmaErica S KlaassenJohan KuiperJacobus BurggraafChristoph J BinderMatthijs MoerlandPublished in: Biology (2020)
In mice vaccination with Streptococcus pneumoniae results in an increase in anti-oxLDL IgM antibodies due to mimicry of anti-phosphorylcholine (present in the cell wall of S. pneumoniae) and anti-oxLDL IgM. In this study we investigated the human translation of this molecular mimicry by vaccination against S. pneumoniae using the Prevenar-13 vaccine. Twenty-four healthy male volunteers were vaccinated with Prevenar-13, either three times, twice or once in a double-blind, placebo-controlled, randomized single center clinical study. Anti-pneumococcal wall, oxLDL and phosphorycholine antibody levels were measured at a fixed serum dilution, as well as circulating lipid levels over the course of 68 weeks. A significant increase in anti-oxLDL IgG and IgM was seen in the group receiving two doses six months apart compared to the placebo. However, these differences were not observed in the groups receiving a single dose, two doses one month apart, or three doses. This study shows that vaccination with Prevenar-13 does not result in robust anti-oxLDL IgM levels in humans. Further research would be required to test alternative pneumococcal-based vaccines, vaccination regimens or study populations, such as cardiovascular disease patients.
Keyphrases
- double blind
- placebo controlled
- cardiovascular disease
- clinical trial
- phase iii
- endothelial cells
- newly diagnosed
- radiation therapy
- open label
- cell wall
- squamous cell carcinoma
- ejection fraction
- randomized controlled trial
- adipose tissue
- metabolic syndrome
- fatty acid
- drug delivery
- cardiovascular events
- single molecule
- skeletal muscle
- cancer therapy
- patient reported outcomes
- induced pluripotent stem cells
- mass spectrometry
- atomic force microscopy
- respiratory tract