Pneumococcal vaccination decreases atherosclerotic lesion formation: molecular mimicry between Strep

Author:  ["Christoph J Binder","Sohvi Hörkkö","Asheesh Dewan","Mi-Kyung Chang","Emily P Kieu","Carl S Goodyear","Peter X Shaw","Wulf Palinski","Joseph L Witztum","Gregg J Silverman"]

Publication:  Nature Medicine

CITE.CC academic search helps you expand the influence of your papers.

Tags:     Medicine

Abstract

During the progression of atherosclerosis, autoantibodies are induced to epitopes of oxidized low-density lipoprotein (oxLDL) and active immunization of hypercholesterolemic mice with oxLDL ameliorates atherogenesis. We unexpectedly found that many autoantibodies to oxLDL derived from 'naive' atherosclerotic mice share complete genetic and structural identity with antibodies from the classic anti-phosphorylcholine B-cell clone, T15, which protect against common infectious pathogens, including pneumococci. To investigate whether in vivo exposure to pneumococci can affect atherogenesis, we immunized Ldlr−/− mice with Streptococcus pneumoniae. This induced high circulating levels of oxLDL-specific IgM and a persistent expansion of oxLDL-specific T15 IgM-secreting B cells primarily in the spleen, which were cross-reactive with pneumococcal determinants. Pneumococcal immunization decreased the extent of atherosclerosis, and plasma from these mice had an enhanced capacity to block the binding of oxLDL to macrophages. These studies show molecular mimicry between epitopes of oxLDL and S. pneumoniae and indicate that these immune responses can have beneficial effects.

Cite this article

Binder, C., Hörkkö, S., Dewan, A. et al. Pneumococcal vaccination decreases atherosclerotic lesion formation: molecular mimicry between Streptococcus pneumoniae and oxidized LDL. Nat Med 9, 736–743 (2003). https://doi.org/10.1038/nm876

View full text

>> Full Text:   Pneumococcal vaccination decreases atherosclerotic lesion formation: molecular mimicry between Strep

Prostaglandin E2–EP4 signaling initiates skin immune responses by promoting migration and maturation

Attenuation of levodopa-induced dyskinesia by normalizing dopamine D3 receptor function