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Search: onr:"swepub:oai:lup.lub.lu.se:98a1cfe6-d564-4054-9baf-c420b5ddf933" > Inhibition of Ather...

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  • Nordin Fredrikson, GunillaMalmö högskola,Lund University,Lunds universitet,Kardiovaskulär forskning - immunitet och ateroskleros,Forskargrupper vid Lunds universitet,Cardiovascular Research - Immunity and Atherosclerosis,Lund University Research Groups,Fakulteten för hälsa och samhälle (HS) (author)

Inhibition of Atherosclerosis in ApoE-Null Mice by Immunization with ApoB-100 Peptide Sequences.

  • Article/chapterEnglish2003

Publisher, publication year, extent ...

  • The Assoc.2003

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  • LIBRIS-ID:oai:lup.lub.lu.se:98a1cfe6-d564-4054-9baf-c420b5ddf933
  • https://lup.lub.lu.se/record/112654URI
  • https://doi.org/10.1161/01.ATV.0000067937.93716.DBDOI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-5111URI

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  • Language:English
  • Summary in:English

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  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

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  • Objective - LDL oxidation is believed to play an important role in the development of atherosclerosis, and oxidized LDL particles have been shown to become targets for the immune system. Immunization of animals with oxidized LDL results in reduction of atherosclerosis, suggesting an atheroprotective effect of this immune response. Methods and Results - Using a polypeptide library covering the complete sequence of apoB-100, a large number of native and malondialdehyde-modified peptide sequences in apoB-100 that are recognized by antibodies in human plasma were identified. We report here that immunization with apoB-100 peptide sequences, against which high levels of IgG and IgM antibodies are present in healthy human controls, reduce atherosclerosis in apoE-null mice by about 60%. Immunizations with these peptides were also found to increase the collagen content of subvalvular lesions. Conclusions - These studies have identified peptide sequences in apoB-100 that induce immune responses, which inhibits atherosclerosis. This suggests a way of developing an immunization therapy for coronary heart disease.

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  • Söderberg, IngridLund University,Lunds universitet,Kardiovaskulär forskning - immunitet och ateroskleros,Forskargrupper vid Lunds universitet,Cardiovascular Research - Immunity and Atherosclerosis,Lund University Research Groups(Swepub:lu)medf-iso (author)
  • Lindholm, MarieLund University,Lunds universitet,Kardiovaskulär forskning - immunitet och ateroskleros,Forskargrupper vid Lunds universitet,Cardiovascular Research - Immunity and Atherosclerosis,Lund University Research Groups(Swepub:lu)medf-mli (author)
  • Dimayuga, Paul (author)
  • Chyu, Kuang-Yuh (author)
  • Shah, Prediman K. (author)
  • Nilsson, JanLund University,Lunds universitet,Kardiovaskulär forskning - immunitet och ateroskleros,Forskargrupper vid Lunds universitet,Cardiovascular Research - Immunity and Atherosclerosis,Lund University Research Groups(Swepub:lu)medf-jni (author)
  • Kardiovaskulär forskning - immunitet och aterosklerosForskargrupper vid Lunds universitet (creator_code:org_t)

Related titles

  • In:Arteriosclerosis, Thrombosis and Vascular Biology: The Assoc.23:5, s. 879-8841524-46361079-5642

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