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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003168naa a2200361 4500
001oai:DiVA.org:liu-46445
003SwePub
008091011s2003 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-464452 URI
024a https://doi.org/10.1046/j.1365-2796.2003.01217.x2 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Jonasson, Lenau Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Kardiologi,Kardiologiska kliniken4 aut0 (Swepub:liu)lenjo59
2451 0a Expansion of peripheral CD8+ T cells in patients with coronary artery disease :b Relation to cytomegalovirus infection
264 1b Wiley,c 2003
338 a print2 rdacarrier
520 a Objectives. The nature of the immune response in coronary artery disease (CAD) is not fully defined. One pathogen that has been linked to atherogenesis, cytomegalovirus (CMV). is known to exert strong and long-lasting effects on peripheral T cells. In the present study, we investigated the effect of prior CMV infection on the immune system in CAD patients. Subjects. Patients with stable angina and angiographically verified CAD (n = 43) and clinically healthy controls (n = 69) were included. Methods. The expression of CD57 and CD28 on peripheral CD4+ and CD8+ T cells was evaluated with three-colour flow cytometry. The findings were related to serological markers of inflammation, T-cell activation and CMV seropositivity. Results. An expansion of CD8+ T cells expressing CD57 but lacking CD28 was seen in the patient group. The numbers of CD8+CD57+ and CD8+ CD28- T-cell subsets were independently related to CMV seropositivity (P < 0.001) but also to CAD per se (P < 0.05). Serum concentrations of C-reactive protein (CRP) and soluble interleukin-2 receptor (sIL-2R) were elevated in the patients but not related to CMV or CD8 + T-cell subsets. Conclusion. A pronounced shift in peripheral T-cell homeostasis was observed in CAD patients. Primarily CMV infection but also CAD per se contributed to the expansion of CD8+ T-cell subsets. The T-cell changes were not related to a systemic inflammatory response but should rather be considered as markers of a chronic antigen exposure and/or immunosenescence in CAD.
653 a Coronary artery disease
653 a Cytomegalovirus
653 a Immune system
653 a T lymphocytes
653 a MEDICINE
653 a MEDICIN
700a Tompa, A.u Department of Microbiology, Ryhov Hospital, Jönköping, Sweden4 aut
700a Wikby, A.u Dept. of Nat. Sci. and Biomedicine, School of Health Sciences, Jönköping University, Jönköping, Sweden4 aut
710a Linköpings universitetb Hälsouniversitetet4 org
773t Journal of Internal Medicined : Wileyg 254:5, s. 472-478q 254:5<472-478x 0954-6820x 1365-2796
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1046/j.1365-2796.2003.01217.x
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-46445
8564 8u https://doi.org/10.1046/j.1365-2796.2003.01217.x

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Tompa, A.
Wikby, A.
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