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Verfasst von:Salbach, Christian [VerfasserIn]   i
 Schlegel, Philipp [VerfasserIn]   i
 Stroikova, Vera [VerfasserIn]   i
 Helmschrott, Matthias [VerfasserIn]   i
 Müller, Anna-Maria [VerfasserIn]   i
 Weiß, Christel [VerfasserIn]   i
 Giannitsis, Evangelos [VerfasserIn]   i
 Frey, Norbert [VerfasserIn]   i
 Raake, Philip [VerfasserIn]   i
 Kaya, Ziya [VerfasserIn]   i
Titel:Increase of cardiac autoantibodies against beta-2-adrenergic receptor during acute cellular heart transplant rejection
Verf.angabe:Christian Salbach, MD, Philipp Schlegel, MD, Vera Stroikova, MD, Matthias Helmschrott, MD, Anna-Maria Mueller, MD, Christel Weiß, PhD, Evangelos Giannitsis, MD, Norbert Frey, MD, Philip Raake, MD, and Ziya Kaya, MD
E-Jahr:2024
Jahr:October 2024
Umfang:6 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 19.11.2024
Titel Quelle:Enthalten in: Transplantation
Ort Quelle:Hagerstown, Md. : Lippincott Williams & Wilkins, 1963
Jahr Quelle:2024
Band/Heft Quelle:108(2024), 10, Seite e327-e332
ISSN Quelle:1534-6080
Abstract:Background. - Acute cellular rejection (ACR) in heart transplant (HTx) recipients may be accompanied by cardiac cell damage with subsequent exposure to cardiac autoantigens and the production of cardiac autoantibodies (aABs). This study aimed to evaluate a peptide array screening approach for cardiac aABs in HTx recipients during ACR (ACR-HTx). - Methods. - In this retrospective single-center observational study, sera from 37 HTx recipients, as well as age and sex-matched healthy subjects were screened for a total of 130 cardiac aABs of partially overlapping peptide sequences directed against structural proteins using a peptide array approach. - Results. - In ACR-HTx, troponin I (TnI) serum levels were found to be elevated. Here, we could identify aABs against beta-2-adrenergic receptor (β-2AR: EAINCYANETCCDFFTNQAY) to be upregulated in ACR-HTx (intensities: 0.80 versus 1.31, P = 0.0413). Likewise, patients positive for β-2AR aABs showed higher TnI serum levels during ACR compared with aAB negative patients (10.0 versus 30.0 ng/L, P = 0.0375). Surprisingly, aABs against a sequence of troponin I (TnI: QKIFDLRGKFKRPTLRRV) were found to be downregulated in ACR-HTx (intensities: 3.49 versus 1.13, P = 0.0025). A comparison in healthy subjects showed the same TnI sequence to be upregulated in non-ACR-HTx (intensities: 2.19 versus 3.49, P = 0.0205), whereas the majority of aABs were suppressed in non-ACR-HTx. - Conclusions. - Our study served as a feasibility analysis for a peptide array screening approach in HTx recipients during ACR and identified 2 different regulated aABs in ACR-HTx. Hence, further multicenter studies are needed to evaluate the prognostic implications of aAB testing and diagnostic or therapeutic consequences.
DOI:doi:10.1097/TP.0000000000005062
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1097/TP.0000000000005062
 kostenfrei: Volltext: https://journals.lww.com/transplantjournal/fulltext/2024/10000/increase_of_cardiac_autoantibodies_against.26.aspx
 DOI: https://doi.org/10.1097/TP.0000000000005062
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1908952520
Verknüpfungen:→ Zeitschrift

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