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Amniotic fluid biomarkers predict the severity of congenital cytomegalovirus infection.
Vorontsov, Olesya; Levitt, Lorinne; Lilleri, Daniele; Vainer, Gilad W; Kaplan, Orit; Schreiber, Licita; Arossa, Alessia; Spinillo, Arseno; Furione, Milena; Alfi, Or; Oiknine-Djian, Esther; Kupervaser, Meital; Nevo, Yuval; Elgavish, Sharona; Yassour, Moran; Zavattoni, Maurizio; Bdolah-Abram, Tali; Baldanti, Fausto; Geal-Dor, Miriam; Zakay-Rones, Zichria; Yanay, Nili; Yagel, Simcha; Panet, Amos; Wolf, Dana G.
Afiliação
  • Vorontsov O; Clinical Virology Unit, Hadassah-Hebrew University Medical Center and Faculty of Medicine.
  • Levitt L; Department of Biochemistry, Institute for Medical Research, Israel-Canada (IMRIC), Faculty of Medicine.
  • Lilleri D; Lautenberg Center for General and Tumor Immunology, Faculty of Medicine, and.
  • Vainer GW; Department of Obstetrics and Gynecology, Hadassah-Hebrew University Medical Center and Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
  • Kaplan O; Department of Microbiology and Virology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Schreiber L; Department of Pathology, Hadassah-Hebrew University Medical Center and Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
  • Arossa A; Clinical Virology Unit, Hadassah-Hebrew University Medical Center and Faculty of Medicine.
  • Spinillo A; Maccabi Healthcare Services, Central Laboratory, Rehovot, Israel.
  • Furione M; Department of Obstetrics and Gynecology, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Alfi O; Department of Obstetrics and Gynecology, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Oiknine-Djian E; Department of Microbiology and Virology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Kupervaser M; Clinical Virology Unit, Hadassah-Hebrew University Medical Center and Faculty of Medicine.
  • Nevo Y; Department of Biochemistry, Institute for Medical Research, Israel-Canada (IMRIC), Faculty of Medicine.
  • Elgavish S; Lautenberg Center for General and Tumor Immunology, Faculty of Medicine, and.
  • Yassour M; Clinical Virology Unit, Hadassah-Hebrew University Medical Center and Faculty of Medicine.
  • Zavattoni M; Department of Biochemistry, Institute for Medical Research, Israel-Canada (IMRIC), Faculty of Medicine.
  • Bdolah-Abram T; Lautenberg Center for General and Tumor Immunology, Faculty of Medicine, and.
  • Baldanti F; The De Botton Protein Profiling Institute of the Nancy and Stephen Grand Israel National Center for Personalized Medicine, Weizmann Institute of Science, Rehovot, Israel.
  • Geal-Dor M; Info-CORE, Bioinformatics Unit of the I-CORE.
  • Zakay-Rones Z; Info-CORE, Bioinformatics Unit of the I-CORE.
  • Yanay N; School of Computer Science and Engineering.
  • Yagel S; Department of Microbiology and Molecular Genetics, IMRIC, Faculty of Medicine, and.
  • Panet A; Department of Microbiology and Virology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Wolf DG; Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.
J Clin Invest ; 132(11)2022 06 01.
Article em En | MEDLINE | ID: mdl-35439172
ABSTRACT
BACKGROUNDCytomegalovirus (CMV) is the most common intrauterine infection, leading to infant brain damage. Prognostic assessment of CMV-infected fetuses has remained an ongoing challenge in prenatal care, in the absence of established prenatal biomarkers of congenital CMV (cCMV) infection severity. We aimed to identify prognostic biomarkers of cCMV-related fetal brain injury.METHODSWe performed global proteome analysis of mid-gestation amniotic fluid samples, comparing amniotic fluid of fetuses with severe cCMV with that of asymptomatic CMV-infected fetuses. The levels of selected differentially excreted proteins were further determined by specific immunoassays.RESULTSUsing unbiased proteome analysis in a discovery cohort, we identified amniotic fluid proteins related to inflammation and neurological disease pathways, which demonstrated distinct abundance in fetuses with severe cCMV. Amniotic fluid levels of 2 of these proteins - the immunomodulatory proteins retinoic acid receptor responder 2 (chemerin) and galectin-3-binding protein (Gal-3BP) - were highly predictive of the severity of cCMV in an independent validation cohort, differentiating between fetuses with severe (n = 17) and asymptomatic (n = 26) cCMV, with 100%-93.8% positive predictive value, and 92.9%-92.6% negative predictive value (for chemerin and Gal-3BP, respectively). CONCLUSIONAnalysis of chemerin and Gal-3BP levels in mid-gestation amniotic fluids could be used in the clinical setting to profoundly improve the prognostic assessment of CMV-infected fetuses.FUNDINGIsrael Science Foundation (530/18 and IPMP 3432/19); Research Fund - Hadassah Medical Organization.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Infecções por Citomegalovirus Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant / Pregnancy Idioma: En Revista: J Clin Invest Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Infecções por Citomegalovirus Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Infant / Pregnancy Idioma: En Revista: J Clin Invest Ano de publicação: 2022 Tipo de documento: Article