Diagnosis of congenital cytomegalovirus infection
AssigneeHadasit Medical Research Services and Development Ltd.
InventorDana Wolf
Life of this patent
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Abstract
The present invention provides biomarkers allowing the diagnosis of symptomatic congenital cytomegalovirus (CMV) infection and in particular to differentiate between symptomatic and asymptomatic infected fetuses, methods of diagnosis of CMV using said biomarkers, diagnostic kits comprising thereof, and use of the kits and methods of diagnosing fetuses infected with a symptomatic congenital cytomegalovirus (CMV).
Claims21
A method of treating a symptomatic congenital human cytomegalovirus (cCMV) infection in a fetus in need thereof, the method comprising:
- administering to the fetus or its mother an anti-CMV active agent selected from valacyclovir and letermovir or administering valganciclovir to the fetus upon its birth, wherein the fetus has been indicated as having a symptomatic cCMV infection by a method comprising:
- (i) determining via an enzyme-linked immunosorbent assay (ELISA) or mass spectrometry a level of at least one biomarker in a biological sample selected from an amniotic fluid;
- blood, plasma or serum of the fetus;
- blood, plasma or serum of an umbilical cord of the fetus;
- a biopsy of a placenta of the fetus' mother;
- and blood or serum of the fetus' mother;
- and
- (ii) comparing the level of the at least one biomarker from the biological sample to its level in a control, wherein a difference in the level of the biomarker in the biological sample compared to the control is indicative of the presence of the symptomatic cCMV infection, wherein the at least one biomarker is selected from Retinoic acid receptor responder protein 2 (RARRES2), Galectin-3-binding protein (LGALS3BP), Transmembrane glycoprotein NMB (GPNMB), Nesprin-1 (SYNE1), Myosin-14 (MYH14), Carboxypeptidase A2 (CPA2), Secretoglobin family 3A member 2 (SCGB3A2)C-reactive protein (CRP), Glutathione S-transferase theta-1 (GSTT1),;
- Carboxypeptidase Q Protein (CPQ);
- Family with sequence similarity 3 member D (FAM3D);, Keratin 17 (KRT17), Carboxypeptidase M (CPM), Platelet-derived growth factor receptor beta (PDGFRB), Angiopoietin-related protein 6 (ANGPTL6), Dermokine (DMKN), Secretogranin-1 (CHGB), A Disintegrin and metalloproteinase domain-containing protein 9 (ADAM9), Growth arrest-specific protein 1 (GAS1), Platelet basic protein (PPBP), Platelet glycoprotein Ib alpha chain (GP1BA), Lysosome-associated membrane glycoprotein 2 (LAMP2), Neurofascin (NFASC), Alcohol dehydrogenase [NADP (+)] (AKR1A1), Heat shock protein beta-1 (HSPB1), Maltase-glucoamylase (MGAM), LAMP2 and Actin alpha 1, skeletal muscle (ACTA1), Mesothelin (MSLN);, Sarcoglycan epsilon (SGCE);, Cell growth regulator with EF hand domain protein 1 (CGREF1);, and Endoplasmic reticulum aminopeptidase 1 (ERAP1).
A method of treating a symptomatic congenital human cytomegalovirus (cCMV) infection in a fetus in need thereof, the method comprising:
- (a) determining via an enzyme-linked immunosorbent assay (ELISA) or mass spectrometry a level of at least one biomarker in a biological sample selected from an amniotic fluid;
- blood, plasma or serum of the fetus;
- blood, plasma or serum of an umbilical cord of the fetus;
- a biopsy of a placenta of the fetus' mother;
- or blood or serum of the fetus' mother;
- (b) comparing the level of at least one biomarker from the biological sample to its level in a control, wherein a difference in the level of the biomarker in the biological sample compared to the control is indicative of the presence of the symptomatic cCMV infection, wherein the at least one biomarker is selected from Retinoic acid receptor responder protein 2 (RARRES2), Galectin-3-binding protein (LGALS3BP), Transmembrane glycoprotein NMB (GPNMB), Nesprin-1 (SYNE1), Myosin-14 (MYH14), Carboxypeptidase A2 (CPA2), Secretoglobin family 3A member 2 (SCGB3A2)C-reactive protein (CRP), Glutathione S-transferase theta-1 (GSTT1), Carboxypeptidase Q Protein (CPQ), Family with sequence similarity 3 member D (FAM3D), Keratin 17 (KRT17), Carboxypeptidase M (CPM), Platelet-derived growth factor receptor beta (PDGFRB), Angiopoietin-related protein 6 (ANGPTL6), Dermokine (DMKN), Secretogranin-1 (CHGB), A Disintegrin and metalloproteinase domain-containing protein 9 (ADAM9), Growth arrest-specific protein 1 (GAS1), Platelet basic protein (PPBP), Platelet glycoprotein Ib alpha chain (GP1BA), Lysosome-associated membrane glycoprotein 2 (LAMP2), Neurofascin (NFASC), Alcohol dehydrogenase [NADP (+)] (AKR1A1), Heat shock protein beta-1 (HSPB1), Maltase-glucoamylase (MGAM), LAMP2 and Actin alpha 1, skeletal muscle (ACTA1), Mesothelin (MSLN), Sarcoglycan epsilon (SGCE), Cell growth regulator with EF hand domain protein 1 (CGREF1), and Endoplasmic reticulum aminopeptidase 1 (ERAP1);
- and
- (c) administering to the fetus or its mother an anti-CMV active agent selected from valacyclovir and letermovir or administering valganciclovir to the fetus upon its birth, wherein the comparing in step (b) indicates that the fetus has a symptomatic cCMV infection.
Dependencies are inferred from the claim text.