Human cytomegalovirus (HCMV) long-term shedding and HCMV-specific immune response in pregnant women with primary HCMV infection.
C FornaraF ZavaglioM FurioneA SarasiniP d'AngeloA ArossaA SpinilloDaniele LilleriF BaldantiPublished in: Medical microbiology and immunology (2022)
Human cytomegalovirus (HCMV) shedding has been extensively investigated in newborns and in young children, however, much less is known about it in immunocompetent adults. Shedding of HCMV was investigated in saliva, vaginal secretions and urine of pregnant women experiencing primary infection along with the development of the HCMV-specific immune response. Thirty-three pregnant women shed HCMV DNA in peripheral biological fluids at least until one year after onset of infection, while in blood HCMV DNA was cleared earlier. Significantly higher levels of viral load were found in vaginal secretions compared to saliva and urine. All subjects examined two years after the onset of infection showed a high avidity index, with IgM persisting in 36% of women. Viral load in blood was directly correlated with levels of HCMV-specific IgM and inversely correlated with levels of IgG specific for the pentameric complex gH/gL/pUL128L; in addition, viral load in blood was inversely correlated with percentage of HCMV-specific CD4 + and CD8 + expressing IL-7R (long-term memory, LTM) while viral load in biological fluids was inversely correlated with percentage of HCMV-specific CD4 + and CD8 + effector memory RA + (T EMRA ). In conclusion, viral shedding during primary infection in pregnancy persists in peripheral biological fluids for at least one year and the development of both antibodies (including those directed toward the pentameric complex) and memory T cells are associated with viral clearance.
Keyphrases
- pregnant women
- immune response
- endothelial cells
- pregnancy outcomes
- sars cov
- rheumatoid arthritis
- dendritic cells
- type diabetes
- epstein barr virus
- multidrug resistant
- cell free
- circulating tumor
- polycystic ovary syndrome
- mass spectrometry
- induced pluripotent stem cells
- disease activity
- systemic lupus erythematosus
- inflammatory response
- preterm infants
- pluripotent stem cells
- skeletal muscle
- diffuse large b cell lymphoma
- idiopathic pulmonary fibrosis
- high resolution