Variation of Complement Protein Levels in Maternal Plasma and Umbilical Cord Blood during Normal Pregnancy: An Observational Study.

complement system pregnancy umbilical cord blood

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
22 Jun 2022
Historique:
received: 31 05 2022
revised: 19 06 2022
accepted: 20 06 2022
entrez: 9 7 2022
pubmed: 10 7 2022
medline: 10 7 2022
Statut: epublish

Résumé

The complement system constitutes a crucial part of the innate immunity, mediating opsonization, lysis, inflammation, and elimination of potential pathogens. In general, there is an increased activity of the complement system during pregnancy, which is essential for maintaining the host's defense and fetal survival. Unbalanced or excessive activation of the complement system in the placenta is associated with pregnancy complications, such as miscarriage, preeclampsia, and premature birth. Nonetheless, the actual clinical value of monitoring the activation of the complement system during pregnancy remains to be investigated. Unfortunately, normal reference values specifically for pregnant women are missing, and for umbilical cord blood (UCB), data on complement protein levels are scarce. Herein, complement protein analyses (C1q, C3, C4, C3d levels, and C3d/C3 ratio) were performed in plasma samples from 100 healthy, non-medicated and non-smoking pregnant women, collected during different trimesters and at the time of delivery. In addition, UCB was collected at all deliveries. Maternal plasma C1q and C3d/C3 ratio showed the highest mean values during the first trimester, whereas C3, C4, and C3d had rising values until delivery. We observed low levels of C1q and C4 as well as increased C3d and C3d/C3 ratio, particularly during the first trimester, as a sign of complement activation in some women. However, the reference limits of complement analyses applied for the general population appeared appropriate for the majority of the samples. As expected, the mean complement concentrations in UCB were much lower than in maternal plasma, due to the immature complement system in neonates.

Identifiants

pubmed: 35806894
pii: jcm11133611
doi: 10.3390/jcm11133611
pmc: PMC9267899
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Muna Saleh (M)

Department of Biomedical and Clinical Sciences, Division of Inflammation and Infection/Rheumatology, Linköping University, SE-581 85 Linköping, Sweden.

Michele Compagno (M)

Rheumatology, Department of Clinical Sciences Malmö, Faculty of Medicine, Lund University, SE-222 42 Lund, Sweden.

Sofia Pihl (S)

Department of Obstetrics and Gynaecology, Linköping University Hospital, SE-581 85 Linköping, Sweden.
Department of Biomedical and Clinical Sciences, Division of Children's and Women's Health, Linköping University, SE-581 85 Linköping, Sweden.

Helena Strevens (H)

Department of Clinical Sciences Lund, Department of Obstetrics and Gynaecology, Lund University, SE-222 42 Lund, Sweden.

Barbro Persson (B)

Rudbeck Laboratory C5:3, Department of Immunology, Genetics and Pathology, Uppsala University, SE-751 85 Uppsala, Sweden.

Jonas Wetterö (J)

Department of Biomedical and Clinical Sciences, Division of Inflammation and Infection/Rheumatology, Linköping University, SE-581 85 Linköping, Sweden.

Bo Nilsson (B)

Rudbeck Laboratory C5:3, Department of Immunology, Genetics and Pathology, Uppsala University, SE-751 85 Uppsala, Sweden.

Christopher Sjöwall (C)

Department of Biomedical and Clinical Sciences, Division of Inflammation and Infection/Rheumatology, Linköping University, SE-581 85 Linköping, Sweden.

Classifications MeSH