1. Clinical associations of complement-activating collectins, collectin-10, collectin-11 and mannose-binding lectin in preterm neonates
- Author
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Gabriela Gajek, Soren W. K. Hansen, Dariusz Jarych, Maja Kufelnicka-Babout, Anna S. Świerzko, Paulina Kobiela, Agnieszka Szala-Poździej, Karolina Chojnacka, Katarzyna Sobczuk, Iwona Domżalska-Popadiuk, Jan Mazela, Jarosław Kalinka, Steffen Thiel, and Maciej Cedzyński
- Subjects
CL-10 ,CL-11 ,collectin ,complement ,mannose-binding lectin (MBL) ,neonate ,Immunologic diseases. Allergy ,RC581-607 - Abstract
IntroductionPremature and low-birthweight infants are at especially high risk of perinatal complications, including impaired thermoregulation, infections and respiratory distress. Such adverse effects and the need for invasive procedures are associated with high mortality among preterms. This study focused on the influence of the innate immune system and tested the levels of collectins, collectin-10 (CL-10), collectin-11 (CL-11) and mannose-binding lectin (MBL) in preterm neonates.MethodsCord blood was collected from 535 preterms (born at gestational age ≤37 weeks). COLEC10 and COLEC11 polymorphisms were analyzed by real-time PCR and those of MBL2 by PCR/PCR-RFLP. The concentrations of collectins in sera from cord blood were determined with ELISA.FindingsLow concentrations of CL-10 in cord sera (G, His219Arg) was more common in preterm premature rupture of membranes (pPROM) cases, compared with corresponding reference groups. Furthermore, C/T or T/T genotypes at COLEC11 at rs3820897 (-9570 C>T) as well as MBL deficiency-associated MBL2 gene variants were more common in preterms diagnosed with RDS than among unaffected newborns.ConclusionThe complement-activating collectins investigated here could be important for maintaining homeostasis in preterm neonates. Despite similar structure and specificity, MBL, CL-10 and CL-11 manifest a different spectrum of clinical associations.
- Published
- 2024
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