Publications by authors named "Cedzynski M"

Introduction: Premature 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.

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  • Surfactant proteins A and D (SP-A and SP-D) are pattern-recognition molecules that help the immune system recognize and clear abnormal or pathogen cells, particularly in the lungs.
  • These proteins contain four distinct structural domains and are produced by certain lung cells, contributing to surfactant function and preventing lung collapse.
  • The review discusses how SP-A and SP-D have both anti- and pro-cancer effects and explores their potential roles in diagnosing and treating various types of cancer.
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The immune system starts to develop early in embryogenesis. However, at birth it is still immature and associated with high susceptibility to infection. Adaptation to extrauterine conditions requires a balance between colonization with normal flora and protection from pathogens.

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Introduction: Toll-like receptors (TLRs) contribute to the innate immune system. They are an element of non-specific immunity, which enables organisms to react quickly to foreign antigens, without being previously exposed to them. TLRs are pattern recognition receptors.

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Introduction: Ficolin-2 is a serum pattern recognition molecule, involved in complement activation the lectin pathway. This study aimed to investigate the association of ficolin-2 concentration in cord blood serum with complications related to premature birth.

Methods: 546 premature neonates were included.

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Single nucleotide polymorphisms (SNPs) localised to the promoter region of the FCN2 gene are known to influence the concentration of ficolin-2 in human serum and therefore potentially have clinical associations. We investigated the relationships between SNPs at positions −986 (A > G), −602 (G > A), −64 (A > C) and −4 (A > G) and clinical complications in 501 preterms. Major alleles at positions −986 and −64 and A/A homozygosity for both polymorphisms were less frequent among babies with very low birthweight (VLBW, ≤1500 g) compared with the reference group (OR = 0.

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O:3 (YeO3) is considered to be associated with reactive arthritis (ReA), and its lipopolysaccharide (LPS) has been detected in synovial fluids from patients. Interestingly, YeO3 wild-type LPS was processed by host cells, resulting in truncated LPS molecules presenting the core region. Previously, we reported the immunogenicity but not adjuvanticity of YeO3 LPSs of wild (S) type, Ra, Rd, or Re chemotypes in mice.

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The complement system is an important branch of the humoral innate immune response that can be activated via three distinct pathways (classical, alternative, lectin), contributing to keeping/restoring homeostasis. It can also interact with cellular innate immunity and with components of acquired immunity. Cross-talk between the complement system and other enzyme-dependent cascades makes it a more influential defence system, but on the other hand, over- or chronic activation can be harmful.

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Ficolin-2 is regarded as an important innate immunity factor endowed with both lectin (carbohydrate recognition) qualities and ability to induce complement activation. The aim of this study was to investigate the association of the 3'-untranslated region (3'UTR) polymorphisms with ficolin-2 expression and perinatal complications in preterm neonates. The sequencing analysis allowed us to identify six 3'UTR polymorphisms with minor allele frequency (MAF) >1%: rs4521835, rs73664188, rs11103564, rs11103565, rs6537958 and rs6537959.

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O:3 is mentioned among the most common arthritogenic pathogens. Bacterial components (including lipopolysaccharide (LPS)) may persist in the joint after eradication of infection. Having an adjuvant activity, LPS may enhance production of anticollagen antibodies, involved in the pathogenesis of rheumatoid arthritis.

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Lung diseases are among the leading causes of morbidity and mortality. Complement activation may prevent a variety of respiratory infections, but on the other hand, could exacerbate tissue damage or contribute to adverse side effects. In this review, the associations of factors specific for complement activation the lectin pathway (LP) with infections of the respiratory system, from birth to adulthood, are discussed.

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A viral infection is detected through germline-encoded pattern-recognition receptors (PRRs) leading to the production of interferons (IFNs) and proinflammatory cytokines. The objective of this study was to investigate the expression of retinoic acid-inducible gene-I (RIG-I)-like receptors (RLRs) in response to viral infection and the selected cytokine responses in the human term placenta. Placental villi and decidual explants were infected with human cytomegalovirus (CMV) or vesicular stomatitis virus (VSV) and cultured ex vivo to study viral infection.

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The Malpuech, Michels, Mingarelli, Carnevale (3MC) syndrome is a rare, autosomal recessive genetic- disorder associated with mutations in the , or genes. The number of 3MC patients with known mutations in these three genes reported so far remains very small. To date, 16 mutations in , 12 mutations in and three in associated with 3MC syndrome have been identified.

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The complement system is activated cascadically via three distinct major routes: classical pathway (CP), alternative pathway (AP) or lectin pathway (LP). The unique factors associated with the latter are collectins (mannose-binding lectin, collectin-10, collectin-11), ficolins (ficolin-1, ficolin-2, ficolin-3) and proteins of the mannose-binding lectin-associated serine protease (MASP) family (MASP-1, MASP-2, MASP-3, MAp19, MAp44). Collectins and ficolins are both pattern-recognising molecules (PRM), reactive against pathogen-associated molecular patterns (PAMP) or danger-associated molecular patterns (DAMP).

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  • Researchers studied the levels of ficolins and mannose-binding lectin (MBL) in 157 patients with acute myeloid leukaemia (AML) compared to 267 healthy individuals.
  • They found that ficolin-1 was significantly lower in AML patients, while ficolin-2, ficolin-3, and MBL were higher, with the highest MBL levels linked to a greater risk of severe infections.
  • Genotyping suggested a specific genetic variant (G/G homozygosity) associated with the disease, and ficolins could serve as potential new biomarkers for diagnosing AML and distinguishing it from other blood cancers.
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  • A study involving 312 patients with multiple myeloma and lymphomas assessed the levels of ficolins (immune proteins) and their genetic polymorphisms before and after high-dose chemotherapy and stem cell transplantation.
  • Findings showed that multiple myeloma patients had significantly lower levels of ficolin-1 and ficolin-2 compared to healthy controls, suggesting a link to the disease itself rather than post-transplant complications.
  • Genetic variations in the ficolin genes were more frequently found in cancer patients, with some polymorphisms associated with a higher risk of infections post-chemotherapy, especially in lymphoma patients.
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  • * Higher numbers of certain genetic variants (MBL2 gene exon 1) were found in tuberculosis patients compared to healthy individuals, while some variations (SFTPA2 +26 C > A SNP) were less common in patients.
  • * Increased levels of specific serum proteins, including ficolin-1, were seen in patients, suggesting ficolin-1 could be a potential marker to distinguish between tuberculosis patients and healthy individuals.
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Inflammatory bowel disease (IBD) refers to disorders associated with progressive inflammatory processes in the gastrointestinal system. IBD consists of two major forms, Crohn's disease (CD), and ulcerative colitis (UC). IBD became a global disease in the 21 century.

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Background: Ficolin-3 is a pattern-recognition molecule with the ability to activate the lectin pathway of complement. It is found in lung, liver and blood, but its physiological role is unclear. We have investigated interaction of recombinant ficolin-3 with malignant cells and tissues.

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  • Congenital heart disease (CHD) often requires surgery and can lead to serious post-operative complications, prompting a study on the innate immune system factors related to these outcomes in pediatric patients.
  • Key findings reveal that low levels of MAp44 are linked to increased complications like low cardiac output syndrome and renal issues, while low MASP-3 and high MASP-1 levels correlate with fatal outcomes.
  • Low ficolin-3 levels are associated with more severe complications, but surprisingly, patients with low ficolin-3 still had a much higher survival rate compared to others, suggesting its potential as a prognostic marker for post-operative recovery.
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  • - This study involved 312 patients with multiple myeloma and lymphomas undergoing high-dose chemotherapy and autologous stem cell transplantation, examining the role of certain gene polymorphisms and serum concentrations of immune-related proteins.
  • - Findings indicated that multiple myeloma patients had a higher prevalence of MBL deficiency genotypes, but this was not linked to hospital infections or recovery of white blood cells, although it correlated with more severe infections during follow-up.
  • - Interestingly, high levels of MBL were associated with prolonged fever and some infections post-chemotherapy, while a notable association between a gene mutation and lymphoma was identified, and overall, the influence of MBL on infections in these patients remains conflicting.
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Lipopolysaccharide (LPS, endotoxin), the main surface antigen and virulence factor of Gram-negative bacteria, is composed of lipid A, core oligosaccharide, and O-specific polysaccharide (O-PS) regions. Each LPS region is capable of complement activation. We have demonstrated that LPS of , an opportunistic human pathogen, reacts strongly with human and murine mannose-binding lectins (MBLs).

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The artificial surface used for cardiopulmonary bypass (CPB) is a crucial factor activating the complement system and thus contributing to the generation of a systemic inflammatory response. The activation of classical and alternative pathways on this artificial surface is well known. In contrast, lectin pathway (LP) activation has not been fully investigated, although noted during CPB in several studies.

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Both complement activation and certain infections (including those with Yersinia sp.) may contribute to the pathogenesis of juvenile idiopathic arthritis (JIA). We investigated factors specific for the lectin pathway of complement: mannose-binding lectin (MBL), ficolins and MBL-associated serine protease-2 (MASP-2), in 144 patients and 98 controls.

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