Increased Levels of serum Pentraxin 3 in Critical Coronavirus Disease-2019 Patients
Pentraxin 3 (PTX3) and ficolin are the plasma phase of pattern recognition receptors (PRRs) and can activate complement through classical and lectin pathways, respectively, which may contribute to disease severity. This study aimed to investigate the association between PTX3 and ficolin with disease...
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Published in | Environmental science and pollution research international Vol. 29; no. 57; pp. 85569 - 85573 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.12.2022
Springer Nature B.V |
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Online Access | Get full text |
ISSN | 0944-1344 1614-7499 1614-7499 |
DOI | 10.1007/s11356-021-15183-9 |
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Abstract | Pentraxin 3 (PTX3) and ficolin are the plasma phase of pattern recognition receptors (PRRs) and can activate complement through classical and lectin pathways, respectively, which may contribute to disease severity. This study aimed to investigate the association between PTX3 and ficolin with disease severity in patients with coronavirus disease-2019 (COVID-19). Seventy-three COVID-19 patients and 25 healthy controls were enrolled in this study. The participants were divided into three groups as follows: 14 patients as the intensive care unit (ICU) group, 59 patients as the non-ICU group, and 25 subjects as the healthy control group. The serum levels of PTX3 and ficolin were measured by enzyme-linked immunosorbent assay (ELISA) kits. Patients in ICU and non-ICU groups had significantly higher levels of PTX3 compared to the healthy control group (
p
= 0.0002 and
p
= 0.0072, respectively). Patients in the ICU group also had an increased amount of PTX3 (1957 ± 1769 pg/ml) compared to non-ICU patients (1220 ± 1784 pg/ml). However, this difference was not significant. On the other hand, serum levels of ficolin were not different among the three groups. PTX3, as an acute phase protein, may contribute to disease severity. Its probable inflammatory role could result from the high activation of the complement system. On the other hand, it could be suggested that ficolin has no crucial role in the disease severity of COVID-19 patients. |
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AbstractList | Pentraxin 3 (PTX3) and ficolin are the plasma phase of pattern recognition receptors (PRRs) and can activate complement through classical and lectin pathways, respectively, which may contribute to disease severity. This study aimed to investigate the association between PTX3 and ficolin with disease severity in patients with coronavirus disease-2019 (COVID-19). Seventy-three COVID-19 patients and 25 healthy controls were enrolled in this study. The participants were divided into three groups as follows: 14 patients as the intensive care unit (ICU) group, 59 patients as the non-ICU group, and 25 subjects as the healthy control group. The serum levels of PTX3 and ficolin were measured by enzyme-linked immunosorbent assay (ELISA) kits. Patients in ICU and non-ICU groups had significantly higher levels of PTX3 compared to the healthy control group (p = 0.0002 and p = 0.0072, respectively). Patients in the ICU group also had an increased amount of PTX3 (1957 ± 1769 pg/ml) compared to non-ICU patients (1220 ± 1784 pg/ml). However, this difference was not significant. On the other hand, serum levels of ficolin were not different among the three groups. PTX3, as an acute phase protein, may contribute to disease severity. Its probable inflammatory role could result from the high activation of the complement system. On the other hand, it could be suggested that ficolin has no crucial role in the disease severity of COVID-19 patients.Pentraxin 3 (PTX3) and ficolin are the plasma phase of pattern recognition receptors (PRRs) and can activate complement through classical and lectin pathways, respectively, which may contribute to disease severity. This study aimed to investigate the association between PTX3 and ficolin with disease severity in patients with coronavirus disease-2019 (COVID-19). Seventy-three COVID-19 patients and 25 healthy controls were enrolled in this study. The participants were divided into three groups as follows: 14 patients as the intensive care unit (ICU) group, 59 patients as the non-ICU group, and 25 subjects as the healthy control group. The serum levels of PTX3 and ficolin were measured by enzyme-linked immunosorbent assay (ELISA) kits. Patients in ICU and non-ICU groups had significantly higher levels of PTX3 compared to the healthy control group (p = 0.0002 and p = 0.0072, respectively). Patients in the ICU group also had an increased amount of PTX3 (1957 ± 1769 pg/ml) compared to non-ICU patients (1220 ± 1784 pg/ml). However, this difference was not significant. On the other hand, serum levels of ficolin were not different among the three groups. PTX3, as an acute phase protein, may contribute to disease severity. Its probable inflammatory role could result from the high activation of the complement system. On the other hand, it could be suggested that ficolin has no crucial role in the disease severity of COVID-19 patients. Pentraxin 3 (PTX3) and ficolin are the plasma phase of pattern recognition receptors (PRRs) and can activate complement through classical and lectin pathways, respectively, which may contribute to disease severity. This study aimed to investigate the association between PTX3 and ficolin with disease severity in patients with coronavirus disease-2019 (COVID-19). Seventy-three COVID-19 patients and 25 healthy controls were enrolled in this study. The participants were divided into three groups as follows: 14 patients as the intensive care unit (ICU) group, 59 patients as the non-ICU group, and 25 subjects as the healthy control group. The serum levels of PTX3 and ficolin were measured by enzyme-linked immunosorbent assay (ELISA) kits. Patients in ICU and non-ICU groups had significantly higher levels of PTX3 compared to the healthy control group (p = 0.0002 and p = 0.0072, respectively). Patients in the ICU group also had an increased amount of PTX3 (1957 ± 1769 pg/ml) compared to non-ICU patients (1220 ± 1784 pg/ml). However, this difference was not significant. On the other hand, serum levels of ficolin were not different among the three groups. PTX3, as an acute phase protein, may contribute to disease severity. Its probable inflammatory role could result from the high activation of the complement system. On the other hand, it could be suggested that ficolin has no crucial role in the disease severity of COVID-19 patients. Pentraxin 3 (PTX3) and ficolin are the plasma phase of pattern recognition receptors (PRRs) and can activate complement through classical and lectin pathways, respectively, which may contribute to disease severity. This study aimed to investigate the association between PTX3 and ficolin with disease severity in patients with coronavirus disease-2019 (COVID-19). Seventy-three COVID-19 patients and 25 healthy controls were enrolled in this study. The participants were divided into three groups as follows: 14 patients as the intensive care unit (ICU) group, 59 patients as the non-ICU group, and 25 subjects as the healthy control group. The serum levels of PTX3 and ficolin were measured by enzyme-linked immunosorbent assay (ELISA) kits. Patients in ICU and non-ICU groups had significantly higher levels of PTX3 compared to the healthy control group ( p = 0.0002 and p = 0.0072, respectively). Patients in the ICU group also had an increased amount of PTX3 (1957 ± 1769 pg/ml) compared to non-ICU patients (1220 ± 1784 pg/ml). However, this difference was not significant. On the other hand, serum levels of ficolin were not different among the three groups. PTX3, as an acute phase protein, may contribute to disease severity. Its probable inflammatory role could result from the high activation of the complement system. On the other hand, it could be suggested that ficolin has no crucial role in the disease severity of COVID-19 patients. |
Author | Mohammadnia-Afrouzi, Mousa Rostami, Ali Bagherzadeh, Mojgan Mirzakhani, Mohammad Shahbazi, Mehdi Moulana, Zahra |
Author_xml | – sequence: 1 givenname: Zahra surname: Moulana fullname: Moulana, Zahra organization: Immunoregulation Research Center, Health Research Institute, Babol University of Medical Sciences, Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences – sequence: 2 givenname: Mojgan surname: Bagherzadeh fullname: Bagherzadeh, Mojgan organization: Immunoregulation Research Center, Health Research Institute, Babol University of Medical Sciences – sequence: 3 givenname: Mohammad surname: Mirzakhani fullname: Mirzakhani, Mohammad organization: Immunoregulation Research Center, Health Research Institute, Babol University of Medical Sciences – sequence: 4 givenname: Ali surname: Rostami fullname: Rostami, Ali organization: Immunoregulation Research Center, Health Research Institute, Babol University of Medical Sciences, Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences – sequence: 5 givenname: Mousa surname: Mohammadnia-Afrouzi fullname: Mohammadnia-Afrouzi, Mousa email: m.mohammadnia@mubabol.ac.ir organization: Immunoregulation Research Center, Health Research Institute, Babol University of Medical Sciences, Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences – sequence: 6 givenname: Mehdi surname: Shahbazi fullname: Shahbazi, Mehdi email: m.shahbazi@mubabol.ac.ir organization: Immunoregulation Research Center, Health Research Institute, Babol University of Medical Sciences |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34212320$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1186_s12985_024_02501_z crossref_primary_10_1177_22840265241287674 crossref_primary_10_3390_cancers14184438 crossref_primary_10_3390_ijms24043537 crossref_primary_10_2147_COPD_S402463 crossref_primary_10_23736_S1825_859X_22_00142_6 crossref_primary_10_1016_j_dci_2023_105064 crossref_primary_10_1016_j_imbio_2023_152393 crossref_primary_10_1007_s40121_022_00730_9 crossref_primary_10_3390_cells12101349 crossref_primary_10_1007_s00383_022_05289_7 |
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ContentType | Journal Article |
Copyright | The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021. |
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Keywords | COVID-19 Ficolin Coronavirus Pentraxin 3 Pattern recognition receptors |
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SubjectTerms | Acute phase proteins Aquatic Pollution Atmospheric Protection/Air Quality Control/Air Pollution blood serum C-Reactive Protein - analysis complement Complement activation Coronavirus - metabolism Coronaviruses COVID-19 COVID-19 - blood COVID-19 - genetics COVID-19 - metabolism COVID-19 infection disease severity Earth and Environmental Science Ecotoxicology Environment Environmental Chemistry Environmental Health Environmental science Enzyme-linked immunosorbent assay Ficolins Humans lectins Novel Corona Virus (COVID-19) in Environmental Engineering Novel Corona Virus (COVID-19) in Environmental Engineering Perspective Pattern recognition Pattern recognition receptors Pentraxins Serum Amyloid P-Component - analysis Serum Amyloid P-Component - metabolism Serum levels Viral diseases Waste Water Technology Water Management Water Pollution Control |
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Title | Increased Levels of serum Pentraxin 3 in Critical Coronavirus Disease-2019 Patients |
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