Association of polymorphisms in long pentraxin 3 and its plasma levels with COVID-19 severity

被引:12
作者
Feitosa, Thiala Alves [1 ]
de Souza Sa, Mirela Vanessa [2 ]
Pereira, Vanessa Cardoso [3 ]
de Andrade Cavalcante, Marton Kaique [4 ,5 ]
Alves Pereira, Valeria Rego [4 ]
Armstrong, Anderson da Costa [6 ]
do Carmo, Rodrigo Feliciano [1 ,2 ]
机构
[1] Univ Fed Vale Sao Francisco, Postgrad Program Biosci, Av Jose de Sa Manicoba S-N, Petrolina, PE, Brazil
[2] Univ Fed Vale Sao Francisco, Coll Pharmaceut Sci, Petrolina, PE, Brazil
[3] Petrolina City Hall, Petrolina, PE, Brazil
[4] Fundacao Oswaldo Cruz, Dept Immunol, Recife, PE, Brazil
[5] Univ Fed Pernambuco, Ctr Biosci, Postgrad Program Therapeut Innovat, Recife, PE, Brazil
[6] Univ Fed Vale Sao Francisco, Dept Med, Petrolina, PE, Brazil
关键词
Coronavirus; COVID-19; Immunity; SARS-CoV-2; PTX3; SNP; PTX3; ASPERGILLOSIS; RECOGNITION; RISK;
D O I
10.1007/s10238-022-00926-w
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
COVID-19 is an infectious respiratory disease caused by SARS-CoV-2. Pentraxin 3 (PTX3) is involved in the activation and regulation of the complement system, demonstrating an important role in the pathogenesis of COVID-19. The aim was to evaluate the association of single nucleotide polymorphisms in PTX3 and its plasma levels with the severity of COVID-19. This is a retrospective cohort study, carried out between August 2020 and July 2021, including patients with confirmed COVID-19 hospitalized in 2 hospitals in the Northeast Region of Brazil. Polymorphisms in PTX3 (rs1840680 and rs2305619) were determined by real-time PCR. PTX3 plasma levels were measured by ELISA. Serum levels of interleukin (IL)-6, IL-8, and IL-10 were determined by flow cytometry. A multivariate logistic regression model was used to identify parameters independently associated with COVID-19 severity. P values < 0.05 were considered significant. The study included 496 patients, classified as moderate (n = 267) and severe (n = 229) cases. The PTX3 AA genotype (rs1840680) was independently associated with protection against severe COVID-19 (P = 0.037; odds ratio = 0.555). PTX3 plasma levels were significantly associated with COVID-19 severity and mortality (P < 0.05). PTX3 levels were significantly correlated with IL-6, IL-8, IL-10, C-reactive protein, total leukocytes, neutrophil-to-lymphocyte ratio, urea, creatinine, ferritin, length of hospital stay, and higher respiratory rate (P < 0.05). Our results revealed a protective effect of the PTX3 AA genotype (rs1840680) on the development of severe forms of COVID-19. Additionally, PTX3 plasma levels were associated with the severity of COVID-19. The results of this study provide evidence of an important role of PTX3 in the immunopathology of COVID-19.
引用
收藏
页码:1225 / 1233
页数:9
相关论文
共 39 条
[1]   Influence of Pentraxin 3 (PTX3) Genetic Variants on Myocardial Infarction Risk and PTX3 Plasma Levels [J].
Barbati, Elisa ;
Specchia, Claudia ;
Villella, Massimo ;
Rossi, Marco Luciano ;
Barlera, Simona ;
Bottazzi, Barbara ;
Crociati, Luisa ;
d'Arienzo, Carmela ;
Fanelli, Raffaele ;
Garlanda, Cecilia ;
Gori, Francesca ;
Mango, Ruggiero ;
Mantovani, Alberto ;
Merla, Giuseppe ;
Nicolis, Enrico B. ;
Pietri, Silvia ;
Presbitero, Patrizia ;
Sudo, Yukio ;
Villella, Alessandro ;
Franzosi, Maria Grazia .
PLOS ONE, 2012, 7 (12)
[2]   Pentraxin 3 protects from MCMV infection and reactivation through TLR sensing pathways leading to IRF3 activation [J].
Bozza, Silvia ;
Bistoni, Francesco ;
Gaziano, Roberta ;
Pitzurra, Lucia ;
Zelante, Teresa ;
Bonifazi, Pierluigi ;
Perruccio, Katia ;
Bellocchio, Silvia ;
Neri, Mariella ;
Iorio, Anna Maria ;
Salvatori, Giovanni ;
De Santis, Rita ;
Calvitti, Mario ;
Doni, Andrea ;
Garlanda, Cecilia ;
Mantovani, Alberto ;
Romani, Luigina .
BLOOD, 2006, 108 (10) :3387-3396
[3]   Macrophage expression and prognostic significance of the long pentraxin PTX3 in COVID-19 [J].
Brunetta, Enrico ;
Folci, Marco ;
Bottazzi, Barbara ;
De Santis, Maria ;
Gritti, Giuseppe ;
Protti, Alessandro ;
Mapelli, Sarah N. ;
Bonovas, Stefanos ;
Piovani, Daniele ;
Leone, Roberto ;
My, Ilaria ;
Zanon, Veronica ;
Spata, Gianmarco ;
Bacci, Monica ;
Supino, Domenico ;
Carnevale, Silvia ;
Sironi, Marina ;
Davoudian, Sadaf ;
Peano, Clelia ;
Landi, Francesco ;
Di Marco, Fabiano ;
Raimondi, Federico ;
Gianatti, Andrea ;
Angelini, Claudio ;
Rambaldi, Alessandro ;
Garlanda, Cecilia ;
Ciccarelli, Michele ;
Cecconi, Maurizio ;
Mantovani, Alberto .
NATURE IMMUNOLOGY, 2021, 22 (01) :19-24
[4]   Lessons learned: new insights on the role of cytokines in COVID-19 [J].
Buszko, Maja ;
Nita-Lazar, Aleksandra ;
Park, Jung-Hyun ;
Schwartzberg, Pamela L. ;
Verthelyi, Daniela ;
Young, Howard A. ;
Rosenberg, Amy S. .
NATURE IMMUNOLOGY, 2021, 22 (04) :404-411
[5]   Genetic variation in PTX3 and plasma levels associated with hepatocellular carcinoma in patients with HCV [J].
Carmo, R. F. ;
Aroucha, D. ;
Vasconcelos, L. R. S. ;
Pereira, L. M. M. B. ;
Moura, P. ;
Cavalcanti, M. S. M. .
JOURNAL OF VIRAL HEPATITIS, 2016, 23 (02) :116-122
[6]   Ten things we learned about COVID-19 [J].
Cecconi, Maurizio ;
Forni, Guido ;
Mantovani, Alberto .
INTENSIVE CARE MEDICINE, 2020, 46 (08) :1590-1593
[7]   COVID-19: A collision of complement, coagulation and inflammatory pathways [J].
Chauhan, Anoop J. ;
Wiffen, Laura J. ;
Brown, Thomas P. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2020, 18 (09) :2110-2117
[8]   PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients [J].
Chiarini, M. ;
Sabelli, C. ;
Melotti, P. ;
Garlanda, C. ;
Savoldi, G. ;
Mazza, C. ;
Padoan, R. ;
Plebani, A. ;
Mantovani, A. ;
Notarangelo, L. D. ;
Assael, B. M. ;
Badolato, R. .
GENES AND IMMUNITY, 2010, 11 (08) :665-670
[9]   Genetic PTX3 Deficiency and Aspergillosis in Stem-Cell Transplantation [J].
Cunha, Cristina ;
Aversa, Franco ;
Lacerda, Joao F. ;
Busca, Alessandro ;
Kurzai, Oliver ;
Grube, Matthias ;
Loeffler, Juergen ;
Maertens, Johan A. ;
Bell, Alain S. ;
Inforzato, Antonio ;
Barbati, Elisa ;
Almeida, Bruno ;
Santos e Sousa, Pedro ;
Barbui, Anna ;
Potenza, Leonardo ;
Caira, Morena ;
Rodrigues, Fernando ;
Salvatori, Giovanni ;
Pagano, Livio ;
Luppi, Mario ;
Mantovani, Alberto ;
Velardi, Andrea ;
Romani, Luigina ;
Carvalho, Agostinho .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 370 (05) :421-432
[10]  
Del Valle DM, 2020, NAT MED, V26, P1636, DOI [10.1038/s41591-020-1051-9, 10.1101/2020.05.28.20115758]