A deficient immune response to SARS-CoV-2 in the nasopharynx is associated with severe COVID-19 pneumonia

被引:3
|
作者
Pita-Martinez, Carlos [1 ]
Perez-Garcia, Felipe [1 ,2 ,3 ,4 ]
Berdices, Ana Virseda [1 ,2 ]
Martin-Vicente, Maria [1 ]
Castilla-Garcia, Lucia [5 ]
Fernandez, Irene Hervas [3 ]
Ventosa, Victoria Gonzalez [3 ]
Munoz-Gomez, Maria Jose [1 ,2 ]
Cuadros-Gonzalez, Juan [3 ,4 ]
Bermejo-Martin, Jesus F. [6 ,7 ]
Resino, Salvador [1 ,2 ]
Martinez, Isidoro [1 ,2 ]
机构
[1] Inst Salud Carlos III, Ctr Nacl Microbiol, Unidad Infecc Viral & Inmunidad, Majadahonda, Spain
[2] Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Infecciosas CIB, Madrid, Spain
[3] Hosp Univ Principe Asturias, Serv Microbiol Clin, Madrid, Spain
[4] Univ Alcala, Fac Med, Dept Biomed & Biotecnol, Madrid, Spain
[5] Hosp Univ Principe Asturias, Serv Hematol & Hemoterapia, Madrid, Spain
[6] Inst Invest Biomed Salamanca, Grp Biomed Res Sepsis BioSepsis, IBSAL, Salamanca, Spain
[7] Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Resp CIBERES, Madrid, Spain
基金
加拿大健康研究院;
关键词
SARS-CoV-2; COVID-19; Pneumonia; Gene expression; Mucosal nasopharynx; Immune response;
D O I
10.1016/j.ijid.2023.06.001
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: We analyzed the expression of inflammatory and antiviral genes in the nasopharynx of SARSCoV-2 infected patients and their association with the severity of COVID-19 pneumonia. Methods: We conducted a cross-sectional study on 223 SARS-CoV-2 infected patients. Clinical data were collected from medical records, and nasopharyngeal samples were collected in the first 24 hours after admission to the emergency room. The gene expression of eight proinflammatory/antiviral genes (plasminogen activator urokinase receptor [ PLAUR ], interleukin [ IL ] -6, IL-8 , interferon [ IFN ] - & beta;, IFN-stimulated gene 15 [ ISG15 ], retinoic acid-inducible gene I [ RIG-I ], C-C motif ligand 5 [ CCL5 ], and chemokine C-XC motif ligand 10 [ CXCL10 ]) were quantified by real-time polymerase chain reaction. Outcome variables were: (i) pneumonia; (ii) severe pneumonia or acute respiratory distress syndrome. Statistical analysis was performed using multivariate logistic regression analyses. Results: We enrolled 84 mild, 88 moderate, and 51 severe/critical cases. High expression of PLAUR (adjusted odds ratio [aOR] = 1.25; P = 0.032, risk factor) and low expression of CXCL10 (aOR = 0.89; P = 0.048, protective factor) were associated with pneumonia. Furthermore, lower values of ISG15 (aOR = 0.88, P = 0.021), RIG-I (aOR = 0.87, P = 0.034), CCL5 (aOR = 0.73, P < 0.001), and CXCL10 (aOR = 0.84, P = 0.002) were risk factors for severe pneumonia/acute respiratory distress syndrome. Conclusion: An unbalanced early innate immune response to SARS-CoV-2 in the nasopharynx, characterized by high expression of PLAUR and low expression of antiviral genes ( ISG15 and RIG-I ), and chemokines ( CCL5 and CXCL10 ), was associated with COVID-19 severity. & COPY; 2023 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页码:126 / 132
页数:7
相关论文
共 50 条
  • [41] SARS-CoV-2 in severe COVID-19 induces a TGF-β-dominated chronic immune response that does not target itself
    Marta Ferreira-Gomes
    Andrey Kruglov
    Pawel Durek
    Frederik Heinrich
    Caroline Tizian
    Gitta Anne Heinz
    Anna Pascual-Reguant
    Weijie Du
    Ronja Mothes
    Chaofan Fan
    Stefan Frischbutter
    Katharina Habenicht
    Lisa Budzinski
    Justus Ninnemann
    Peter K. Jani
    Gabriela Maria Guerra
    Katrin Lehmann
    Mareen Matz
    Lennard Ostendorf
    Lukas Heiberger
    Hyun-Dong Chang
    Sandy Bauherr
    Marcus Maurer
    Günther Schönrich
    Martin Raftery
    Tilmann Kallinich
    Marcus Alexander Mall
    Stefan Angermair
    Sascha Treskatsch
    Thomas Dörner
    Victor Max Corman
    Andreas Diefenbach
    Hans-Dieter Volk
    Sefer Elezkurtaj
    Thomas H. Winkler
    Jun Dong
    Anja Erika Hauser
    Helena Radbruch
    Mario Witkowski
    Fritz Melchers
    Andreas Radbruch
    Mir-Farzin Mashreghi
    Nature Communications, 12
  • [42] Changes in the immune response against SARS-CoV-2 in individuals with severe COVID-19 treated with high dose of vitamin D
    Torres, Montserrat
    Casado, Guiomar
    Vigon, Lorena
    Rodriguez-Mora, Sara
    Mateos, Elena
    Ramos-Martin, Fernando
    Lopez-Wolf, Daniel
    Sanz-Moreno, Jose
    Ryan-Murua, Pablo
    Luisa Taboada-Martinez, Maria
    Rosa Lopez-Huertas, Maria
    Cervero, Miguel
    Coiras, Mayte
    BIOMEDICINE & PHARMACOTHERAPY, 2022, 150
  • [43] Is SARS-CoV-2 associated with liver dysfunction in COVID-19 patients?
    Ali, Nurshad
    CLINICS AND RESEARCH IN HEPATOLOGY AND GASTROENTEROLOGY, 2020, 44 (04) : E84 - E86
  • [44] SARS-CoV-2 Role of viral load in severe forms of Covid-19
    Derrien, Elisa
    ACTUALITES PHARMACEUTIQUES, 2021, 60 (604): : 5 - 5
  • [45] Activated Platelets Harbor SARS-CoV-2 during Severe COVID-19
    Agbani, Ejaife O.
    Schneider, Prism
    McDonald, Braedon
    Skeith, Leslie
    Poon, Man-Chiu
    Lee, Adrienne
    THROMBOSIS AND HAEMOSTASIS, 2022, 122 (02) : 308 - 309
  • [46] Inflammasomes are activated in response to SARS-CoV-2 infection and are associated with COVID-19 severity in patients
    Rodrigues, Tamara S.
    de Sa, Keyla S. G.
    Ishimoto, Adriene Y.
    Becerra, Amanda
    Oliveira, Samuel
    Almeida, Leticia
    Goncalves, Augusto, V
    Perucello, Debora B.
    Andrade, Warrison A.
    Castro, Ricardo
    Veras, Flavio P.
    Toller-Kawahisa, Juliana E.
    Nascimento, Daniele C.
    de Lima, Mikhael H. F.
    Silva, Camila M. S.
    Caetite, Diego B.
    Martins, Ronaldo B.
    Castro, Italo A.
    Pontelli, Marjorie C.
    de Barros, Fabio C.
    do Amaral, Natalia B.
    Giannini, Marcela C.
    Bonjorno, Leticia P.
    Lopes, Maria Isabel F.
    Santana, Rodrigo C.
    Vilar, Fernando C.
    Auxiliadora-Martins, Maria
    Luppino-Assad, Rodrigo
    de Almeida, Sergio C. L.
    de Oliveira, Fabiola R.
    Batah, Sabrina S.
    Li Siyuan
    Benatti, Maira N.
    Cunha, Thiago M.
    Alves-Filho, Jose C.
    Cunha, Fernando Q.
    Cunha, Larissa D.
    Frantz, Fabiani G.
    Kohlsdorf, Tiana
    Fabro, Alexandre T.
    Arruda, Eurico
    de Oliveira, Rene D. R.
    Louzada-Junior, Paulo
    Zamboni, Dario S.
    JOURNAL OF EXPERIMENTAL MEDICINE, 2021, 218 (03):
  • [47] Evaluation of SARS-CoV-2 in Tears of Patients with Moderate to Severe COVID-19
    Arora, Ritu
    Goel, Ruchi
    Kumar, Sumit
    Chhabra, Mohit
    Saxena, Sonal
    Manchanda, Vikas
    Pumma, Palak
    OPHTHALMOLOGY, 2021, 128 (04) : 494 - 503
  • [48] SARS-CoV-2 in Urine May Predict a Severe Evolution of COVID-19
    Perrella, Alessandro
    Brita, Mario
    Coletta, Francesco
    Cotena, Simona
    De Marco, GiamPaola
    Longobardi, Adele
    Sala, Crescenzo
    Sannino, Dania
    Tomasello, Antonio
    Perrella, Marco
    Russo, Giuseppe
    Tarsitano, Marina
    Chetta, Massimo
    Della Monica, Matteo
    Orlando, Valentina
    Coscioni, Enrico
    Villani, Romolo
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (18)
  • [49] Impaired Cellular Immunity to SARS-CoV-2 in Severe COVID-19 Patients
    Ni, Ling
    Cheng, Meng-Li
    Feng, Yu
    Zhao, Hui
    Liu, Jingyuan
    Ye, Fang
    Ye, Qing
    Zhu, Gengzhen
    Li, Xiaoli
    Wang, Pengzhi
    Shao, Jing
    Deng, Yong-Qiang
    Wei, Peng
    Chen, Fang
    Qin, Cheng-Feng
    Wang, Guoqing
    Li, Fan
    Zeng, Hui
    Dong, Chen
    FRONTIERS IN IMMUNOLOGY, 2021, 12
  • [50] Autoimmunity and Immunodeficiency in Severe SARS-CoV-2 Infection and Prolonged COVID-19
    Garmendia, Jenny Valentina
    Garcia, Alexis Hipolito
    De Sanctis, Claudia Valentina
    Hajduch, Marian
    De Sanctis, Juan Bautista
    CURRENT ISSUES IN MOLECULAR BIOLOGY, 2023, 45 (01) : 33 - 50