Autoimmunity is a hallmark of post-COVID syndrome

Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against sel...

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Published inJournal of translational medicine Vol. 20; no. 1; pp. 129 - 5
Main Authors Rojas, Manuel, Rodríguez, Yhojan, Acosta-Ampudia, Yeny, Monsalve, Diana M., Zhu, Chengsong, Li, Quan-Zhen, Ramírez-Santana, Carolina, Anaya, Juan-Manuel
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Published England BioMed Central Ltd 16.03.2022
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Abstract Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against self-antigens and infectious agents were evaluated by an antigen array chip for 116 IgG and 104 IgM antibodies. Thirty pre-pandemic healthy individuals were included as a control group. The median age of patients was 49 years (IQR: 37.8 to 55.3). There were 47 males. The median post-COVID time was 219 (IQR: 143 to 258) days. Latent autoimmunity and polyautoimmunity were found in 83% and 62% of patients, respectively. Three patients developed an overt autoimmune disease. IgG antibodies against IL-2, CD8B, and thyroglobulin were found in more than 10% of the patients. Other IgG autoantibodies, such as anti-interferons, were positive in 5–10% of patients. Anti-SARS-CoV-2 IgG antibodies were found in > 85% of patients and were positively correlated with autoantibodies, age, and body mass index (BMI). Few autoantibodies were influenced by age and BMI. There was no effect of gender on the over- or under-expression of autoantibodies. IgG anti-IFN-λ antibodies were associated with the persistence of respiratory symptoms. In summary, autoimmunity is characteristic of PCS, and latent autoimmunity correlates with humoral response to SARS-CoV-2.
AbstractList Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against self-antigens and infectious agents were evaluated by an antigen array chip for 116 IgG and 104 IgM antibodies. Thirty pre-pandemic healthy individuals were included as a control group. The median age of patients was 49 years (IQR: 37.8 to 55.3). There were 47 males. The median post-COVID time was 219 (IQR: 143 to 258) days. Latent autoimmunity and polyautoimmunity were found in 83% and 62% of patients, respectively. Three patients developed an overt autoimmune disease. IgG antibodies against IL-2, CD8B, and thyroglobulin were found in more than 10% of the patients. Other IgG autoantibodies, such as anti-interferons, were positive in 5-10% of patients. Anti-SARS-CoV-2 IgG antibodies were found in > 85% of patients and were positively correlated with autoantibodies, age, and body mass index (BMI). Few autoantibodies were influenced by age and BMI. There was no effect of gender on the over- or under-expression of autoantibodies. IgG anti-IFN-λ antibodies were associated with the persistence of respiratory symptoms. In summary, autoimmunity is characteristic of PCS, and latent autoimmunity correlates with humoral response to SARS-CoV-2.
Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against self-antigens and infectious agents were evaluated by an antigen array chip for 116 IgG and 104 IgM antibodies. Thirty pre-pandemic healthy individuals were included as a control group. The median age of patients was 49 years (IQR: 37.8 to 55.3). There were 47 males. The median post-COVID time was 219 (IQR: 143 to 258) days. Latent autoimmunity and polyautoimmunity were found in 83% and 62% of patients, respectively. Three patients developed an overt autoimmune disease. IgG antibodies against IL-2, CD8B, and thyroglobulin were found in more than 10% of the patients. Other IgG autoantibodies, such as anti-interferons, were positive in 5-10% of patients. Anti-SARS-CoV-2 IgG antibodies were found in > 85% of patients and were positively correlated with autoantibodies, age, and body mass index (BMI). Few autoantibodies were influenced by age and BMI. There was no effect of gender on the over- or under-expression of autoantibodies. IgG anti-IFN-[lambda] antibodies were associated with the persistence of respiratory symptoms. In summary, autoimmunity is characteristic of PCS, and latent autoimmunity correlates with humoral response to SARS-CoV-2. Keywords: Post-COVID syndrome, Post-COVID, Long COVID, Post-acute COVID-19, COVID-19, Autoimmunity, Autoantibodies, Latent autoimmunity, Antigen array
Abstract Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against self-antigens and infectious agents were evaluated by an antigen array chip for 116 IgG and 104 IgM antibodies. Thirty pre-pandemic healthy individuals were included as a control group. The median age of patients was 49 years (IQR: 37.8 to 55.3). There were 47 males. The median post-COVID time was 219 (IQR: 143 to 258) days. Latent autoimmunity and polyautoimmunity were found in 83% and 62% of patients, respectively. Three patients developed an overt autoimmune disease. IgG antibodies against IL-2, CD8B, and thyroglobulin were found in more than 10% of the patients. Other IgG autoantibodies, such as anti-interferons, were positive in 5–10% of patients. Anti-SARS-CoV-2 IgG antibodies were found in > 85% of patients and were positively correlated with autoantibodies, age, and body mass index (BMI). Few autoantibodies were influenced by age and BMI. There was no effect of gender on the over- or under-expression of autoantibodies. IgG anti-IFN-λ antibodies were associated with the persistence of respiratory symptoms. In summary, autoimmunity is characteristic of PCS, and latent autoimmunity correlates with humoral response to SARS-CoV-2.
Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against self-antigens and infectious agents were evaluated by an antigen array chip for 116 IgG and 104 IgM antibodies. Thirty pre-pandemic healthy individuals were included as a control group. The median age of patients was 49 years (IQR: 37.8 to 55.3). There were 47 males. The median post-COVID time was 219 (IQR: 143 to 258) days. Latent autoimmunity and polyautoimmunity were found in 83% and 62% of patients, respectively. Three patients developed an overt autoimmune disease. IgG antibodies against IL-2, CD8B, and thyroglobulin were found in more than 10% of the patients. Other IgG autoantibodies, such as anti-interferons, were positive in 5-10% of patients. Anti-SARS-CoV-2 IgG antibodies were found in > 85% of patients and were positively correlated with autoantibodies, age, and body mass index (BMI). Few autoantibodies were influenced by age and BMI. There was no effect of gender on the over- or under-expression of autoantibodies. IgG anti-IFN-λ antibodies were associated with the persistence of respiratory symptoms. In summary, autoimmunity is characteristic of PCS, and latent autoimmunity correlates with humoral response to SARS-CoV-2.Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against self-antigens and infectious agents were evaluated by an antigen array chip for 116 IgG and 104 IgM antibodies. Thirty pre-pandemic healthy individuals were included as a control group. The median age of patients was 49 years (IQR: 37.8 to 55.3). There were 47 males. The median post-COVID time was 219 (IQR: 143 to 258) days. Latent autoimmunity and polyautoimmunity were found in 83% and 62% of patients, respectively. Three patients developed an overt autoimmune disease. IgG antibodies against IL-2, CD8B, and thyroglobulin were found in more than 10% of the patients. Other IgG autoantibodies, such as anti-interferons, were positive in 5-10% of patients. Anti-SARS-CoV-2 IgG antibodies were found in > 85% of patients and were positively correlated with autoantibodies, age, and body mass index (BMI). Few autoantibodies were influenced by age and BMI. There was no effect of gender on the over- or under-expression of autoantibodies. IgG anti-IFN-λ antibodies were associated with the persistence of respiratory symptoms. In summary, autoimmunity is characteristic of PCS, and latent autoimmunity correlates with humoral response to SARS-CoV-2.
Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship between SARS-CoV-2 and autoimmunity in PCS, a clinical and serological assessment on 100 patients was done. Serum antibody profiles against self-antigens and infectious agents were evaluated by an antigen array chip for 116 IgG and 104 IgM antibodies. Thirty pre-pandemic healthy individuals were included as a control group. The median age of patients was 49 years (IQR: 37.8 to 55.3). There were 47 males. The median post-COVID time was 219 (IQR: 143 to 258) days. Latent autoimmunity and polyautoimmunity were found in 83% and 62% of patients, respectively. Three patients developed an overt autoimmune disease. IgG antibodies against IL-2, CD8B, and thyroglobulin were found in more than 10% of the patients. Other IgG autoantibodies, such as anti-interferons, were positive in 5-10% of patients. Anti-SARS-CoV-2 IgG antibodies were found in > 85% of patients and were positively correlated with autoantibodies, age, and body mass index (BMI). Few autoantibodies were influenced by age and BMI. There was no effect of gender on the over- or under-expression of autoantibodies. IgG anti-IFN-[lambda] antibodies were associated with the persistence of respiratory symptoms. In summary, autoimmunity is characteristic of PCS, and latent autoimmunity correlates with humoral response to SARS-CoV-2.
ArticleNumber 129
Audience Academic
Author Ramírez-Santana, Carolina
Acosta-Ampudia, Yeny
Zhu, Chengsong
Li, Quan-Zhen
Rojas, Manuel
Monsalve, Diana M.
Rodríguez, Yhojan
Anaya, Juan-Manuel
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  surname: Acosta-Ampudia
  fullname: Acosta-Ampudia, Yeny
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  fullname: Monsalve, Diana M.
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  givenname: Chengsong
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  fullname: Zhu, Chengsong
– sequence: 6
  givenname: Quan-Zhen
  surname: Li
  fullname: Li, Quan-Zhen
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  surname: Anaya
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Cites_doi 10.1016/j.jtauto.2021.100091
10.1093/infdis/jiac017
10.1016/j.jtauto.2022.100140
10.1126/sciimmunol.abl4340
10.1186/s12967-021-03184-8
10.1016/j.jaut.2017.07.003
10.1016/j.autrev.2011.10.004
10.1186/s12967-020-02464-z
10.1016/j.autrev.2021.102947
10.1186/s12967-020-02524-4
10.1038/s41467-021-25509-3
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Issue 1
Keywords Autoimmunity
COVID-19
Post-COVID
Autoantibodies
Post-COVID syndrome
Latent autoimmunity
Antigen array
Long COVID
Post-acute COVID-19
Language English
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References J-M Anaya (3328_CR3) 2021; 4
W-T Ma (3328_CR8) 2017; 83
GJ Tobón (3328_CR9) 2012; 11
Y Acosta-Ampudia (3328_CR1) 2022; 1
Y Liu (3328_CR5) 2021; 19
3328_CR7
P Bastard (3328_CR4) 2021; 6
L Camacho-Domínguez (3328_CR10) 2022; 1
A De Lorenzo (3328_CR11) 2020; 18
D Maguire (3328_CR12) 2020; 18
SE Chang (3328_CR2) 2021; 12
J-M Anaya (3328_CR6) 2021; 20
34965855 - J Transl Med. 2021 Dec 30;19(1):524
References_xml – volume: 4
  start-page: 100091
  year: 2021
  ident: 3328_CR3
  publication-title: J Transl Autoimmun.
  doi: 10.1016/j.jtauto.2021.100091
– ident: 3328_CR7
– volume: 1
  start-page: jiac017
  year: 2022
  ident: 3328_CR1
  publication-title: J Infect Dis.
  doi: 10.1093/infdis/jiac017
– volume: 1
  start-page: 10014.0
  year: 2022
  ident: 3328_CR10
  publication-title: J Transl Autoimmun.
  doi: 10.1016/j.jtauto.2022.100140
– volume: 6
  start-page: 1
  year: 2021
  ident: 3328_CR4
  publication-title: Sci Immunol.
  doi: 10.1126/sciimmunol.abl4340
– volume: 19
  start-page: 524
  year: 2021
  ident: 3328_CR5
  publication-title: J Transl Med
  doi: 10.1186/s12967-021-03184-8
– volume: 83
  start-page: 95
  year: 2017
  ident: 3328_CR8
  publication-title: J Autoimmun
  doi: 10.1016/j.jaut.2017.07.003
– volume: 11
  start-page: 259
  year: 2012
  ident: 3328_CR9
  publication-title: Autoimmun Rev.
  doi: 10.1016/j.autrev.2011.10.004
– volume: 18
  start-page: 299
  year: 2020
  ident: 3328_CR11
  publication-title: J Transl Med
  doi: 10.1186/s12967-020-02464-z
– volume: 20
  start-page: 102947
  year: 2021
  ident: 3328_CR6
  publication-title: Autoimmun Rev.
  doi: 10.1016/j.autrev.2021.102947
– volume: 18
  start-page: 354
  year: 2020
  ident: 3328_CR12
  publication-title: J Transl Med
  doi: 10.1186/s12967-020-02524-4
– volume: 12
  start-page: 5417
  year: 2021
  ident: 3328_CR2
  publication-title: Nat Commun
  doi: 10.1038/s41467-021-25509-3
– reference: 34965855 - J Transl Med. 2021 Dec 30;19(1):524
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Snippet Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the relationship...
Abstract Autoimmunity has emerged as a characteristic of the post-COVID syndrome (PCS), which may be related to sex. In order to further investigate the...
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StartPage 129
SubjectTerms Adult
Antibodies, Viral - blood
Autoimmunity
COVID-19
Demographic aspects
Health aspects
Humans
Immunoglobulin M - blood
Long COVID
Male
Middle Aged
Post-acute COVID-19
Post-COVID
Post-COVID syndrome
SARS-CoV-2
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Title Autoimmunity is a hallmark of post-COVID syndrome
URI https://www.ncbi.nlm.nih.gov/pubmed/35296346
https://www.proquest.com/docview/2640328769
https://pubmed.ncbi.nlm.nih.gov/PMC8924736
https://doaj.org/article/0899b56d3134457697930c51497c598a
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