» Articles » PMID: 34987516

Presence of Anti-MDA5 Antibody and Its Value for the Clinical Assessment in Patients With COVID-19: A Retrospective Cohort Study

Overview
Journal Front Immunol
Date 2022 Jan 6
PMID 34987516
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Striking similarities have been found between coronavirus disease 2019 (COVID-19) and anti-melanoma differentiation-associated gene 5 (MDA5) antibody (Ab)-related dermatomyositis, implying a shared autoinflammatory aberrance. Herein, we aim to investigate whether the anti-MDA5 Ab is present in COVID-19 and correlates with the severity and adverse outcome of COVID-19 patients.

Methods And Findings: We retrospectively recruited 274 adult inpatients with COVID-19 in this study, including 48, 164, and 62 cases of deaths, severe, and non-severe patients respectively. The anti-MDA5 Ab was determined by ELISA and verified by Western Blotting, which indicated that the positive rate of anti-MDA5 Ab in COVID-19 patients was 48.2% (132/274). The clinical and laboratory features, as well as outcomes between patients with positive and negative anti-MDA5 Ab were compared and we found that the anti-MDA5 Ab positive patients tended to represent severe disease (88.6% 66.9%, <0.0001). We also demonstrated that the titer of anti-MDA5 Ab was significantly elevated in the non-survivals (5.95 ± 5.16 8.22 ± 6.64, =0.030) and the positive rate was also higher than that in the survivals (23.5% 12.0%, =0.012). Regarding severe COVID-19 patients, we found that high titer of anti-MDA5 Ab (≥10.0 U/mL) was more prevalent in the non-survivals (31.2% 14.0%, =0.006). Moreover, a dynamic analysis of anti-MDA5 Ab was conducted at different time-points of COVID-19, which revealed that early profiling of anti-MDA5 Ab could distinguish severe patients from those with non-severe ones.

Conclusions: Anti-MDA5 Ab was prevalent in the COVID-19 patients and high titer of this antibody is correlated with severe disease and unfavorable outcomes.

Citing Articles

Recognition of Idiopathic Inflammatory Myopathies Underlying Interstitial Lung Diseases.

Morina G, Sambataro D, Libra A, Palmucci S, Colaci M, La Rocca G Diagnostics (Basel). 2025; 15(3).

PMID: 39941205 PMC: 11817385. DOI: 10.3390/diagnostics15030275.


Outcome of COVID-19 in patients with idiopathic inflammatory myopathy during the Omicron wave in China: A longitudinal observational study.

Li Y, Tian X, Sun C, Wei Y, Jiang W, He L PLoS One. 2025; 20(2):e0317319.

PMID: 39928605 PMC: 11809795. DOI: 10.1371/journal.pone.0317319.


Autoantibodies as potential prognostic factors for clinical outcomes related to COVID-19: a systematic review of inception prospective cohort studies with GRADE recommendations.

Araujo F, Amaral A, Silva H, Santos J, Mendonca V, Oliveira V Braz J Med Biol Res. 2025; 58:e13965.

PMID: 39907423 PMC: 11793148. DOI: 10.1590/1414-431X2024e13965.


Monocyte-macrophage dynamics as key in disparate lung and peripheral immune responses in severe anti-melanoma differentiation-associated gene 5-positive dermatomyositis-related interstitial lung disease.

Shi J, Pei X, Peng J, Wu C, Lv Y, Wang X Clin Transl Med. 2025; 15(2):e70226.

PMID: 39902678 PMC: 11791760. DOI: 10.1002/ctm2.70226.


MDA5 Is a Major Determinant of Developing Symptoms in Critically Ill COVID-19 Patients.

Maiti A Clin Rev Allergy Immunol. 2024; 67(1-3):58-72.

PMID: 39460899 DOI: 10.1007/s12016-024-09008-z.


References
1.
Kawasumi H, Gono T, Kawaguchi Y, Kaneko H, Katsumata Y, Hanaoka M . IL-6, IL-8, and IL-10 are associated with hyperferritinemia in rapidly progressive interstitial lung disease with polymyositis/dermatomyositis. Biomed Res Int. 2014; 2014:815245. PMC: 3988788. DOI: 10.1155/2014/815245. View

2.
Zhou F, Yu T, Du R, Fan G, Liu Y, Liu Z . Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet. 2020; 395(10229):1054-1062. PMC: 7270627. DOI: 10.1016/S0140-6736(20)30566-3. View

3.
Ruan Q, Yang K, Wang W, Jiang L, Song J . Clinical predictors of mortality due to COVID-19 based on an analysis of data of 150 patients from Wuhan, China. Intensive Care Med. 2020; 46(5):846-848. PMC: 7080116. DOI: 10.1007/s00134-020-05991-x. View

4.
Ledford H . Coronavirus breakthrough: dexamethasone is first drug shown to save lives. Nature. 2020; 582(7813):469. DOI: 10.1038/d41586-020-01824-5. View

5.
Park A, Iwasaki A . Type I and Type III Interferons - Induction, Signaling, Evasion, and Application to Combat COVID-19. Cell Host Microbe. 2020; 27(6):870-878. PMC: 7255347. DOI: 10.1016/j.chom.2020.05.008. View