Protective role of anti-SARS-CoV-2 antibody responses against vital organ related long COVID symptoms.

Publication date: Jul 03, 2025

COVID-19 pandemic continues to challenge the world with a major public health problem, long COVID (LC), which is estimated to affect over 400 million people worldwide. Many unknowns remain regarding the mechanisms involved in LC. We investigated the impact of anti-SARS-CoV-2 antibody and IFN-γ responses on the development of LC and its various phenotypes. We studied a cohort of 137 convalescents following predominantly mild COVID-19 during the first pandemic wave (2020) and up to one-year post-infection. We found 45% of LC cases that were associated with a greater number and duration of acute-phase symptoms. Cardiovascular and/or gastrointestinal symptoms in the acute phase were associated to protection against LC development, while pulmonary, otorhinolaryngological, musculoskeletal and other symptoms were associated with increased risk of LC development. Regarding LC phenotypes, we observed risk associations and potentially deleterious effects of anti-SARS-CoV-2 antibodies for LC symptoms classified as general or other. In contrast, for vital organ-related LC symptoms, we found only protective associations, particularly for cardiovascular symptoms, which indeed had a low prevalence in LC (16%). Collectively, our data suggest that anti-SARS-CoV-2 antibodies play a protective role against vital organ-related LC symptoms, especially cardiovascular symptoms, but are insufficient in preventing or limiting other highly prevalent LC symptoms, such as neurological, psychiatric and pulmonary.

Open Access PDF

Concepts Keywords
Antibodies Adult
Organ Aged
Otorhinolaryngological Antibodies, Viral
Pandemic Antibodies, Viral
Cardiovascular protection
COVID-19
Female
Humans
Humoral responses
IgA anti-NP protection
Long COVID phenotypes
Male
Middle Aged
Post-Acute COVID-19 Syndrome
SARS-CoV-2

Semantics

Type Source Name
disease IDO role
disease MESH long COVID
disease MESH COVID-19 pandemic
disease MESH infection
drug DRUGBANK Coenzyme M
disease IDO symptom
disease MESH viral infections
disease MESH immune tolerance
disease MESH autoimmunity
disease MESH myalgic encephalomyelitis
disease IDO pathogen
disease MESH inflammation
disease MESH convalescence
disease IDO blood
disease IDO assay
drug DRUGBANK Aspartame
disease MESH Depression
disease MESH Derealization
disease MESH Dry eyes
disease MESH tachycardia
disease IDO production
disease IDO process
pathway REACTOME Immune System
disease IDO protein

Original Article

(Visited 2 times, 1 visits today)

Leave a Comment

Your email address will not be published. Required fields are marked *