Yukari Magawa Jhosiene, Jacintho Lucas Cauê, Alves Ferreira Marcelo, Ramos Oliveira Jamille, Rahal Guaragna Machado Rafael, Kuramoto Takara Andreia, Moreno Lima de Oliveira Renata, Cesario Lima Ariane, Sasahara Greyce Luri, Lopes Adami Flávia, Xavier Medeiros Giuliana, de Souza Apostolico Juliana, Ruz Fernandes Edgar, Bruna Leal de Oliveira Danielle, Durigon Edison Luiz, Giavina Bianchi Pedro, Boscardin Silvia Beatriz, Santoro Rosa Daniela, Cunha-Neto Edecio, Kalil Jorge, Coelho Verônica, Souza Santos Keity
Departamento de Clínica Médica, Disciplina de Alergia e Imunologia Clínica, Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP, Brazil.
Laboratório de Imunologia, LIM19, Instituto do Coração (InCor), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, (HCFMUSP), São Paulo, SP, Brazil.
Sci Rep. 2025 Jul 3;15(1):23705. doi: 10.1038/s41598-025-04152-8.
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.
新冠疫情持续以长期新冠(LC)这一重大公共卫生问题挑战着世界,据估计全球有超过4亿人受到影响。关于长期新冠所涉及的机制仍有许多未知之处。我们研究了抗SARS-CoV-2抗体和IFN-γ反应对长期新冠及其各种表型发展的影响。我们研究了一组在第一波疫情(2020年)期间主要经历轻度新冠感染且感染后长达一年的137名康复者。我们发现45%的长期新冠病例与急性期症状的数量和持续时间增加有关。急性期的心血管和/或胃肠道症状与预防长期新冠的发生有关,而肺部、耳鼻喉科、肌肉骨骼和其他症状与长期新冠发生风险增加有关。关于长期新冠的表型,我们观察到抗SARS-CoV-2抗体与归类为一般或其他的长期新冠症状存在风险关联以及潜在有害影响。相比之下,对于与重要器官相关的长期新冠症状,我们仅发现了保护性关联,特别是对于心血管症状,其在长期新冠中的患病率确实较低(16%)。总体而言,我们的数据表明,抗SARS-CoV-2抗体对与重要器官相关的长期新冠症状,尤其是心血管症状,起到保护作用,但在预防或限制其他高度普遍的长期新冠症状方面,如神经、精神和肺部症状,作用不足。