de Sá Nathalia Beatriz Ramos, Macieira Karine Venegas, Coelho Mariana Rosa Inacio, Goulart Milena Neira, Ribeiro-Alves Marcelo, Rosadas Leonardo Azevedo da Silva, Geraldo Kim Mattos, Ribeiro Maria Pia Diniz, Cardoso Sandra Wagner, Grinsztejn Beatriz, Veloso Valdiléa G, Cazote Andressa da Silva, de Almeida Dalziza Victalina, Giacoia-Gripp Carmem Beatriz Wagner, Côrtes Fernanda Heloise, Morgado Mariza Gonçalves
Laboratório de AIDS & Imunologia Molecular, Instituto Oswaldo Cruz (IOC), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.
Laboratório de Pesquisa Clínica em IST e AIDS, Instituto Nacional de Infectologia Evandro Chagas (INI), FIOCRUZ, Rio de Janeiro 21040-360, Brazil.
Viruses. 2025 Jan 13;17(1):91. doi: 10.3390/v17010091.
Severe COVID-19 presents a variety of clinical manifestations associated with inflammatory profiles. People living with HIV (PLWH) could face a higher risk of hospitalization and mortality from COVID-19, depending on their immunosuppression levels. This study describes inflammatory markers in COVID-19 clinical outcomes with and without HIV infection.
We analyzed 112 inpatients of the Hospital Center for COVID-19 (INI/FIOCRUZ), including 22 cases of COVID-19 in PLWH (COVID/PLWH group). Plasma samples were tested for a panel of 15 cytokines by Luminex. Sociodemographic, clinical, and laboratory data were collected from patients' clinical records.
COVID-19 individuals were stratified according to the WHO clinical severity profiles at hospitalization. Significant differences in clinical scores, symptoms (coughs), and the occurrence of HIV infection were found among the groups. Clinical blood parameters and plasma cytokines were analyzed among COVID-19 groups with distinct severity profiles. Critical COVID-19 cases showed higher levels of inflammatory markers (Bilirubin, D-dimer, PCR, and urea, as well as IL-8, IL-10, TNF-α, INF-α, IL-1β, IL-17A, IL-23, IL-6) than moderate and severe groups. The COVID/PLWH group had lower CD4 counts (64 cells/mm) and cytokine levels than other COVID-19 patients.
Overall, critically ill COVID-19 patients exhibited heightened inflammatory responses, while COVID/PLWH demonstrated unique immunological characteristics without increased mortality risk.
重症新型冠状病毒肺炎(COVID-19)呈现出多种与炎症特征相关的临床表现。感染人类免疫缺陷病毒(HIV)的人(PLWH)根据其免疫抑制水平,可能面临更高的因COVID-19住院和死亡风险。本研究描述了合并或未合并HIV感染的COVID-19患者临床结局中的炎症标志物。
我们分析了COVID-19医院中心(INI/FIOCRUZ)的112名住院患者,其中包括22例PLWH中的COVID-19病例(COVID/PLWH组)。通过Luminex检测血浆样本中的15种细胞因子。从患者临床记录中收集社会人口统计学、临床和实验室数据。
COVID-19患者根据住院时世界卫生组织的临床严重程度分类进行分层。各亚组在临床评分、症状(咳嗽)和HIV感染发生率方面存在显著差异。对具有不同严重程度分类的COVID-19亚组患者的临床血液参数和血浆细胞因子进行了分析。重症COVID-19病例的炎症标志物(胆红素、D-二聚体、C反应蛋白和尿素,以及白细胞介素-8、白细胞介素-10、肿瘤坏死因子-α、干扰素-α、白细胞介素-1β、白细胞介素-17A、白细胞介素-23、白细胞介素-6)水平高于中度和重度组。COVID/PLWH组的CD4细胞计数(64个细胞/mm³)和细胞因子水平低于其他COVID-19患者。
总体而言,重症COVID-19患者表现出炎症反应增强,而COVID/PLWH组表现出独特的免疫特征,且死亡风险未增加。