Efficacy of convalescent plasma therapy in improving survival in non-immunized COVID-19 patients.

Publication date: Jun 24, 2025

Convalescent plasma (CP), obtained from individuals who have recovered from COVID-19, has been widely explored as a potential therapeutic option, particularly in the absence of vaccines and monoclonal antibody treatments. This study aimed to evaluate the effectiveness of CP therapy in improving survival among non-immunized COVID-19 patients hospitalized in Brazil. This retrospective unicentric cohort study was conducted at a private hospital in Campo Largo, ParancE1, Brazil, from July 2020 to February 2021. A total of 245 hospitalized COVID-19 patients were included, confirmed by RT-qPCR or antigen testing. Patients were divided into two groups: those receiving CP alongside standard treatment (n=100) and those receiving standard treatment alone (n=145). Survival outcomes were assessed using Kaplan-Meier analysis and Cox regression, while inflammatory responses were evaluated through C-reactive protein (CRP) measurements. Patients treated with CP had a significantly higher survival rate (91%) compared to the control group (82. 8%) (P=0. 0363). The survival benefit persisted throughout the follow-up period, with a 2. 25-fold lower risk of death in the CP group after adjusting for age (P=0. 0480). However, no significant differences in CRP levels were observed between groups at discharge, suggesting that CP’s benefits may be mediated through immune modulation rather than direct anti-inflammatory effects. Our findings indicate that CP therapy significantly improves survival in non-immunized COVID-19 patients, reinforcing its potential role in settings with limited access to advanced treatments. Future studies should explore CP’s mechanisms of action and its integration into broader therapeutic strategies.

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Concepts Keywords
Death Adult
February Aged
July Antibodies, Viral
Vaccines Antibodies, Viral
Brazil
C-Reactive Protein
C-Reactive Protein
COVID-19
COVID-19 Serotherapy
Female
Humans
Immunization, Passive
Kaplan-Meier Estimate
Male
Middle Aged
Retrospective Studies
SARS-CoV-2
Survival Rate
Treatment Outcome

Semantics

Type Source Name
disease MESH COVID-19
disease MESH death
disease IDO role
disease MESH Long Covid
pathway REACTOME Reproduction
disease MESH asymptomatic infections
disease MESH pneumonia
disease MESH acute respiratory distress syndrome
drug DRUGBANK Azelaic acid
disease MESH influenza
disease IDO immune response
pathway KEGG Influenza A
disease MESH viral load
disease IDO symptom
disease MESH respiratory infections
pathway KEGG Viral replication
disease IDO intervention
disease IDO host
disease IDO protein
drug DRUGBANK Angiotensin II
disease IDO infectivity
disease MESH inflammation
disease MESH complications
disease MESH Emergency
drug DRUGBANK Indoleacetic acid
disease MESH dyspnea
disease MESH lung injury
disease MESH abnormalities
disease IDO history
disease MESH anaphylactic reactions
disease IDO blood
drug DRUGBANK Oxygen
drug DRUGBANK Methionine
disease MESH infection
disease MESH hepatitis
disease MESH syphilis
disease MESH Chagas disease
pathway KEGG Chagas disease
disease IDO process
disease MESH comorbidity
drug DRUGBANK Trestolone
disease MESH bacterial pneumonia
disease MESH multiple organ dysfunction syndrome
disease MESH hypertension
disease MESH neoplasia
drug DRUGBANK Coenzyme M
drug DRUGBANK Aspartame
drug DRUGBANK Sulfasalazine
disease MESH viral infections
disease MESH functional status
disease MESH obesity
disease MESH secondary infections
disease IDO cell
disease MESH etiology
disease MESH critically ill
disease IDO replication
drug DRUGBANK Ranitidine
disease MESH syndrome

Original Article

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