COVID‐19 in a lung transplant recipient: Exploring the diagnostic role of circulating exosomes and the clinical impact of advanced immunosuppression
Autor: | Kellie J Goodlet, Sandhya Bansal, Ashwini Arjuna, Thalachallour Mohanakumar, Sofya Tokman, Ashraf Omar, Hesham Mohamed, Rajat Walia, Michael D Nailor, Bhuvin Buddhdev, Hesham Abdelrazek |
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Rok vydání: | 2020 |
Předmět: |
Globulin
medicine.medical_treatment Case Report Case Reports Human leukocyte antigen 030230 surgery 03 medical and health sciences 0302 clinical medicine medicine Lung transplant recipient Transplantation Lung biology business.industry Immunosuppression respiratory system Microvesicles respiratory tract diseases Infectious Diseases medicine.anatomical_structure Methylprednisolone Immunology biology.protein 030211 gastroenterology & hepatology Antibody business medicine.drug |
Zdroj: | Transplant Infectious Disease |
ISSN: | 1399-3062 1398-2273 |
Popis: | Exosomes isolated from plasma of lung transplant recipients with allograft injury contain donor‐derived lung self‐antigens (collagen V and Kα1 tubulin) and human leukocyte antigen (HLA) molecules. We present a case of a 76‐year‐old, female lung transplant recipient treated for acute cellular rejection with methylprednisolone and anti‐thymocyte globulin, who subsequently contracted SARS‐CoV‐2 and developed a sharp increase in the mean fluorescent intensity of anti‐HLA antibodies. Analysis of circulating exosomes during rejection, but before SARS‐CoV‐2 infection, revealed the presence of lung self‐antigens and HLA class II molecules. After the patient contracted SARS‐CoV‐2, exosomes with the SARS‐CoV‐2 spike protein were also found. After resolution of infectious symptoms, exosomes with SARS‐CoV‐2 spike protein were no longer detected; however, exosomes with lung self‐antigens and HLA class II molecules persisted, which coincided with a progressive decline in spirometric flows, suggesting chronic lung allograft dysfunction. We propose that the analysis of circulating exosomes may be used to detect allograft injury mediated by both rejection and infection. Furthermore, the detection of exosomes containing viral proteins may be helpful in identifying allograft injury driven by viral pathogens. |
Databáze: | OpenAIRE |
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