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Tytuł pozycji:

Prospective Clinical, Virologic, and Immunologic Assessment of COVID-19 in Transplant Recipients.

Tytuł:
Prospective Clinical, Virologic, and Immunologic Assessment of COVID-19 in Transplant Recipients.
Autorzy:
Marinelli T; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Ferreira VH; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Ierullo M; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Ku T; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Lilly L; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Kim SJ; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Schiff J; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Sidhu A; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
McDonald M; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Hosseini-Moghaddam SM; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Husain S; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Rotstein C; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Majchrzak-Kita B; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Kulasingam V; Department of Biochemistry, University Health Network, Toronto, ON, Canada.
Humar A; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Kumar D; Multi-Organ Transplant Program, University Health Network, Toronto, ON, Canada.
Źródło:
Transplantation [Transplantation] 2021 Oct 01; Vol. 105 (10), pp. 2175-2183.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: Hagerstown, MD : Lippincott Williams & Wilkins
Original Publication: Baltimore, Williams & Wilkins.
MeSH Terms:
Organ Transplantation*
SARS-CoV-2*
Viral Load*
Antibodies, Viral/*blood
COVID-19/*immunology
Adult ; Aged ; COVID-19/virology ; Female ; Humans ; Male ; Middle Aged ; Prospective Studies ; Severity of Illness Index ; Transplant Recipients ; Virus Shedding
References:
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Transplantation. 2021 Jan 1;105(1):138-150. (PMID: 32941394)
Transplantation. 2021 Jul 1;105(7):1445-1448. (PMID: 33606483)
Am J Transplant. 2020 Nov;20(11):3149-3161. (PMID: 32786152)
N Engl J Med. 2021 Feb 11;384(6):533-540. (PMID: 33369366)
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Substance Nomenclature:
0 (Antibodies, Viral)
Entry Date(s):
Date Created: 20210621 Date Completed: 20211011 Latest Revision: 20240403
Update Code:
20240403
PubMed Central ID:
PMC8487707
DOI:
10.1097/TP.0000000000003860
PMID:
34149003
Czasopismo naukowe
Background: Several studies have described the clinical features of COVID-19 in solid-organ transplant recipients. However, many have been retrospective or limited to more severe cases (hospitalized) and have not routinely included serial virological sampling (especially in outpatients) and immunologic assessment.
Methods: Transplant patients diagnosed with COVID-19 based on a respiratory sample PCR were prospectively followed up to 90 d. Patients provided consent for convalescent serum samples and serial nasopharyngeal swabs for SARS-CoV-2 antibody (antinucleoprotein and anti-RBD) and viral load, respectively.
Results: In the 161 SOT recipients diagnosed with COVID-19, the spectrum of disease ranged from asymptomatic infection (4.3%) to hospitalization (60.6%), supplemental oxygen requirement (43.1%), mechanical ventilation (22.7%), and death (15.6%). Increasing age (OR, 1.031; 95% CI, 1.001-1.062; P = 0.046) and ≥2 comorbid conditions (OR, 3.690; 95% CI, 1.418-9.615; P = 0.007) were associated with the need for supplemental oxygen. Allograft rejection was uncommon (3.7%) despite immunosuppression modification. Antibody response at ≥14 d postsymptoms onset was present in 90% (anti-RBD) and 76.7% (anti-NP) with waning of anti-NP titers and stability of anti-RBD over time. Median duration of nasopharyngeal positivity was 10.0 d (IQR, 5.5-18.0) and shedding beyond 30 d was observed in 6.7% of patients. The development of antibody did not have an impact on viral shedding.
Conclusions: This study demonstrates the spectrum of COVID-19 illness in transplant patients. Risk factors for severe disease are identified. The majority form antibody by 2 wk with differential stability over time. Prolonged viral shedding was observed in a minority of patients. Reduction of immunosuppression was a safe strategy.
(Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.)

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