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Prevalence and predictors of SARS-CoV-2 antibodies among solid organ transplant recipients with confirmed infection.
Burack, Daniel; Pereira, Marcus R; Tsapepas, Demetra S; Harren, Patricia; Farr, Maryjane A; Arcasoy, Selim; Cohen, David J; Mohan, Sumit; Emond, Jean C; Hod, Eldad A; Verna, Elizabeth C.
  • Burack D; Department of Medicine, Columbia University College of Physicians & Surgeons, New York, New York.
  • Pereira MR; Department of Medicine, Division of Infectious Disease, Columbia University College of Physicians & Surgeons, New York, New York.
  • Tsapepas DS; Department of Surgery, Columbia University College of Physicians & Surgeons, New York, New York.
  • Harren P; Department of Surgery, Columbia University College of Physicians & Surgeons, New York, New York.
  • Farr MA; Department of Medicine, Division of Cardiology, Columbia University College of Physicians & Surgeons, New York, New York.
  • Arcasoy S; Department of Medicine, Division of Division of Pulmonary, Allergy and Critical Care Medicine, Columbia University College of Physicians & Surgeons, New York, New York.
  • Cohen DJ; Department of Medicine, Division of Nephrology, Columbia University College of Physicians & Surgeons, New York, New York.
  • Mohan S; Department of Medicine, Division of Nephrology, Columbia University College of Physicians & Surgeons, New York, New York.
  • Emond JC; Department of Surgery, Columbia University College of Physicians & Surgeons, New York, New York.
  • Hod EA; Center for Liver Disease and Transplantation, Columbia University College of Physicians & Surgeons, New York, New York.
  • Verna EC; Department of Pathology, Columbia University College of Physicians & Surgeons, New York, New York.
Am J Transplant ; 21(6): 2254-2261, 2021 06.
Article in English | MEDLINE | ID: covidwho-1085302
ABSTRACT
It remains uncertain whether immunocompromised patients including solid organ transplant (SOT) recipients will have a robust antibody response to SARS-CoV-2 infection. We enrolled all adult SOT recipients at our center with confirmed SARS-CoV-2 infection who underwent antibody testing with a single commercially available anti-nucleocapsid antibody test at least 7 days after diagnosis in a retrospective cohort. Seventy SOT recipients were studied (56% kidney, 19% lung, 14% liver ± kidney, and 11% heart ± kidney recipients). Thirty-six (51%) had positive anti-nucleocapsid antibody testing, and 34 (49%) were negative. Recipients of a kidney allograft were less likely to have positive antibody testing compared to those who did not receive a kidney (p = .04). In the final multivariable model, the years from transplant to diagnosis (OR 1.26, p = .002) and baseline immunosuppression with more than two agents (OR 0.26, p = .03) were significantly associated with the antibody test result, controlling for kidney transplantation. In conclusion, among SOT recipients with confirmed infection, only 51% of patients had detectable anti-nucleocapsid antibodies, and transplant-related variables including the level and nature of immunosuppression were important predictors. These findings raise the concern that SOT recipients with COVID-19 may be less likely to form SARS-CoV-2 antibodies.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Organ Transplantation / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Limits: Adult / Humans Language: English Journal: Am J Transplant Journal subject: Transplantation Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Organ Transplantation / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Limits: Adult / Humans Language: English Journal: Am J Transplant Journal subject: Transplantation Year: 2021 Document Type: Article