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High-titer post-vaccine COVID-19 convalescent plasma for immunocompromised patients during the first omicron surge.
Tayyar, Ralph; Wong, Lisa Kanata; Dahlen, Alex; Shu, Elaine; Pandey, Suchitra; Liu, Anne Y.
  • Tayyar R; Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Wong LK; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
  • Dahlen A; Stanford Blood Center, Stanford, California, USA.
  • Shu E; Quantitative Sciences Unit, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Pandey S; Stanford Blood Center, Stanford, California, USA.
  • Liu AY; Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
Transpl Infect Dis ; 25(2): e14055, 2023 Apr.
Article in English | MEDLINE | ID: covidwho-2283716
ABSTRACT

BACKGROUND:

Transplant and hematologic malignancy patients have high Coronavirus disease 2019 (COVID-19) mortality and impaired vaccination responses. Omicron variant evades several monoclonal antibodies previously used in immunocompromised patients. Polyclonal COVID-19 convalescent plasma (CCP) may provide broader neutralizing capacity against new variants at high titers. Vaccination increases severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) titer in convalescent donors.

METHODS:

We conducted a retrospective chart review of hospitalized immunocompromised patients with COVID-19 who received high-titer CCP during the first omicron surge, collected from vaccinated donors within 6 months of pre-omicron COVID-19. Data on safety and outcomes were extracted.

RESULTS:

A total of 44 immunocompromised patients were included, 59.1% with solid organ transplant, 22.7% with hematopoietic cell transplant, 11.4% with hematologic malignancy, and 6.8% with autoimmune disease. Overall, 95% of CCP units transfused were from recently recovered and vaccinated donors and had SARS-CoV-2 antibody results 8- to 37-fold higher than the Food and Drug Administration's cutoff for high-titer CCP. There were two mild transfusion reactions. A total of 30-day mortality was 4.5%. There were no differences in 100-day mortality by underlying diagnosis, levels of immunosuppression, and timing of CCP administration. Patients with higher immunosuppression had significantly higher mean World Health Organization clinical progression scores at 30-day post-CCP compared to those with lower immunosuppression.

CONCLUSIONS:

CCP is a safe, globally available treatment for immunocompromised patients with COVID-19. Mortality was lower in our cohort than that of COVID-19 patients with similar immunocompromising conditions. Post-vaccine CCP with very high titers should be prioritized for study in immunocompromised patients. Post-vaccine CCP has the potential to keep pace with new variants by overcoming mutations at sufficiently high titer.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vaccines / Hematopoietic Stem Cell Transplantation / Hematologic Neoplasms / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Transpl Infect Dis Journal subject: Transplantation Year: 2023 Document Type: Article Affiliation country: Tid.14055

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vaccines / Hematopoietic Stem Cell Transplantation / Hematologic Neoplasms / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Transpl Infect Dis Journal subject: Transplantation Year: 2023 Document Type: Article Affiliation country: Tid.14055