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Outpatient treatment with concomitant vaccine-boosted convalescent plasma for patients with immunosuppression and COVID-19.
Ripoll, Juan G; Tulledge-Scheitel, Sidna M; Stephenson, Anthony A; Ford, Shane; Pike, Marsha L; Gorman, Ellen K; Hanson, Sara N; Juskewitch, Justin E; Miller, Alex J; Zaremba, Solomiia; Ovrom, Erik A; Razonable, Raymund R; Ganesh, Ravindra; Hurt, Ryan T; Fischer, Erin N; Derr, Amber N; Eberle, Michele R; Larsen, Jennifer J; Carney, Christina M; Theel, Elitza S; Parikh, Sameer A; Kay, Neil E; Joyner, Michael J; Senefeld, Jonathon W.
Affiliation
  • Ripoll JG; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Tulledge-Scheitel SM; Division of Community Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Stephenson AA; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Ford S; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Pike ML; Department of Nursing, Mayo Clinic, Rochester, Rochester, Minnesota, USA.
  • Gorman EK; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Hanson SN; Department of Family Medicine, Mayo Clinic Health Care System, Mankato, Minnesota, USA.
  • Juskewitch JE; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Miller AJ; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Zaremba S; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Ovrom EA; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Razonable RR; Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Ganesh R; Division of General Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Hurt RT; Division of General Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Fischer EN; Department of Nursing, Mayo Clinic, Rochester, Rochester, Minnesota, USA.
  • Derr AN; Division of Hematology and Infusion Therapy, Rochester, Minnesota, USA.
  • Eberle MR; Mayo Clinic Health System Northwest Wisconsin, Eau Claire, Wisconsin, USA.
  • Larsen JJ; Division of Hematology and Infusion Therapy, Rochester, Minnesota, USA.
  • Carney CM; Mayo Clinic Health System, Red Wing, Minnesota, USA.
  • Theel ES; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Parikh SA; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Kay NE; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
  • Joyner MJ; Department of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
  • Senefeld JW; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota, USA.
mBio ; 15(5): e0040024, 2024 May 08.
Article in En | MEDLINE | ID: mdl-38602414
ABSTRACT
Although severe coronavirus disease 2019 (COVID-19) and hospitalization associated with COVID-19 are generally preventable among healthy vaccine recipients, patients with immunosuppression have poor immunogenic responses to COVID-19 vaccines and remain at high risk of infection with SARS-CoV-2 and hospitalization. In addition, monoclonal antibody therapy is limited by the emergence of novel SARS-CoV-2 variants that have serially escaped neutralization. In this context, there is interest in understanding the clinical benefit associated with COVID-19 convalescent plasma collected from persons who have been both naturally infected with SARS-CoV-2 and vaccinated against SARS-CoV-2 ("vax-plasma"). Thus, we report the clinical outcome of 386 immunocompromised outpatients who were diagnosed with COVID-19 and who received contemporary COVID-19-specific therapeutics (standard-of-care group) and a subgroup who also received concomitant treatment with very high titer COVID-19 convalescent plasma (vax-plasma group) with a specific focus on hospitalization rates. The overall hospitalization rate was 2.2% (5 of 225 patients) in the vax-plasma group and 6.2% (10 of 161 patients) in the standard-of-care group, which corresponded to a relative risk reduction of 65% (P = 0.046). Evidence of efficacy in nonvaccinated patients cannot be inferred from these data because 94% (361 of 386 patients) of patients were vaccinated. In vaccinated patients with immunosuppression and COVID-19, the addition of vax-plasma or very high titer COVID-19 convalescent plasma to COVID-19-specific therapies reduced the risk of disease progression leading to hospitalization.IMPORTANCEAs SARS-CoV-2 evolves, new variants of concern (VOCs) have emerged that evade available anti-spike monoclonal antibodies, particularly among immunosuppressed patients. However, high-titer COVID-19 convalescent plasma continues to be effective against VOCs because of its broad-spectrum immunomodulatory properties. Thus, we report clinical outcomes of 386 immunocompromised outpatients who were treated with COVID-19-specific therapeutics and a subgroup also treated with vaccine-boosted convalescent plasma. We found that the administration of vaccine-boosted convalescent plasma was associated with a significantly decreased incidence of hospitalization among immunocompromised COVID-19 outpatients. Our data add to the contemporary data providing evidence to support the clinical utility of high-titer convalescent plasma as antibody replacement therapy in immunocompromised patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunization, Passive / Immunocompromised Host / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 / COVID-19 Serotherapy / Hospitalization Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: MBio Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Immunization, Passive / Immunocompromised Host / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 / COVID-19 Serotherapy / Hospitalization Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: MBio Year: 2024 Type: Article Affiliation country: United States