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Clinical Results with a B Cell Activating Anti-CD73 Antibody for the Immunotherapy of COVID-19
Richard A Miller; Pramod Guru; Philippe Bauer; Jorge Robles; Christian Tomaszewski; J. Scott Overcash; Michael Waters; Miriam Cameron; Julián Olalla Sierra; Haider Mashhedi; Mehrdad Mobasher; James Janc; Jenny A. Rudnick; Shenshen Hu; William B. Jones; Long Kwei; Suresh Mahabhashyam; Stephen B. Willingham; Gerard Criner.
Afiliação
  • Richard A Miller; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Pramod Guru; Mayo Clinic, Jacksonville, FL, USA
  • Philippe Bauer; Mayo Clinic, Rochester, MN, USA
  • Jorge Robles; El Centro Regional Medical Center, El Centro, CA, USA
  • Christian Tomaszewski; El Centro Regional Medical Center, El Centro, CA, USA; University of California, San Diego, CA, USA
  • J. Scott Overcash; Sharp Grossmont Hospital, La Mesa, CA, USA
  • Michael Waters; Sharp Chula Vista Medical Center, Chula Vista, CA, USA
  • Miriam Cameron; Holy Cross Hospital, Silver Spring, MD, USA
  • Julián Olalla Sierra; Hospital Costa del Sol, Marbella, Spain
  • Haider Mashhedi; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Mehrdad Mobasher; Corvus Pharmaceuticals, Burlingame, CA, USA
  • James Janc; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Jenny A. Rudnick; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Shenshen Hu; Corvus Pharmaceuticals, Burlingame, CA, USA
  • William B. Jones; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Long Kwei; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Suresh Mahabhashyam; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Stephen B. Willingham; Corvus Pharmaceuticals, Burlingame, CA, USA
  • Gerard Criner; Temple University Hospital, Philadelphia, PA, USA
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21263406
ABSTRACT
Robust polyclonal humoral immune responses have the potential to generate a diverse set of antibodies to neutralize and eliminate viruses such as SARS-CoV-2 and protect against transmission, re-infection and the evolution of variants that evade immunity. CD73 is present on subsets of human B and T cells where it plays a role in lymphocyte activation and migration. CD73 also functions as an ectoenzyme that converts AMP into immunosuppressive adenosine. We have developed a humanized anti-CD73 antibody, mupadolimab (CPI-006), that blocks CD73 enzymatic activity and activates CD73POS B cells, thereby inducing differentiation into plasmablasts, immunoglobulin class switching, and antibody secretion independent of the adenosine modulatory activity. These effects suggest mupadolimab may enhance the magnitude, diversity, and duration of anti-viral responses in patients with COVID-19. This hypothesis was tested in a dose escalation phase 1 trial in 29 hospitalized patients with COVID-19. Single doses of 0.3 mg/kg - 5 mg/kg mupadolimab were well tolerated with no drug related adverse events. Doses greater than 0.3 mg/kg resulted in rapid generation of IgG and IgM to SARS-CoV-2 significantly above titers measured in convalescent controls, with elevated IgG titers sustained for more than 6 months beyond presentation of symptoms. Based on these findings, a randomized double-blind, placebo-controlled Phase 3 study in hospitalized patients was initiated. The primary endpoint was proportion of patients alive and free from respiratory failure within 28 days. This trial was discontinued early during the period of waning COVID-19 incidence after enrolling 40 patients. Although underpowered, results from this trial suggest improvement in the primary and key secondary endpoints in patients treated with single doses of 2 mg/kg and 1 mg/kg compared to placebo. The presumed mechanism of action, stimulation of B cells, may represent a novel approach to immunotherapy of COVID-19 and other viral infections.
Licença
cc_by_nc_nd
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Observational_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Experimental_studies / Observational_studies / Prognostic_studies / Rct Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint