4.7 Article

Oral Immunotherapy With Human Secretory Immunoglobulin A Improves Survival in the Hamster Model of Clostridioides difficile Infection

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 224, 期 8, 页码 1394-1397

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiab087

关键词

Clostridioides difficile infection; secretory IgA; immunotherapy

资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health [1R43DK10972901A1, 3R43DK109729-01A1S1]
  2. Business Accelerator Award from Ann Arbor SPARK, Ann Arbor, MI
  3. PreviPharma, GmbH, Mannheim, Germany

向作者/读者索取更多资源

Co-administration of human secretory IgA with subtherapeutic vancomycin can enhance survival in the Clostridioides difficile infection hamster model. Passive immunization with sIgA can be administered orally and prevent death in a partially treated CDI hamster model.
Coadministration of human secretory IgA (sIgA) together with subtherapeutic vancomycin enhanced survival in the Clostridioides difficile infection (CDI) hamster model. Vancomycin (5 or 10 mg/kg x 5 days) plus healthy donor plasma sIgA/monomeric IgA (TID x 21 days) or hyperimmune sIgA/monomeric IgA (BID x 13 days) enhanced survival. Survival was improved compared to vancomycin alone, P = .018 and .039 by log-rank Mantel-Cox, for healthy and hyperimmune sIgA, respectively. Passive immunization with sIgA (recombinant human secretory component plus IgA dimer/polymer from pooled human plasma) can be administered orally and prevents death in a partially treated CDI hamster model.

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