A previously treated severe haemophilia A patient developed high-titre inhibitor after vaccinations

Author:

Li Zekun1ORCID,Chen Zhenping1,Cheng Xiaoling1ORCID,Wu Xinyi1,Li Gang1,Zhen Yingzi1,Poon Man-Chiu2,Wu Runhui1

Affiliation:

1. Hemophilia Work Group, Hematology Oncology Center, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s Health, Beijing, China

2. Departments of Medicine, Pediatrics and Oncology, University of Calgary, Cumming School of Medicine, and Southern Alberta Rare Blood and Bleeding Disorders Comprehensive Care program, Foothills Hospital, Alberta Health Services, Calgary, AB, Canada

Abstract

The factor VIII (FVIII)-neutralizing antibody (inhibitor) seen in 25%–30% of patients with severe haemophilia A (SHA). Vaccination is a non-genetic risk factor of inhibitor development as ‘danger signal’ which may provide a pro-inflammatory microenvironment to increase FVIII immunogenicity. We reported a previously treated SHA patient postponed the first vaccination to 15-month age received diphtheria-pertussis-tetanus intramuscularly. At 18-month age, the patient received Hepatitis A intramuscularly and Varicella Zoster Virus subcutaneously with 2 weeks interval and FVIII infusion was given <24 h prior for each. Successive bleedings occurred 1 week later with inefficacy of FVIII replacement. High-titre inhibitor was tested at 117 exposure days. This case suggested that continuous vaccinations in close proximity to FVIII could induce inhibitor. The relationship between vaccination and FVIII immunogenicity still needs to be revealed by further study.

Funder

beijing municipal science and technology commission

Capitals Funds for Health Improvement and Research of China

National Science and Technology Key Projects

Beijing Natural Science Foundation of China

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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