A Protein Epitope Targeted by the Antibody Response to Kawasaki Disease

Author:

Rowley Anne H123,Baker Susan C4,Arrollo David3,Gruen Leah J3,Bodnar Tetyana1,Innocentini Nancy3,Hackbart Matthew4,Cruz-Pulido Yazmin E4,Wylie Kristine M56,Kim Kwang-Youn A7,Shulman Stanford T13

Affiliation:

1. Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA

2. Department of Microbiology/Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA

3. Ann and Robert H. Lurie Children’s Hospital of Chicago, Chicago, Illinois, USA

4. Department of Microbiology and Immunology, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois, USA

5. Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA

6. McDonnell Genome Institute, Washington University School of Medicine, St Louis, Missouri, USA

7. Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA

Abstract

Abstract Background Kawasaki disease (KD) is the leading cause of childhood acquired heart disease in developed nations and can result in coronary artery aneurysms and death. Clinical and epidemiologic features implicate an infectious cause but specific antigenic targets of the disease are unknown. Peripheral blood plasmablasts are normally highly clonally diverse but the antibodies they encode are approximately 70% antigen-specific 1–2 weeks after infection. Methods We isolated single peripheral blood plasmablasts from children with KD 1–3 weeks after onset and prepared 60 monoclonal antibodies (mAbs). We used the mAbs to identify their target antigens and assessed serologic response among KD patients and controls to specific antigen. Results Thirty-two mAbs from 9 of 11 patients recognize antigen within intracytoplasmic inclusion bodies in ciliated bronchial epithelial cells of fatal cases. Five of these mAbs, from 3 patients with coronary aneurysms, recognize a specific peptide, which blocks binding to inclusion bodies. Sera from 5/8 KD patients day ≥ 8 after illness onset, compared with 0/17 infant controls (P < .01), recognized the KD peptide antigen. Conclusions These results identify a protein epitope targeted by the antibody response to KD and provide a means to elucidate the pathogenesis of this important worldwide pediatric problem.

Funder

National Institute of Allergy and Infectious Diseases

Feitler Family

Max Goldenberg Foundation

Center for Kawasaki Disease

National Cancer Institute

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Cited by 30 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Kawasaki Disease and Multisystem Inflammatory Syndrome in Children;Rheumatic Disease Clinics of North America;2023-08

2. Multisystem Inflammatory Syndrome in Children and Kawasaki Disease;Rheumatic Disease Clinics of North America;2023-08

3. Analysis of Plasmablasts From Children With Kawasaki Disease Reveals Evidence of a Convergent Antibody Response to a Specific Protein Epitope;The Journal of Infectious Diseases;2023-02-18

4. Kawasaki Disease;Principles and Practice of Pediatric Infectious Diseases;2023

5. SARS-CoV-2–Related Mitigation Measures and Insights Into Kawasaki Disease;JAMA Pediatrics;2022-12-01

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3