Your browser doesn't support javascript.
loading
A Protein Epitope Targeted by the Antibody Response to Kawasaki Disease.
Rowley, Anne H; Baker, Susan C; Arrollo, David; Gruen, Leah J; Bodnar, Tetyana; Innocentini, Nancy; Hackbart, Matthew; Cruz-Pulido, Yazmin E; Wylie, Kristine M; Kim, Kwang-Youn A; Shulman, Stanford T.
Affiliation
  • Rowley AH; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Baker SC; Department of Microbiology/Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Arrollo D; Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
  • Gruen LJ; Department of Microbiology and Immunology, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois, USA.
  • Bodnar T; Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
  • Innocentini N; Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
  • Hackbart M; Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
  • Cruz-Pulido YE; Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
  • Wylie KM; Department of Microbiology and Immunology, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois, USA.
  • Kim KA; Department of Microbiology and Immunology, Loyola University Chicago, Stritch School of Medicine, Maywood, Illinois, USA.
  • Shulman ST; Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
J Infect Dis ; 222(1): 158-168, 2020 06 16.
Article in En | MEDLINE | ID: mdl-32052021
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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Cells / Antibodies, Monoclonal / Antibody Formation / Mucocutaneous Lymph Node Syndrome / Epitopes Limits: Female / Humans / Infant / Male Country/Region as subject: America do norte Language: En Journal: J Infect Dis Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Cells / Antibodies, Monoclonal / Antibody Formation / Mucocutaneous Lymph Node Syndrome / Epitopes Limits: Female / Humans / Infant / Male Country/Region as subject: America do norte Language: En Journal: J Infect Dis Year: 2020 Document type: Article Affiliation country: United States