Frontiers in Immunology (Mar 2020)
Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies
- Mahya Dezfouli,
- Mahya Dezfouli,
- Sofia Bergström,
- Lillemor Skattum,
- Lillemor Skattum,
- Hassan Abolhassani,
- Hassan Abolhassani,
- Maja Neiman,
- Monireh Torabi-Rahvar,
- Clara Franco Jarava,
- Andrea Martin-Nalda,
- Juana M. Ferrer Balaguer,
- Charlotte A. Slade,
- Charlotte A. Slade,
- Anja Roos,
- Luis M. Fernandez Pereira,
- Margarita López-Trascasa,
- Luis I. Gonzalez-Granado,
- Luis M. Allende-Martinez,
- Yumi Mizuno,
- Yusuke Yoshida,
- Vanda Friman,
- Åsa Lundgren,
- Asghar Aghamohammadi,
- Nima Rezaei,
- Manuel Hernández-Gonzalez,
- Ulrika von Döbeln,
- Lennart Truedsson,
- Toshiro Hara,
- Shigeaki Nonoyama,
- Jochen M. Schwenk,
- Peter Nilsson,
- Lennart Hammarström
Affiliations
- Mahya Dezfouli
- Division of Clinical Immunology and Transfusion Medicine, Department of Laboratory Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden
- Mahya Dezfouli
- Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology & SciLifeLab, Stockholm, Sweden
- Sofia Bergström
- Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology & SciLifeLab, Stockholm, Sweden
- Lillemor Skattum
- Department of Laboratory Medicine, Section of Microbiology, Immunology and Glycobiology, Lund University, Lund, Sweden
- Lillemor Skattum
- Clinical Immunology and Transfusion Medicine, Region Skåne, Lund, Sweden
- Hassan Abolhassani
- Division of Clinical Immunology and Transfusion Medicine, Department of Laboratory Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden
- Hassan Abolhassani
- Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
- Maja Neiman
- Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology & SciLifeLab, Stockholm, Sweden
- Monireh Torabi-Rahvar
- Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
- Clara Franco Jarava
- Immunology Department, Vall d'Hebron Research Institute, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain
- Andrea Martin-Nalda
- Pediatric Infectious Diseases and Immunodeficiencies Unit, Vall d'Hebron Research Institute, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain
- Juana M. Ferrer Balaguer
- Immunology, Hospital Universitari Son Espases/Institut d'Investigació Sanitària Illes Balears, Palma, Spain
- Charlotte A. Slade
- 0Royal Melbourne Hospital, Melbourne, VIC, Australia
- Charlotte A. Slade
- 1The Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia
- Anja Roos
- 2Department of Microbiology and Immunology, Sint Antonius Hospital, Nieuwegein, Netherlands
- Luis M. Fernandez Pereira
- 3Department of Immunology, Hospital San Pedro de Alcántara, Cáceres, Spain
- Margarita López-Trascasa
- 4Departamento de Medicina, Hospital La Paz Institute for Health Research (IdiPAZ), Universidad Autónoma de Madrid and Complement Research Group, Madrid, Spain
- Luis I. Gonzalez-Granado
- 5Primary Immunodeficiencies Unit, Department of Pediatrics, University Hospital 12 de Octubre, Research Institute Hospital 12 Octubre (I+12), Madrid, Spain
- Luis M. Allende-Martinez
- 6Immunology Department, University Hospital 12 de Octubre, Research Institute Hospital 12 Octubre (I+12), Madrid, Spain
- Yumi Mizuno
- 7Fukuoka Children's Hospital, Kyushu University, Fukuoka, Japan
- Yusuke Yoshida
- 8Department of Pediatrics, National Defense Medical College, Saitama, Japan
- Vanda Friman
- 9Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
- Åsa Lundgren
- 0Departments of Infectious Diseases, Central Hospital, Kristianstad, Sweden
- Asghar Aghamohammadi
- Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
- Nima Rezaei
- Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
- Manuel Hernández-Gonzalez
- Immunology Department, Vall d'Hebron Research Institute, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain
- Ulrika von Döbeln
- 1Division of Metabolic Diseases, Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital Solna, Stockholm, Sweden
- Lennart Truedsson
- Department of Laboratory Medicine, Section of Microbiology, Immunology and Glycobiology, Lund University, Lund, Sweden
- Toshiro Hara
- 7Fukuoka Children's Hospital, Kyushu University, Fukuoka, Japan
- Shigeaki Nonoyama
- 8Department of Pediatrics, National Defense Medical College, Saitama, Japan
- Jochen M. Schwenk
- Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology & SciLifeLab, Stockholm, Sweden
- Peter Nilsson
- Division of Affinity Proteomics, Department of Protein Science, KTH Royal Institute of Technology & SciLifeLab, Stockholm, Sweden
- Lennart Hammarström
- Division of Clinical Immunology and Transfusion Medicine, Department of Laboratory Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden
- DOI
- https://doi.org/10.3389/fimmu.2020.00455
- Journal volume & issue
-
Vol. 11
Abstract
The clinical outcomes of primary immunodeficiencies (PIDs) are greatly improved by accurate diagnosis early in life. However, it is not common to consider PIDs before the manifestation of severe clinical symptoms. Including PIDs in the nation-wide newborn screening programs will potentially improve survival and provide better disease management and preventive care in PID patients. This calls for the detection of disease biomarkers in blood and the use of dried blood spot samples, which is a part of routine newborn screening programs worldwide. Here, we developed a newborn screening method based on multiplex protein profiling for parallel diagnosis of 22 innate immunodeficiencies affecting the complement system and respiratory burst function in phagocytosis. The proposed method uses a small fraction of eluted blood from dried blood spots and is applicable for population-scale performance. The diagnosis method is validated through a retrospective screening of immunodeficient patient samples. This diagnostic approach can pave the way for an earlier, more comprehensive and accurate diagnosis of complement and phagocytic disorders, which ultimately lead to a healthy and active life for the PID patients.
Keywords
- primary immunodeficiency
- complement deficiencies
- phagocytic disorders
- presymptomatic diagnosis
- newborn screening
- dried blood spot