Elevated immune response in the brain of autistic patients
This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF-α, IL-6 and GM-CSF), Th1 cytokine (IFN-γ) and chemokine (IL-8) were significantly increased in the brain...
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Published in | Journal of neuroimmunology Vol. 207; no. 1; pp. 111 - 116 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
15.02.2009
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Subjects | |
Online Access | Get full text |
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Abstract | This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF-α, IL-6 and GM-CSF), Th1 cytokine (IFN-γ) and chemokine (IL-8) were significantly increased in the brains of ASD patients compared with the controls. However the Th2 cytokines (IL-4, IL-5 and IL-10) showed no significant difference. The Th1/Th2 ratio was also significantly increased in ASD patients. Conclusion: ASD patients displayed an increased innate and adaptive immune response through the Th1 pathway, suggesting that localized brain inflammation and autoimmune disorder may be involved in the pathogenesis of ASD. |
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AbstractList | Abstract This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF-α, IL-6 and GM-CSF), Th1 cytokine (IFN-γ) and chemokine (IL-8) were significantly increased in the brains of ASD patients compared with the controls. However the Th2 cytokines (IL-4, IL-5 and IL-10) showed no significant difference. The Th1/Th2 ratio was also significantly increased in ASD patients. Conclusion: ASD patients displayed an increased innate and adaptive immune response through the Th1 pathway, suggesting that localized brain inflammation and autoimmune disorder may be involved in the pathogenesis of ASD. This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF-alpha, IL-6 and GM-CSF), Th1 cytokine (IFN-gamma) and chemokine (IL-8) were significantly increased in the brains of ASD patients compared with the controls. However the Th2 cytokines (IL-4, IL-5 and IL-10) showed no significant difference. The Th1/Th2 ratio was also significantly increased in ASD patients.UNLABELLEDThis study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF-alpha, IL-6 and GM-CSF), Th1 cytokine (IFN-gamma) and chemokine (IL-8) were significantly increased in the brains of ASD patients compared with the controls. However the Th2 cytokines (IL-4, IL-5 and IL-10) showed no significant difference. The Th1/Th2 ratio was also significantly increased in ASD patients.ASD patients displayed an increased innate and adaptive immune response through the Th1 pathway, suggesting that localized brain inflammation and autoimmune disorder may be involved in the pathogenesis of ASD.CONCLUSIONASD patients displayed an increased innate and adaptive immune response through the Th1 pathway, suggesting that localized brain inflammation and autoimmune disorder may be involved in the pathogenesis of ASD. This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF-alpha, IL-6 and GM-CSF), Th1 cytokine (IFN-gamma) and chemokine (IL-8) were significantly increased in the brains of ASD patients compared with the controls. However the Th2 cytokines (IL-4, IL-5 and IL-10) showed no significant difference. The Th1/Th2 ratio was also significantly increased in ASD patients. ASD patients displayed an increased innate and adaptive immune response through the Th1 pathway, suggesting that localized brain inflammation and autoimmune disorder may be involved in the pathogenesis of ASD. This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF-α, IL-6 and GM-CSF), Th1 cytokine (IFN-γ) and chemokine (IL-8) were significantly increased in the brains of ASD patients compared with the controls. However the Th2 cytokines (IL-4, IL-5 and IL-10) showed no significant difference. The Th1/Th2 ratio was also significantly increased in ASD patients. Conclusion: ASD patients displayed an increased innate and adaptive immune response through the Th1 pathway, suggesting that localized brain inflammation and autoimmune disorder may be involved in the pathogenesis of ASD. This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed that proinflammatory cytokines (TNF- alpha , IL-6 and GM-CSF), Th1 cytokine (IFN- gamma ) and chemokine (IL-8) were significantly increased in the brains of ASD patients compared with the controls. However the Th2 cytokines (IL-4, IL-5 and IL-10) showed no significant difference. The Th1/Th2 ratio was also significantly increased in ASD patients. Conclusion: ASD patients displayed an increased innate and adaptive immune response through the Th1 pathway, suggesting that localized brain inflammation and autoimmune disorder may be involved in the pathogenesis of ASD. |
Author | Li, Xiaohong Ji, Lina Sheikh, Ashfaq M. Chauhan, Abha Brown, Ted Patil, Sangita Chauhan, Ved Li, Xiu-Min Malik, Mazhar |
AuthorAffiliation | b Department of Pediatrics, Mount Sinai School of Medicine, New York, NY 10029 a Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, New York, NY 10314 |
AuthorAffiliation_xml | – name: a Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, New York, NY 10314 – name: b Department of Pediatrics, Mount Sinai School of Medicine, New York, NY 10029 |
Author_xml | – sequence: 1 givenname: Xiaohong surname: Li fullname: Li, Xiaohong email: xiaohong.li@mssm.edu organization: Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, NY 10314, New York, United States – sequence: 2 givenname: Abha surname: Chauhan fullname: Chauhan, Abha organization: Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, NY 10314, New York, United States – sequence: 3 givenname: Ashfaq M. surname: Sheikh fullname: Sheikh, Ashfaq M. organization: Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, NY 10314, New York, United States – sequence: 4 givenname: Sangita surname: Patil fullname: Patil, Sangita organization: Department of Pediatrics, Mount Sinai School of Medicine, NY 10029, New York, United States – sequence: 5 givenname: Ved surname: Chauhan fullname: Chauhan, Ved organization: Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, NY 10314, New York, United States – sequence: 6 givenname: Xiu-Min surname: Li fullname: Li, Xiu-Min organization: Department of Pediatrics, Mount Sinai School of Medicine, NY 10029, New York, United States – sequence: 7 givenname: Lina surname: Ji fullname: Ji, Lina organization: Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, NY 10314, New York, United States – sequence: 8 givenname: Ted surname: Brown fullname: Brown, Ted organization: Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, NY 10314, New York, United States – sequence: 9 givenname: Mazhar surname: Malik fullname: Malik, Mazhar organization: Department of Neurochemistry, NY State Institute for Basic Research in Developmental Disabilities, NY 10314, New York, United States |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19157572$$D View this record in MEDLINE/PubMed |
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Snippet | This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our results showed... Abstract This study determined immune activities in the brain of ASD patients and matched normal subjects by examining cytokines in the brain tissue. Our... |
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SubjectTerms | Adolescent Adult Allergy and Immunology Autistic Disorder - immunology Autistic Disorder - pathology Autistic spectrum disorders (ASD) Brain - immunology Brain - pathology Case-Control Studies Chemokines - metabolism Child Child, Preschool Cytokines Cytokines - metabolism Female Flow cytometry method Humans Immune response Inflammation Male Multiplexed bead analysis Neurology Statistics, Nonparametric Th1 Cells - immunology Th2 Cells - immunology Young Adult |
Title | Elevated immune response in the brain of autistic patients |
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