Differential Frequency of CD8+ T Cell Subsets in Multiple Sclerosis Patients with Various Clinical Patterns

Autor: Mohammad Ali Sahraian, Maryam Izad, Rozita Doosti, Masoumeh Beheshti, Zahra Salehi, Ehsan Janzamin
Jazyk: angličtina
Rok vydání: 2016
Předmět:
Male
Physiology
Cellular differentiation
lcsh:Medicine
Pathogenesis
CD8-Positive T-Lymphocytes
Pathology and Laboratory Medicine
Gastroenterology
0302 clinical medicine
Immune Physiology
Cellular types
Cytotoxic T cell
lcsh:Science
Innate Immune System
Multidisciplinary
medicine.diagnostic_test
Immune cells
Healthy subjects
Neurodegenerative Diseases
Cell Differentiation
Hematology
Body Fluids
Blood
Neurology
White blood cells
Cytokines
Female
Anatomy
Research Article
Adult
Cell biology
Blood cells
medicine.medical_specialty
Multiple Sclerosis
Patients
Immunology
T cells
Cytotoxic T cells
Autoimmune Diseases
Flow cytometry
03 medical and health sciences
Internal medicine
Remission phase
medicine
Humans
Medicine and health sciences
Biology and life sciences
business.industry
Multiple sclerosis
lcsh:R
Molecular Development
medicine.disease
Demyelinating Disorders
Health Care
Animal cells
Immune System
Clinical Immunology
lcsh:Q
Clinical Medicine
business
030217 neurology & neurosurgery
CD8
Developmental Biology
030215 immunology
Zdroj: PLoS ONE, Vol 11, Iss 7, p e0159565 (2016)
PLoS ONE
ISSN: 1932-6203
Popis: Recent evidence points to a pathogenic role for CD8+ cytotoxic T (Tc) cells in Multiple sclerosis (MS). Based on cytokine profile, Tc cells can be divided into different subsets: IFN-γ (Tc1), IL-4 (Tc2), IL-10 (Tc10), IL-17 (Tc17), IL-21 (Tc21), IL-22 (Tc22) and TNF-α producing cells. In this study we evaluated the frequency of Tc cell subsets and the serum level of Tc17 differentiation cytokines in MS patients with different clinical patterns. We analyzed Tc cell subsets percentage in peripheral blood of relapsing-remitting (RRMS) (n = 28), secondary-progressive (SPMS) (n = 10) and primary-progressive (PPMS) (n = 4) MS patients in comparison to healthy controls (n = 15) using flow cytometry. Serum level of TGF-β, IL-6 and IL-23 were measured by ELISA. We showed elevated levels of Tc1 and Tc17 cells in SPMS and RRMS patients in relapse phase, respectively (P = 0.04). Interestingly, the percentage of TNF-α producing CD8+ T cells in relapse and remission phase of RRMS and SPMS patients were higher than controls (P = 0.01, P = 0.004, P = 0.01, respectively) and Tc21 increased in remission phase of RRMS compared to SPMS (P = 0.03). We also found higher frequency of CD8+ IFN-γ+ TNF-α+ IL-17+ T cells in relapse phase of RRMS compared to remission phase, SPMS patients and controls (P = 0.01, P = 0.004 and P = 0.02, respectively). TGF- β increased in sera of RRMS patients in remission phase (P = 0.03) and SPMS (P = 0.05) compared to healthy subjects. Increased level of Tc17 and CD8+ IFN-γ+ TNF-α+ IL-17+ T cells in relapse phase highlights the critical role of IL-17 in RRMS pathogenesis.
Databáze: OpenAIRE