2016
Decreased Numbers of CD57(+)CD3(-) Cells Identify Potential Innate Immune Differences in Patients with Autism Spectrum Disorder
SINISCALCO, Dario; Tatjana MIJATOVIC; Eugene BOSMANS; Alessandra CIRILLO; Peter KRUŽLIAK et. al.Základní údaje
Originální název
Decreased Numbers of CD57(+)CD3(-) Cells Identify Potential Innate Immune Differences in Patients with Autism Spectrum Disorder
Autoři
SINISCALCO, Dario (380 Itálie); Tatjana MIJATOVIC (380 Itálie); Eugene BOSMANS (56 Belgie); Alessandra CIRILLO (56 Belgie); Peter KRUŽLIAK (703 Slovensko, domácí); Vincent C. LOMBARDI (840 Spojené státy); Kenny DE MEIRLEIR (840 Spojené státy) a Nicola ANTONUCCI (380 Itálie)
Vydání
In vivo, ATHENS, Greece : International Institute of Anticancer Research, 2016, 0258-851X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30212 Surgery
Stát vydavatele
Řecko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 0.953
Kód RIV
RIV/00216224:14110/16:00100477
Organizační jednotka
Lékařská fakulta
UT WoS
000371066900002
Klíčová slova anglicky
Autism; CD57(+)CD3(-) lymphocytes; HNK-1; immune dysfunction
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 17. 5. 2018 12:32, Soňa Böhmová
Anotace
V originále
Background/Aim: Autism spectrum disorders (ASD) are complex, and severe heterogeneous neurodevelopmental pathologies with accepted but complex immune system abnormalities. Additional knowledge regarding potential immune dysfunctions may provide a greater understanding of this malady. The aim of this study was to evaluate the CD57(+)CD3(-) mature lymphocyte subpopulation of natural killer cells as a marker of immune dysfunction in ASD. Materials and Methods: Three-color flow cytometry-based analysis of fresh peripheral blood samples from children with autism was utilized to measure CD57(+)CD3(-) lymphocytes. Results. A reduction of CD57(+)CD3(-) lymphocyte count was recorded in a significant number of patients with autism. Discussion and conclusion: We demonstrated that the number of peripheral CD57(+)CD3(-) cells in children with autism often falls below the clinically accepted normal range. This implies that a defect in the counter-regulatory functions necessary for balancing pro-inflammatory cytokines exists, thus opening the way to chronic inflammatory conditions associated with ASD.