Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Polyclonal, newly derived T cells with low expression of inhibitory molecule PD-1 in tonsils define the phenotype of lymphocytes in children with Periodic Fever, Aphtous Stomatitis, Pharyngitis and Adenitis (PFAPA) syndrome

D. Petra, K. Petra, K. Michaela, K. Daniela, H. Petr, K. Ladislav, K. Rami, H. Ondrej, K. Zdenek, D. Pavla, K. Tomas, F. Eva,

. 2015 ; 65 (1) : 139-147.

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc15022829

Grantová podpora
NT14343 MZ0 CEP - Centrální evidence projektů

PURPOSE: PFAPA syndrome is a benign, recurrent inflammatory disease of childhood. Tonsillectomy is one of the therapeutic options with a yet unexplained biological mechanism. We tested whether specific lymphocyte subsets recruited from blood to human tonsils participate in PFAPA pathogenesis. METHODS: Paired tonsils/peripheral blood (PB) samples were investigated (a) from children with PFAPA that successfully resolved after tonsillectomy (n=10) (b) from children with obstructive sleep apnoea syndrome as controls (n=10). The lymphocyte profiles were analysed using 8-colour flow cytometry, immunoglobulin (IGH) and T-cell receptor (TCR) gene rearrangements via PCR and next generation sequencing; a TREC/KREC analysis was performed using qPCR. RESULTS: The PFAPA tonsils in the asymptomatic phase had a lower percentage of B-lymphocytes than controls; T-lymphocyte counts were significantly higher in PB. The percentages of cytotoxic CD8pos T-lymphocytes were approximately 2-fold higher in PFAPA tonsils; the transitional B cells and naïve stages of both the CD4pos and CD8pos T-lymphocytes with a low expression of PD-1 molecule and high numbers of TREC were also increased. With the exception of elevated plasmablasts, no other differences were significant in PB. The expression levels of CXCL10, CXCL9 and CCL19 genes were significantly higher in PFAPA tonsils. The IGH/TCR pattern showed no clonal/oligoclonal expansion. DNA from the Epstein-Barr virus, Human Herpervirus-6 or adenovirus was detected in 7 of 10 PFAPA tonsils but also in 7 of 9 controls. CONCLUSIONS: Our findings suggest that the uninhibited, polyclonal response of newly derived lymphocytes participate in the pathogenesis of PFAPA. Because most of the observed changes were restricted to tonsils and were not present in PB, they partly explain the therapeutic success of tonsillectomy in PFAPA syndrome.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc15022829
003      
CZ-PrNML
005      
20181211140729.0
007      
ta
008      
150709s2015 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.molimm.2015.01.004 $2 doi
035    __
$a (PubMed)25656804
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Dytrych, Petra $u Department of ENT, Charles University, 2nd Faculty of Medicine, Charles University Prague and University Hospital Motol, Czech Republic. $7 xx0228232
245    10
$a Polyclonal, newly derived T cells with low expression of inhibitory molecule PD-1 in tonsils define the phenotype of lymphocytes in children with Periodic Fever, Aphtous Stomatitis, Pharyngitis and Adenitis (PFAPA) syndrome / $c D. Petra, K. Petra, K. Michaela, K. Daniela, H. Petr, K. Ladislav, K. Rami, H. Ondrej, K. Zdenek, D. Pavla, K. Tomas, F. Eva,
520    9_
$a PURPOSE: PFAPA syndrome is a benign, recurrent inflammatory disease of childhood. Tonsillectomy is one of the therapeutic options with a yet unexplained biological mechanism. We tested whether specific lymphocyte subsets recruited from blood to human tonsils participate in PFAPA pathogenesis. METHODS: Paired tonsils/peripheral blood (PB) samples were investigated (a) from children with PFAPA that successfully resolved after tonsillectomy (n=10) (b) from children with obstructive sleep apnoea syndrome as controls (n=10). The lymphocyte profiles were analysed using 8-colour flow cytometry, immunoglobulin (IGH) and T-cell receptor (TCR) gene rearrangements via PCR and next generation sequencing; a TREC/KREC analysis was performed using qPCR. RESULTS: The PFAPA tonsils in the asymptomatic phase had a lower percentage of B-lymphocytes than controls; T-lymphocyte counts were significantly higher in PB. The percentages of cytotoxic CD8pos T-lymphocytes were approximately 2-fold higher in PFAPA tonsils; the transitional B cells and naïve stages of both the CD4pos and CD8pos T-lymphocytes with a low expression of PD-1 molecule and high numbers of TREC were also increased. With the exception of elevated plasmablasts, no other differences were significant in PB. The expression levels of CXCL10, CXCL9 and CCL19 genes were significantly higher in PFAPA tonsils. The IGH/TCR pattern showed no clonal/oligoclonal expansion. DNA from the Epstein-Barr virus, Human Herpervirus-6 or adenovirus was detected in 7 of 10 PFAPA tonsils but also in 7 of 9 controls. CONCLUSIONS: Our findings suggest that the uninhibited, polyclonal response of newly derived lymphocytes participate in the pathogenesis of PFAPA. Because most of the observed changes were restricted to tonsils and were not present in PB, they partly explain the therapeutic success of tonsillectomy in PFAPA syndrome.
650    _2
$a Adenoviridae $x genetika $x izolace a purifikace $7 D000256
650    _2
$a B-lymfocyty $x imunologie $7 D001402
650    _2
$a CD8-pozitivní T-lymfocyty $x imunologie $7 D018414
650    _2
$a chemokin CCL19 $x biosyntéza $7 D054415
650    _2
$a chemokin CXCL10 $x biosyntéza $7 D054357
650    _2
$a chemokin CXCL9 $x biosyntéza $7 D054370
650    _2
$a dítě $7 D002648
650    _2
$a předškolní dítě $7 D002675
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a horečka neznámého původu $x komplikace $x imunologie $x chirurgie $7 D005335
650    _2
$a virus Epsteinův-Barrové $x genetika $x izolace a purifikace $7 D004854
650    _2
$a lidský herpesvirus 6 $x genetika $x izolace a purifikace $7 D015654
650    _2
$a lidé $7 D006801
650    _2
$a kojenec $7 D007223
650    _2
$a lymfadenitida $x komplikace $x imunologie $x chirurgie $7 D008199
650    _2
$a počet lymfocytů $7 D018655
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a krční mandle $x cytologie $x imunologie $x chirurgie $7 D014066
650    _2
$a faryngitida $x komplikace $x imunologie $x chirurgie $7 D010612
650    _2
$a antigeny CD279 $x biosyntéza $7 D061026
650    _2
$a receptory antigenů T-buněk $x genetika $7 D011948
650    _2
$a obstrukční spánková apnoe $x imunologie $x chirurgie $7 D020181
650    _2
$a aftózní stomatitida $x komplikace $x imunologie $x chirurgie $7 D013281
650    _2
$a T-lymfocyty - podskupiny $x imunologie $7 D016176
650    _2
$a tonzilektomie $7 D014068
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Petra, Krol $u Pediatric Rheumatology Unit, Department of Pediatrics and Adolescent Medicine, Charles University Prague, and General University Hospital in Prague, 1st Faculty of Medicine, Czech Republic.
700    1_
$a Kotrová, Michaela $u CLIP, Department of Paediatric Haematology/Oncology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic. $7 xx0209776
700    1_
$a Daniela, Kuzilkova $u CLIP, Department of Paediatric Haematology/Oncology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic.
700    1_
$a Hubáček, Petr, $u CLIP, Department of Paediatric Haematology/Oncology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic; Department of Medical Microbiology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic. $d 1978- $7 xx0075829
700    1_
$a Krol, Ladislav $u CLIP, Department of Paediatric Haematology/Oncology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic. $7 _AN046471
700    1_
$a Rami, Katra $u Department of ENT, Charles University, 2nd Faculty of Medicine, Charles University Prague and University Hospital Motol, Czech Republic.
700    1_
$a Hrušák, Ondřej, $u CLIP, Department of Paediatric Haematology/Oncology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic. $d 1965- $7 xx0036691
700    1_
$a Kabelka, Zdeněk, $u Department of ENT, Charles University, 2nd Faculty of Medicine, Charles University Prague and University Hospital Motol, Czech Republic. $d 1951-2014 $7 xx0053507
700    1_
$a Doležalová, Pavla, $u Pediatric Rheumatology Unit, Department of Pediatrics and Adolescent Medicine, Charles University Prague, and General University Hospital in Prague, 1st Faculty of Medicine, Czech Republic. $d 1960- $7 nlk20040158529
700    1_
$a Kalina, Tomáš, $u CLIP, Department of Paediatric Haematology/Oncology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic. $d 1975 říjen 11.- $7 xx0060125
700    1_
$a Froňková, Eva, $u CLIP, Department of Paediatric Haematology/Oncology, 2nd Faculty of Medicine, Charles University in Prague and University Hospital Motol, Czech Republic. Electronic address: eva.fronkova@lfmotol.cuni.cz. $d 1977- $7 xx0105058
773    0_
$w MED00003395 $t Molecular immunology $x 1872-9142 $g Roč. 65, č. 1 (2015), s. 139-147
856    41
$u https://pubmed.ncbi.nlm.nih.gov/25656804 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20150709 $b ABA008
991    __
$a 20181211140852 $b ABA008
999    __
$a ok $b bmc $g 1083168 $s 905822
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 65 $c 1 $d 139-147 $i 1872-9142 $m Molecular immunology $n Mol Immunol $x MED00003395
GRA    __
$a NT14343 $p MZ0
LZP    __
$a Pubmed-20150709

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...