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  1. AU="Berta, László"
  2. AU="Barzilay, Regina"
  3. AU="Schmidt, Michael Rahbek"
  4. AU=Tack J
  5. AU="Oh, Hye Min"
  6. AU=Gaffen Sarah L AU=Gaffen Sarah L
  7. AU="Schmitt, Christine"
  8. AU="McKay, Jackie"
  9. AU="Bellissimo, Catherine A"
  10. AU="Desai, Urja"
  11. AU="Chini, Maria Giovanna"
  12. AU="Xiao, Difei"
  13. AU="Ryan, Chris"
  14. AU="Omar Bazighifan"
  15. AU="Corominas Galbany, Jordi"
  16. AU=Fox Norma E
  17. AU="Hamilton, Shelia M"
  18. AU="Nichols, J Wylie"
  19. AU="Pesce R."
  20. AU="Gambitta, P"
  21. AU="Imran, Aqeel"
  22. AU="Sharma, Yashoda"
  23. AU="Kosai, Jordyn"
  24. AU="Aroca Ferri, María"
  25. AU="Laba, Stephanie"
  26. AU="Kim, Ye-Sel"

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  1. Artikel ; Online: Cytokine production pattern of T lymphocytes in neonatal arterial ischemic stroke during the first month of life-a case study.

    Bajnok, Anna / Berta, László / Orbán, Csaba / Tulassay, Tivadar / Toldi, Gergely

    Journal of neuroinflammation

    2018  Band 15, Heft 1, Seite(n) 191

    Abstract: Background: The perinatal period carries the highest risk for stroke in childhood; however, the pathophysiology is poorly understood and preventive, prognostic, and therapeutic strategies are not available. A new pathophysiological model describes the ... ...

    Abstract Background: The perinatal period carries the highest risk for stroke in childhood; however, the pathophysiology is poorly understood and preventive, prognostic, and therapeutic strategies are not available. A new pathophysiological model describes the development of neonatal arterial ischemic stroke (NAIS) as the combined result of prenatal inflammation and hypoxic-ischemic insult. Neuroinflammation and a systemic inflammatory response are also important features of NAIS. Identifying key players of the inflammatory system is in the limelight of current research.
    Case presentation: We present four NAIS cases, in whom detailed analysis of intracellular and plasma cytokine levels are available from the first month of life. All neonates were admitted with the initial diagnosis of hypoxic ischemic encephalopathy (HIE); however, early MRI examination revealed NAIS. Blood samples were collected between 3 and 6 h of life, at 24 h, 72 h, 1 week, and 1 month of life. Peripheral blood mononuclear cells were assessed with flow cytometry and plasma cytokine levels were measured. Pooled data from the cohort of four NAIS patients were compared to infants with HIE. At 6 and 72 h of age, the prevalence of IL10+ CD8+ lymphocytes remained lower in NAIS. At 6 h, CD8+ lymphocytes in NAIS produced more IL-17. At 72 h, CD8+ cells produced more IL-6 in severe HIE than in NAIS, but IL-6 production remained elevated in CD8 cells at 1 month in NAIS, while it decreased in HIE. At 1 week, the prevalence of TGF-β + lymphocytes prone to enter the CNS was elevated in NAIS. On the other hand, by 1 month of age, the prevalence of TGF-β + CD4+ lymphocytes decreased in NAIS compared to HIE. At 72 h, we found elevated plasma levels of IL-5, MCP-1, and IL-17 in NAIS. By 1 month, plasma levels of IL-4, IL-12, and IL-17 decreased in NAIS but remained elevated in HIE.
    Conclusions: Differences in the cytokine network are present between NAIS and HIE. CD8 lymphocytes appear to shift towards the pro-inflammatory direction in NAIS. The inflammatory response appears to be more pronounced at 72 h in NAIS but decreases faster, reaching lower plasma levels of inflammatory markers at 1 month.
    Mesh-Begriff(e) Adolescent ; Cytokines/metabolism ; Female ; Gestational Age ; Humans ; Hypoxia-Ischemia, Brain/complications ; Infant ; Leukocytes, Mononuclear/metabolism ; Leukocytes, Mononuclear/pathology ; Lymphocyte Count ; Magnetic Resonance Imaging ; Male ; Stroke/diagnostic imaging ; Stroke/etiology ; Stroke/pathology ; T-Lymphocytes/metabolism
    Chemische Substanzen Cytokines
    Schlagwörter covid19
    Sprache Englisch
    Erscheinungsdatum 2018-06-22
    Erscheinungsland England
    Dokumenttyp Case Reports ; Journal Article
    ISSN 1742-2094
    ISSN (online) 1742-2094
    DOI 10.1186/s12974-018-1229-y
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: The role of B7 family costimulatory molecules and indoleamine 2,3-dioxygenase in primary Sjögren's syndrome and systemic sclerosis.

    Legány, Nóra / Berta, László / Kovács, László / Balog, Attila / Toldi, Gergely

    Immunologic research

    2017  Band 65, Heft 3, Seite(n) 622–629

    Abstract: B7 costimulatory molecules are present on antigen-presenting cells (APCs) and influence intracellular expression of indoleamine 2,3-dioxygenase (IDO), a molecule with important immunoregulatory functions. We determined the frequency of activated (CD11b+) ...

    Abstract B7 costimulatory molecules are present on antigen-presenting cells (APCs) and influence intracellular expression of indoleamine 2,3-dioxygenase (IDO), a molecule with important immunoregulatory functions. We determined the frequency of activated (CD11b+) monocytes expressing B7-1, B7-2, B7-H1, and B7-H2 molecules, and that of CD3+ and CD4+ T cells expressing the corresponding CD28, CTLA-4, PD-1, and ICOS receptors in peripheral blood samples of 20 healthy adults and 9 SSc and 15 pSS patients using flow cytometry. We also examined the intracellular expression of IDO. The expression of CD28 was lower in both SSc and pSS patients. The frequency of CTLA-4 was increased in pSS. The expression of ICOS, a stimulator of T cell activation, was elevated in pSS, but not in SSc, while that of its corresponding costimulatory molecule, B7-H2, was strongly decreased in SSc compared to controls. The frequency of PD-1 expressing T lymphocytes was decreased in both pSS and SSc. The frequency of IDO-expressing APCs, as well as intracellular IDO content in T cells was higher in pSS than in controls. Our investigation identified a number of differences in B7 costimulation between SSc and pSS patients which may play a role in the distinct pathogenesis and clinical features of these autoimmune disorders.
    Sprache Englisch
    Erscheinungsdatum 2017-06
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 632857-x
    ISSN 1559-0755 ; 0257-277X
    ISSN (online) 1559-0755
    ISSN 0257-277X
    DOI 10.1007/s12026-016-8880-0
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Favorable Outcome After Single-kidney Transplantation From Small Donors in Children: A Match-controlled CERTAIN Registry Study.

    Schild, Raphael / Carvajal Abreu, Karla / Büscher, Anja / Kanzelmeyer, Nele / Lezius, Susanne / Krupka, Kai / Weitz, Marcus / Prytula, Agnieszka / Printza, Nikoleta / Berta, László / Saygılı, Seha Kamil / Sellier-Leclerc, Anne-Laure / Spartà, Giuseppina / Marks, Stephen D / Kemper, Markus J / König, Sabine / Topaloglu, Rezan / Müller, Dominik / Klaus, Günter /
    Weber, Stefanie / Oh, Jun / Herden, Uta / Carraro, Andrea / Dello Strologo, Luca / Ariceta, Gema / Hoyer, Peter / Tönshoff, Burkhard / Pape, Lars

    Transplantation

    2024  

    Abstract: Background: Kidney transplantation (KTx) from small donors is associated with inferior graft survival in registry studies, whereas single-center studies show favorable results.: Methods: We compared 175 pediatric KTx from small donors ≤20 kg (SDKTx) ... ...

    Abstract Background: Kidney transplantation (KTx) from small donors is associated with inferior graft survival in registry studies, whereas single-center studies show favorable results.
    Methods: We compared 175 pediatric KTx from small donors ≤20 kg (SDKTx) with 170 age-matched recipients from adult donors (ADKTx) from 20 centers within the Cooperative European Paediatric Renal Transplant Initiative registry. Graft survival and estimated glomerular filtration rate (eGFR) were analyzed by Cox regression and mixed models. Detailed data on surgical and medical management were tested for association with graft survival.
    Results: One-year graft survival was lower after SDKTx compared with ADKTx (90.9% versus 96.5%; odds ratio of graft loss, 2.92; 95% confidence interval [CI], 1.10-7.80; P = 0.032), but 5-y graft survival was comparable (90.9% versus 92.7%; adjusted hazard ratio of graft loss 1.9; 95% CI, 0.85-4.25; P = 0.119). SDKTx recipients had an annual eGFR increase of 8.7 ± 6.2 mL/min/1.73 m² compared with a decrease of 6.9 ± 5.7 mL/min/1.73 m² in ADKTx recipients resulting in a superior 5-y eGFR (80.5 ± 25.5 in SDKTx versus 65.7 ± 23.1 mL/min/1.73 m² in ADKTx; P = 0.008). At 3 y posttransplant, eGFR after single SDKTx was lower than after en bloc SDKTx (86.6 ± 20.4 versus 104.6 ± 35.9; P = 0.043) but superior to ADKTx (68.1 ± 23.9 mL/min/1.73 m²). Single-kidney SDKTx recipients had a lower rate of hypertension at 3 y than ADKTx recipients (40.0% versus 64.7%; P = 0.008).
    Conclusions: Compared with ADKTx, 5-y graft function is superior in SDKTx and graft survival is similar, even when performed as single KTx. Utilizing small donor organs, preferably as single kidneys in experienced centers, is a viable option to increase the donor pool for pediatric recipients.
    Sprache Englisch
    Erscheinungsdatum 2024-04-30
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 208424-7
    ISSN 1534-6080 ; 0041-1337
    ISSN (online) 1534-6080
    ISSN 0041-1337
    DOI 10.1097/TP.0000000000004993
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: T-Cell Subsets in Rheumatoid Arthritis Patients on Long-Term Anti-TNF or IL-6 Receptor Blocker Therapy.

    Dulic, Sonja / Vásárhelyi, Zsófia / Sava, Florentina / Berta, László / Szalay, Balázs / Toldi, Gergely / Kovács, László / Balog, Attila

    Mediators of inflammation

    2017  Band 2017, Seite(n) 6894374

    Abstract: Data on the impact of biological therapies on the T-cell phenotype in rheumatoid arthritis are limited. Here, we prospectively measured the percentages of 15 circulating T-cell subtypes using flow cytometry. We obtained transversal and longitudinal data ... ...

    Abstract Data on the impact of biological therapies on the T-cell phenotype in rheumatoid arthritis are limited. Here, we prospectively measured the percentages of 15 circulating T-cell subtypes using flow cytometry. We obtained transversal and longitudinal data in 30 anti-TNF responders, 19 secondary anti-TNF nonresponders, and 43 IL-6R antagonist responders, before, 8 weeks and at least 6 months after biological therapy. Untreated RA patients and healthy controls were also included. The important findings are the following: (1) the proportion of regulatory T-cells (Tregs) which are decreased in untreated RA patients becomes normal in all long-term-treated groups; (2) in anti-TNF responders as well as in nonresponders, the frequencies of naïve CD4+ and CD8+ cells are lower, whereas those of proinflammatory Th1, Th2, and Th17 cells and HLA-DR+-activated cells are higher than those in untreated RA or healthy controls; (3) in IL-6R responders, Th1 proportion is decreased, while that of Th2 and Th17 is increased as compared to that in anti-TNF-treated patients and controls; (4) pending confirmation, a CD4CD69 ratio < 2.43 at baseline, could be useful to predict a good therapeutic response to anti-TNF therapy. This study provides comprehensive information regarding the long-term impacts of those biological therapies on the ecotaxis of T-cells in RA. The ClinicalTrials.gov registration number of our study is NCT03266822.
    Mesh-Begriff(e) Adalimumab/therapeutic use ; Adult ; Aged ; Antibodies, Monoclonal/therapeutic use ; Antibodies, Monoclonal, Humanized/therapeutic use ; Arthritis, Rheumatoid/drug therapy ; Arthritis, Rheumatoid/immunology ; CD4-Positive T-Lymphocytes/metabolism ; CD8-Positive T-Lymphocytes/metabolism ; Certolizumab Pegol/therapeutic use ; Cross-Sectional Studies ; Etanercept/therapeutic use ; Female ; Flow Cytometry ; Humans ; Infliximab/therapeutic use ; Male ; Middle Aged ; Receptors, Interleukin-6/antagonists & inhibitors ; Receptors, Interleukin-6/metabolism ; T-Lymphocyte Subsets/metabolism ; T-Lymphocytes, Regulatory/metabolism ; Th17 Cells/metabolism ; Th2 Cells/metabolism ; Tumor Necrosis Factor-alpha/antagonists & inhibitors ; Tumor Necrosis Factor-alpha/metabolism
    Chemische Substanzen Antibodies, Monoclonal ; Antibodies, Monoclonal, Humanized ; Receptors, Interleukin-6 ; Tumor Necrosis Factor-alpha ; golimumab (91X1KLU43E) ; Infliximab (B72HH48FLU) ; Adalimumab (FYS6T7F842) ; tocilizumab (I031V2H011) ; Etanercept (OP401G7OJC) ; Certolizumab Pegol (UMD07X179E)
    Sprache Englisch
    Erscheinungsdatum 2017-10-25
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 1137605-3
    ISSN 1466-1861 ; 0962-9351
    ISSN (online) 1466-1861
    ISSN 0962-9351
    DOI 10.1155/2017/6894374
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Impact of aging on calcium influx and potassium channel characteristics of T lymphocytes.

    Kollár, Szonja / Berta, László / Vásárhelyi, Zsófia Eszter / Balog, Attila / Vásárhelyi, Barna / Rigó, János / Toldi, Gergely

    Oncotarget

    2015  Band 6, Heft 15, Seite(n) 13750–13756

    Abstract: Adaptive immunity and T cell function are affected by aging. Calcium influx patterns, regulated by Kv1.3 and IKCa1 potassium channels, influence T cell activation. We aimed to compare calcium influx kinetics in CD8, Th1 and Th2 cells in human peripheral ... ...

    Abstract Adaptive immunity and T cell function are affected by aging. Calcium influx patterns, regulated by Kv1.3 and IKCa1 potassium channels, influence T cell activation. We aimed to compare calcium influx kinetics in CD8, Th1 and Th2 cells in human peripheral blood samples obtained from five different age groups (cord blood, 10-15 ys, 25-40 ys, 45-55 ys, 60-75 ys).We measured calcium influx using flow cytometry in samples treated with or without specific inhibitors of Kv1.3 and IKCa1 channels (MGTX and TRAM, respectively).Calcium influx was higher in Th1 cells of adults, however, its extent decreased again with aging. Importantly, these changes were not detected in Th2 cells, where the pattern of calcium influx kinetics is similar throughout all investigated age groups. MGTX had a more pronounced inhibitory effect on calcium influx in Th2 cells, while in Th1 cells the same was true for TRAM in the 25-40 ys and 45-55 ys groups. Calcium influx of CD8 cells were inhibited to a similar extent by both applied inhibitors in these groups, and had no effect in the elderly.Altered lymphocyte potassium channel inhibitory patterns, regulators of calcium influx kinetics, might contribute to the development of age-related changes of T cell function.
    Mesh-Begriff(e) Adolescent ; Adult ; Age Factors ; Aged ; CD8-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/metabolism ; Calcium/blood ; Child ; Female ; Fetal Blood/cytology ; Fetal Blood/metabolism ; Humans ; Infant, Newborn ; Lymphocyte Activation ; Male ; Middle Aged ; Potassium Channels/blood ; T-Lymphocytes/immunology ; T-Lymphocytes/metabolism ; Th1 Cells/immunology ; Th1 Cells/metabolism ; Th2 Cells/immunology ; Th2 Cells/metabolism ; Young Adult
    Chemische Substanzen Potassium Channels ; Calcium (SY7Q814VUP)
    Sprache Englisch
    Erscheinungsdatum 2015-05-30
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2560162-3
    ISSN 1949-2553 ; 1949-2553
    ISSN (online) 1949-2553
    ISSN 1949-2553
    DOI 10.18632/oncotarget.3808
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Distinct cytokine patterns may regulate the severity of neonatal asphyxia-an observational study.

    Bajnok, Anna / Berta, László / Orbán, Csaba / Veres, Gábor / Zádori, Dénes / Barta, Hajnalka / Méder, Ünőke / Vécsei, László / Tulassay, Tivadar / Szabó, Miklós / Toldi, Gergely

    Journal of neuroinflammation

    2017  Band 14, Heft 1, Seite(n) 244

    Abstract: Background: Neuroinflammation and a systemic inflammatory reaction are important features of perinatal asphyxia. Neuroinflammation may have dual aspects being a hindrance, but also a significant help in the recovery of the CNS. We aimed to assess ... ...

    Abstract Background: Neuroinflammation and a systemic inflammatory reaction are important features of perinatal asphyxia. Neuroinflammation may have dual aspects being a hindrance, but also a significant help in the recovery of the CNS. We aimed to assess intracellular cytokine levels of T-lymphocytes and plasma cytokine levels in moderate and severe asphyxia in order to identify players of the inflammatory response that may influence patient outcome.
    Methods: We analyzed the data of 28 term neonates requiring moderate systemic hypothermia in a single-center observational study. Blood samples were collected between 3 and 6 h of life, at 24 h, 72 h, 1 week, and 1 month of life. Neonates were divided into a moderate (n = 17) and a severe (n = 11) group based on neuroradiological and amplitude-integrated EEG characteristics. Peripheral blood mononuclear cells were assessed with flow cytometry. Cytokine plasma levels were measured using Bioplex immunoassays. Components of the kynurenine pathway were assessed by high-performance liquid chromatography.
    Results: The prevalence and extravasation of IL-1b + CD4 cells were higher in severe than in moderate asphyxia at 6 h. Based on Receiver operator curve analysis, the assessment of the prevalence of CD4+ IL-1β+ and CD4+ IL-1β+ CD49d+ cells at 6 h appears to be able to predict the severity of the insult at an early stage in asphyxia. Intracellular levels of TNF-α in CD4 cells were increased at all time points compared to 6 h in both groups. At 1 month, intracellular levels of TNF-α were higher in the severe group. Plasma IL-6 levels were higher at 1 week in the severe group and decreased by 1 month in the moderate group. Intracellular levels of IL-6 peaked at 24 h in both groups. Intracellular TGF-β levels were increased from 24 h onwards in the moderate group.
    Conclusions: IL-1β and IL-6 appear to play a key role in the early events of the inflammatory response, while TNF-α seems to be responsible for prolonged neuroinflammation, potentially contributing to a worse outcome. The assessment of the prevalence of CD4+ IL-1β+ and CD4+ IL-1β+ CD49d+ cells at 6 h appears to be able to predict the severity of the insult at an early stage in asphyxia.
    Mesh-Begriff(e) Asphyxia Neonatorum/blood ; Asphyxia Neonatorum/immunology ; Cytokines/blood ; Female ; Humans ; Infant, Newborn ; Male
    Chemische Substanzen Cytokines
    Sprache Englisch
    Erscheinungsdatum 2017-12-12
    Erscheinungsland England
    Dokumenttyp Journal Article ; Observational Study
    ISSN 1742-2094
    ISSN (online) 1742-2094
    DOI 10.1186/s12974-017-1023-2
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: B7 costimulation and intracellular indoleamine 2,3-dioxygenase expression in umbilical cord blood and adult peripheral blood.

    Grozdics, Enikő / Berta, László / Gyarmati, Béla / Veres, Gábor / Zádori, Dénes / Szalárdy, Levente / Vécsei, László / Tulassay, Tivadar / Toldi, Gergely

    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

    2014  Band 20, Heft 10, Seite(n) 1659–1665

    Abstract: Alterations in the expression of B7 costimulatory molecules and their receptors, as well as differences in the tryptophan (TRP) catabolic pathway, may influence immunological reactivity of umbilical cord blood (UCB) compared with adult peripheral blood ( ... ...

    Abstract Alterations in the expression of B7 costimulatory molecules and their receptors, as well as differences in the tryptophan (TRP) catabolic pathway, may influence immunological reactivity of umbilical cord blood (UCB) compared with adult peripheral blood (APB) T lymphocytes. We determined the frequency of activated (CD11b(+)) monocytes expressing B7-1, B7-2, B7-H1, and B7-H2, and that of T cells and CD4(+) T helper cells expressing CD28, cytotoxic T lymphocyte antigen 4 (CTLA-4), programmed death-1 receptor, and inducible costimulator of T cells in UCB and APB samples using flow cytometry. We also examined the intracellular expression of indoleamine 2,3-dioxygenase (IDO) applying flow cytometry and plasma levels of TRP, kynurenine (KYN), and kynurenic acid using high-performance liquid chromatography. The level of CTLA-4 expression on CD4 cells was higher in UCB compared with in APB, indicating that the possibility of CD28-mediated costimulation may be decreased. The level of the corresponding costimulator molecule, B7-2, was also elevated. Therefore, this inhibitory relation may function to a higher extent in UCB than in APB. The plasma KYN to TRP (K/T) ratio was 2-fold higher in UCB compared with APB. However, the capacity of UCB monocytes to produce IDO compared with APB monocytes was lower, and reverse signaling via B7-2 in UCB monocytes was found to be immature, which suggests that the observed increase in K/T ratio may be due to placental, rather than fetal, overexpression of IDO in competent cells. These factors may all contribute to the previously observed reduced reactivity of UCB T lymphocytes compared to APB T cells.
    Mesh-Begriff(e) Adult ; B7 Antigens/genetics ; B7 Antigens/immunology ; CD28 Antigens/genetics ; CD28 Antigens/immunology ; CTLA-4 Antigen/genetics ; CTLA-4 Antigen/immunology ; Fetal Blood/cytology ; Fetal Blood/immunology ; Gene Expression Regulation ; Humans ; Indoleamine-Pyrrole 2,3,-Dioxygenase/genetics ; Indoleamine-Pyrrole 2,3,-Dioxygenase/immunology ; Infant, Newborn ; Kynurenic Acid/immunology ; Kynurenic Acid/metabolism ; Kynurenine/immunology ; Kynurenine/metabolism ; Monocytes/cytology ; Monocytes/immunology ; Primary Cell Culture ; Programmed Cell Death 1 Receptor/genetics ; Programmed Cell Death 1 Receptor/immunology ; Signal Transduction ; T-Lymphocytes, Cytotoxic/cytology ; T-Lymphocytes, Cytotoxic/immunology ; T-Lymphocytes, Helper-Inducer/cytology ; T-Lymphocytes, Helper-Inducer/immunology ; Tryptophan/immunology ; Tryptophan/metabolism
    Chemische Substanzen B7 Antigens ; CD28 Antigens ; CTLA-4 Antigen ; Indoleamine-Pyrrole 2,3,-Dioxygenase ; PDCD1 protein, human ; Programmed Cell Death 1 Receptor ; Kynurenine (343-65-7) ; Tryptophan (8DUH1N11BX) ; Kynurenic Acid (H030S2S85J)
    Sprache Englisch
    Erscheinungsdatum 2014-10
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1474865-4
    ISSN 1523-6536 ; 1083-8791
    ISSN (online) 1523-6536
    ISSN 1083-8791
    DOI 10.1016/j.bbmt.2014.06.008
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: B7 costimulation and intracellular indoleamine-2,3-dioxygenase (IDO) expression in peripheral blood of healthy pregnant and non-pregnant women.

    Grozdics, Enikő / Berta, László / Bajnok, Anna / Veres, Gábor / Ilisz, István / Klivényi, Péter / Rigó, János / Vécsei, László / Tulassay, Tivadar / Toldi, Gergely

    BMC pregnancy and childbirth

    2014  Band 14, Seite(n) 306

    Abstract: Background: B7 costimulatory molecules are expressed on antigen presenting cells (APCs) and are important regulators of T cell activation. We investigated the role of the B7 family of costimulatory molecules in the development of the systemic maternal ... ...

    Abstract Background: B7 costimulatory molecules are expressed on antigen presenting cells (APCs) and are important regulators of T cell activation. We investigated the role of the B7 family of costimulatory molecules in the development of the systemic maternal immune tolerance during healthy pregnancy (HP). We also aimed to investigate the intracellular expression of indoleamine-2,3-dioxygenase (IDO) and plasma levels of tryptophane (TRP), kynurenine (KYN) and kynurenic acid (KYNA), important molecules with immunoregulatory properties, in order to describe their potential contribution to the pregnancy-specific maternal immune tolerance.
    Methods: We determined the frequency of activated (CD11b+) monocytes expressing B7-1, B7-2, B7-H1, and B7-H2, and that of T cells and CD4+ T helper cells expressing CD28, CTLA-4, PD-1, and ICOS in peripheral blood samples of healthy pregnant (HP) and non-pregnant (NP) women using flow cytometry. We also examined the intracellular expression of IDO applying flow cytometry and plasma levels of TRP, KYN and KYNA using high-performance liquid chromatography.
    Results: A significant increase in the prevalence of CD28+ T cells was observed in HP compared to NP women. At the same time a decrease was shown in the expression of CTLA-4 on these cells. The frequency of CD80+ monocytes was lower in HP women. The prevalence of IDO-expressing T cells and monocytes was higher in HP compared to NP women. Plasma KYN, KYNA and TRP levels were lower, while at the same time, the KYN/TRP ratio was higher in HP than in NP women.
    Conclusions: Costimulation via CD28 may not contribute to the immunosuppressive environment, at least in the third trimester of pregnancy. The development of the pregnancy-specific immune tolerance in the mechanism of B7 costimulation may be more related to the altered expression of B7 proteins on APCs rather than that of their receptors on T cells. The elevated intracellular IDO expression in monocytes and T cells, as well as higher plasma enzymatic IDO activity are likely to contribute to the systemic immunosuppressive environment in the third trimester characteristic for healthy gestation.
    Mesh-Begriff(e) Adult ; B7 Antigens/analysis ; CD28 Antigens/analysis ; CD4 Lymphocyte Count ; CTLA-4 Antigen/analysis ; Female ; Flow Cytometry ; Humans ; Immune Tolerance/physiology ; Indoleamine-Pyrrole 2,3,-Dioxygenase/analysis ; Kynurenic Acid/blood ; Kynurenine/blood ; Monocytes/chemistry ; Pregnancy/immunology ; Programmed Cell Death 1 Receptor/analysis ; T-Lymphocytes/chemistry ; Tryptophan/blood
    Chemische Substanzen B7 Antigens ; CD28 Antigens ; CTLA-4 Antigen ; Indoleamine-Pyrrole 2,3,-Dioxygenase ; PDCD1 protein, human ; Programmed Cell Death 1 Receptor ; Kynurenine (343-65-7) ; Tryptophan (8DUH1N11BX) ; Kynurenic Acid (H030S2S85J)
    Sprache Englisch
    Erscheinungsdatum 2014-09-04
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1471-2393
    ISSN (online) 1471-2393
    DOI 10.1186/1471-2393-14-306
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: Diterpenoids from Euphorbia peplus

    Hohmann, Judit / Evanics, Ferenc / Berta, László / Bartók, Tibor

    Planta Medica

    2000  Band 66, Heft 03, Seite(n) 291–294

    Abstract: From a pro-inflammatory active extract of EUPHORBIA PEPLUS, two new diterpene polyesters based on the pepluane and jatrophane skeletons were isolated, together with four known ingenane and jatrophane diterpenes. The structures were determined on the ... ...

    Abstract From a pro-inflammatory active extract of EUPHORBIA PEPLUS, two new diterpene polyesters based on the pepluane and jatrophane skeletons were isolated, together with four known ingenane and jatrophane diterpenes. The structures were determined on the basis of extensive NMR studies. Ingenol 3-angelate, which was obtained for the first time from this plant, is an irritant toxin with high activity.
    Sprache Englisch
    Erscheinungsdatum 2000-01-01
    Erscheinungsort Stuttgart ; New York
    Dokumenttyp Artikel
    ZDB-ID 123545-x
    ISSN 1439-0221 ; 0032-0943
    ISSN (online) 1439-0221
    ISSN 0032-0943
    DOI 10.1055/s-2000-8568
    Datenquelle Thieme Verlag

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