In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults. / Müller, K; Zak, M; Nielsen, S; Pedersen, F K; de Nully, P; Bendtzen, K.

I: Pediatric Allergy and Immunology, Bind 7, Nr. 3, 01.08.1996, s. 117-24.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Müller, K, Zak, M, Nielsen, S, Pedersen, FK, de Nully, P & Bendtzen, K 1996, 'In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults', Pediatric Allergy and Immunology, bind 7, nr. 3, s. 117-24.

APA

Müller, K., Zak, M., Nielsen, S., Pedersen, F. K., de Nully, P., & Bendtzen, K. (1996). In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults. Pediatric Allergy and Immunology, 7(3), 117-24.

Vancouver

Müller K, Zak M, Nielsen S, Pedersen FK, de Nully P, Bendtzen K. In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults. Pediatric Allergy and Immunology. 1996 aug. 1;7(3):117-24.

Author

Müller, K ; Zak, M ; Nielsen, S ; Pedersen, F K ; de Nully, P ; Bendtzen, K. / In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults. I: Pediatric Allergy and Immunology. 1996 ; Bind 7, Nr. 3. s. 117-24.

Bibtex

@article{000a557a3f6744d686740c449a2a4354,
title = "In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults",
abstract = "Age related differences in immunological reactions include variations in the in vitro functions of blood mononuclear cells (MNC). In an attempt to understand the mechanism behind these differences we examined age related differences in the phenotype profiles of MNC in parallel with the in vitro production of interleukin IL-6, tumour necrosis factor alpha (TNF alpha) and interferon gamma (IFNg) in neonates, children and adults. In cultures without added polyclonal activators IL-6 and TNF alpha levels in children were 3-6 times higher than those of umbilical cords and adults. However, using optimal in vitro stimulation (E. coli lipopolysaccharide (LPS), phytohaemmagglutinin or pokeweed mitogen (PWM)) no significant differences in the levels of these cytokines were observed. The levels of IFNg in PWM driven cultures followed a different pattern with comparable levels in children and adults, and unmeasurable levels in cord blood MNC. Flow cytometry analysis of the phenotypic distribution of MNC revealed age related differences in the expression of CD3, CD4, CD8, CD14, CD19, CD45RA, CD45R0, CD2, LFA-1, ICAM-1 and LFA-3. Correlation studies did not indicate that the observed differences in cytokine production could be ascribed to differences in the frequency of monocytes, T cells or B cells. The TNF alpha levels in suboptimally stimulated cultures correlated negatively with the expression of LFA-3 and positively with CD45RA, while IFNg correlated positively with CD2, LFA-1, CD45R0 and CD8. In conclusion, the study provides evidence of age related differences in the production of TNF alpha, IL-6 and IFNg among neonates, children and adults. These differences may to some extent be caused by differences in the expression of cell surface molecules involved in cellular interactions and signalling.",
keywords = "Adult, Age Factors, Antigens, CD, Antigens, CD58, B-Lymphocytes, Cells, Cultured, Child, Child, Preschool, Enzyme-Linked Immunosorbent Assay, Female, Fetal Blood, Flow Cytometry, HLA-DR Antigens, Humans, Infant, Newborn, Intercellular Adhesion Molecule-1, Interferon-gamma, Interleukin-6, Leukocytes, Mononuclear, Lipopolysaccharides, Lymphocyte Function-Associated Antigen-1, Male, Monocytes, Phytohemagglutinins, Pokeweed Mitogens, Pregnancy, T-Lymphocytes, Tumor Necrosis Factor-alpha",
author = "K M{\"u}ller and M Zak and S Nielsen and Pedersen, {F K} and {de Nully}, P and K Bendtzen",
year = "1996",
month = aug,
day = "1",
language = "English",
volume = "7",
pages = "117--24",
journal = "Pediatric Allergy and Immunology, Supplement",
issn = "0906-5784",
publisher = "Wiley-Blackwell",
number = "3",

}

RIS

TY - JOUR

T1 - In vitro cytokine production and phenotype expression by blood mononuclear cells from umbilical cords, children and adults

AU - Müller, K

AU - Zak, M

AU - Nielsen, S

AU - Pedersen, F K

AU - de Nully, P

AU - Bendtzen, K

PY - 1996/8/1

Y1 - 1996/8/1

N2 - Age related differences in immunological reactions include variations in the in vitro functions of blood mononuclear cells (MNC). In an attempt to understand the mechanism behind these differences we examined age related differences in the phenotype profiles of MNC in parallel with the in vitro production of interleukin IL-6, tumour necrosis factor alpha (TNF alpha) and interferon gamma (IFNg) in neonates, children and adults. In cultures without added polyclonal activators IL-6 and TNF alpha levels in children were 3-6 times higher than those of umbilical cords and adults. However, using optimal in vitro stimulation (E. coli lipopolysaccharide (LPS), phytohaemmagglutinin or pokeweed mitogen (PWM)) no significant differences in the levels of these cytokines were observed. The levels of IFNg in PWM driven cultures followed a different pattern with comparable levels in children and adults, and unmeasurable levels in cord blood MNC. Flow cytometry analysis of the phenotypic distribution of MNC revealed age related differences in the expression of CD3, CD4, CD8, CD14, CD19, CD45RA, CD45R0, CD2, LFA-1, ICAM-1 and LFA-3. Correlation studies did not indicate that the observed differences in cytokine production could be ascribed to differences in the frequency of monocytes, T cells or B cells. The TNF alpha levels in suboptimally stimulated cultures correlated negatively with the expression of LFA-3 and positively with CD45RA, while IFNg correlated positively with CD2, LFA-1, CD45R0 and CD8. In conclusion, the study provides evidence of age related differences in the production of TNF alpha, IL-6 and IFNg among neonates, children and adults. These differences may to some extent be caused by differences in the expression of cell surface molecules involved in cellular interactions and signalling.

AB - Age related differences in immunological reactions include variations in the in vitro functions of blood mononuclear cells (MNC). In an attempt to understand the mechanism behind these differences we examined age related differences in the phenotype profiles of MNC in parallel with the in vitro production of interleukin IL-6, tumour necrosis factor alpha (TNF alpha) and interferon gamma (IFNg) in neonates, children and adults. In cultures without added polyclonal activators IL-6 and TNF alpha levels in children were 3-6 times higher than those of umbilical cords and adults. However, using optimal in vitro stimulation (E. coli lipopolysaccharide (LPS), phytohaemmagglutinin or pokeweed mitogen (PWM)) no significant differences in the levels of these cytokines were observed. The levels of IFNg in PWM driven cultures followed a different pattern with comparable levels in children and adults, and unmeasurable levels in cord blood MNC. Flow cytometry analysis of the phenotypic distribution of MNC revealed age related differences in the expression of CD3, CD4, CD8, CD14, CD19, CD45RA, CD45R0, CD2, LFA-1, ICAM-1 and LFA-3. Correlation studies did not indicate that the observed differences in cytokine production could be ascribed to differences in the frequency of monocytes, T cells or B cells. The TNF alpha levels in suboptimally stimulated cultures correlated negatively with the expression of LFA-3 and positively with CD45RA, while IFNg correlated positively with CD2, LFA-1, CD45R0 and CD8. In conclusion, the study provides evidence of age related differences in the production of TNF alpha, IL-6 and IFNg among neonates, children and adults. These differences may to some extent be caused by differences in the expression of cell surface molecules involved in cellular interactions and signalling.

KW - Adult

KW - Age Factors

KW - Antigens, CD

KW - Antigens, CD58

KW - B-Lymphocytes

KW - Cells, Cultured

KW - Child

KW - Child, Preschool

KW - Enzyme-Linked Immunosorbent Assay

KW - Female

KW - Fetal Blood

KW - Flow Cytometry

KW - HLA-DR Antigens

KW - Humans

KW - Infant, Newborn

KW - Intercellular Adhesion Molecule-1

KW - Interferon-gamma

KW - Interleukin-6

KW - Leukocytes, Mononuclear

KW - Lipopolysaccharides

KW - Lymphocyte Function-Associated Antigen-1

KW - Male

KW - Monocytes

KW - Phytohemagglutinins

KW - Pokeweed Mitogens

KW - Pregnancy

KW - T-Lymphocytes

KW - Tumor Necrosis Factor-alpha

M3 - Journal article

C2 - 9116875

VL - 7

SP - 117

EP - 124

JO - Pediatric Allergy and Immunology, Supplement

JF - Pediatric Allergy and Immunology, Supplement

SN - 0906-5784

IS - 3

ER -

ID: 33494082