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1.
Mol Cell Endocrinol ; 563: 111855, 2023 03 01.
Article in English | MEDLINE | ID: mdl-36646303

ABSTRACT

The pro-inflammatory cytokine, chemokine (C-C motif) ligand 20 (CCL20), is emerging as a therapeutic target for immune-based therapies. Cooperative regulation of CCL20 by glucocorticoids and progestins used in endocrine therapy and pro-inflammatory mediators could modulate immune function and affect disease outcomes. We show that glucocorticoids as well as medroxyprogesterone acetate (MPA), the progestin widely used in injectable contraception in sub-Saharan Africa, cooperate with pro-inflammatory mediators to upregulate CCL20 protein and/or mRNA in human peripheral blood mononuclear cells (PBMCs) and human cervical cell lines. Changes in CCL20 mRNA levels were shown to be synergistic, as assessed by Chou analysis, cell- and gene-specific and to involve transcriptional regulation, with a requirement for a nuclear factor kappa B (NF-κB) site and glucocorticoid receptor (GR) involvement. The novel results suggest a mechanism whereby MPA, like glucocorticoids, may impact inflammation both systemically and in the genital tract in patients using MPA and/or glucocorticoid therapy.


Subject(s)
Glucocorticoids , Medroxyprogesterone Acetate , Humans , Medroxyprogesterone Acetate/pharmacology , Glucocorticoids/pharmacology , Glucocorticoids/metabolism , Leukocytes, Mononuclear/metabolism , Progestins/metabolism , Receptors, Glucocorticoid/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Chemokine CCL20/genetics , Chemokine CCL20/metabolism
2.
Bioanalysis ; 13(15): 1183-1193, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34114884

ABSTRACT

Aim: Serological assays for the detection of anti-SARS coronavirus-2 (SARS-CoV-2) antibodies are essential to the response to the global pandemic. A ligand binding-based serological assay was validated for the semiquantitative detection of IgG, IgM, IgA and neutralizing antibodies (nAb) against SARS-CoV-2 in serum. Results: The assay demonstrated high levels of diagnostic specificity and sensitivity (85-99% for all analytes). Serum IgG, IgM, IgA and nAb correlated positively (R2 = 0.937, R2 = 0.839, R2 = 0.939 and R2 = 0.501, p < 0.001, respectively) with those measured in dried blood spot samples collected using the hemaPEN® microsampling device (Trajan Scientific and Medical, Victoria, Australia). In vitro SARS-CoV-2 pseudotype neutralization correlated positively with the solid phase nAb signals in convalescent donors (R2 = 0.458, p < 0.05). Conclusion: The assay is applicable in efficacy studies, infection monitoring and postmarketing surveillance following vaccine rollout.


Subject(s)
COVID-19/blood , Dried Blood Spot Testing/methods , High-Throughput Screening Assays/methods , SARS-CoV-2/pathogenicity , Biological Assay , Healthy Volunteers , Humans , Reproducibility of Results
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