Fine-tuning of T lymphocytes in autoimmunity: genetic association of CTLA-4 variants and Graves’ disease revisited

2003 ◽  
Vol 59 (5) ◽  
pp. 555-557 ◽  
Author(s):  
Klaus Badenhoop ◽  
Christian Seidl
Author(s):  
A.M. Madec ◽  
J. Orgiazzi ◽  
A. Stefanutti ◽  
N. Genetet ◽  
B. Genetet ◽  
...  
Keyword(s):  

2010 ◽  
Vol 1804 (3) ◽  
pp. 592-597 ◽  
Author(s):  
Richard V. Parry ◽  
Stephanie J. Harris ◽  
Stephen G. Ward

2019 ◽  
Vol 47 (1) ◽  
pp. 329-337 ◽  
Author(s):  
Ralf Fliegert ◽  
Jörg Heeren ◽  
Friedrich Koch-Nolte ◽  
Viacheslav O. Nikolaev ◽  
Christian Lohr ◽  
...  

Abstract Adenine nucleotides (AdNs) play important roles in immunity and inflammation. Extracellular AdNs, such as adenosine triphosphate (ATP) or nicotinamide adenine dinucleotide (NAD) and their metabolites, act as paracrine messengers by fine-tuning both pro- and anti-inflammatory processes. Moreover, intracellular AdNs derived from ATP or NAD play important roles in many cells of the immune system, including T lymphocytes, macrophages, neutrophils and others. These intracellular AdNs are signaling molecules that transduce incoming signals into meaningful cellular responses, e.g. activation of immune responses against pathogens.


AIDS ◽  
2010 ◽  
Vol 24 (17) ◽  
pp. 2619-2628 ◽  
Author(s):  
Michael S Bennett ◽  
Aviva Joseph ◽  
Hwee L Ng ◽  
Harris Goldstein ◽  
Otto O Yang

2021 ◽  
Vol 67 (6) ◽  
pp. 39-49
Author(s):  
M. A. Dudina ◽  
S. A. Dogadin ◽  
A. A. Savchenko ◽  
V. D. Belenyuk

BACKGROUND: Effective control of autoimmune inflammation in Graves’ disease determines necessity to study the T helper (Th) and cytotoxic T-lymphocytes dysfunction, as well as the level of regulatory T-cells (Treg) activation in patients with Graves’ disease on thyrostatic medication, which will clarify the immunomodulatory effects of long-term thiamazole treatment serve as targets for more specific therapies.AIM: To study the phenotypic composition of T-lymphocytes in the peripheral blood of patients with Graves’ disease to assess the direction of immune response depending on thimazole-induced euthyroidism duration.MATERIALS AND METHODS: A single-center, cohort, continuous, open-label, controlled trial was conducted to assess the phenotypic composition of T-lymphocytes in peripheral blood in women with Graves’ disease on long-term thiamazole treatment. The phenotypic composition of T-lymphocytes was determined by flow cytometry using direct immunofluorescence with conjugated FITC monoclonal antibodies depending on the duration of thimazole-induced euthyroidism of long-term thiamazole treatment.RESULTS: The study included 135 women with Graves’ disease, mean age 43.09±12.81 years, 120 (88.91%) with a relapse of the disease and 15 (11.09%) with newly diagnosed hyperthyroidism. An increase of activated CD3+CD4+CD25+ was found in patients with Graves’ disease with a duration of thimazole-induced euthyroidism 5–8 months and 9–12 months, respectively, Me=0.94 (0.48–1.45), p=0.020) and Me=0.95 (0.41–1.80), p=0.025), in control group — Me=0.12 (0.03–0.68). Compared to the control an increase of CD4+CD25+CD127Low (Treg) was found in patients with a duration of thimazole-induced euthyroidism 5–8 and 9–12 months. The content of Treg in peripheral blood in Graves’ disease patients with a duration of thimazole-induced euthyroidism more than 12 months decreases, but remains elevated relative to the control.CONCLUSION: In patients with Graves’ disease with a duration of thimazole-induced euthyroidism 5–8 months and 9–12 months the level of Treg has been increased. The increase of activated Th (CD3+CD4+CD25+) persists independently of thimazole-induced euthyroidism. In patients with Graves’ disease with a duration of thimazole-induced euthyroidism for more than 12 months, there is a compensatory increase in regulatory T-lymphocyte, and the total number of T-helpers is restored to the control.


1991 ◽  
Vol 124 (6) ◽  
pp. 630-636 ◽  
Author(s):  
R. Paschke ◽  
N. Brückner ◽  
R. Schmeidl ◽  
P. Pfiester ◽  
K. H. Usadel

Abstract. It has been proposed that intrathyroidal lymphocytes, localized in specific anatomical sites might have distinct, pathophysiologically relevant functions in Graves' disease. However, most studies of intrathyroidal lymphocytes were restricted to two lymphocyte locations and used semiquantitative methods. Therefore we used seven anatomically different lymphoid compartments to classify and evaluate by quantitative representative methods the total intrathyroidal lymphocytic infiltration and the staining indexes for immunoglobulin-producing plasmocytes and primed T cells (CD45RO), which provide maximum help to pokeweed mitogen-stimulated immunoglobulin synthesis in 36 thyroid glands from patients with Graves' disease. We found only 3.4% of all intrathyroidal lymphocytes intraepithelially. However, only intraepithelial lymphocytes showed a significantly higher staining index for primed T cells compared with several other compartments. There was also a high staining index for immunoglobulin-producing lymphocytes in this compartment. Kappa- and lambda-positive plasmocytes were found in a polyclonal distribution (kappa:lambda=64.1: 35.9) in all compartments. This increased incidence of CD45RO-positive T lymphocytes and of immunoglobulin-producing lymphocytes among the intraepithelial lymphocytes suggests a distinct pathophysiological function of lymphocytes in peripolesis in Graves' disease. Furthermore, there is a polyclonal intrathyroidal immunoglobulin synthesis.


Gene ◽  
2013 ◽  
Vol 512 (2) ◽  
pp. 300-304 ◽  
Author(s):  
Ting Guo ◽  
Ya'nan Huo ◽  
Wei Zhu ◽  
Fanghua Xu ◽  
Changqin Liu ◽  
...  

Immunobiology ◽  
2016 ◽  
Vol 221 (1) ◽  
pp. 56-62 ◽  
Author(s):  
Yi Fang ◽  
Yanyan Li ◽  
Jing Zeng ◽  
Jingjing Wang ◽  
Ran Liu ◽  
...  

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