Phenotypic characterization of peripheral blood innate immune cell subpopulations in women with endometriosis before and after surgery

2021 ◽  
Vol 10_2021 ◽  
pp. 93-102
Author(s):  
Korotkova T.D. Korotkova ◽  
Krechetova L.V. Krechetova ◽  
Inviyaeva E.V. Inviyaeva ◽  
Vtorushina V.V. Vtorushina V ◽  
Vanko L.V. Vanko ◽  
...  
2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Rossella Cianci ◽  
Simona Frosali ◽  
Danilo Pagliari ◽  
Paola Cesaro ◽  
Lucio Petruzziello ◽  
...  

Background/Aim. Uncomplicated diverticular disease (UDD) is a frequent condition in adults. The pathogenesis of symptoms remains unknown. Bacteria are able to interact with Toll-like receptors (TLRs) and to induce inflammation through both innate immunity and T-cell recruitment. We investigated the pattern of TLRs 2 and 4 and the intestinal homing in patients with UDD before and after a course of Rifaximin.Methods. Forty consecutive patients with UDD and 20 healthy asymptomatic subjects were enrolled. Among UDD patients, 20 were assigned to a 2-month course of treatment with Rifaximin 1.2 g/day for 15 days/month and 20 received placebo. Blood sample and colonic biopsies were obtained from patients and controls. The samples were collected and analyzed at baseline and at the end of treatment. Flow cytometry was performed using monoclonal antibodies (CD3, CD4, CD8, CD103, TCR-gamma/delta, CD14, TLR2, and TLR4).Results. In UDD, TLR2 and TLR4 expression on immune cell subpopulations from blood and mucosa of the affected colon are altered as compared with controls. Rifaximin treatment induced significant modifications of altered conditions.Conclusions. Our data show the role of TLRs in the development of inflammation in UDD. TLRs distribution is altered in UDD and these alterations are reversed after antibiotic treatment. This trial is registered with ClinicalTrials.gov:NCT02068482.


2020 ◽  
Author(s):  
Leonard Daniël Samson ◽  
A. Mieke H. Boots ◽  
José A. Ferreira ◽  
H. Susan J. Picavet ◽  
Lia G. H. De Rond ◽  
...  

Abstract Background: With advancing age, the composition of leukocyte subpopulations in peripheral blood is known to change, but how this change differs between men and women and how it relates to frailty is poorly understood. Thus, our aim in this exploratory study was to investigate whether frailty is associated with changes in immune cell subpopulations and whether associations differ between men and women. Therefore, we performed in-depth immune cell phenotyping by enumerating a total of 37 subsets of T cells, B cells, NK cells, monocytes, and neutrophils in peripheral blood of 289 elderly people between 60-87 years of age. Associations between frailty and each immune cell subpopulation were tested separately in men and women and were adjusted for age and CMV serostatus. In addition, a random forest algorithm was used to predict a participant’s frailty score based on enumeration of immune cell subpopulations. Results: In an association study, frailty was observed to be associated with increases in numbers of neutrophils in both men and in women. Furthermore, sex-specific associations were found. Frailer women, but not men, showed higher numbers of total and CD16^-^ monocytes and lower numbers of CD56^+^ T cells. Overall, the accuracy of the predictions in the random forest analysis was low (9.2% explained variance in men and 12.2% in women). Yet, the random forest analysis confirmed all associations mentioned above, but did not confirm a possible negative association in women between frailty and late differentiated CD4^+^ TemRA cells. Moreover, the random forest analysis revealed additional relationships with frailty, with frailer men showing higher CD16^+^ monocyte and lower naïve B cell numbers. Other important variables for predicting frailty were plasmablast numbers in men and total T cell numbers in women. Conclusions: We report on observed associations of frailty with elevated myeloid cell numbers in men and women. In-depth immune cellular profiling also revealed sex-specific associations of frailty with several immune subpopulations. However, an expected positive association between frailty and memory T cells was not observed. We hope that our study will prompt further investigation into the immune mechanisms associated with the development of frailty in men and women.


2011 ◽  
Vol 3 (5) ◽  
pp. 530-540 ◽  
Author(s):  
Jih-Jin Tsai ◽  
Yen-Hua Jen ◽  
Jung-San Chang ◽  
Hui-Mien Hsiao ◽  
Sansanee Noisakran ◽  
...  

2019 ◽  
Vol 97 (4) ◽  
pp. 416-426 ◽  
Author(s):  
Emily M Mulcahy ◽  
Margaret A Cooley ◽  
Helen McGuire ◽  
Suzanne Asad ◽  
Barbara Fazekas de St Groth ◽  
...  

2016 ◽  
Vol 72 (3) ◽  
pp. 531-534 ◽  
Author(s):  
H. Al-Khalifa ◽  
A. Al-Nasser ◽  
M. Al-Bahouh ◽  
G. Ragheb ◽  
S. Al-Qalaf ◽  
...  

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