2022
DOI: 10.1016/j.clim.2022.109166
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Peripheral immunophenotypes associated with the flare in the systemic lupus erythematosus patients with low disease activity state

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Cited by 3 publications
(3 citation statements)
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“…The present study was performed in an attempt to estimate a possible correlation between T cell immunity and DN B lymphocytes in patients with SLE. DN B cells consist of a certain subpopulation, which is significantly increased in the elderly but also in several chronic inflammatory diseases, including SLE [ 7 , 11 , 16 , 17 , 18 ]. Their origin, function, and differential status is still unclear, as they carry characteristics of both naïve, switched memory, and immune-exhausted cells [ 6 , 7 ].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The present study was performed in an attempt to estimate a possible correlation between T cell immunity and DN B lymphocytes in patients with SLE. DN B cells consist of a certain subpopulation, which is significantly increased in the elderly but also in several chronic inflammatory diseases, including SLE [ 7 , 11 , 16 , 17 , 18 ]. Their origin, function, and differential status is still unclear, as they carry characteristics of both naïve, switched memory, and immune-exhausted cells [ 6 , 7 ].…”
Section: Discussionmentioning
confidence: 99%
“…SLE, as well as other systemic autoimmune diseases, is associated with a significant increase in DN B lymphocytes, both DN1 and DN2. From those, DN2 B cells are most important, as they act as antigen-presenting cells and stimulate T cell response, differentiate into antibody and cytokine-secreting cells, and modulate immune response, sustained autoimmunity, and inflammation [ 16 , 17 , 18 , 19 ]. DN2 B lymphocytes share similar characteristics with naïve B lymphocytes, such as the absence of CXCR5, CD24, and CD38 surface molecules, which are common in the rest of peripheral B lymphocyte subsets, but also retain a unique phenotype, expressing CD69, HLA-DR, CD86, and the regulatory receptors CD32b and CD22, and lacking the lymph node homing receptor L-selectin (CD62L) [ 7 , 9 , 20 ].…”
Section: Discussionmentioning
confidence: 99%
“…The pathogenesis of SLE is likely based on genetic susceptibility factors of the body due to infection, ultraviolet (UV) irradiation, and other factors, inducing immune disorders that result in an abnormal activation of autoreactive T and B lymphocytes, the production of a large number of autoantibodies, immune complex formation and deposition, which lead to deregulated inflammation and multiorgan injuries ( George and Tsokos, 2011 ; Lech and Anders, 2013 ; Marianthi Kiriakidou and Cathy Lee Ching, 2020 ). Jian Zheng ( Zheng et al, 2022 )analyzed the B and T cell subsets comparing SLE patients in the low activity phase and healthy controls, and the T and B cell axes showed abnormalities, and the proportion of double negative B cells and CD8 + T cells was significantly reduced, the results indicated that the immune phenotype and the incidence of the disease were closely related. Autophagy affects the pathogenesis of SLE in many ways.…”
Section: Autophagy and Immunological Aberrations In Slementioning
confidence: 99%