The Imbalance of B-Lymphocyte Subsets in Subjects with Different Glucose Tolerance: Relationship with Metabolic Parameter and Disease Status

B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D (n=60), impaired glucose regulation (IGR, n=73), and normal gluco...

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Published inJournal of Diabetes Research Vol. 2017; no. 2017; pp. 1 - 9
Main Authors Wang, Xiangbing, Zhou, Z. G., Huang, Gan, Deng, Chao, Xiang, Yufei, Tan, Tingting, Ren, Zhihui, Cao, Chuqing, Liu, Bingwen
Format Journal Article
LanguageEnglish
Published Cairo, Egypt Hindawi Publishing Corporation 01.01.2017
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John Wiley & Sons, Inc
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Abstract B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D (n=60), impaired glucose regulation (IGR, n=73), and normal glucose tolerance (NGT, n=169) by flow cytometry. T2D subjects had an increased percentage of CD19+CD23+ (B-2) cells and a decreased percentage of CD19+CD23− (B-1) cells attributing to CD19+CD23−CD5− (B-1b) cells, but not CD19+CD23−CD5+ (B-1a) cells, compared to NGT and IGR subjects. The proportion of CD19+CD5+CD1dhi (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.
AbstractList B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D (n=60), impaired glucose regulation (IGR, n=73), and normal glucose tolerance (NGT, n=169) by flow cytometry. T2D subjects had an increased percentage of CD19+CD23+ (B-2) cells and a decreased percentage of CD19+CD23− (B-1) cells attributing to CD19+CD23−CD5− (B-1b) cells, but not CD19+CD23−CD5+ (B-1a) cells, compared to NGT and IGR subjects. The proportion of CD19+CD5+CD1dhi (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.
B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D (n = 60), impaired glucose regulation (IGR, n = 73), and normal glucose tolerance (NGT, n = 169) by flow cytometry. T2D subjects had an increased percentage of CD19+CD23+ (B-2) cells and a decreased percentage of CD19+CD23- (B-1) cells attributing to CD19+CD23-CD5- (B-1b) cells, but not CD19+CD23-CD5+ (B-1a) cells, compared to NGT and IGR subjects. The proportion of CD19+CD5+CD1dhi (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D (n = 60), impaired glucose regulation (IGR, n = 73), and normal glucose tolerance (NGT, n = 169) by flow cytometry. T2D subjects had an increased percentage of CD19+CD23+ (B-2) cells and a decreased percentage of CD19+CD23- (B-1) cells attributing to CD19+CD23-CD5- (B-1b) cells, but not CD19+CD23-CD5+ (B-1a) cells, compared to NGT and IGR subjects. The proportion of CD19+CD5+CD1dhi (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.
B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D (n = 60), impaired glucose regulation (IGR, n = 73), and normal glucose tolerance (NGT, n = 169) by flow cytometry. T2D subjects had an increased percentage of [CD19.sup.+][CD23.sup.+] (B-2) cells and a decreased percentage of [CD19.sup.+][CD23.sup.-] (B-1) cells attributing to [CD19.sup.+][CD23.sup.-][CD5.sup.-] (B-1b) cells, but not [CD19.sup.+][CD23.sup.-][CD5.sup.+] (B-1a) cells, compared to NGT and IGR subjects. The proportion of [CD19.sup.+][CD5.sup.+][CD1d.sup.hi] (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.
B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D ( n = 60 ), impaired glucose regulation (IGR, n = 73 ), and normal glucose tolerance (NGT, n = 169 ) by flow cytometry. T2D subjects had an increased percentage of CD19 + CD23 + (B-2) cells and a decreased percentage of CD19 + CD23 − (B-1) cells attributing to CD19 + CD23 − CD5 − (B-1b) cells, but not CD19 + CD23 − CD5 + (B-1a) cells, compared to NGT and IGR subjects. The proportion of CD19 + CD5 + CD1d hi (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.
B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D ( = 60), impaired glucose regulation (IGR, = 73), and normal glucose tolerance (NGT, = 169) by flow cytometry. T2D subjects had an increased percentage of CD19 CD23 (B-2) cells and a decreased percentage of CD19 CD23 (B-1) cells attributing to CD19 CD23 CD5 (B-1b) cells, but not CD19 CD23 CD5 (B-1a) cells, compared to NGT and IGR subjects. The proportion of CD19 CD5 CD1d (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.
B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype and frequency of B-lymphocyte subsets in subjects recently diagnosed with T2D ( n = 60), impaired glucose regulation (IGR, n = 73), and normal glucose tolerance (NGT, n = 169) by flow cytometry. T2D subjects had an increased percentage of CD19 + CD23 + (B-2) cells and a decreased percentage of CD19 + CD23 − (B-1) cells attributing to CD19 + CD23 − CD5 − (B-1b) cells, but not CD19 + CD23 − CD5 + (B-1a) cells, compared to NGT and IGR subjects. The proportion of CD19 + CD5 + CD1d hi (B10) cells did not differ between the IGR or T2D group and NGT controls. Of note, HbA1c and triglyceride showed a positive correlation with B-2 cells but an inverse correlation with B-1 and B-1b cells, which were independently associated with the presence of T2D by logistic regression models. In summary, this study shows an unbalanced proinflammatory phenotype of B-cell subsets correlated with glycemia and lipidemia in patients with T2D. Our data provide new insight into chronic activation of the immune system and subclinical inflammation in T2D. Further prospective studies are warranted to confirm our observations.
Audience Academic
Author Zhou, Z. G.
Tan, Tingting
Wang, Xiangbing
Cao, Chuqing
Deng, Chao
Ren, Zhihui
Xiang, Yufei
Liu, Bingwen
Huang, Gan
AuthorAffiliation 3 Division of Endocrinology, Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA
1 Department of Metabolism & Endocrinology, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China
2 Key Laboratory of Diabetes Immunology, Central South University, Ministry of Education, National Clinical Research Center for Metabolic Diseases, Changsha, Hunan 410011, China
AuthorAffiliation_xml – name: 1 Department of Metabolism & Endocrinology, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, China
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Snippet B lymphocytes are involved in inflammation and are related to insulin resistance in obesity and type 2 diabetes (T2D). This study investigated the phenotype...
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SubjectTerms Adult
Antibodies
Antigens, CD19 - immunology
B cells
B-Lymphocyte Subsets - immunology
B-Lymphocytes - immunology
Blood Glucose - metabolism
Blood pressure
Body mass index
Care and treatment
Case-Control Studies
CD5 Antigens - immunology
Cholesterol
Cytokines
Diabetes
Diabetes Mellitus, Type 2 - immunology
Diabetes Mellitus, Type 2 - metabolism
Diagnosis
Female
Flow Cytometry
Glucose
Glucose Intolerance - immunology
Glucose Intolerance - metabolism
Glucose tolerance tests
Glycated Hemoglobin A - metabolism
Humans
Inflammation
Insulin Resistance
Laboratories
Lipoproteins
Logistic Models
Male
Metabolism
Middle Aged
Obesity
Peptides
Plasma
Receptors, IgE - immunology
Regulation
Software
Triglycerides
Triglycerides - metabolism
Type 2 diabetes
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Title The Imbalance of B-Lymphocyte Subsets in Subjects with Different Glucose Tolerance: Relationship with Metabolic Parameter and Disease Status
URI https://search.emarefa.net/detail/BIM-1174386
https://dx.doi.org/10.1155/2017/5052812
https://www.ncbi.nlm.nih.gov/pubmed/28491871
https://www.proquest.com/docview/2407644713
https://www.proquest.com/docview/1897804894
https://pubmed.ncbi.nlm.nih.gov/PMC5410374
https://doaj.org/article/99c8f2acf24a4da2beda7a88cf003d30
Volume 2017
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