An age-related numerical and functional deficit in CD19+CD24hiCD38hi B cells is associated with an increase in systemic autoimmunity

Aging Cell

Volumn 12, Issue 5, 2013, Pages 873-881

  Duggal, Niharika A ^a   Upton, Jane ^a   Phillips, Anna C ^a   Sapey, Elizabeth ^a   Lord, Janet M ^a  

^a UNIVERSITY DEPARTMENT OF MEDICINE   (United Kingdom)

Author keywords

Autoimmunity; B cells; Cellular immunology; Inflammation; Rheumatoid factor

Indexed keywords

B7 ANTIGEN; CD19 ANTIGEN; CD24 ANTIGEN; CD3 ANTIGEN; CD38 ANTIGEN; CD40 ANTIGEN; CD40 LIGAND; CD86 ANTIGEN; INTERLEUKIN 10; RHEUMATOID FACTOR; STAT3 PROTEIN; TOLL LIKE RECEPTOR;

ADULT; AGED; AGING; ARTICLE; AUTOIMMUNITY; B LYMPHOCYTE; CD4+ T LYMPHOCYTE; CYTOKINE PRODUCTION; CYTOKINE RELEASE; HUMAN; HUMAN CELL; IMMUNE RESPONSE; IMMUNOREGULATION; IMMUNOSUPPRESSIVE TREATMENT; NORMAL HUMAN; PHENOTYPE; PRE B LYMPHOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; T LYMPHOCYTE;

MURINAE;

AUTOIMMUNITY; B CELLS; CELLULAR IMMUNOLOGY; INFLAMMATION; RHEUMATOID FACTOR;

ADULT; AGED; AGED, 80 AND OVER; AGING; ANTIGENS, CD; AUTOIMMUNITY; B-LYMPHOCYTES; CELL DIFFERENTIATION; FEMALE; HUMANS; MALE; MIDDLE AGED; SIGNAL TRANSDUCTION; YOUNG ADULT;

EID: 84883817362     PISSN: 14749718     EISSN: 14749726     Source Type: Journal    
DOI: 10.1111/acel.12114     Document Type: Article

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