IgG Subclasses and Isotypes of VH4-34 Encoded Antibodies

被引:8
作者
Bhat, Neelima M. [1 ]
Kshirsagar, Mihir A. [1 ]
Bieber, Marcia M. [1 ]
Teng, Nelson N. H. [1 ]
机构
[1] Stanford Univ, Sch Med, Div Gynecol Oncol, Dept Gynecol & Obstet, Stanford, CA 94305 USA
关键词
9G4; autoantibodies; HCV; IM; SLE; SYSTEMIC-LUPUS-ERYTHEMATOSUS; MEMORY B-CELLS; MONOCLONAL-ANTIBODIES; GENE SEGMENT; CLASS SWITCH; ANTIGEN; AUTOANTIBODIES; CHILDREN; MUTATION; DISEASE;
D O I
10.3109/08820139.2015.1015682
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
VH4-34 gene encoded autoantibodies are elevated in systemic lupus erythematosus (SLE) and in other diseases associated with B-cell hyperproliferation/dysfunction. One of the autoantigens recognized by VH4-34-encoded antibodies are branched/linear poly N-acetyl lactosamine chains. Since the anti-carbohydrate response in humans is dominated by the IgG2 subclass, here we tested whether VH4-34 encoded IgG showed similar subclass segregation. Serum samples from SLE, infectious mononucleosis, nasopharyngeal carcinoma and hepatitis-C were analyzed. Levels of VH4-34-encoded IgM and IgA isotypes were also tested. VH4-34-IgM and IgA were elevated in all four clinical conditions. VH4-34-IgG was detected in the IgG1 and IgG3 subclass but not in the IgG2 and IgG4 subclass. Interestingly, VH4-34-IgG3 was also detected in serum samples of normal healthy adults. These observations are discussed in context of the VH4-34 gene regulation. VH4-34 repertoire development is of interest since it is the only human VH gene profoundly overrepresented in the naive repertoire but counter-selected for antibody secretion. VH4-34 B-cell could thus become a unique tool to inspect germinal center independent/dependent pathways of subclass and isotype-specific antibody secretion.
引用
收藏
页码:400 / 410
页数:11
相关论文
共 41 条
[41]   Human immunoglobulin selection associated with class switch and possible tolerogenic origins for Cδ class-switched B cells [J].
Zheng, NY ;
Wilson, K ;
Wang, XJ ;
Boston, A ;
Kolar, G ;
Jackson, SM ;
Liu, YJ ;
Pascual, V ;
Capra, JD ;
Wilson, PC .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (08) :1188-1201