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
[1]   9G4+Antibodies Isolated from HIV-Infected Patients Neutralize HIV-1 and Have Distinct Autoreactivity Profiles [J].
Alcena, Danielle C. ;
Kobie, James J. ;
Kaminski, Denise A. ;
Rosenberg, Alexander F. ;
Mattiacio, Jonelle L. ;
Brewer, Matthew ;
Dewhurst, Stephen ;
Dykes, Carrie ;
Jin, Xia ;
Keefer, Michael C. ;
Sanz, Ignacio .
PLOS ONE, 2013, 8 (12)
[2]   The anergic B cell [J].
Andrews, Sarah F. ;
Wilson, Patrick C. .
BLOOD, 2010, 115 (24) :4976-4978
[3]   T Cell-Independent IgA Class Switch Recombination Is Restricted to the GALT and Occurs Prior to Manifest Germinal Center Formation [J].
Bergqvist, Peter ;
Stensson, Anneli ;
Lycke, Nils Y. ;
Bemark, Mats .
JOURNAL OF IMMUNOLOGY, 2010, 184 (07) :3545-3553
[4]   Human memory B cells originate from three distinct germinal center-dependent and -independent maturation pathways [J].
Berkowska, Magdalena A. ;
Driessen, Gertjan J. A. ;
Bikos, Vasilis ;
Grosserichter-Wagener, Christina ;
Stamatopoulos, Kostas ;
Cerutti, Andrea ;
He, Bing ;
Biermann, Katharina ;
Lange, Johan F. ;
van der Burg, Mirjam ;
van Dongen, Jacques J. M. ;
van Zelm, Menno C. .
BLOOD, 2011, 118 (08) :2150-2158
[5]  
Bhat Neelima M, 2004, Hum Antibodies, V13, P63
[6]  
BHAT NM, 1993, J IMMUNOL, V151, P5011
[7]  
Bhat NM, 2002, J RHEUMATOL, V29, P2114
[8]   Rapid cytotoxicity of human B lymphocytes induced by VH4-34 (VH4.21) gene-encoded monoclonal antibodies .2. [J].
Bhat, NM ;
Bieber, MM ;
Hsu, FJ ;
Chapman, CJ ;
Spellerberg, M ;
Stevenson, FK ;
Teng, NNH .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 108 (01) :151-159
[9]   Serum IgG1 and IgG2 antibody responses to Porphyromonas gingivalis in patients with periodontitis [J].
Booth, V ;
Solakoglu, Ö ;
Bavisha, N ;
Curtis, MA .
ORAL MICROBIOLOGY AND IMMUNOLOGY, 2006, 21 (02) :93-99
[10]   PRODUCTION OF HUMAN MONOCLONAL IGG ANTIBODIES AGAINST RHESUS (D) ANTIGEN [J].
BRON, D ;
FEINBERG, MB ;
TENG, NNH ;
KAPLAN, HS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (10) :3214-3217