Characterisation of the immunoglobulin variable region gene usage encoding the murine anti-ganglio side antibody repertoire

被引:30
作者
Boffey, J
Odaka, M
Nicoll, D
Wagner, ER
Townson, K
Bowes, T
Conner, J
Furukawa, K
Willison, HJ [1 ]
机构
[1] So Gen Hosp, Inst Neurol Sci, Univ Dept Neurol, Glasgow G51 4TF, Lanark, Scotland
[2] Glasgow Caledonian Univ, Dept Biol Sci, Glasgow G4 0BA, Lanark, Scotland
[3] Nagoya Univ, Sch Med, Dept Biochem 2, Nagoya, Aichi 466, Japan
基金
英国惠康基金;
关键词
GD3; synthase; ganglioside; neuropathy; monoclonal antibody; variable region gene;
D O I
10.1016/j.jneuroim.2005.04.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neuropathogenic murine antibodies reactive with terminal disialylgalactose epitopes are innate and preferentially encoded by the VH7183.3b gene. Here we have studied antibodies reactive with internal galactose-linked disialosyl epitopes and the terminal trisaccharide of GT1b. Antibodies were of moderate affinity and unmutated. Anti-GD1b antibodies were often encoded by the VH10.2b heavy and gi38e light chain genes. Anti-GT1b antibodies with broader glycan binding patterns were encoded by VHQ52 and VHJ558 family genes. These data indicate that the discrete specificities of ganglioside-binding antibodies are dictated by particular patterns of V gene usage residing within the innate B cell repertoire. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:92 / 103
页数:12
相关论文
共 41 条
[11]   Germline diversity of the expressed BALB/c VhJ558 gene family [J].
Haines, BB ;
Angeles, CV ;
Parmelee, AP ;
McLean, PA ;
Brodeur, PH .
MOLECULAR IMMUNOLOGY, 2001, 38 (01) :9-18
[12]   Anti-disialoside antibodies kill perisynaptic Schwann cells and damage motor nerve terminals via membrane attack complex in a murine model of neuropathy [J].
Halstead, SK ;
O'Hanlon, GM ;
Humphreys, PD ;
Morrison, DB ;
Morgan, BP ;
Todd, AJ ;
Plomp, JJ ;
Willison, HJ .
BRAIN, 2004, 127 :2109-2123
[13]   The primary antibody repertoire of normal, immunodeficient and autoimmune mice is characterized by differences in V gene expression [J].
Kaushik, A ;
Lim, W .
RESEARCH IN IMMUNOLOGY, 1996, 147 (01) :9-26
[14]   IMGT, the international ImMunoGeneTics database® [J].
Lefranc, MP .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :307-310
[15]   High-affinity anti-ganglioside IgG antibodies raised in complex ganglioside knockout mice: Reexamination of GD1a immunolocalization [J].
Lunn, MPT ;
Johnson, LA ;
Fromholt, SE ;
Itonori, S ;
Huang, J ;
Vyas, AA ;
Hildreth, JEK ;
Griffin, JW ;
Schnaar, RL ;
Sheikh, KA .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (01) :404-412
[16]   T-cell-dependent antibody response to the dominant epitope of streptococcal polysaccharide, N-acetyl-glucosamine, is cross-reactive with cardiac myosin [J].
Malkiel, S ;
Liao, L ;
Cunningham, MW ;
Diamond, B .
INFECTION AND IMMUNITY, 2000, 68 (10) :5803-5808
[17]   Marginal zone and B1B cells unite in the early response against T-independent blood-borne particulate antigens [J].
Martin, F ;
Oliver, AM ;
Kearney, JF .
IMMUNITY, 2001, 14 (05) :617-629
[18]   B1 cells: similarities and differences with other B cell subsets [J].
Martin, F ;
Kearney, JF .
CURRENT OPINION IN IMMUNOLOGY, 2001, 13 (02) :195-201
[19]   Molecular analysis of cross-reactive anti-myosin/anti-streptococcal mouse monoclonal antibodies [J].
Mertens, NMJ ;
Galvin, JE ;
Adderson, EE ;
Cunningham, MW .
MOLECULAR IMMUNOLOGY, 2000, 37 (15) :901-913
[20]   Complex gangliosides as autoantibody targets at the neuromuscular junction in Miller Fisher syndrome: A current perspective [J].
O'Hanlon, GM ;
Bullens, RWM ;
Plomp, JJ ;
Willison, HJ .
NEUROCHEMICAL RESEARCH, 2002, 27 (7-8) :697-709