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1 recently have raised several monoclonal IgG anti-ganglioside antibodies.
2 mice that received systemically administered anti-ganglioside antibodies.
3 s a postinfectious autoimmune neuropathy and anti-ganglioside antibodies (Abs) are strongly associate
5 GBS, and in particular its association with anti-ganglioside antibodies and a primary axonal neuropa
6 nstrate first, that both GBS sera containing anti-ganglioside antibodies and monoclonal anti-ganglios
7 ediated injury over this time scale and that anti-ganglioside antibodies and the cholera toxin B subu
8 tissues contribute to target recognition by anti-ganglioside antibodies and this observation provide
9 major unexpected pathway by which pathogenic anti-ganglioside antibodies, and potentially other gangl
10 eview those studies, which clearly show that anti-ganglioside antibodies are capable of binding to NM
11 In axonal forms of Guillain-Barre syndrome, anti-ganglioside antibodies bind gangliosides on nerve s
12 investigated whether endocytic clearance of anti-ganglioside antibodies by nerve terminals might als
13 injury are not completely resolved: (i) some anti-ganglioside antibodies can cross-react with glycopr
15 g anti-ganglioside antibodies and monoclonal anti-ganglioside antibodies cause neuronal cell lysis by
16 sive transfer with systemically administered anti-ganglioside antibodies did not cause nerve fiber de
19 ransmitter recycling, are able to endocytose anti-ganglioside antibodies from the cell surface so rap
20 cluding our own, have studied the effects of anti-ganglioside antibodies in ex vivo and in vivo exper
22 pathological evidence to support a role for anti-ganglioside antibodies in mediating nerve terminal
24 ally be used for screening of (i) pathogenic anti-ganglioside antibodies in patients with immune-medi
26 ues, we developed and characterized a simple anti-ganglioside antibody-mediated cytotoxicity assay.
27 brane pool appears to be more susceptible to anti-ganglioside antibody-mediated injury than the GM1 p
30 lysing electrophysiologically the effects of anti-ganglioside antibodies on nerve function, possibly
31 from human and animal studies indicates that anti-ganglioside antibodies play a primary neuropathogen
32 ization with a melanoma cell vaccine induced anti-ganglioside antibody responses in melanoma patients
33 s implanted with an intraperitoneal clone of anti-ganglioside antibody-secreting hybridoma developed
34 inals of neuromuscular junctions, from where anti-ganglioside antibody was retrogradely transported t
35 in 81% of AMAN and 50% of AIDP patients, and anti-ganglioside antibodies were common in both Campylob
37 e immunostained to differing levels with the anti-ganglioside antibodies, whereas neural cells from m
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