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1 apoptotic cells, oxidized phospholipids, and bacterial polysaccharides.
2 r the ABC transporter-dependent synthesis of bacterial polysaccharides.
3 s identified here by probing a microarray of bacterial polysaccharides.
4  for in vivo generation of novel tailor-made bacterial polysaccharides.
5 onses to T-independent (TI) antigens such as bacterial polysaccharides.
6 T-independent type II (TI-2) Ab responses to bacterial polysaccharides.
7 Kdo is also found in a small number of other bacterial polysaccharides.
8  exceeding those formed by immunization with bacterial polysaccharides.
9 found in furanose configuration in plant and bacterial polysaccharides.
10  insight for a wide group of closely related bacterial polysaccharide acetyltransferases.
11  the previously observed differences between bacterial polysaccharide and NP-Ficoll immunogenicity.
12 Antibodies were then analyzed for binding to bacterial polysaccharide and to renal antigens.
13 wn that anti-DNA antibodies cross-react with bacterial polysaccharide and, thus, might be elicited by
14 t a mechanism for the weak immunogenicity of bacterial polysaccharides and explain the previously obs
15 gies employed to generate antibodies against bacterial polysaccharides and proteins rely on the avail
16 unological data related to Ab recognition of bacterial polysaccharides and should be applicable to ot
17 lent cations are important bridging ions for bacterial polysaccharides and since they may play regula
18                                     Although bacterial polysaccharides are considered to be T cell-in
19                            Surface-expressed bacterial polysaccharides are often immunodominant, prot
20 nstrate that Abs generated against conserved bacterial polysaccharides are reactive with and dampen t
21               Immunologic paradigms classify bacterial polysaccharides as T cell-independent antigens
22 s similar to those encoded by genes of other bacterial polysaccharide biosynthesis loci.
23 ohydrates) can substitute for one another in bacterial polysaccharide biosynthesis, even if the enzym
24 on-based signaling network, which alters the bacterial polysaccharide biosynthesis.
25 rve as model systems for the biosynthesis of bacterial polysaccharides by ATP-binding cassette transp
26                               The lengths of bacterial polysaccharides can be critical for their biol
27               Thus, production of Sia-capped bacterial polysaccharide capsules that mimic human cell
28 temic immunization with vaccines composed of bacterial polysaccharides chemically coupled to suitable
29 quivalent to a proline-rich motif of several bacterial polysaccharide co-polymerases and a superfamil
30  aureus, it seems clear that factors such as bacterial polysaccharide components are involved in atta
31 us polysaccharide and with a number of other bacterial polysaccharides containing ribitol and glycero
32  addressed by conjugate vaccines composed of bacterial polysaccharide covalently attached to protein
33 haride protein conjugate vaccines consist of bacterial polysaccharides covalently linked to carrier p
34                                              Bacterial polysaccharides, despite their rich structural
35       Despite this conservation, exposure to bacterial polysaccharides during innate-like B lymphocyt
36 demonstrates that some Abs generated against bacterial polysaccharides engage fungal pathogens and pr
37                    Previously, we found that bacterial polysaccharides enhance poliovirus stability a
38                                     CM101, a bacterial polysaccharide exotoxin produced by group B St
39 PS expressed and demonstrate the fluidity of bacterial polysaccharide expression in response to envir
40                            Pretreatment with bacterial polysaccharide immune globulin led to a signif
41 on of a panel of monosaccharide analogs into bacterial polysaccharides in a highly homogenous manner
42 ysaccharides may uncover novel functions for bacterial polysaccharides in nature, and may lead to the
43 on method was developed in the Laboratory of Bacterial Polysaccharides in the Center for Biologics Ev
44 hetic oligosaccharides, glycoconjugates, and bacterial polysaccharide inhibitors to inhibit the bindi
45  the innate and adaptive immune responses to bacterial polysaccharides is discussed.
46 ion of complex carbohydrates, especially for bacterial polysaccharides, is determination of the absol
47  cell independent type 2 (TI-2) Ags, such as bacterial polysaccharides, is severely impaired in X-lin
48 nd reovirus can be stabilized by bacteria or bacterial polysaccharides, limiting inactivation and aid
49 bstitution that is heretofore unknown in the bacterial polysaccharide literature.
50                                              Bacterial polysaccharide lyases depolymerize GAGs in bet
51 indeed recently showed that response against bacterial polysaccharides mobilize marginal zone B cells
52           The recently discovered fungal and bacterial polysaccharide monooxygenases (PMOs) are capab
53 In this study, we investigated the effect of bacterial polysaccharides on B cell responses to BAFF an
54   The capacity of metal-dependent fungal and bacterial polysaccharide oxygenases, termed GH61 and CBM
55 nd can be readily adapted for use with other bacterial polysaccharide preparations as well.
56                                              Bacterial polysaccharides (PS) are T-independent type 2
57                                              Bacterial polysaccharides (PS) are type 2 T-independent
58 adapted the purpald assay for measurement of bacterial polysaccharides (PS) containing substituted an
59                               Conjugation of bacterial polysaccharides (PS) to protein carriers confe
60 us gut microorganism Bacteroides fragilis, a bacterial polysaccharide (PSA) directs the cellular and
61 of Cell, Kasper and colleagues reveal that a bacterial polysaccharide, PSA, produced by the commensal
62 ds identically, a screening of more than 300 bacterial polysaccharides revealed highly diverging avid
63 illustrate a molecular approach for relating bacterial polysaccharide structure to function, provide
64 ed very similar binding specificities toward bacterial polysaccharides, suggesting that domains 4-7 a
65                         Pel is a GalNAc-rich bacterial polysaccharide that contributes to the structu
66   PAM galactan is one of a growing number of bacterial polysaccharides that exhibit antibiofilm activ
67 polysaccharide is one of a growing number of bacterial polysaccharides that exhibit broad-spectrum, n
68                        Covalent linkage of a bacterial polysaccharide to a protein greatly enhances t
69                        Covalent linkage of a bacterial polysaccharide to an immunogenic protein great
70  conjugate vaccines achieve this by coupling bacterial polysaccharides to a carrier protein that recr
71 as been developed to confirm the identity of bacterial polysaccharides used to formulate a polyvalent
72                                            A bacterial polysaccharide utilization locus (PUL) is a se
73                   Neonatal immunization with bacterial polysaccharide vaccines results in attenuated
74 ved levels with those quoted in studies with bacterial polysaccharide vaccines that had been quantifi
75 age mannose receptor to a range of different bacterial polysaccharides was investigated.
76 xpressing antibodies specific for individual bacterial polysaccharides were expanded in the IgM+ memo
77               These studies demonstrate that bacterial polysaccharides with a distinct charge motif a
78                                     However, bacterial polysaccharides with a zwitterionic charge mot
79   T cells activated in vitro by zwitterionic bacterial polysaccharides (Zps) known to induce abscess