ライフサイエンスコーパス: bacterial polysaccharide

1 apoptotic cells, oxidized phospholipids, and bacterial polysaccharides.

2 r the ABC transporter-dependent synthesis of bacterial polysaccharides.

3 Kdo is also found in a small number of other bacterial polysaccharides.

4 s identified here by probing a microarray of bacterial polysaccharides.

5 for in vivo generation of novel tailor-made bacterial polysaccharides.

6 onses to T-independent (TI) antigens such as bacterial polysaccharides.

7 T-independent type II (TI-2) Ab responses to bacterial polysaccharides.

8 exceeding those formed by immunization with bacterial polysaccharides.

9 insight for a wide group of closely related bacterial polysaccharide acetyltransferases.

10 the previously observed differences between bacterial polysaccharide and NP-Ficoll immunogenicity.

11 Antibodies were then analyzed for binding to bacterial polysaccharide and to renal antigens.

12 wn that anti-DNA antibodies cross-react with bacterial polysaccharide and, thus, might be elicited by

13 t a mechanism for the weak immunogenicity of bacterial polysaccharides and explain the previously obs

14 unological data related to Ab recognition of bacterial polysaccharides and should be applicable to ot

15 lent cations are important bridging ions for bacterial polysaccharides and since they may play regula

16 Although bacterial polysaccharides are considered to be T cell-in

17 Surface-expressed bacterial polysaccharides are often immunodominant, prot

18 nstrate that Abs generated against conserved bacterial polysaccharides are reactive with and dampen t

19 Immunologic paradigms classify bacterial polysaccharides as T cell-independent antigens

20 s similar to those encoded by genes of other bacterial polysaccharide biosynthesis loci.

21 ohydrates) can substitute for one another in bacterial polysaccharide biosynthesis, even if the enzym

22 rve as model systems for the biosynthesis of bacterial polysaccharides by ATP-binding cassette transp

23 The lengths of bacterial polysaccharides can be critical for their biol

24 Thus, production of Sia-capped bacterial polysaccharide capsules that mimic human cell

25 temic immunization with vaccines composed of bacterial polysaccharides chemically coupled to suitable

26 quivalent to a proline-rich motif of several bacterial polysaccharide co-polymerases and a superfamil

27 aureus, it seems clear that factors such as bacterial polysaccharide components are involved in atta

28 us polysaccharide and with a number of other bacterial polysaccharides containing ribitol and glycero

29 addressed by conjugate vaccines composed of bacterial polysaccharide covalently attached to protein

30 Bacterial polysaccharides, despite their rich structural

31 Despite this conservation, exposure to bacterial polysaccharides during innate-like B lymphocyt

32 demonstrates that some Abs generated against bacterial polysaccharides engage fungal pathogens and pr

33 CM101, a bacterial polysaccharide exotoxin produced by group B St

34 PS expressed and demonstrate the fluidity of bacterial polysaccharide expression in response to envir

35 Pretreatment with bacterial polysaccharide immune globulin led to a signif

36 on of a panel of monosaccharide analogs into bacterial polysaccharides in a highly homogenous manner

37 ysaccharides may uncover novel functions for bacterial polysaccharides in nature, and may lead to the

38 on method was developed in the Laboratory of Bacterial Polysaccharides in the Center for Biologics Ev

39 hetic oligosaccharides, glycoconjugates, and bacterial polysaccharide inhibitors to inhibit the bindi

40 the innate and adaptive immune responses to bacterial polysaccharides is discussed.

41 ion of complex carbohydrates, especially for bacterial polysaccharides, is determination of the absol

42 cell independent type 2 (TI-2) Ags, such as bacterial polysaccharides, is severely impaired in X-lin

43 bstitution that is heretofore unknown in the bacterial polysaccharide literature.

44 Bacterial polysaccharide lyases depolymerize GAGs in bet

45 The recently discovered fungal and bacterial polysaccharide monooxygenases (PMOs) are capab

46 In this study, we investigated the effect of bacterial polysaccharides on B cell responses to BAFF an

47 The capacity of metal-dependent fungal and bacterial polysaccharide oxygenases, termed GH61 and CBM

48 nd can be readily adapted for use with other bacterial polysaccharide preparations as well.

49 Bacterial polysaccharides (PS) are T-independent type 2

50 Bacterial polysaccharides (PS) are type 2 T-independent

51 adapted the purpald assay for measurement of bacterial polysaccharides (PS) containing substituted an

52 Conjugation of bacterial polysaccharides (PS) to protein carriers confe

53 us gut microorganism Bacteroides fragilis, a bacterial polysaccharide (PSA) directs the cellular and

54 of Cell, Kasper and colleagues reveal that a bacterial polysaccharide, PSA, produced by the commensal

55 ds identically, a screening of more than 300 bacterial polysaccharides revealed highly diverging avid

56 illustrate a molecular approach for relating bacterial polysaccharide structure to function, provide

57 ed very similar binding specificities toward bacterial polysaccharides, suggesting that domains 4-7 a

58 PAM galactan is one of a growing number of bacterial polysaccharides that exhibit antibiofilm activ

59 polysaccharide is one of a growing number of bacterial polysaccharides that exhibit broad-spectrum, n

60 Covalent linkage of a bacterial polysaccharide to a protein greatly enhances t

61 Covalent linkage of a bacterial polysaccharide to an immunogenic protein great

62 conjugate vaccines achieve this by coupling bacterial polysaccharides to a carrier protein that recr

63 as been developed to confirm the identity of bacterial polysaccharides used to formulate a polyvalent

64 A bacterial polysaccharide utilization locus (PUL) is a se

65 Neonatal immunization with bacterial polysaccharide vaccines results in attenuated

66 ved levels with those quoted in studies with bacterial polysaccharide vaccines that had been quantifi

67 age mannose receptor to a range of different bacterial polysaccharides was investigated.

68 xpressing antibodies specific for individual bacterial polysaccharides were expanded in the IgM+ memo

69 These studies demonstrate that bacterial polysaccharides with a distinct charge motif a

70 However, bacterial polysaccharides with a zwitterionic charge mot

71 T cells activated in vitro by zwitterionic bacterial polysaccharides (Zps) known to induce abscess