ライフサイエンスコーパス: serum immunoglobulin G

1 proliferation in the presence of respective serum immunoglobulin G.

2 e deficiency, characterized by low levels of serum immunoglobulin G, A, and/or M with loss of antibod

3 ly correlated with the level of prechallenge serum immunoglobulin G against the O127 lipopolysacchari

4 l aplasia, several vaccine/pathogen-specific serum immunoglobulin G and A (IgG and IgA) titers remain

5 Neutralizing antibody responses, serum immunoglobulin G and A, and nasal wash specimen im

6 Antral gastritis, anti-H. pylori serum immunoglobulin G, and atrophy all increased, but w

7 or, CVD 915(pTETlpp) elicited high titers of serum immunoglobulin G anti-fragment C.

8 Only conjugates with O acetyls elicited serum immunoglobulin G anti-LPS with bactericidal activi

9 ith the level of protection correlating with serum immunoglobulin G anti-protective antigen titers.

10 l immunoglobulin A antiamebic antibodies and serum immunoglobulin G antiamebic antibodies.

11 VRP resulted in high levels of DENV-specific serum immunoglobulin G antibodies and significant titers

12 Although serum immunoglobulin G antibodies are significantly high

13 ll-length block 2 antigens showed that human serum immunoglobulin G antibodies induced by infection c

14 orbent assays (ELISAs) for quantification of serum immunoglobulin G antibodies specific for N. mening

15 uced specific secretory immunoglobulin A and serum immunoglobulin G antibodies that persisted at subs

16 concentrations and neutralizing activity of serum immunoglobulin G antibodies to the RSV prefusion (

17 tion, as well as the specificity, of anti-P1 serum immunoglobulin G antibodies were demonstrated in g

18 It was shown that serum immunoglobulin G antibodies were produced against

19 d formation, an impaired ability to generate serum immunoglobulin G antibodies, and significant inhib

20 treated patients with LA have high levels of serum immunoglobulin G antibodies, and sometimes low lev

21 cator of inflammation), or edentulism and 2) serum immunoglobulin G antibody response to Aggregatibac

22 e also developed sustained anti-H. hepaticus serum immunoglobulin G antibody responses and elevated a

23 Less marked, but significant, anti-SREHP serum immunoglobulin G antibody responses were also indu

24 d animalls developed sustained anti-H. felis serum immunoglobulin G antibody responses.

25 PI) owing to the presence of highly elevated serum immunoglobulin G antibody titers with a high avidi

26 cant levels of salivary immunoglobulin A and serum immunoglobulin G antibody to the respective inject

27 A serum immunoglobulin G autoantibody (NMO-IgG) serves as

28 All conjugates elicited high levels of serum immunoglobulin G both to the polysaccharides and t

29 There was a slight increase in serum immunoglobulin G (IgG) against the MS11 strain and

30 Serologic markers such as serum immunoglobulin G (IgG) and antinuclear antibody le

31 although FspA1 induced the highest levels of serum immunoglobulin G (IgG) and fecal IgA.

32 ity to S. typhimurium severely depressed the serum immunoglobulin G (IgG) and IgA anti-FrgC response

33 -CAT construct induced significant levels of serum immunoglobulin G (IgG) and IgA antibody to both pa

34 Recall responses were seen in serum immunoglobulin G (IgG) and IgA following boosting

35 with Invaplex was found to enhance anti-OVA serum immunoglobulin G (IgG) and IgA responses and induc

36 oximately 2-week intervals and evaluated for serum immunoglobulin G (IgG) and IgG subclass and for sa

37 Despite production of serum immunoglobulin G (IgG) and IgM (median titers of 1

38 throughout the experiment and evaluated for serum immunoglobulin G (IgG) and IgM and salivary IgA an

39 In mice i.n. challenged with H10407, serum immunoglobulin G (IgG) and IgM antibodies were mea

40 or no bacteria in the liver and lungs, high serum immunoglobulin G (IgG) and IgM antibody titers, an

41 lpha stimulated strong antigen (Ag)-specific serum immunoglobulin G (IgG) and IgM responses, while MI

42 ion of mice with CVLPs induced gp41-specific serum immunoglobulin G (IgG) and intestinal secretory Ig

43 lones were found to stimulate high levels of serum immunoglobulin G (IgG) and mucosal IgA antibodies

44 luenza virus showed significant increases in serum immunoglobulin G (IgG) and mucosal IgA antibodies

45 oxin (CT) A2 and B subunits (CTA2/B) develop serum immunoglobulin G (IgG) and mucosal IgA antibody re

46 hesizing either PspA fusion protein elicited serum immunoglobulin G (IgG) and mucosal IgA responses a

47 The levels of antigen-specific serum immunoglobulin G (IgG) and mucosal IgA were higher

48 cific gamma interferon-producing T cells and serum immunoglobulin G (IgG) and mucosal IgA.

49 hK63 or LThR72 exhibited high titers of both serum immunoglobulin G (IgG) and mucosal secretory IgA a

50 ed animals demonstrated significantly higher serum immunoglobulin G (IgG) and salivary IgA antibody l

51 Both peptides readily induced serum immunoglobulin G (IgG) and salivary IgA antipeptid

52 astric tissue, histology, and measurement of serum immunoglobulin G (IgG) and salivary IgA.

53 The specificity of anti-P1 serum immunoglobulin G (IgG) and secretory IgA antibodie

54 enuation elicited higher Salmonella-specific serum immunoglobulin G (IgG) and/or mucosal secretory-Ig

55 later, significant reductions were seen for serum immunoglobulin G (IgG) antibodies at week 14 and f

56 Serum immunoglobulin G (IgG) antibodies have been implic

57 recombinant proteins were reacted with human serum immunoglobulin G (IgG) antibodies in Western immun

58 We investigated the ability of serum immunoglobulin G (IgG) antibodies to periodontal b

59 Low maternally derived serum immunoglobulin G (IgG) antibodies to Streptococcus

60 ta provide evidence that a critical level of serum immunoglobulin G (IgG) antibodies to the surface p

61 were found to be immunogenic since elevated serum immunoglobulin G (IgG) antibodies without a specif

62 Oral and i.p. vaccines elicited O11-specific serum immunoglobulin G (IgG) antibodies, but IgA was obs

63 isms are found and the induction of specific serum immunoglobulin G (IgG) antibodies, we examined the

64 ay was used to measure the seroprevalence of serum immunoglobulin G (IgG) antibody among NHANES parti

65 We determined pneumococcal serum immunoglobulin G (IgG) antibody concentrations aga

66 ria during the study interval, and increased serum immunoglobulin G (IgG) antibody levels substantiat

67 nce of P. gingivalis in dental plaque and of serum immunoglobulin G (IgG) antibody levels to P. gingi

68 GFPuv-specific serum immunoglobulin G (IgG) antibody responses were ana

69 oPn produced greater titers of MoPn-specific serum immunoglobulin G (IgG) antibody than mice that rec

70 zed by enzyme-linked immunosorbent assay for serum immunoglobulin G (IgG) antibody to Aggregatibacter

71 Levels of serum immunoglobulin G (IgG) antibody to GTF or CAT in t

72 Serum immunoglobulin G (IgG) antibody, induced by subcut

73 rticular) demonstrated significantly reduced serum immunoglobulin G (IgG) antibody, salivary IgA anti

74 train RB51 (SRB51) produced small amounts of serum immunoglobulin G (IgG) but no IgM antibody to smoo

75 Ribi had the highest levels of PorB-specific serum immunoglobulin G (IgG) by enzyme-linked immunosorb

76 New serum immunoglobulin G (IgG) detected by whole-cell enzy

77 mean titer (GMTs) and 4-fold rise of anti-Vi serum immunoglobulin G (IgG) enzyme-linked immunosorbent

78 ntigenic MDI-albumin products, as defined by serum immunoglobulin G (IgG) from MDI-exposed workers, w

79 Aberrant serum immunoglobulin G (IgG) glycosylation and its immun

80 immunosorbent assay to measure beta-specific serum immunoglobulin G (IgG) levels and used it to compa

81 Significant anti-GLU serum immunoglobulin G (IgG) levels were seen in groups

82 Smoking is also known to reduce serum immunoglobulin G (IgG) levels.

83 haride (PS) conjugate vaccines may prime for serum immunoglobulin G (IgG) memory responses to meningo

84 transplantations indicate that low levels of serum immunoglobulin G (IgG) negatively impact outcomes.

85 Overall, 23% of patients developed either a serum immunoglobulin G (IgG) response (9%) or sputum IgA

86 . denticola induced a significant (400-fold) serum immunoglobulin G (IgG) response compared to that i

87 Anamnestic anti-SEB serum immunoglobulin G (IgG) responses were elicited in

88 ized with replication-defective HSV, durable serum immunoglobulin G (IgG) responses were elicited.

89 e the long-term course of H. pylori-specific serum immunoglobulin G (IgG) responses with respect to s

90 were effective in eliciting antigen-specific serum immunoglobulin G (IgG) responses, and these respon

91 s evokes large increases in antigen-specific serum immunoglobulin G (IgG) responses.

92 fold increase over the prechallenge anti-SMV serum immunoglobulin G (IgG) titer, mostly subclass IgG1

93 were consistent with significantly declined serum immunoglobulin G (IgG) titers for HHV-6 of MS pati

94 ckerboard analyses of eight plaque bacteria, serum immunoglobulin G (IgG) titers to 17 bacteria, and

95 Serum immunoglobulin G (IgG) titers to 28 pneumococcal p

96 B) toxoid in saline elicited higher anti-SEB serum immunoglobulin G (IgG) titers when the toxoid was

97 Binding activity of patient serum immunoglobulin G (IgG) to HupB did not correlate w

98 colonization, 9 of 40 patients developed new serum immunoglobulin G (IgG) to OMP CD, as measured by e

99 ollowing infection and who had developed new serum immunoglobulin G (IgG) to their infecting strain w

100 eleased from bovine fetuin, polyclonal human serum immunoglobulin G (IgG), and human alpha1-acid glyc

101 he most effective means of immunization: the serum immunoglobulin G (IgG), IgA, and IgM anti-fragment

102 We measured serum immunoglobulin G (IgG), IgM, and IgA antibodies to

103 increased class switched memory B cells and serum immunoglobulin G (IgG).

104 s resulted in the induction of FimA-specific serum (immunoglobulin G [IgG] and IgA) and salivary (IgA

105 adermal comparative tuberculin skin test and serum immunoglobulin G [IgG] responses) against a range

106 vated during primary infections (acute-phase serum immunoglobulin G [IgG] titers, <25), compared with

107 nses (HI, antibody-secreting cell [ASC], and serum immunoglobulin G [IgG]) in 15 LRs and 25 control H

108 minent specific anti-CtxB responses in vivo (serum immunoglobulin G [IgG], P </= 0.05; serum IgA, P <

109 ortal vein diameter, splenomegaly, increased serum immunoglobulin G level, and increasing number of a

110 tly improved liver histology (P = 0.005) and serum immunoglobulin G levels (P = 0.0002).

111 We compared serum immunoglobulin G levels and toxin-neutralizing ant

112 The serum immunoglobulin G levels correlated with protection

113 P. gingivalis-specific serum immunoglobulin G levels were significantly elevate

114 , with a 44% reduction in intracardiomyocyte serum immunoglobulin G localization in het-treated-8 mic

115 cination geometric mean titre of LT-specific serum immunoglobulin G of 3400.29, compared with 315.41

116 asma could not be duplicated by pooled human serum, immunoglobulin G, or fibrinogen, whether used sep

117 Serum immunoglobulin G profiling by proteome microarray

118 Serum immunoglobulin G reactivity to Hsp10 and Hsp60 ant

119 the naturally infected SCID/NCr mice had no serum immunoglobulin G response against H. hepaticus.

120 vaccine doses elicited a strong PA-specific serum immunoglobulin G response with a geometric mean ti

121 Only LAM-reactive serum immunoglobulin G responses were significantly incr

122 ufficient to decrease P. gingivalis-specific serum immunoglobulin G responses, but lower antibody tit

123 osted 4 weeks later induced higher levels of serum immunoglobulin G specific for PspA and for outer m

124 Serum immunoglobulin G subclass levels and antibody tite

125 The serum immunoglobulin G subclass profiles were indicative

126 he vhs(-)/ICP8(-) mutant showed prechallenge serum immunoglobulin G titers comparable to those immuni

127 a clinical oral-health examination, and had serum immunoglobulin G titers measured against 19 period

128 of variants with ChoP correlates with higher serum immunoglobulin G titers to LPS containing this str

129 Vi stimulates serum immunoglobulin G Vi antibodies, whereas Ty21a, whi

130 A low serum immunoglobulin G was associated with number of inf

131 Subgingival P. endodontalis levels and serum immunoglobulin G were associated with a higher EL

132 ut adjuvant stimulated induction of specific serum immunoglobulin G, whereas antigen alone or admixed