ライフサイエンスコーパス: serum immunoglobulin

1 s of peripheral mature B cells and decreased serum immunoglobulin.

2 east or by immobilized protein A/G to remove serum immunoglobulin.

3 me activated in the presence of neutralizing serum immunoglobulin.

4 mbers showed progressive loss of B cells and serum immunoglobulins.

5 nd central memory T cells and an increase in serum immunoglobulins.

6 vestigated the prevalence of abnormally high serum immunoglobulin A (IgA) and IgG anti-gliadin antibo

7 nses; all volunteers who received H10407 had serum immunoglobulin A (IgA) and IgG responses, and all

8 Serum immunoglobulin A (IgA) and immunoglobulin G (IgG),

9 for RV1 and RV5 to correlate anti-rotavirus serum immunoglobulin A (IgA) antibody titers vs efficacy

10 Monomeric serum immunoglobulin A (IgA) can contribute to the devel

11 Half of the volunteers mounted a positive serum immunoglobulin A (IgA) response to S. flexneri lip

12 fetuin, bovine submaxillary gland mucin, and serum immunoglobulin A (IgA).

13 Elevated serum immunoglobulin A and immunoglobulin G titers were

14 s female family members showed only elevated serum immunoglobulin A levels.

15 H. pylori serum immunoglobulin A, IgG, and IgG subclass responses

16 trifluoroacetylated protein adduct-specific serum immunoglobulin and hepatotoxicity were reduced.

17 oved B-cell function with increases in total serum immunoglobulin and increased splenic mitogen respo

18 inflammation and hyperresponsiveness (AHR), serum immunoglobulin and splenic T cells were assessed.

19 erved as lesser allergic phenotypes, reduced serum immunoglobulins and allergic mediators, lower mast

20 methods included flow cytometry, analysis of serum immunoglobulins and autoantibodies, lymphocyte sti

21 Serum immunoglobulins and complement factors, peripheral

22 Ptpn6(f/f);CD19-cre mice exhibited elevated serum immunoglobulins and impaired antibody responses to

23 tive IgE, which is the least abundant of the serum immunoglobulins and occurs at subnanomolar levels,

24 scores during the last 8 weeks of treatment, serum immunoglobulins and safety assessments.

25 Allergen-specific serum immunoglobulins and total immunoglobulin E in diff

26 lasma cells within the bone marrow, elevated serum immunoglobulin, and osteolytic bone disease.

27 in early B-cell development, near absence of serum immunoglobulin, and recurrent bacterial infections

28 Eosinophil recruitment, cytokine production, serum immunoglobulins, and airway histology were analyze

29 sponse (ASR), anaphylaxis, body temperature, serum immunoglobulins, and mouse mast cell protease-1 (m

30 ignificant reductions in lymphocyte count or serum immunoglobulin, anticardiolipin antibody, or rubel

31 In 10% to 20% of patients, the serum immunoglobulins are higher than expected or the on

32 d activation parameters are normal; however, serum immunoglobulins are increased and kidney function

33 iency associated with partial persistence of serum immunoglobulin arising from a missense mutation in

34 nificantly reduced titers of IgG2a and IgG2b serum immunoglobulins as well as autoantibodies, but mai

35 solated using the device was consistent with serum immunoglobulin assays that are commonly used in MM

36 Ku70-deficient mice lacked mature B cells or serum immunoglobulin but, unexpectedly, reproducibly dev

37 als produced significantly less IgG1 and IgE serum immunoglobulins, but maintained comparable levels

38 than did those of their corresponding total serum immunoglobulin classes.

39 d a normal immune cell repertoire, unchanged serum immunoglobulin concentrations and an intact immune

40 While total serum immunoglobulin concentrations decline following CT

41 ations depended on DCs, in contrast to total serum immunoglobulin concentrations, suggesting an effec

42 B and T cell zones and resulted in elevated serum immunoglobulin concentrations.

43 sistent with eradication of B-lineage cells, serum immunoglobulins decreased to very low levels after

44 ogeneous and miniscule fraction of the total serum immunoglobulin displaying identical properties oth

45 sponses, characterized by increases in total serum immunoglobulin E (IgE) and specific serum IgG1 lev

46 While serum immunoglobulin E (IgE) concentration has been show

47 Elevated serum Immunoglobulin E (IgE) levels and increased airway

48 This study examined the association between serum immunoglobulin E (IgE) levels for a panel of commo

49 Total serum immunoglobulin E (IgE) levels were significantly l

50 al hyperresponsiveness (BHR), elevated total serum immunoglobulin E (IgE) levels, and skin tests posi

51 dies of intermediate phenotypes, one each on serum immunoglobulin E (IgE) levels, blood eosinophil co

52 Total serum immunoglobulin E (IgE) levels, for example, show s

53 ent of CD4-CD8- peripheral T cells, elevated serum immunoglobulin E (IgE), and possible pulmonary inf

54 cts on markers of Th2 inflammation, reducing serum immunoglobulin E (IgE), chemokine ligands 13 and 1

55 However, the level of a systemic Th2 marker, serum immunoglobulin E (IgE), correlated significantly w

56 ypersensitivity (DTH) to SEA; high levels of serum immunoglobulin E (IgE); a strong T2 cytokine pheno

57 Serum immunoglobulin E against eight common inhalant and

58 d with asthma phenotypes, such as high total serum immunoglobulin E and bronchial hyperresponsiveness

59 Total serum immunoglobulin E and FEV1 predicted levels were no

60 ti-TNF-alpha-treated mice exhibited elevated serum immunoglobulin E and inhibition of the anticryptoc

61 levels at year 1 and repeated assessments of serum immunoglobulin E antibodies (year 1, 4.5, 6), atop

62 the allergen specificity, allergen-specific serum immunoglobulin E concentration, or individual labo

63 Allergen-specific serum immunoglobulin E concentrations ranged from 0.1 to

64 Allergen-specific serum immunoglobulin E detection and quantification have

65 Allergen-specific serum immunoglobulin E determination with the fluoroimmu

66 nome-scan data set and incorporate the total serum immunoglobulin E level in the analysis.

67 Serum immunoglobulin E levels were increased in IL-13Ral

68 eukin-4 production by NKT cells, to increase serum immunoglobulin E levels, and to promote the genera

69 so had reduced T2 cytokine production and no serum immunoglobulin E production.

70 he accumulation of eosinophils and levels of serum immunoglobulin E were increased in NFAT1 -/- mice.

71 ormed with asthma, AHR, lung function, total serum immunoglobulin E, and blood eosinophil levels.

72 -OIT-FDEIA groups, except for level of total serum immunoglobulin E.

73 es on swIg(+) cells until they disappear and serum immunoglobulin falls to a low level, in which case

74 Levels of total serum immunoglobulins fell, although the mean values eac

75 The serum immunoglobulin FLC ratio is an important additiona

76 An abnormal serum immunoglobulin free light chain (FLC) ratio at dia

77 one marrow plasmacytosis, extremely abnormal serum immunoglobulin free light chain ratio, and multipl

78 C-reactive protein, human interleukin-6, and serum immunoglobulin free light chains decreased with th

79 Natural serum immunoglobulin from mice was able to bind to the b

80 n ovarian cancer phage display library using serum immunoglobulins from an ovarian cancer patient as

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

109 Serum immunoglobulin G (IgG) antibodies have been implic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

129 We studied the prognostic relevance of serum immunoglobulin G (IgG) elevated above the upper li

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

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

132 ale C57BL/6 mice treated daily with purified serum immunoglobulin G (IgG) from patients with longstan

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

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

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

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

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

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

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

140 Serum immunoglobulin G (IgG) responses were analyzed lon

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

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

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

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

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

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

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

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

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

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

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

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

153 Thirty-four glycopeptides from human serum immunoglobulin G (IgG) tryptic digests were obviou

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 Although serum immunoglobulin G antibodies are significantly high

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

188 The serum immunoglobulin G levels correlated with protection

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

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

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

192 Serum immunoglobulin G profiling by proteome microarray

193 Serum immunoglobulin G reactivity to Hsp10 and Hsp60 ant

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

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

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

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

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

199 Serum immunoglobulin G subclass levels and antibody tite

200 The serum immunoglobulin G subclass profiles were indicative

201 ked immunosorbent assay (ELISA) to determine serum immunoglobulin G titers against Shigella LPS.

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

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

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

205 Antimeasles serum immunoglobulin G titers were quantified using enzy

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

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

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

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

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

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

212 proliferation in the presence of respective serum immunoglobulin G.

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

214 s well as the production of antigen-specific serum immunoglobulin G1 (IgG1) and IgG2a antibodies.

215 wever, there was an increase in the level of serum immunoglobulin G1 (IgG1) and IgG2b as well as a mi

216 fected with wild-type H. hepaticus developed serum immunoglobulin G1 (IgG1) and IgG2c responses again

217 Also, virus-specific serum immunoglobulin G1 (IgG1) levels were greatly reduc

218 i antibody levels in serum showed a dominant serum immunoglobulin G1 (IgG1) response in immunized C57

219 Oral F1-V mice had higher prechallenge serum immunoglobulin G1 (IgG1) titers than s.c. F1-V mic

220 sponse, including the levels of RSV-specific serum immunoglobulin G1 (IgG1), IgG2a, IgA, and total Ig

221 onstrated an increased level of CVB3-binding serum immunoglobulin G1 in mice inoculated with CVB3-PL2

222 le, VirB9, VirB10, and CTP are recognized by serum immunoglobulin G2 (IgG2) and stimulate memory T-ly

223 Patients with LJP have elevated levels of serum immunoglobulin G2 (IgG2), and this is most strikin

224 e demonstrated between the levels of anti-P1 serum immunoglobulin G2a (IgG2a) and IgG2b, but not of I

225 e vector and passenger antigen, resulting in serum immunoglobulin G2a (IgG2a) and modest mucosal IgA

226 mRNAs; high levels of antibody, particularly serum immunoglobulin G2a (IgG2a) and respiratory IgA; an

227 hat oral reovirus infection elicits specific serum immunoglobulin G2a (IgG2a), while parenteral reovi

228 by the production of high titers of specific serum immunoglobulin G2a antibody and the production of

229 n the dermis and subcutaneous fat, increased serum immunoglobulin G2a levels, and lymphadenopathy ass

230 al immunization with LT-R72 induced a potent serum immunoglobulin G2a response, indicating that this

231 he cecum, as well as elevated Th1-associated serum immunoglobulin G2a(b) compared to infection of B6

232 Elevated serum immunoglobulin G4 (sIgG4) is a feature of autoimmu

233 ry sclerosing cholangitis but with increased serum immunoglobulin G4 and infiltrating immunoglobulin

234 r predilection and is associated with normal serum immunoglobulin G4 levels.

235 o rotavirus infection, we analyzed levels of serum immunoglobulin (Ig) A and IgG antibodies to variou

236 Significant serum immunoglobulin (Ig) A and IgG antibody responses t

237 ek 6 (predicted peak of pollen) to determine serum immunoglobulin (Ig) E concentrations and Treg perc

238 Serum immunoglobulin (Ig) E concentrations associated wi

239 red orally without adjuvant, and they elicit serum immunoglobulin (Ig) G and intestinal IgA responses

240 pithelial antigen that reacted strongly with serum immunoglobulin (Ig) G from the mouse model of BA w

241 Notably, serum immunoglobulin (Ig) isotypes and kidney Ig/C3 depo

242 ever, in the absence of constant reexposure, serum immunoglobulin (Ig) levels rapidly decline and ful

243 samples were collected for quantification of serum immunoglobulin (Ig) levels, specific antibodies ag

244 Consistent with B-lymphocyte increases, serum immunoglobulin (Ig) M, IgG, and IgE were significa

245 fective B-cell function characterized by low serum immunoglobulin (Ig) M, low IgM antibody production

246 We evaluated serum immunoglobulin (Ig) proteins as predictors of NHL

247 ) cell cytotoxic activity and were devoid of serum immunoglobulin (Ig) throughout a 37-week lifespan.

248 f antibody effector functions by retargeting serum immunoglobulin (Ig).

249 ymic stromal lymphopoietin, IL-5 and IL-13), serum immunoglobulin (Ig)E and airway hyper-responsivene

250 In both cases, total serum immunoglobulin (Ig)E level was >1000 IU/mL and fun

251 re examined pulmonary pathophysiological and serum immunoglobulin (Ig)E responses in mice of 12 inbre

252 We hypothesized that serum immunoglobulin (Ig)G antibody levels against BspA

253 No baseline serum immunoglobulin (Ig)G antibody or splenic CD4+ T-ce

254 ing checkerboard DNA-DNA hybridizations, and serum immunoglobulin (Ig)G levels were measured against

255 ity to carriage did not correlate with total serum immunoglobulin (Ig)G to the homotypic capsular pol

256 pression, mutant mice had elevated levels of serum immunoglobulin (Ig)G1, IgG2b, and IgE and produced

257 Deficiency of serum immunoglobulin (Ig)M is associated with the develo

258 CAR bacillus-specific serum immunoglobulins (immunoglobulin M [IgM], IgG1, IgG

259 long-lived plasma cells, which produce most serum immunoglobulin, is central to humoral immunity.

260 re was widespread variation in the levels of serum immunoglobulin isotypes as well as in the percenta

261 o, and baseline levels of the Th2-controlled serum immunoglobulin isotypes, IgE and IgG1, were also s

262 ith baseline levels, we noted an increase in serum immunoglobulin levels across all classes, and a re

263 Serum immunoglobulin levels and lymphocyte phenotypes an

264 Despite this, patients had normal serum immunoglobulin levels and normal antigen-specific

265 Despite normal B-lymphocyte numbers, serum immunoglobulin levels decreased with age.

266 Previous studies examined the serum immunoglobulin levels in relation to coronary arte

267 Absolute numbers of lymphocyte subsets and serum immunoglobulin levels were all within normal range

268 Serum immunoglobulin levels were also elevated in HIV-in

269 Serum immunoglobulin levels were also markedly reduced i

270 ; CD5(+) peritoneal B cells were absent, and serum immunoglobulin levels were markedly reduced.

271 Serum immunoglobulin levels were measured by enzyme-link

272 Similar effects on the serum immunoglobulin levels were observed immediately af

273 ) is characterized by variable reductions in serum immunoglobulin levels which cause most ICF patient

274 rently normal lymphocyte development, normal serum immunoglobulin levels, and the capacity to respond

275 in viremic individuals, and correlated with serum immunoglobulin levels, particularly IgG.

276 not associated with significant decreases in serum immunoglobulin levels.

277 ma cells in tonsils appeared normal, as were serum immunoglobulin levels.

278 flow cytometry of blood B-cell subsets, and serum immunoglobulin levels.

279 cell numbers; immune complex, complement, or serum immunoglobulin levels; delayed type hypersensitivi

280 was associated with higher brain CFU, lower serum immunoglobulin M (IgM) and IgG responses to glucur

281 cryptocococcal pulmonary infection elicited serum immunoglobulin M (IgM) and IgG to the capsular pol

282 of peritoneal B1 B cells, and correction of serum immunoglobulin M (IgM) and IgG(3) levels.

283 Interestingly, anti-Bordetella serum immunoglobulin M (IgM) levels were significantly l

284 (+)CD4(-) T cells, and decreases in elevated serum immunoglobulin M and inflammatory markers includin

285 At best response, median serum immunoglobulin M declined from 3,520 to 821 mg/dL,

286 production, comprising approximately 90% of serum immunoglobulin M in ATA micro kappa mice.

287 se with nonsense CXCR4 mutations have higher serum immunoglobulin M levels and incidence of symptomat

288 88 show lower bone marrow disease burden and serum immunoglobulin M levels but show an increased risk

289 vement declined from 55% to 10% (P = .0004), serum immunoglobulin M levels declined from 4,830 to 1,1

290 ysts had no detectable mature T and B cells, serum immunoglobulin M, or even Thy-1(+) and B220(+) pre

291 Passive transfer of normal mouse serum, immunoglobulin M (IgM) from normal mouse serum, o

292 higher bone marrow (BM) disease involvement, serum immunoglobulin-M levels, and symptomatic disease r

293 CXCR4(WILDTYPE (WT)) had intermediate BM and serum immunoglobulin-M levels; those with MYD88(WT)CXCR4

294 luble and membrane-bound TGF-beta as well as serum immunoglobulin production are high in these mice.

295 ural killer cells, lymphocyte phenotype, and serum immunoglobulin subclass levels were evaluated.

296 scue of mature B cells with normal levels of serum immunoglobulins, together with complete rescue of

297 enzyme-linked immunosorbent assay, specific serum immunoglobulin was detected as early as 134 days p

298 Serum immunoglobulin was purified by protein A/G chromat

299 Furthermore, mice deficient in serum immunoglobulin were equally protected and this pro

300 ically by inadequate quantity and quality of serum immunoglobulins with increased susceptibility to i