ライフサイエンスコーパス: antibody-secreting cell

1 icroneutralisation titres, and the number of antibody secreting cells.

2 le to screening both bacterial and mammalian antibody secreting cells.

3 systemic antigen-specific IgG(+) and IgA(+) antibody secreting cells.

4 stigation of differentiation of B cells into antibody secreting cells.

5 ndrial homeostasis and alterations in GC and antibody-secreting cells.

6 tion of the preexisting and newly-developing antibody-secreting cells.

7 on, class switching and differentiation into antibody-secreting cells.

8 ant increases in the numbers of specific IgA antibody-secreting cells.

9 um responses and developed S. typhi-specific antibody-secreting cells.

10 ntibody to hepatitis pre-S or pre-S-specific antibody-secreting cells.

11 rotavirus, as determined by assay of mucosal antibody-secreting cells.

12 sion and the differentiation of B cells into antibody-secreting cells.

13 ing, and increased the numbers of anti-HIV-1 antibody-secreting cells.

14 emory B cells and no evidence of circulating antibody-secreting cells.

15 ero-mammary link may exist for food-specific antibody-secreting cells.

16 T-dependent B cell memory and high affinity antibody-secreting cells.

17 rapid conversion of naive B cells to mature antibody-secreting cells.

18 ntibodies (blood and stool) and RBD-specific antibody-secreting cells.

19 the TIV group and correlated with number of antibody-secreting cells.

20 nd facilitates differentiation of long-lived antibody-secreting cells.

21 tiation of Foxp3+ regulatory T cells and IgA antibody-secreting cells.

22 ional and morphological differentiation into antibody-secreting cells.

23 d native antigens and differentiate into VLR antibody-secreting cells.

24 The increase in frequency of donor-specific antibody-secreting cells after renal transplantation ind

25 ncies of memory B cells and antigen-specific antibody-secreting cells after vaccination.

26 ease in antibody titer, reduced frequency of antibody secreting cells, an absence of affinity maturat

27 a, and this colonization induced significant antibody-secreting cell and enzyme-linked immunosorbent

28 cific B and T cells after i.n. immunization, antibody-secreting cells and antigen-responsive T cells

29 also led to increased levels of HIV-specific antibody-secreting cells and B cell-associated chemokine

30 NP-specific antibody-secreting cells and heightened frequencies of g

31 carrier protein, leading to large numbers of antibody-secreting cells and high titers of high-affinit

32 Moreover, significantly lower numbers of IgG antibody-secreting cells and lower levels of CD4(+)-T-ce

33 irus strain correlate with low production of antibody-secreting cells and memory B cells recognizing

34 veals the capacity of memBcs to develop into antibody-secreting cells and present an idea for a new c

35 RSV-specific, T-cell-dependent neutralizing antibody-secreting cells and RSV-specific memory respons

36 (NV-specific IgA and immunoglobulin G [IgG] antibody-secreting cells and total and NV-specific IgA a

37 y lower levels of germinal center formation, antibody-secreting cells, and circulating influenza viru

38 l center (GC) reaction, increased anti-gp120 antibody-secreting cells, and increased anti-gp120 funct

39 indings show that memory B cells and natural antibody-secreting cells are BLyS-independent and sugges

40 We identified antibody-secreting cells as the major splenic B cell pop

41 Immunoglobulin in cerebral spinal fluid and antibody secreting cells (ASC) within the central nervou

42 Antibody-secreting cell (ASC) and memory B-cell (MBC) re

43 The transcriptional network regulating antibody-secreting cell (ASC) differentiation has been e

44 ly elevated circulating immunoglobulin (Ig)G antibody-secreting cell (ASC) frequencies and hypergamma

45 vestigated the kinetics of the FMDV-specific antibody-secreting cell (ASC) response following homolog

46 A dose-related, immunoglobulin A antibody-secreting cell (ASC) response to S. flexneri 2a

47 measure local and systemic isotype-specific antibody-secreting cell (ASC) responses to individual st

48 IgG responses, and all but one volunteer had antibody-secreting cell (ASC) responses.

49 Isotype-specific antibody-secreting cells (ASC were enumerated at selecte

50 In vivo antigen-activated antibody-secreting cells (ASC) (effector B cells) and in

51 on-isotype-switched, memory (Bmem) cells and antibody-secreting cells (ASC) accumulate in various mod

52 id differentiation to become HA-specific IgG antibody-secreting cells (ASC) after activation in non-T

53 aluated immunoglobulin M (IgM), IgA, and IgG antibody-secreting cells (ASC) and cytokine-secreting ce

54 Antibody-secreting cells (ASC) and serum antibody titers

55 r immunoglobulin A (IgA) and IgG circulating antibody-secreting cells (ASC) and stimulated memory B c

56 responses were determined from the number of antibody-secreting cells (ASC) in blood measured by enzy

57 ified by the frequency of influenza-specific antibody-secreting cells (ASC) in peripheral blood, was

58 ibody titers, and significant numbers of IgG antibody-secreting cells (ASC) in the spleen and tracheo

59 induced activation and differentiation into antibody-secreting cells (ASC) of CBC but not IBC when t

60 F-specific antibodies and fewer 23F-specific antibody-secreting cells (ASC) than did BALB/c or (CBA/J

61 hat were associated with the localization of antibody-secreting cells (ASC) to the bone marrow.

62 cle-treated mice, virus-specific IgM and IgG antibody-secreting cells (ASC) were decreased 22- and 45

63 To assess correlates of protection, antibody-secreting cells (ASC) were enumerated in intest

64 The highest numbers of antibody-secreting cells (ASC), both IgA and IgG, were d

65 potent and selective chemoattractant for IgA antibody-secreting cells (ASC), efficiently recruiting I

66 FMDV-specific antibody-secreting cells (ASC), predominantly IgM, were

67 rast, in STV there was a lack of circulating antibody-secreting cells (ASC), reflecting the local muc

68 nature and homing potentials of circulating antibody-secreting cells (ASC).

69 IgM(-) memory B cells (B(mem)), and CD138(+) antibody-secreting cells (ASC).

70 rders are often associated with retention of antibody-secreting cells (ASC).

71 We analyzed the humoral responses (HI, antibody-secreting cell [ASC], and serum immunoglobulin

72 ibody responses (measured by quantitation of antibody-secreting cells [ASC] in intestinal and systemi

73 Antibody secreting cells (ASCs) are critical effector ce

74 anut IgE levels, symptoms, or numbers of IgE antibody secreting cells (ASCs) in the BM.

75 ples were collected for serological profile, antibody secreting cells (ASCs), and analysis of ASC hom

76 entification and recovery of target specific antibody secreting cells (ASCs).

77 pecificity and duration of circulating human antibody-secreting cells (ASCs) after vaccination have b

78 oglobulin A (IgA) and immunoglobulin G (IgG) antibody-secreting cells (ASCs) and influenza virus-spec

79 Antigen-specific B cells bifurcate into antibody-secreting cells (ASCs) and memory B cells (MBCs

80 ted a robust expansion of the virus-specific antibody-secreting cells (ASCs) and memory B cells in th

81 Antibody-secreting cells (ASCs) are isolated from whole

82 Antibody-secreting cells (ASCs) are present in the CNS a

83 rbent assay (ELISA), and total IgG and dsDNA antibody-secreting cells (ASCs) by enzyme-linked immunos

84 was to test the contribution of allospecific antibody-secreting cells (ASCs) from different anatomica

85 on in secondary lymphoid organs, a subset of antibody-secreting cells (ASCs) homes to the bone marrow

86 pecific immunoglobulin A (IgA), IgG, and IgM antibody-secreting cells (ASCs) in a dose-responsive man

87 ons through the generation of class-switched antibody-secreting cells (ASCs) in germinal centers.

88 Germinal centers and antibody-secreting cells (ASCs) in spleens and IgG depos

89 s-specific antibodies and rotavirus-specific antibody-secreting cells (ASCs) in the circulation to pr

90 otype, magnitude, and tissue distribution of antibody-secreting cells (ASCs) in the intestinal and sy

91 The accumulation of immunoglobulin (Ig)A antibody-secreting cells (ASCs) in the lactating mammary

92 B cell differentiation into antibody-secreting cells (ASCs) is a tightly regulated p

93 0, 1, and 3 months, and serum antibodies and antibody-secreting cells (ASCs) were assessed.

94 Frequencies of influenza-specific antibody-secreting cells (ASCs) were measured by enzyme-

95 ced memory T cell responses or PnPS-specific antibody-secreting cells (ASCs) were responsible for ser

96 s erythematosus (SLE) courses with surges of antibody-secreting cells (ASCs) whose origin, diversity

97 ) and immunoglobulin G (IgG), fecal IgA, IgA antibody-secreting cells (ASCs), and IFN-gamma productio

98 d and tested by ELISpot for antigen-specific antibody-secreting cells (ASCs).

99 out IL-6 as a differentiation factor for IgM antibody-secreting cells (ASCs).

100 ng immunoglobulin G (IgG) antibodies and IgG antibody-secreting cells (ASCs).

101 ulting from significantly reduced numbers of antibody-secreting cells (ASCs).

102 he CNS were primarily CD8(+) T cells and IgM antibody-secreting cells (ASCs).

103 differentiation of autoreactive B cells into antibody-secreting cells, but it is not necessary for th

104 y enzyme-linked immunosorbent assay and lung antibody secreting cells by enzyme-linked immunospot ass

105 ed using Luminex assays and the frequency of antibody-secreting cells by ELISpot.

106 relied on conversion of memory B cells into antibody-secreting cells by in vitro culture.

107 tavirus-specific, immunoglobulin A-producing antibody-secreting cell concentration in antibiotic-trea

108 9, 39, 278, and 233 for immunoglobulin (IgA) antibody-secreting cell counts; 401, 201, 533, and 284 f

109 mbers of bone marrow plasma cells and spleen antibody-secreting cells detected in the MN group.

110 Thus, antibody-secreting cells do not exclusively control the

111 increases in the frequency of donor-specific antibody-secreting cells eight weeks after transplantati

112 charide (LPS)-specific immunoglobulin (Ig) A antibody-secreting cells (enzyme-linked immunospot [ELIS

113 logy for cellular infiltration, and measured antibody-secreting cells (enzyme-linked immunospot assay

114 moniae infection exaggerates early antiviral antibody-secreting cell formation, and at later times, l

115 sponding decrease in secondary high-affinity antibody-secreting cell formation.

116 differentiation, and spleen and bone marrow antibody-secreting cell frequencies were 10-fold higher

117 were characterized and compared to those of antibody-secreting cells from untreated ITP spleens and

118 o evaluate the diversity of antigen-specific antibody-secreting cells generated during an in vivo hum

119 virus from the lung and enhanced humoral and antibody-secreting cell immune responses after 100% surv

120 imulated immunoglobulin A-producing anti-LPS antibody-secreting cells in 60, 91, and 100% of subjects

121 uce protective CD8(+) T cells and long-lived antibody-secreting cells in CD4KO mice.

122 ibody responses and in higher frequencies of antibody-secreting cells in corresponding draining cervi

123 ), and the numbers of Campylobacter-specific antibody-secreting cells in peripheral blood failed to i

124 CCR9 can be expressed on IgM as well as IgA antibody-secreting cells in response to acute intestinal

125 Human B cells proliferate and turn into antibody-secreting cells in response to TLR3, TLR7 and T

126 i.n. immunization induced predominantly IgA antibody-secreting cells in salivary glands and IgA and

127 We enumerated donor-specific antibody-secreting cells in the blood of nine renal allo

128 We sought to quantify B-cell populations and antibody-secreting cells in the blood of patients with A

129 BALB/b mice had 25-fold more MHV-specific antibody-secreting cells in the central nervous system,

130 monoclonal antibodies (hMAbs) directly from antibody-secreting cells in the circulation of immunized

131 antly enhanced the number of AgI/II-specific antibody-secreting cells in the draining superficial cer

132 LPS in lung lavages and specific IgG and IgA antibody-secreting cells in the lungs and spleen.

133 ollicular helper (GC Tfh) and GC B cells and antibody-secreting cells in the spleen and bone marrow i

134 igen-specific immunoglobulin G (IgG) and IgA antibody-secreting cells in the spleen and draining lymp

135 ing cells in salivary glands and IgA and IgG antibody-secreting cells in the superficial and central

136 raoral immunization also induced IgA and IgG antibody-secreting cells in the superficial and central

137 d virus-specific antibodies in the serum and antibody-secreting cells in their secondary lymphoid org

138 The frequency of antibody-secreting cells in tissues, postulated to funct

139 eting cells, including listeria-specific IgA antibody-secreting cells, in the lamina propria of the s

140 patients, and a 10-fold decrease in anti-DNA antibody-secreting cell lines was found after treatment

141 subcutaneous (neck) immunization induced IgG antibody-secreting cells mainly in the draining facial l

142 stribution and maintenance of these critical antibody-secreting cells may serve as potential therapeu

143 eutralizing antibodies, mucosal and systemic antibody-secreting cells, memory B cells, and gamma inte

144 oth total and RV-specific murine IgM and IgA antibody-secreting cells migrate efficiently to CCL28 (t

145 y lower measles-specific antibody levels and antibody-secreting cell numbers were also observed, indi

146 1, 3, and 4 showed a significant increase in antibody-secreting cells on ELISPOT.

147 rise from B220(+) memory B cells and produce antibody-secreting cells on rechallenge with antigen.

148 NV-specific memory B cells but not antibody-secreting cells persisted 180 days after infect

149 ts suggest strategies to remove xenoreactive antibody-secreting cells prior to transplantation.

150 Antibody-secreting cells producing antilipopolysaccharid

151 In these mice, antibody-secreting cells recognizing multivalent antigen

152 ti-BLyS treatment, yet the number of natural antibody-secreting cells remained constant.

153 Most vaccinees had an IgA antibody-secreting cell response against colonization fa

154 ix volunteers that received 10(4) CFU had an antibody-secreting cell response, and four had a serum I

155 ived 10(3) CFU excreted SC602 and had an IgA antibody-secreting cell response.

156 ling in the development of anti-WNV-specific antibody-secreting cell responses and memory B cell resp

157 Although many of the volunteers generated antibody-secreting cell responses to Vi, only 2 of the 3

158 Antibody-secreting cell responses were biased toward IgA

159 compared to rLBNSE, could differentiate into antibody-secreting cells, resulting in rapid and potent

160 lipopolysaccharide responses, as measured by antibody-secreting cell, serum, or fecal antibody levels

161 differentiation, which cooperate to generate antibody-secreting cells that cause the deposition of an

162 ic IgM(+) MBCs proliferated and gave rise to antibody-secreting cells that dominated the early second

163 The level of circulating antibody-secreting cells that make anti-galalpha1-3gal a

164 -cells to proliferate and differentiate into antibody-secreting cells that morphologically resemble p

165 ant increase in the iliac lymph nodes of IgA antibody-secreting cells to p27 (P < 0.02), CD8-suppress

166 in these children differentiated quickly to antibody-secreting cells to the new vaccine antigens.

167 B lymphocytes differentiate into antibody-secreting cells under the antigen-specific cont

168 ver, in vitro differentiation of memBcs into antibody-secreting cells was 6.1-, 2.6-, and 3.7-fold si

169 are required for B-cell differentiation into antibody-secreting cells, we found that MM cells inheren

170 In addition, specific antibody-secreting cells were detectable in the lamina p

171 Long-lived antibody-secreting cells were detected in the bone marro

172 F protein-specific antibody-secreting cells were detected in the bone marro

173 Circulating antibody-secreting cells were enumerated using enzyme-li

174 were detected in lung lavages, and specific antibody-secreting cells were isolated from the spleen a

175 Antibody production and the frequency of antibody-secreting cells were significantly elevated in

176 in a dramatic reduction of antigen-specific antibody-secreting cells, whereas deletion of relb had n

177 f-HA causes a population of immunoglobulin G antibody-secreting cells, which dominate the primary res

178 ly polarized antibody repertoire in CD138(+) antibody-secreting cells within the PLN.