ライフサイエンスコーパス: secreting cell

1 f relatively high-frequency, single-cytokine secreting cells.

2 cytokine IL-22 is often coproduced by IL-17-secreting cells.

3 tly, the skin-homing B1 cells included IL-10-secreting cells.

4 TCR transgenic CD4(+) T cells into IFN-gamma-secreting cells.

5 increased the numbers of anti-HIV-1 antibody-secreting cells.

6 man intestinal epithelial cells into insulin-secreting cells.

7 alisation titres, and the number of antibody secreting cells.

8 raining the respiratory tract, mostly as IgM-secreting cells.

9 ells and no evidence of circulating antibody-secreting cells.

10 ic adenosine monophosphate (cAMP) in insulin-secreting cells.

11 eening both bacterial and mammalian antibody secreting cells.

12 stinal cells into glucose-responsive insulin-secreting cells.

13 tor 4 inhibitor reduced the formation of IgM-secreting cells.

14 erentiation into mature CD27(-)CD44(+) IL-17-secreting cells.

15 ent B cell memory and high affinity antibody-secreting cells.

16 nversion of naive B cells to mature antibody-secreting cells.

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

18 l monomeric IgA-secreting cells and some IgG-secreting cells.

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

20 ane but not the endosomal system in Hedgehog-secreting cells.

21 reased frequency of proinflammatory cytokine-secreting cells.

22 secreted proteins in-well for highly active secreting cells.

23 ation models when delivered by lentivirus or secreting cells.

24 own of ABF-1 potentiates the formation of Ab-secreting cells.

25 eduction in pathogenic autoantibodies and Ab-secreting cells.

26 olation of multiple, low-frequency, cytokine-secreting cells.

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

28 of differentiation of B cells into antibody secreting cells.

29 Instead, it reduced the number of Ab-secreting cells.

30 do not proliferate or differentiate into Ab-secreting cells.

31 ic Abs and low numbers of Ag-experienced, Ab-secreting cells.

32 ecombination (CSR) and differentiate into Ig-secreting cells.

33 r ability to differentiate into autoantibody-secreting cells.

34 tasis through coordinated actions of hormone-secreting cells.

35 s as well as class-switched high-affinity Ab-secreting cells.

36 ifferentiation of B cells into memory and Ab-secreting cells.

37 Th9 cells attenuated the percentage of IL-9-secreting cells.

38 act, and generate regulatory T cells and IgA-secreting cells.

39 nd also self-renewed and persisted as IL-17A-secreting cells.

40 metry phenotypically characterized IFN-gamma-secreting cells.

41 TI-2 memory B cells and long-lived antibody secreting cells.

42 important cross-talk between classes of SFP-secreting cells.

43 nd maturation into broadly-reacting antibody-secreting cells.

44 development of pathogenic ICOS(+) IFN-gamma-secreting cells.

45 meostasis and alterations in GC and antibody-secreting cells.

46 ry link may exist for food-specific antibody-secreting cells.

47 he naive T cells into antigen-specific IL-22-secreting cells.

48 ar helper cells and tonsillar Ag-specific Ab-secreting cells.

49 wer Peyer's patches and lower numbers of IgA-secreting cells.

50 nsity for conversion into functional insulin-secreting cells.

51 via pulmonary alpha-1,3-glucan-specific IgA-secreting cells.

52 2-secreting, but lower portions of IFN-gamma-secreting, cells.

53 In insulin secreting cells a surprisingly large fraction of total r

54 er (GC) reaction leading to production of Ab-secreting cells (AbSCs).

55 n of human embryonic stem cells into insulin-secreting cells, achieving an elusive goal for regenerat

56 tive autophagy but are capable of forming Ab-secreting cells after rechallenge with Ags.

57 ease in frequency of donor-specific antibody-secreting cells after renal transplantation indicates th

58 memory B cells and antigen-specific antibody-secreting cells after vaccination.

59 and overexpression of CTSH protected insulin-secreting cells against cytokine-induced apoptosis.

60 In this study, we analyzed Ab-secreting cell and Ab responses in 20 hospitalized COVID

61 t fully reconstitute the pool of natural IgM-secreting cells and circulating IgM levels.

62 d in the differentiation of IL-17- and IL-22-secreting cells and elevation of mRNA that encode signat

63 ells differentiate into slow-growing acetate-secreting cells and fast-growing CO2-secreting cells, an

64 easures the number and intensity of cytokine-secreting cells and has excellent dynamic range with rap

65 uced injury contain increased numbers of IgA-secreting cells and have IgA deposits in sinusoids.

66 NP-specific antibody-secreting cells and heightened frequencies of germinal c

67 stimation of the presence of type 2 cytokine-secreting cells and highlight IL-2 as a critical compone

68 nderstanding of sensory pathways in incretin secreting cells and highlights the therapeutic potential

69 protein expression, and stability in insulin-secreting cells and isolated rodent islets of Langerhans

70 in correlate with low production of antibody-secreting cells and memory B cells recognizing that stra

71 Unlike memory T cells, spontaneous Ab secreting cells and memory B cells specific to influenza

72 mmune response involves the generation of Ab-secreting cells and memory B cells through a process cal

73 higher levels of envelope-specific antibody-secreting cells and memory B cells, higher IgG antibody

74 or the Ag-neutralization potential of the Ab-secreting cells and memory cells generated upon immuniza

75 uration from immature via mature/naive to Ig-secreting cells and memory cells.

76 capacity of memBcs to develop into antibody-secreting cells and present an idea for a new classifica

77 also notable differences between S7 insulin-secreting cells and primary human beta cells.

78 with the detection of splenic Vi-specific Ab-secreting cells and protective Ab in Rag1-deficient B1b

79 ific, T-cell-dependent neutralizing antibody-secreting cells and RSV-specific memory responses.

80 dress this basic question at the level of Ab-secreting cells and serum IgG using a pair of isogenic s

81 n mammals, specifically in all monomeric IgA-secreting cells and some IgG-secreting cells.

82 prevents the differentiation of autoantibody-secreting cells and the recurrence of autoimmune arthrit

83 Nevertheless, the numbers of alloantibody-secreting cells and the serum titers of antidonor IgG al

84 ific IgA and immunoglobulin G [IgG] antibody-secreting cells and total and NV-specific IgA and IgG me

85 faces, act locally as 'professional cytokine-secreting cells' and thereby establish peri-vascular mic

86 acetate-secreting cells and fast-growing CO2-secreting cells, and a large population growing at inter

87 evels of germinal center formation, antibody-secreting cells, and circulating influenza virus-specifi

88 ion promoted the massive accumulation of IgM-secreting cells, and cutaneous immunization directed bot

89 (GC) reaction, increased anti-gp120 antibody-secreting cells, and increased anti-gp120 functional avi

90 emory in the lung, long-lived bone marrow Ab-secreting cells, and influenza-specific IgG Ab.

91 specific and almost entirely made up of IgG-secreting cells, and plasmablasts reached very high numb

92 se of exocrine zymogen and endocrine hormone secreting cells; and (ii) elevated presence of innate im

93 Accordingly, more OVA-specific IgG1-secreting cells are present in spleen and fewer in the b

94 oach allergen, alpha-1,3-glucan-specific IgA-secreting cells are present in the lungs of mice immuniz

95 We identified antibody-secreting cells as the major splenic B cell population t

96 rough the generation of parasite-specific Ab-secreting cells, as well as germinal center and memory B

97 -specific serum IgG, systemic and mucosal Ab-secreting cells, as well as IFN-gamma, TNF-alpha, IL-2,

98 Antibody-secreting cell (ASC) and memory B-cell (MBC) responses w

99 transcriptional network regulating antibody-secreting cell (ASC) differentiation has been extensivel

100 cific defect in IgG2a switch and impaired Ab-secreting cell (ASC) differentiation.

101 Ab-secreting cell (ASC) expansion and survival are importan

102 Human Ab-secreting cell (ASC) populations in circulation are not

103 d the kinetics of the FMDV-specific antibody-secreting cell (ASC) response following homologous and h

104 on-gamma (IFN-gamma) and long-lived antibody-secreting cell (ASC) responses, the roles for IFN-gamma

105 e-switched, memory (Bmem) cells and antibody-secreting cells (ASC) accumulate in various models of ce

106 Antibody-secreting cells (ASC) and serum antibody titers were ass

107 otropic viral infections, with antibody (Ab)-secreting cells (ASC) contributing to local protection.

108 the frequency of influenza-specific antibody-secreting cells (ASC) in peripheral blood, was significa

109 Ab-secreting cells (ASC) or plasma cells are essential comp

110 These Ab-secreting cells (ASC) originate from peritoneal cavity-r

111 ed mice, virus-specific IgM and IgG antibody-secreting cells (ASC) were decreased 22- and 457-fold in

112 FMDV-specific antibody-secreting cells (ASC), predominantly IgM, were evident a

113 ed IgG switching and differentiation into Ab-secreting cells (ASC)-a finding that coincided with incr

114 mory B cells (B(mem)), and CD138(+) antibody-secreting cells (ASC).

115 ted with local accumulation of antibody (Ab)-secreting cells (ASC).

116 nly a fraction differentiating into antibody-secreting cells (ASC).

117 analyzed the humoral responses (HI, antibody-secreting cell [ASC], and serum immunoglobulin G [IgG])

118 A (IgA) and immunoglobulin G (IgG) antibody-secreting cells (ASCs) and influenza virus-specific CD4(

119 gen-specific B cells bifurcate into antibody-secreting cells (ASCs) and memory B cells (MBCs) after i

120 ust expansion of the virus-specific antibody-secreting cells (ASCs) and memory B cells in the periphe

121 Antibody secreting cells (ASCs) are critical effector cells and l

122 Antibody-secreting cells (ASCs) are present in the CNS and become

123 the measurement of Mp-specific IgM antibody-secreting cells (ASCs) by enzyme-linked immunospot (ELIS

124 ent of Mp-specific immunoglobulin M antibody-secreting cells (ASCs) by enzyme-linked immunospot assay

125 st the contribution of allospecific antibody-secreting cells (ASCs) from different anatomical compart

126 (Mp)-specific immunoglobulin (Ig)M antibody-secreting cells (ASCs) improved diagnosis of Mp infectio

127 gh the generation of class-switched antibody-secreting cells (ASCs) in germinal centers.

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

129 that an enrichment of autoreactive dsDNA Ab-secreting cells (ASCs) in the kidney of lupus-prone mice

130 and the homing molecule expression of IgA Ab-secreting cells (ASCs) induced by intrarectal immunizati

131 B cell differentiation into antibody-secreting cells (ASCs) is a tightly regulated process un

132 Antibody-secreting cells (ASCs) or plasma cells secrete antibodie

133 HBsAg-specific antibody-secreting cells (ASCs) response was not different betwee

134 an last a lifetime due to a subset of the Ab-secreting cells (ASCs) that is long lived.

135 HPV-specific antibody secreting cells (ASCs) were present in the tumour microe

136 atosus (SLE) courses with surges of antibody-secreting cells (ASCs) whose origin, diversity and contr

137 unoglobulin G (IgG), fecal IgA, IgA antibody-secreting cells (ASCs), and IFN-gamma production were ev

138 as a differentiation factor for IgM antibody-secreting cells (ASCs).

139 ion and recovery of target specific antibody secreting cells (ASCs).

140 globulin G (IgG) antibodies and IgG antibody-secreting cells (ASCs).

141 om significantly reduced numbers of antibody-secreting cells (ASCs).

142 nal changes leading to the development of Ab-secreting cells (ASCs).

143 eir subsequent differentiation into antibody-secreting cells (ASCs).

144 ike signaling responses in the biology of Ab-secreting cells (ASCs).

145 and demonstrate by ELISPOT that these are Ab-secreting cells (ASCs).

146 ansgenic mice, we traced newly generated IgA-secreting cells at steady state and after oral immunizat

147 g-specific IgG3-secreting cells, but not IgM-secreting cells, at both early (day 5) and late (week 6)

148 le to convert adult fibroblasts into insulin-secreting cells, avoiding both a stable pluripotent stag

149 identification and sorting of individual Ab-secreting cells based on their Ag reactivity.

150 in B cells reduces the numbers of IgA(+) Ab-secreting cells both in vitro and in vivo, suggesting th

151 iation of autoreactive B cells into antibody-secreting cells, but it is not necessary for their initi

152 oth splenic and bone marrow Ag-specific IgG3-secreting cells, but not IgM-secreting cells, at both ea

153 ntrinsic roles in regulating formation of Ab-secreting cells by controlling the activity of Blimp1 an

154 Luminex assays and the frequency of antibody-secreting cells by ELISpot.

155 t that the implantation of encapsulated GDNF-secreting cells can deliver GDNF in a sustained, targete

156 It is known that GLP-1 secreting cells can sense glucose to promote electrical

157 In insulin-secreting cells, catechol estrogens produced rapid activ

158 b titers and formation of extrafollicular Ab-secreting cells compared with controls.

159 pecific, immunoglobulin A-producing antibody-secreting cell concentration in antibiotic-treated mice.

160 w endogenous Spl expression level in insulin-secreting cells contributes to their extraordinary vulne

161 ents, with the cytokine concentration around secreting cells decaying sharply across only a few cell

162 ntation of pancreatic progenitors or insulin-secreting cells derived from human embryonic stem cells

163 We used IgA1-secreting cells derived from the circulation of IgAN pat

164 ercytokinemia, identifying the hypercytokine-secreting cell, developing consensus criteria for diagno

165 genetic and phenotypic program leading to Ab-secreting cell differentiation in vitro and in vivo.

166 tment consisted of a total of 5 x 108 GM-CSF-secreting cells distributed equally among 3 lymph node r

167 Thus, antibody-secreting cells do not exclusively control the sialylati

168 how that skin accumulation of B cells and Ab-secreting cells during inflammation increases local Ab t

169 tion inhibition titers, IgA(+) and IgG(+) Ab-secreting cells, effector CD4 or CD8 T cell frequencies

170 in the frequency of donor-specific antibody-secreting cells eight weeks after transplantation.

171 ess B cell breadth, Mus musculus (BALB/c) Ab-secreting cells elicited by a candidate COBRA hemaggluti

172 tinin (HA) (termed P1) were compared with Ab-secreting cells elicited by historical H1N1 vaccine stra

173 Overexpression of SOX4 in the human insulin-secreting cell EndoC-betaH2 interfered with granule empt

174 of Ab secretion and form large numbers of Ab-secreting cells even in the absence of cognate Ags.

175 ll proliferation and differentiation into Ab-secreting cells ex vivo and stronger T cell-independent

176 tion correlated strongly with large antibody-secreting cell expansion and early production of high co

177 7 was inhibited by physical removal of IL-17-secreting cells, exposure to recombinant transforming gr

178 Serotonin-secreting cells expressed a number of mast cell genes bu

179 In insulin-secreting cells, expression of NADPH oxidase (NOX), a po

180 hope for self-renewal of functional insulin-secreting cells following beta-cell failure, a historica

181 but without degradation, we find that model secreting cells form clumps without streaming.

182 With degradation, the model secreting cells form streams and efficiently transverse

183 fection exaggerates early antiviral antibody-secreting cell formation, and at later times, levels of

184 decrease in secondary high-affinity antibody-secreting cell formation.

185 tiation, and spleen and bone marrow antibody-secreting cell frequencies were 10-fold higher in aged m

186 binding site on Mcl1 mRNA protected insulin-secreting cells from apoptosis triggered by miR-29 or cy

187 ROCKII inhibitor H1152 as increasing insulin secreting cells from hPSCs and improving beta-cell matur

188 ions of FTY720, which prevents egress of IgA-secreting cells from Peyer's patches.

189 racterized and compared to those of antibody-secreting cells from untreated ITP spleens and from heal

190 oliferation, but it is also essential for Ab-secreting cell function and differentiation in vivo.

191 en clonal expansion of memory B cells and Ab-secreting cell generation are inhibited.

192 ZIKV-specific Ab-secreting cells, germinal center reactions, and monocyte

193 Recently, IL-17A-secreting cells have been found in lung lavage, invoking

194 h pure Ag, we analyze the frequencies of IgG-secreting cells (IgG-SCs) in the spleen, as well as for

195 stellate cells (HSCs), the primary collagen-secreting cell in liver, and queried against a transcrip

196 SARS-CoV-2 nucleocapsid protein-specific Ab-secreting cells in all 20 COVID-19 patients using a mult

197 ression of ABF-1 reduced the formation of Ab-secreting cells in an in vitro differentiation system of

198 enters, and the frequency of SIV-specific Ab-secreting cells in B cell zones.

199 Vi-specific IgG in serum and IgG(+) antibody-secreting cells in bone marrow.

200 r induction of neutralizing Abs, and more Ab-secreting cells in bone marrow.

201 ctive CD8(+) T cells and long-lived antibody-secreting cells in CD4KO mice.

202 The rapid induction of interferon-gamma-secreting cells in ferrets previously infected with H1N1

203 On average >70% of IgG-secreting cells in individuals with severe secondary DEN

204 es of hepatitis and increased numbers of IgA-secreting cells in liver, compared with mice given contr

205 ted with low frequencies of ZIKV-specific Ab-secreting cells in lymph nodes and bone marrow, correlat

206 n B cells proliferate and turn into antibody-secreting cells in response to TLR3, TLR7 and TLR9, but

207 vels and the number of HSV-specific antibody-secreting cells in secondary lymphoid tissues were unaff

208 hen these cells were reprogrammed into IL-17-secreting cells in Skint-1 mutant mice, they required PL

209 We enumerated donor-specific antibody-secreting cells in the blood of nine renal allograft rec

210 to quantify B-cell populations and antibody-secreting cells in the blood of patients with AD, patien

211 which activates the LPA receptor 1 in FGF23-secreting cells in the bone and bone marrow.

212 al antibodies (hMAbs) directly from antibody-secreting cells in the circulation of immunized human vo

213 helper (GC Tfh) and GC B cells and antibody-secreting cells in the spleen and bone marrow in respons

214 ndicate an increase in the frequency of IgG1-secreting cells in the spleen of SjS(s) mice compared to

215 greement with this finding, the number of Ab-secreting cells in the spleens of IkappaBNS KO mice was

216 pecific antibodies in the serum and antibody-secreting cells in their secondary lymphoid organs, part

217 , which is implicated in the loss of insulin-secreting cells in type II diabetics.

218 17-HDHA increased the number of Ab-secreting cells in vitro and the number of HA-specific A

219 timuli and differentiate into immunoglobulin-secreting cells in vitro.

220 ns will progressively convert into IFN-gamma-secreting cells in vivo as they differentiate into effec

221 that these previously unappreciated cytokine-secreting cells, including ILC1 (IFN-gamma-expressing NK

222 Differentiation of B cells into Ab-secreting cells induces changes in gene transcription, I

223 e monitored for the presence of autoantibody-secreting cells, inflammatory cytokines, and joint infla

224 endent and -independent antigen-specific IgM-secreting cells into skin.

225 Instead, its induction in alae-secreting cells is controlled by a specific developmenta

226 ing cells were most abundant early and IL-17-secreting cells late.

227 ic ablation of beta-arrestin 2 in an insulin-secreting cell line and mouse pancreatic islets, respect

228 LUTag) and in vivo in mice using the insulin-secreting cell line INS-1 832/13 as reference.

229 Using the insulin-secreting cell line INS-1E, we found that glucose stimul

230 the spleen and a quiescent population of Ab-secreting cells maintained in the bone marrow for a long

231 a predetermined reservoir to replenish IL-17-secreting cells may have implications in balancing the T

232 n and maintenance of these critical antibody-secreting cells may serve as potential therapeutic targe

233 life and that vaccines that induce IFN-gamma-secreting cells might, in some situations, be less prote

234 g tissue eosinophils and inflammation, mucus-secreting cell (MSC) numbers, type 2-associated cytokine

235 easles-specific antibody levels and antibody-secreting cell numbers were also observed, indicating a

236 maintenance of Ag-specific Ig titers and Ab-secreting cell numbers.

237 ulocyte macrophage colony-stimulating factor-secreting cells of hitherto unknown function in atherosc

238 tions are common in APAs resembling cortisol-secreting cells of the adrenal zona fasciculata but are

239 a subset of APAs resembling the aldosterone-secreting cells of the adrenal zona glomerulosa.

240 ly being scaffolding or extracellular matrix-secreting cells on which organ systems are built, stroma

241 including the expansion of specific IFNgamma secreting cells or production of influenza-specific anti

242 out increasing the number of Env-specific Ab-secreting cells or the Ab-binding titers measured after

243 lls and a higher proportion of interleukin 2-secreting cells (P = .01 and P = .002, respectively).

244 an average of 3253 IgA and 1227 IgG antibody-secreting cells per million peripheral blood mononuclear

245 NV-specific memory B cells but not antibody-secreting cells persisted 180 days after infection.

246 l differentiation toward a CD27(+)CD38(+) Ab-secreting cell phenotype.

247 Partially differentiated antigen-secreting cells (plasmablasts) have long been regarded a

248 27(neg)CD11c(+)CXCR5(neg) (DN2) pre-antibody secreting cell (pre-ASC) subset.

249 ls in vitro and the number of HA-specific Ab-secreting cells present in the bone marrow.

250 rts by positive selection of Ag-specific, Ab-secreting cells prior to hybridoma fusion and validation

251 d by limiting the distance over which enzyme-secreting cells provide benefits to neighbors, resulting

252 Here we show that proton-secreting cells (PSCs) differentiate in the X. laevis la

253 espondingly, less specific IgE- and more IgA-secreting cells resided in the spleen in the 9cRA groups

254 ignificantly reduced for IgG-, IgM-, and IgA-secreting cells, respectively.

255 ovel mechanisms by which professional proton-secreting cells respond to extracellular cues to modulat

256 us better understand how professional proton-secreting cells respond to extracellular cues to modulat

257 gs induce, in mice and monkeys, an IFN-gamma-secreting cell response that significantly reduces viral

258 he development of anti-WNV-specific antibody-secreting cell responses and memory B cell responses ind

259 ice, suggesting that the epitope-specific Ab-secreting cell responses measured after boost are indepe

260 Antibody-secreting cell responses were biased toward IgA, while m

261 to rLBNSE, could differentiate into antibody-secreting cells, resulting in rapid and potent secondary

262 of PPD-specific interferon gamma (IFNgamma) secreting cells (SFU) were compared, with the more susce

263 milar frequencies of stalk-reactive antibody-secreting cells, showing that HA head immunodominance is

264 e detected in parallel with longer-lived IgG-secreting cells, suggesting ongoing and parallel input t

265 iation, which cooperate to generate antibody-secreting cells that cause the deposition of antibodies

266 MBCs proliferated and gave rise to antibody-secreting cells that dominated the early secondary respo

267 Studies also identified IL-17A-secreting cells that expressed IFN-gamma, but their abun

268 duced B cells to differentiate into antibody-secreting cells that produced DSAs.

269 nd they developed into memory B cells and Ab-secreting cells that were capable of producing parasite-

270 sms permit the B cell precursors of these Ab-secreting cells to exist within the normal B cell repert

271 nt CXCR3-mediated migration of antiviral IgM-secreting cells to the infected CNS was dependent on CD4

272 children differentiated quickly to antibody-secreting cells to the new vaccine antigens.

273 creatic beta-cells; the loss of this insulin-secreting cell type underlies type 1 diabetes.

274 erular cells from a renin- to erythropoietin-secreting cell type, presumably in response to HIF-2 acc

275 itro differentiation of memBcs into antibody-secreting cells was 6.1-, 2.6-, and 3.7-fold significant

276 a substantial number of antigen-specific IgA-secreting cells was found in the liver.

277 tional HSV-specific, CD8(+) gamma interferon-secreting cells was significantly decreased.

278 ately the distributions of affinities of IgG-secreting cells we measure in mice immunized against Tet

279 optogenetic, glucagon-like peptide-1 (GLP-1) secreting cells, we conducted light-controlled therapy u

280 nterparts in lymphoid tissues, cutaneous IgM-secreting cells were completely dependent on survival fa

281 IgG-secreting cells were detected by enzyme-linked immunospo

282 F protein-specific antibody-secreting cells were detected in the bone marrows of VLP

283 IFN-gamma-secreting cells were most abundant early and IL-17-secre

284 and short-lived and long-lived autoantibody-secreting cells were nearly undetectable in the CD19 mAb

285 n a human xenogeneic GVHD model, human IL-21-secreting cells were present in the colon of GVHD recipi

286 , IpaD, and dmLT-specific serum IgG- and IgG-secreting cells were produced following i.d. immunizatio

287 ody production and the frequency of antibody-secreting cells were significantly elevated in NP, and t

288 IgA, as well as mucosal and systemic IgA Ab-secreting cells, were seemingly absent.

289 ovide help to B cells for developing into Ab-secreting cells, were similar between responders and non

290 -10 (P<0.05) with reduced IFN-gamma (P<0.05) secreting cells when compared with group 1.

291 nchyme give rise to glucose-sensing, insulin-secreting cells when transplanted in vivo.

292 s-signaling-driven cell proliferation of the secreting cells, whereas conditioned supernatant from th

293 matic reduction of antigen-specific antibody-secreting cells, whereas deletion of relb had no effect.

294 cells preferentially differentiated into Ab-secreting cells, whereas in the primary response, H-2K(d

295 eo) mice contained diminished numbers of IgA-secreting cells, while elevated germinal center B cells

296 with a special focus on the identity of IgE-secreting cells ("who"), their location ("where"), and t

297 of hydrogels in the encapsulation of insulin secreting cells with a special emphasis on hydrogels des

298 ells are CD4(+) T cells that select antibody secreting cells with high antigenic affinity in germinal

299 Treatment of insulin-secreting cells with unloaded DIANAs did not impair cell

300 zed antibody repertoire in CD138(+) antibody-secreting cells within the PLN.