ライフサイエンスコーパス: secreting cell

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

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

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

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

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

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

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

8 reased frequency of proinflammatory cytokine-secreting cells.

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

10 ation models when delivered by lentivirus or secreting cells.

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

12 eduction in pathogenic autoantibodies and Ab-secreting cells.

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

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

15 of differentiation of B cells into antibody secreting cells.

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

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

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

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

20 r ability to differentiate into autoantibody-secreting cells.

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

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

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

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

25 metry phenotypically characterized IFN-gamma-secreting cells.

26 tates differentiation of long-lived antibody-secreting cells.

27 f Foxp3+ regulatory T cells and IgA antibody-secreting cells.

28 ferentiation into type 1 and type 2 cytokine-secreting cells.

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

30 of IgM secretion and higher incidence of IgM-secreting cells.

31 y reduced numbers of early viral-specific Ab-secreting cells.

32 morphological differentiation into antibody-secreting cells.

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

34 nsity for conversion into functional insulin-secreting cells.

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

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

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

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

39 man intestinal epithelial cells into insulin-secreting cells.

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

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

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

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

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

45 eening both bacterial and mammalian antibody secreting cells.

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

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

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

49 secreted by monocytes (percent of TNF-alpha secreting cells: 20.4+/-4.8 vs. 1.2+/-0.5 vs. 1.4+/-0.6

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

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

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

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

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

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

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

57 Many of the IL-17-secreting cells also secrete TNF and some secrete IL-2.

58 rable frequencies of PLP-specific, IFN-gamma-secreting cells and also induced Ag-specific proliferati

59 to increased levels of HIV-specific antibody-secreting cells and B cell-associated chemokines and cyt

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

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

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

63 wed significant increase in interferon-gamma-secreting cells and frequency of WT1 tetramer-positive C

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

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

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

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

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

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

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

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

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

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

74 ish novel actions for NA and G(z) in insulin-secreting cells and possibly other cell types.

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

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

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

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

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

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

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

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

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

84 elicited improved antibody, gamma interferon-secreting cell, and cytotoxic T-lymphocyte responses com

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

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

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

88 nage a trois" involving NK cells, IL-2/IL-15-secreting cells, and infected macrophages.

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

90 tory responses, reduced T. cruzi-specific Ab-secreting cells, and significantly less mucosal T. cruzi

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

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

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

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

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

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

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

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

99 d Staphylococcus aureus Cowan-induced IgG Ab-secreting cell (ASC) frequency, HCV and tetanus-specific

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

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

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

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

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

105 activation and differentiation into antibody-secreting cells (ASC) of CBC but not IBC when the B cell

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

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

108 obulin in cerebral spinal fluid and antibody secreting cells (ASC) within the central nervous system

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

110 STV there was a lack of circulating antibody-secreting cells (ASC), reflecting the local mucosal effe

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

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

113 often associated with retention of antibody-secreting cells (ASC).

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

115 y and duration of circulating human antibody-secreting cells (ASCs) after vaccination have been well

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

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

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

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

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

121 ay (ELISA), and total IgG and dsDNA antibody-secreting cells (ASCs) by enzyme-linked immunospot assay

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

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

124 Germinal centers and antibody-secreting cells (ASCs) in spleens and IgG deposition and

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

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

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

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

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

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

131 collected for serological profile, antibody secreting cells (ASCs), and analysis of ASC homing recep

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

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

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

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

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

137 re primarily CD8(+) T cells and IgM antibody-secreting cells (ASCs).

138 induce transient increases in circulating Ab-secreting cells (ASCs).

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

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

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

142 lasmablasts and spontaneous H1N1-specific Ab-secreting cells at T1.

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

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

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

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

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

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

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

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

151 n conversion of memory B cells into antibody-secreting cells by in vitro culture.

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

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

154 of much higher levels of PLP-specific, IL-17-secreting cells compared with CpG 1826/IFA.

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

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

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

158 and frequencies of autoantigen-specific, Ab-secreting cells declined upon CEP-33779 treatment.

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

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

161 bone marrow plasma cells and spleen antibody-secreting cells detected in the MN group.

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

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

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

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

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

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

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

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

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

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

172 7 was inhibited by physical removal of IL-17-secreting cells, exposure to recombinant transforming gr

173 We found that the ghrelin-secreting cells express high levels of mRNA encoding bet

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

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

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

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

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

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

180 ation of single-cell IgG secretion rates and secreting cell frequencies in human B cell populations.

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

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

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

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

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

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

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

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

189 um autoantibody titers, splenic autoantibody-secreting cells, germinal centers, and the splenic T hel

190 te neuronal responses to neurotrophic factor-secreting cell grafts placed within sites of right C7 he

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

192 ction of the following: 1) the number of IgG-secreting cells (IgG-SC), and 2) the secretion rate of e

193 m the lung and enhanced humoral and antibody-secreting cell immune responses after 100% survival from

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

195 y B cells and ex vivo H1N1-stimulated IgG Ab-secreting cells in an ELISPOT assay.

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

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

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

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

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

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

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

203 gh modest increase in the frequency of IL-17-secreting cells in lymphocytes from long-term patients w

204 like cells similar to the endogenous insulin-secreting cells in mice.

205 very low frequencies of isotype-switched IgG-secreting cells in mouse spleens, until at least 3 wk po

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

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

208 a result of an adenoma arising from the ACTH-secreting cells in the anterior pituitary.

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 and had elevated numbers of IgG2c- and IgG2b-secreting cells in the bone marrow.

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

213 xpressed on the basolateral membrane of acid-secreting cells in the renal outer medullary collecting

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

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

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

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

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

219 17-HDHA increased the number of Ab-secreting cells in vitro and the number of HA-specific A

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

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

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

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

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

225 th AD or from the conditioned media of Abeta-secreting cells into experimental animals.

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 ng antibodies, mucosal and systemic antibody-secreting cells, memory B cells, and gamma interferon-se

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

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

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

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

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

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

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

241 Mucus-secreting cells of the stomach epithelium provide a prot

242 directly on beta(1) receptors on the ghrelin-secreting cells of the stomach.

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

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

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

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

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

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

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

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

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

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

253 he gill epithelium, where the subset of base-secreting cells resides.

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

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

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

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

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

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

260 carry IgE Ag receptors and give rise to IgE-secreting cells should provide longer term efficacy.

261 In this region, a specialized group of acid-secreting cells similar to mammalian gastric parietal ce

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

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

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

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

266 The IgM-secreting cells that we have identified were maintained

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

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

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

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

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

272 equired for the specification of the hormone-secreting cell types of the pituitary gland underlie sev

273 B lymphocytes differentiate into antibody-secreting cells under the antigen-specific control of fo

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

275 No significant population of IFN-gamma-secreting cells was detectable when posttransplantation

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

277 elopment demonstrated that progression to Ab-secreting cells was impaired in IkappaBNS KO B cells.

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

279 rism after CBT, and no significant IFN-gamma-secreting cells were detected after similar stimulations

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

281 gM, IgA, and IgE and a high proportion of Ig-secreting cells were detected in mut/mut mice.

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 CD56(+) NK cells were predominantly cytokine-secreting cells, whereas DN NK possessed both functions.

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

296 The IgM-secreting cells, which exhibited characteristics of both

297 ry lymphoid tissue and contains autoantibody-secreting cells, which may escape from normal censoring

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

299 In human arthritis the majority of IL-17-secreting cells within the joint express a cytokine phen

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