ライフサイエンスコーパス: adoptively

1 ts shows that the resorption response can be adoptively acquired.

2 onal region and alternative splicing, and of adoptively administering them to patients with relapsed

3 MOG-specific CD8 T cells could also suppress adoptively induced disease using wild-type MOG35-55-spec

4 proach for ovarian and other tumors in which adoptively infused gammadelta T cells are targeted using

5 fector memory T (Tem) cells were transferred adoptively to allergen-sensitized animals before allerge

6 Using allotype markers, it is possible to adoptively transfer memory B cells into a naive mouse an

7 rized DCs from sulfatide-treated animals can adoptively transfer protection into naive mice.

8 tch, we compared the therapeutic efficacy of adoptively transfer Treg with or without donor specifici

9 Furthermore, we demonstrate that adoptively transferred (5M)CAR-CTLs can mitigate type I

10 r protection of nude mice was achieved using adoptively transferred 1.0 and 0.1 million, but not 0.01

11 Monitoring the adoptively transferred 2D2 T cells over time demonstrate

12 man islet cells under the kidney capsule and adoptively transferred 5 x 10(6) splenocytes from 6-week

13 Alternatively, macrophages could be adoptively transferred after ex vivo genetic modificatio

14 mation and goblet cell hyperplasia driven by adoptively transferred Ag-specific CD4(+) Th2 cells.

15 rejection and augmented the proliferation of adoptively transferred alloantigen-specific CD4(+) T cel

16 Adoptively transferred allogeneic HSCs migrated to the s

17 bnAb-engineered primary mouse B cells can be adoptively transferred and vaccinated in immunocompetent

18 Adoptively transferred antigen-specific CD4(+) T cells f

19 lated significantly greater proliferation of adoptively transferred antigen-specific CD8(+) T cells i

20 Adoptively transferred antigen-specific T cells that rec

21 l was carried out to evaluate the ability of adoptively transferred autologous T cells transduced wit

22 o 70% of patients with melanoma who received adoptively transferred autologous tumor-infiltrating lym

23 In sharp contrast, adoptively transferred autoreactive T cells from Kindlin

24 When adoptively transferred back to the individual, the genet

25 pDCs and T-cell cultures were adoptively transferred before heterotopic heart transpla

26 Stimulation of adoptively transferred bioluminescent MPhis and B-1a cel

27 ion profiles of other chemokine receptors of adoptively transferred BLT1(+)/(+) and BLT1(-)/(-) CD8(+

28 Furthermore, adoptively transferred caIKKbeta T cells showed diminish

29 ptor CCR2; 2) compared with CCR2(+/+) cells, adoptively transferred CCR2(-/-) bone marrow-derived DCs

30 Adoptively transferred CD18(hypo) PL/J Tregs were more i

31 To test this, we adoptively transferred CD27low NK cells into Rag1-/-T-be

32 28 also enhanced the suppressive capacity of adoptively transferred CD4(+) nTregs by increasing the s

33 Adoptively transferred CD4(+)CD25(-) T cells were conver

34 Adoptively transferred CD70-specific T cells induced sus

35 -infiltrating myeloid cells is important for adoptively transferred CD8(+) cytotoxic T cells to destr

36 intravascular adhesion and extravasation of adoptively transferred CD8(+) effectors that is indispen

37 imal expansion, trafficking, and function of adoptively transferred CD8(+) T cells are parameters tha

38 In contrast, adoptively transferred CD8(+) T cells enter and leave th

39 Adoptively transferred CD8(+) T cells from Ang II-infuse

40 In vivo expansion of adoptively transferred CD8(+) T cells is a critical dete

41 and TLR/CD40 agonists augmented expansion of adoptively transferred CD8(+) T cells, delayed tumor gro

42 role in expansion and antitumor efficacy of adoptively transferred CD8(+) T cells.

43 ion, persistence and anti-tumour capacity of adoptively transferred CD8(+) T cells.

44 ipient mice supported the rapid expansion of adoptively transferred CD8+ T cells against melanoma.

45 To our surprise, an adoptively transferred CD8gamma13 T-cell clone was remar

46 d humans correlates with both a high dose of adoptively transferred cells and cells with a minimally

47 We postulate that adoptively transferred cells are able to expand in respo

48 ere treated with DNA-HSP65, CpG/CFP, or with adoptively transferred cells from immunized mice.

49 ith or without cotransplanted kidneys and/or adoptively transferred cells from long-term tolerant (LT

50 wine received class I mismatched kidney with adoptively transferred cells from LTT SLA(dd) recipients

51 in the spleen (where a major portion of the adoptively transferred cells homed) and in the eyes, whe

52 henotypic and functional characterization of adoptively transferred cells in ACT-responsive and nonre

53 lds promise to increase the effectiveness of adoptively transferred cells in both experimental and cl

54 t the lifespan, safety, and functionality of adoptively transferred cells in the presence of autologo

55 However, adoptively transferred cells isolated from the lamina pr

56 T-cell expansion improved the persistence of adoptively transferred cells, reduced tumor growth, and

57 r infusion, might improve the persistence of adoptively transferred cells.

58 vity, and intratumoral cytokine secretion by adoptively transferred cells.

59 , distribution, or tumor accumulation of the adoptively transferred cells.

60 f T cell tolerogenesis, we further show that adoptively transferred central but not effector memory T

61 e clinical efficacy and anatomic location of adoptively transferred chemokine receptor-deficient CD4(

62 Long-term survival of adoptively transferred chimeric Ag receptor (CAR) T cell

63 hermore, immune reconstitution included both adoptively transferred clonotypes and endogenous clonoty

64 Using a novel approach, we adoptively transferred conventional T cells expressing t

65 tive optical control of Ca(2+) signalling in adoptively transferred CTLs enhances T cell activation a

66 was sufficient to induce the recruitment of adoptively transferred CTLs to islets.

67 kade might enhance the antitumor activity of adoptively transferred CTLs.

68 Strikingly, we found that the activity of adoptively transferred DGKzeta(-/-) T cells relied partl

69 ressing the diabetogenic AI4 T-cell receptor adoptively transferred disease to otherwise unmanipulate

70 We found that low doses of adoptively transferred donor CD4(+) iNKT cells protect f

71 curs in the presence of rapamycin or whether adoptively transferred donor Th9 cells would augment or

72 We investigated the use of adoptively transferred donor-derived cytomegalovirus (CM

73 C function after HCT could be augmented with adoptively transferred donor-derived DC.

74 engineered T cells to overexpress TRAIL and adoptively transferred donor-type unsorted TRAIL+ T cell

75 Furthermore, effector CD8(+) T cells adoptively transferred during the effector phase fail to

76 d that persistence and antitumor activity of adoptively transferred effector T cells deficient in TGF

77 TEa cells were adoptively transferred either into B6 recipients that re

78 k macrophage dynamics in dysferlinopathy, we adoptively transferred enhanced green fluorescent protei

79 enhanced green fluorescent protein mice were adoptively transferred following carotid injury.

80 Splenocytes adoptively transferred from mice with HF, but not from s

81 o far reported only limited tumor control by adoptively transferred gamma9delta2T cells.

82 Adoptively transferred gammadelta T cells isolated from

83 We show that adoptively transferred GFP(+) sorted mature follicular B

84 Adoptively transferred Grp78(-/+) CD8alphabeta(+) T cell

85 ivo microscopy corroborated proliferation of adoptively transferred hematopoietic progenitors in the

86 Here, we evaluate the use of adoptively transferred HIV vaccine-induced subtype C Env

87 We adoptively transferred HLA-A2-matched peripheral blood m

88 CID/IL2Rg(null) mice, but the persistence of adoptively transferred HSPC-NK cells was not affected.

89 lonal antibodies of desired specificity from adoptively transferred human B cells.

90 Mice with adoptively transferred HuR KO Th17 cells had delayed ini

91 Adoptively transferred IELps parked better in the intest

92 cial pathogenic role played by IL-21 in T1D, adoptively transferred IFN-gamma-deficient CpG-proBs did

93 For the in vivo study, we adoptively transferred ILC2s and CD4(+) T cells into Il7

94 We find, however, that adoptively transferred immune T cells eradicate well-est

95 the proliferation of the allospecific Tregs adoptively transferred in an antigen-dependent manner.

96 revent graft-versus-host disease (GVHD) when adoptively transferred in murine models of hematopoietic

97 CD86, in expansion and antitumor efficacy of adoptively transferred in vitro-primed CD8(+) T cells re

98 sCD200 serum adoptively transferred increased graft survival to naive

99 We adoptively transferred innate IL-13-producing cells to i

100 bakeri-infected mice prevented colitis when adoptively transferred into a murine model of inflammato

101 Lastly, MZ, but not follicular, B cells adoptively transferred into B-cell-deficient muMT mice r

102 s plus B-cell-depleted wild-type splenocytes adoptively transferred into B-cell-deficient muMT mice r

103 el was established whereby DsRedOTI-Tc cells adoptively transferred into B6 mice bearing either a ova

104 from IL-6-deficient or wild-type donors were adoptively transferred into BALB/c mice.

105 cs of CD4-mediated help, CD4(+) T cells were adoptively transferred into CD4-deficient mice at variou

106 entiation under these conditions, cells were adoptively transferred into CD8-deficient mice, and lung

107 Monoclonal T. gondii-specific CD8 T cells adoptively transferred into coinfected mice recapitulate

108 Young donor B cells were adoptively transferred into congenic recipients and allo

109 ed with cytokines (GM-CSF, IL-4, IL-33) were adoptively transferred into eosinophil-deficient recipie

110 when FcgammaR(+/+) dendritic cells (DCs) are adoptively transferred into FcgammaR(-/-) mice, uptake a

111 When adoptively transferred into IL-13(-/-) mice, both wild-t

112 Nevertheless, when adoptively transferred into immunodeficient Rai(+/+) mic

113 city to MYHCA acquired a Treg phenotype when adoptively transferred into infarcted mice, which mediat

114 atic DKO NK cells show reduced survival when adoptively transferred into lymphopenic hosts.

115 Interestingly, WT B cells adoptively transferred into lyn(-/-) mice showed increas

116 RPE cell-induced MDSCs were adoptively transferred into mice immunized with interpho

117 om unstressed control mice were isolated and adoptively transferred into naive lymphopenic Rag2(-/-)

118 These memory B cells adoptively transferred into naive mice without memory T

119 itiate immunity (both skin and airways) when adoptively transferred into naive mice.

120 elta T cells in this model, these cells were adoptively transferred into naive recipients.

121 hermore, p47(phox-/-) DCs pulsed with Lm and adoptively transferred into naive WT mice elicited Ab ti

122 Also, human ILC2s and Treg cells were adoptively transferred into NOD SCID gammaC-deficient mi

123 ts with undetectable plasma viral loads were adoptively transferred into NOD.Cg-Prkdc(scid)Il2rg(tm1W

124 ogenic than their wild-type counterpart when adoptively transferred into NOD.Rag1(-/-) recipients, ev

125 tiple lymphoid tissues, and were lethal when adoptively transferred into normal recipient mice.

126 Also, autophagy-deficient ILC2s were adoptively transferred into Rag(-/-)GC(-/-) mice, which

127 1(-) thymocytes from Rag1((-)/(-)) mice were adoptively transferred into Rag1((-)/(-))Ly5.1 congenic

128 d capable of inducing stromal keratitis when adoptively transferred into Rag1(-/-) mice, with 95% of

129 of miR-15b/16 in conventional CD4(+) T cells adoptively transferred into Rag2(-/-) mice increased the

130 , which could by themselves mediate AHR when adoptively transferred into Rag2(-/-); Il2rg(-/-) mice t

131 ILC2(10)s were also adoptively transferred into Rag2(-/-)gammac(-/-) mice, w

132 genic cells specific to hen egg lysozyme are adoptively transferred into recipients that express hen

133 When adoptively transferred into syngeneic naive mice, the by

134 When adoptively transferred into the joint, FAPalpha(+)THY1(-

135 ulation responsible, primed CD8 T cells were adoptively transferred into tumor-bearing immunocompromi

136 cells from ovalbumin (OVA)-primed mice were adoptively transferred into wild-type (WT) hosts.

137 Furthermore, IRF3(-/-) OT1 cells adoptively transferred into wild-type hosts also produce

138 T cell-dependent anti-parasite immunity when adoptively transferred into WT mice.

139 MDSCs and potently promote tumor growth when adoptively transferred into WT mice.

140 In vivo, the number of adoptively transferred Kindlin-3-deficient T effectors w

141 t of infection from a high-dose inoculum, we adoptively transferred large numbers of T cells that wer

142 roscopy of lymph node explants revealed that adoptively transferred lymphocytes accumulated at lympha

143 e tumor cells that are not recognized by the adoptively transferred lymphocytes.

144 Fluorescent imaging analyses revealed that adoptively transferred M2r macrophages specifically home

145 The brain accumulation of adoptively transferred macrophages was evaluated by vari

146 Adoptively transferred mast cells or M2 macrophages reve

147 d in C57BL/6J-Kit(W-sh/W-sh) mice containing adoptively transferred mast cells that were either wild

148 Notably, both adoptively transferred mature KIR(+) NK cells and immatu

149 Furthermore, the adoptively transferred memory cells responded to tumor r

150 d allergy symptoms that could be restored by adoptively transferred MMC9s.

151 was assessed by quantifying proliferation of adoptively transferred monoclonal T-cell receptor transg

152 experiments revealed that the recruitment of adoptively transferred monocytes and neutrophils to the

153 sed expression within primary tumors, as the adoptively transferred MSC develop carcinoma-associated

154 Finally, adoptively transferred MSCs in complement deficient mice

155 Here we trace the fate of adoptively transferred murine NK cells and make the surp

156 but Nlrx1(-/-) mice are more susceptible to adoptively transferred myelin-reactive T cells.

157 Finally, the ability of adoptively transferred naive CD8 T cells to protect RAG(

158 Adoptively transferred naive HEL-specific CD4(+) T cells

159 We also adoptively transferred naive IL-4Ralpha(-/lox) or IL-4Ra

160 e immune milieu, CTX preconditioning allowed adoptively transferred naive tumor-specific CD4+ T cells

161 Importantly, 20% to 30% of the adoptively transferred neutrophils acquired CD11c and MH

162 Second, adoptively transferred neutrophils isolated from G-CSF-p

163 However, to expand the scope of adoptively transferred NK cell homing to various maligna

164 o optimize the in vivo cytokine milieu where adoptively transferred NK cells compete with other lymph

165 Clinical trials on adoptively transferred NK cells in patients with solid t

166 poxia, and transgenic expression of IL-15 in adoptively transferred NKT cells dramatically enhanced t

167 In vivo, adoptively transferred NO-Tregs potently attenuated expe

168 to augmenting both endogenous leukocytes and adoptively transferred ones by informing specificity, in

169 le, we show that CD154 expression identifies adoptively transferred or endogenous Ag-specific CD4(+)

170 Using adoptively transferred OT-2 cells, we show that the Ag t

171 Responses of adoptively transferred OT-II T cells were greater in MPO

172 gely abrogated the proliferative response of adoptively transferred OVA peptide-specific-transgenic C

173 In addition, the ability of adoptively transferred OVA-activated T cells to home to

174 jection, we used a transgenic model in which adoptively transferred ovalbumin (OVA)-specific cytotoxi

175 o not required to promote disease induced by adoptively transferred pathogenic CD4(+) T cells.

176 Adoptively transferred PC1(lo) cells secreted significan

177 Importantly, adoptively transferred PD-1 KO CD8 central memory T (T(C

178 Additionally, adoptively transferred PD-1 KO T(EM) phenotype cells con

179 y, we evaluated the antileukemia activity of adoptively transferred polyclonal cancer antigen-reactiv

180 e mouse spleen and promoted the migration of adoptively transferred pre-activated B cells to the T/B

181 knock-in mice (termed HKIR) were relieved in adoptively transferred recipients in the presence of Sle

182 ntly inhibited antidonor immune responses in adoptively transferred recipients.

183 sed suppressive activity of other subsets in adoptively transferred recipients.

184 In summary, adoptively transferred S1pr3(-/-) BMDCs prevent kidney I

185 We compared the effects of adoptively transferred SOCS3(-/-) and SOCS3(+/+) bone ma

186 Furthermore, adoptively transferred splenic CD8 memory phenotype T ce

187 pled to inadequate cardiac commitment of the adoptively transferred stem cells compromises the improv

188 However, the majority of adoptively transferred stem cells delivered to damaged m

189 Both tumor growth and metastases of adoptively transferred syngeneic Lewis lung carcinoma (L

190 Adoptively transferred T cell receptor (TCR)-transgenic

191 n epigenetic regulation impeding efficacy of adoptively transferred T cells and other approaches that

192 results in increased antitumor immunity when adoptively transferred T cells are presensitized, but de

193 is shown that effector cytokines secreted by adoptively transferred T cells expressing a chimeric Ag

194 In this context, dose minimization of adoptively transferred T cells might be warranted for th

195 We now report adoptively transferred T cells or whole splenocytes from

196 GM-CSF secreted by the adoptively transferred T cells recruited peripheral F4/8

197 esponse and may help prevent inactivation of adoptively transferred T cells thereby improving therape

198 cell surface marker for in vivo tracking of adoptively transferred T cells using both flow cytometry

199 Finally, adoptively transferred T cells were capable of reducing

200 e control of cytotoxic effector functions of adoptively transferred T cells with outstanding spatial

201 sed the population size and functionality of adoptively transferred T cells within the tumor.

202 hich host tumor Ag cross-presentation primes adoptively transferred T cells, which remain functional

203 tors (CARs) determine the overall potency of adoptively transferred T cells.

204 th sustained influx and proliferation of the adoptively transferred T cells.

205 t protected by ST-246 alone or by 10 million adoptively transferred T cells.

206 vivo expansion and polyfunctionality of the adoptively transferred T cells.

207 th increased CTL activity and persistence of adoptively transferred T cells.

208 imarily on the expansion and survival of the adoptively transferred T cells.

209 tors (CARs) direct tumor cell recognition of adoptively transferred T cells.

210 wn to enhance the antimalignancy activity of adoptively transferred T cells.

211 ular tumor microenvironment which suppresses adoptively transferred T cells.

212 al for immunotherapeutic intervention, using adoptively transferred T cells.

213 similarly augmented antitumor effects of the adoptively transferred T cells.

214 Using mice and adoptively transferred T lymphocytes lacking the small G

215 Adoptively transferred T(EM) cells from hypertensive mic

216 Adoptively transferred T-cell receptor (TCR)-engineered

217 athway potentiates the antitumor activity of adoptively transferred Tc17 cells.

218 COS ligand reduced the antitumor activity of adoptively transferred Tc17 cells.

219 Phenotypic analysis revealed that adoptively transferred Tc9 cells secreted IL-2 and were

220 tide injection, in vivo Helios expression in adoptively transferred TCR transgenic T cells was more r

221 activation, proliferation, and expansion of adoptively transferred TEa cells in an Ag-specific manne

222 Adoptively transferred TEa cells in skin-graft recipient

223 By contrast, virtually all adoptively transferred TEa cells were exhausted in CB6F1

224 In this study, we show that activation of adoptively transferred Th cells during primary influenza

225 Interestingly, adoptively transferred Th17 cells demonstrated plasticit

226 Here, we explored the role of adoptively transferred third-party CD4(+) iNKT cells for

227 h2-, or IL-17-producing CD4(+) T cells, were adoptively transferred to APP/PS1 mice at 6 to 7 mo of a

228 ) T cells from Il17a fate-mapping mice, were adoptively transferred to assess their persistence in ge

229 Furthermore, when adoptively transferred to Il7r(-/-) mice, which lack ILC

230 endritic cells cultured with SA-IVIg or IVIg adoptively transferred to mice before OVA challenge indu

231 purified graft-reactive CD4CD25 T cells were adoptively transferred to mice-bearing skin allograft.

232 enes and induced airway hyperreactivity when adoptively transferred to mice.

233 GMSCs were adoptively transferred to multiple low-dose streptozotoc

234 In gain-of-function experiments, B-1a cells, adoptively transferred to muMT mice with EAE, restored t

235 ice fed either control or fish oil diet were adoptively transferred to naive recipient mice.

236 pment of functional Bmem cells that could be adoptively transferred to naive recipients.

237 erior activity against tuberculosis could be adoptively transferred to naive, syngeneic mice by CD4(+

238 Bone marrow-derived DCs (BMDCs) were adoptively transferred to nonsensitized WT mice.

239 that this decreased responsiveness could be adoptively transferred to other mice.

240 Pulmonary basophils were adoptively transferred to OVA-sensitized hosts to assess

241 have demonstrated impressive responses when adoptively transferred to patients with advanced chronic

242 vivo when Il1ra knockout myeloid cells were adoptively transferred to PTEN null mice.

243 cells were sorted by flow cytometry and were adoptively transferred to recipient mice through tail ve

244 cells specific to hen egg lysozyme (HEL) are adoptively transferred to recipients and induce inflamma

245 e, T cell-dependent myeloma control could be adoptively transferred to secondary recipients and was m

246 against EAE when A2AAR(-/-) lymphocytes were adoptively transferred to T cell-deficient A2AAR(+/+) mi

247 yte-restricted adiponectin gene promoter was adoptively transferred to wild-type recipient mice.

248 have evolved from a hypothetical mediator of adoptively transferred tolerance to a well-defined popul

249 Adoptively transferred total T cells from immunized mice

250 PC survival niches and their functioning, we adoptively transferred traceable Blimp-1-(GFP) PCs into

251 Adoptively transferred Treg cells prevented spontaneous

252 D-1 ligand negated the protective ability of adoptively transferred Tregs in IRI.

253 gs, and prevents loss of Foxp3 expression in adoptively transferred Tregs in mice.

254 tion and expansion and/or persistence of the adoptively transferred tumor antigen-specific T cells in

255 Adoptively transferred tumor-infiltrating T lymphocytes

256 the survival and effector differentiation of adoptively transferred tumor-reactive CD8(+) T-cells.

257 mediated expansion and antitumor efficacy of adoptively transferred tumor-specific CD8(+) T cells wer

258 Adoptively transferred tumor-specific T cells offer the

259 ancer immunosurveillance and the efficacy of adoptively transferred tumour-specific T cells.

260 ring effector phase of chronic infection, we adoptively transferred virus-specific day 8 effector CD8

261 Adoptively transferred virus-specific T cells (VSTs) gen

262 has demonstrated the safety and efficacy of adoptively transferred virus-specific T cells for the pr

263 miquimod-treated skin of CCR6(-/-) mice, but adoptively transferred wild-type (CCR6(+/+)) gammadeltaT

264 Adoptively transferred wild-type CD4(+) T cells accumula

265 We found that adoptively transferred wild-type Tregs protected wild-ty

266 cell function was investigated in Rag1 mice adoptively transferred with alloprimed IgG1 B cells.

267 In RAG(-/-) recipients of skin allografts adoptively transferred with CD4(+) T cells, we show that

268 C57BL/6 Rag1(-/-) mice adoptively transferred with HDAC10(-/-) but not wild Tre

269 In addition, the recipient mice that are adoptively transferred with JKAP-knockout T cells show e

270 xaggerated response in DeltaLC mice could be adoptively transferred with liver CD49a(+) NK cells.

271 Mice were adoptively transferred with myeloid cells and treated wi

272 equently, STING(-/-) mice, or wild-type mice adoptively transferred with STING(-/-) bone marrow, are

273 The disease may be adoptively transferred with T lymphocytes and is class I

274 STAT6(-/-) mice adoptively transferred with Th2/Th17 cells had decreased

275 persistence and function of T cells that are adoptively transferred with the graft.

276 Importantly, mice adoptively transferred with Ubc12 knockdown CD4(+) T cel

277 However, Nfil3/Rag1 double-knockout mice adoptively transferred with wild-type CD4(+) T cells dev

278 ID mice but did occur in SCID mice that were adoptively transferred with wild-type T cells, indicatin

279 ompared with T cell-deficient mice that were adoptively transferred with wild-type T cells.

280 in part due to increased M2 macrophages, we adoptively transferred wt macrophages into Cd14(-/-) mic

281 ce were almost completely protected from the adoptively transferred, aggressive form of T1D caused by

282 55)-induced CD8 T cells could also attenuate adoptively transferred, CD4 T cell-mediated EAE.

283 The tracking of adoptively transferred, fluorescently labeled WT and alp

284 tantly, induced genetic deletion of Orai1 in adoptively transferred, MOG-specific T cells was able to

285 allergic airway inflammation (AAI) driven by adoptively transferred, traceable ovalbumin-experienced

286 cells exclusively generated B-1a cells when adoptively transferred, whereas sorted CD93(+)IgM(+)CD5(

287 ettings where virus-specific CD8 T cells are adoptively transferred.

288 y functional and could confer tolerance when adoptively transferred.

289 ent T-cell alterations, could be restored by adoptively transferring CCR8-expressing monocytes/macrop

290 cDC-mediated induction pulmonary allergy by adoptively transferring house dust mite (HDM)-pulsed bon

291 nd that providing an accelerated response by adoptively transferring large numbers of antiviral T cel

292 se inhibitor Nor-NOHA but were reproduced by adoptively transferring MDSC or injecting arginase 1 to

293 ion in a genetically deficient strain and by adoptively transferring NK cells into NK-deficient mice.

294 or effective antitumor immunity was shown by adoptively transferring purified CD27(low)KLRG1(+) NK ce

295 progressive depigmentation was evaluated by adoptively transferring purified Treg or using rapamycin

296 By adoptively transferring Rorc(fm+) ILCs into recipient mi

297 f regulatory T (Treg) cells was evaluated by adoptively transferring Treg cells from milk EPIT-treate

298 CD4 depletion was completely neutralized by adoptively transferring tumor-specific Foxp3(+) T cells.

299 Alternatively, adoptively transferring vaccine-primed T cells from Jh(-

300 ly used as a marker for tracking donor cells adoptively transplanted into recipient animals.