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 CHS) to haptens, and their T cells failed to adoptively transfer CHS.

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

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

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

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

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

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

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

14 Adoptively transferred allogeneic HSCs migrated to the s

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

16 Adoptively transferred antigen-specific T cells that rec

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

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

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

20 nic B cell numbers, survival and function of adoptively transferred B cells, Th cell function, and de

21 Even small numbers of adoptively transferred B10 cells dramatically suppressed

22 When adoptively transferred back to the individual, the genet

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

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

25 Furthermore, adoptively transferred caIKKbeta T cells showed diminish

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

27 We adoptively transferred CD11b(+) cells that were cocultur

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

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

30 28 also enhanced the suppressive capacity of adoptively transferred CD4(+) nTregs by increasing the s

31 Recent evidence suggests that adoptively transferred CD4(+) T cells can trigger endoge

32 dow for optimal effector differentiation for adoptively transferred CD4(+) T cells.

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

34 Adoptively transferred CD70-specific T cells induced sus

35 , and specific cellular interactions between adoptively transferred CD8 T cells and specific CNS cell

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

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

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

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

40 ells, causing them to enhance the effects of adoptively transferred CD8(+) T cells.

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

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

43 A drastically augments effector functions of adoptively transferred CD8+ T cells.

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

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

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

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

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

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

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

51 However, adoptively transferred cells isolated from the lamina pr

52 or cells significantly reduced the number of adoptively transferred cells that entered into the perit

53 icide genes can install a 'safety switch' on adoptively transferred cells to allow ablation if necess

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

55 By tracking adoptively transferred cells, we show that purified graf

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

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

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

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

60 targeted BCR transgenic mice, we showed that adoptively transferred cFLIP-deficient follicular B cell

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

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

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

64 Adoptively transferred CTLs persisted in the blood up to

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

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

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

68 at this single SNP developed spontaneous or adoptively transferred diabetes at comparable rates and

69 we expanded CD98-null T cells in vitro, they adoptively transferred diabetes, establishing that impai

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

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

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

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

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

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

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

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

78 s to generate the damaging Ab repertoire, we adoptively transferred either MZBs or follicular B cells

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

80 ted in the worsening of actively induced and adoptively transferred experimental autoimmune encephalo

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

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

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

84 Adoptively transferred gammadelta T cells isolated from

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

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

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

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

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

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

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

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

96 sCD200 serum adoptively transferred increased graft survival to naive

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

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

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

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

101 CD8 T effector cells (Tc17) from OT-1 mice, adoptively transferred into B16-OVA tumor-bearing mice,

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

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

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

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

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

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

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

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

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

111 ly, neutrophils generated in this way can be adoptively transferred into live animals and tracked dur

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

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

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

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

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

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

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

119 ecipients, serum from presensitized rats was adoptively transferred into naive WF rats.

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

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

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

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

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

125 1(-) thymocytes from Rag1((-)/(-)) mice were adoptively transferred into Rag1((-)/(-))Ly5.1 congenic

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

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

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

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

130 by the spontaneous proliferation of T cells adoptively transferred into specific pathogen-free (SPF)

131 When adoptively transferred into syngeneic naive mice, the by

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

133 wild-type counterparts, C5aR(-/-) mast cells adoptively transferred into W/Wv mice were not competent

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

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

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

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

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

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

140 irect effects of Psgl-1, because Psgl-1(+/+) adoptively transferred leukocytes did not exhibit enhanc

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

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

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

144 Adoptively transferred mast cells or M2 macrophages reve

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

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

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

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

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

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

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

152 x virus-thymidine kinase (TK) gene] when the adoptively transferred MSC developed endothelial-like ch

153 Finally, adoptively transferred MSCs in complement deficient mice

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

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

156 Combinations of adoptively transferred N-alpha-syn and vasoactive intest

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

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

159 l population was successfully outcompeted by adoptively transferred naive T cells, and (iii) demonstr

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

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

167 confirmed by experiments in which MBCs were adoptively transferred or depleted before secondary chal

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

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

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

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

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

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

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

175 Adoptively transferred PC1(lo) cells secreted significan

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

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

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

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

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

181 ntly inhibited antidonor immune responses in adoptively transferred recipients.

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

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

184 tion, and clonal expansion of endogenous and adoptively transferred Salmonella-specific CD4 T cells w

185 Furthermore, adoptively transferred splenic CD8 memory phenotype T ce

186 Adoptively transferred splenic NK cells that migrate to

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 d manner and lends itself to manipulation of adoptively transferred T cells and characterizing specif

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

191 These data show that adoptively transferred T cells can be expanded and activ

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

193 F/VEGFR-2 axis can increase extravasation of adoptively transferred T cells into the tumor and improv

194 studies also demonstrate that persistence of adoptively transferred T cells is associated with therap

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

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

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

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

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

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

206 ular tumor microenvironment which suppresses adoptively transferred T cells.

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

208 similarly augmented antitumor effects 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 tors (CARs) determine the overall potency of adoptively transferred T cells.

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

213 Adoptively transferred T(EM) cells from hypertensive mic

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

215 Through the use of adoptively transferred T-cells, bone marrow chimeras, an

216 In vivo, adoptively transferred Tc17 cells lost the IL-17-secreti

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

223 Interestingly, adoptively transferred Th17 cells demonstrated plasticit

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

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

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

227 normal-mouse infection site tissue Mphi were adoptively transferred to burned mice at the MRSA infect

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

229 uman peripheral blood mononuclear cells were adoptively transferred to immunodeficient mice lacking a

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 GMSCs were adoptively transferred to multiple low-dose streptozotoc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

247 Adoptively transferred total T cells from immunized mice

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

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

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

251 s) have potent anti-inflammatory effects, we adoptively transferred Tregs into infected C57BL/6 and R

252 ously published studies of ex vivo-activated adoptively transferred tumor antigen-specific CD8+ T cel

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

254 Adoptively transferred tumor-infiltrating T lymphocytes

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

256 t for survival and proper differentiation of adoptively transferred tumor-specific CD4(+) T cells.

257 Adoptively transferred tumor-specific T cells offer the

258 We adoptively transferred uveitis to naive mice using BM ce

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

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

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

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

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

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

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

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

267 ficantly reduced in wild-type recipient mice adoptively transferred with DNFB immunity generated in P

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

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

270 Mice were adoptively transferred with myeloid cells and treated wi

271 nted onto C57BL/6-RAG-1-deficient recipients adoptively transferred with purified sorted CD4CD25 T ce

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 Moreover, IL-4Ralpha(-/-) mice adoptively transferred with wild-type macrophages had a

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

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

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

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

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

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 turation, a significantly higher fraction of adoptively transferred, tumor-reactive (reporter) CD8(+)

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

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 By adoptively transferring splenocytes from individual lymp

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

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

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