ライフサイエンスコーパス: adoptive transfer

1 protection against Francisella novicida upon adoptive transfer.

2 134.5 mutant in vivo mediate protection upon adoptive transfer.

3 rise to intestinal CD8alphaalpha IELs after adoptive transfer.

4 otective effects of gammadelta T cells after adoptive transfer.

5 vo modification and expansion of T cells for adoptive transfer.

6 ponse to injury, both endogenously and after adoptive transfer.

7 or T cells and impairs persistence following adoptive transfer.

8 ell receptor transgenic CD4(+) T cells after adoptive transfer.

9 transcription polymerase chain reaction, and adoptive transfer.

10 ry and remodeling, and retain this memory on adoptive transfer.

11 mained detectable from 6 h through 7 d after adoptive transfer.

12 c cells from DNFB-fed mice to inhibit ACD on adoptive transfer.

13 he pathogenesis of Pneumocystis pneumonia by adoptive transfer.

14 in vitro coculture assays and a rat model of adoptive transfer after IR, we determined that CDC-condi

15 Using adoptive transfer and B cell depletion strategies, we de

16 Adoptive transfer and cell depletion studies demonstrate

17 ntary murine GVHD models, we determined that adoptive transfer and early accumulation of beta2 integr

18 Using a single-cell adoptive transfer and spleen biopsy method, we found tha

19 Adoptive transfer and survival experiments show that MDS

20 ted in T-cell receptor beta knockout mice by adoptive transfer, and bone turnover, bone mineral densi

21 s of clodronate liposome-mediated depletion, adoptive transfer, and treatment with recombinant cytoki

22 Using a combination of knockout mice, adoptive transfers, and depletion studies, we recently f

23 ix metalloproteinase-8 in sepsis by using an adoptive transfer approach and alternative sepsis models

24 kout mixed bone marrow chimera as well as an adoptive transfer approach, we show that CD4 T cell-intr

25 muridarum and Chlamydia trachomatis Using an adoptive-transfer approach, we show that naive Tg CD4 T

26 Finally, adoptive transfer assays in vivo revealed a reduced anti

27 Increases in the number of Eo-MDSC by adoptive transfer caused a significant exacerbation of i

28 Vgamma2Vdelta2 T cells for adoptive transfer displayed central/effector memory and

29 ole is especially controversial in models of adoptive transfer EAE in which no adjuvant and no TLR li

30 ther administering low-level TLR2 ligands in adoptive transfer EAE induces TLR2 tolerance and attenua

31 In adoptive transfer EAE models, Bhlhe40-deficient Th1 and

32 ed a critical period for TLR2 involvement in adoptive transfer EAE.

33 ta inhibition in CD8(+) T cells destined for adoptive transfer, enhancing their survival and also the

34 the T cells occurred after priming using an adoptive transfer experimental autoimmune encephalomyeli

35 ice display significantly reduced active and adoptive-transfer experimental autoimmune encephalomyeli

36 ability of isolated Tregs to inhibit IRI in adoptive transfer experiments and protected mice from ci

37 Results from adoptive transfer experiments between WT and CD73(-/-) m

38 BrdU labeling and adoptive transfer experiments confirm more rapid product

39 increased mortality after LPS challenge, and adoptive transfer experiments confirmed that neutrophil-

40 In vivo adoptive transfer experiments further indicated the impo

41 We performed a series of adoptive transfer experiments in mice to better understa

42 nt mice, IL-17F-neutralizing antibodies, and adoptive transfer experiments into Rag1(-/-) mice demons

43 Adoptive transfer experiments revealed that intrahepatic

44 Adoptive transfer experiments revealed that MoMFs primar

45 Adoptive transfer experiments revealed that the thymic n

46 Adoptive transfer experiments show that antibiotic admin

47 Adoptive transfer experiments showed reduced airway eosi

48 Bone marrow chimeric and adoptive transfer experiments suggested that Mincle sign

49 In adoptive transfer experiments they persist in high numbe

50 Additional adoptive transfer experiments together with flow cytomet

51 In our first model, adoptive transfer experiments were followed by cecal lig

52 A series of adoptive transfer experiments with genetically engineere

53 ergy and anaphylaxis, various knockout mice, adoptive transfer experiments, and in vitro assays to id

54 In adoptive transfer experiments, DN T cells significantly

55 nic function of intestinal DCs was tested by adoptive transfer experiments, ex vivo hapten presentati

56 In our adoptive transfer experiments, matrix metalloproteinase-

57 In adoptive transfer experiments, wild type, but not Tnfa(-

58 ytometry, in vitro proliferation assays, and adoptive transfer experiments.

59 Using adoptive-transfer experiments and ovariectomized mice, w

60 mation preceded the formation of LLPCs in an adoptive transfer immunization system, which allowed for

61 the production of multi-VSTs for allogeneic adoptive transfer immunotherapy.

62 derived VSTs confer protection in vivo after adoptive transfer in 70% to 90% of recipients.

63 in response to TPO, and persist longer after adoptive transfer in immunodeficient human TPO-transgeni

64 s CD19 CAR T cells both early and late after adoptive transfer in mice, resulting in complete and per

65 immunospots, cytotoxicity assays as well as adoptive transfer in NOD/SCID/IL2Rgamma mice were used t

66 These T cells induced diabetes after adoptive transfer, indicating their pathogenicity.

67 Th2/Th17 adoptive transfer induced a mixed asthma phenotype chara

68 in 1 receptor antagonist (Kineret(R)) in the adoptive transfer inoculum significantly reduces microgl

69 shown by pre-treatment of monocytes prior to adoptive transfer into an on-going murine peritonitis mo

70 from these tissues initiated infection after adoptive transfer into naive hosts.

71 ation in vitro and in vivo in the PLNs after adoptive transfer into NOD recipients.

72 and CD4 T cells were more diabetogenic upon adoptive transfer into NOD.Rag recipients due to a skewi

73 , our studies suggest that regulatory T cell adoptive transfer may alleviate thrombolytic treatment-i

74 Thus, regulatory T cell adoptive transfer may be useful as a cell-based therapy

75 Their selection, expansion, and/or adoptive transfer may support strategies to eradicate HI

76 tudy, we investigated the role of RIAM in an adoptive transfer model for type I diabetes and report t

77 functionality of tolDCs was confirmed in the adoptive transfer model of NOD-SCID mice where tolDCs de

78 We used an adoptive transfer model to elucidate the kinetics of the

79 We developed a novel adoptive transfer model to investigate the cellular requ

80 In a lymphopaenic mouse adoptive transfer model, naive Mettl3-deficient T cells

81 pacts on the development of colitis using an adoptive transfer model.

82 er EAU was abrogated by BET inhibitors in an adoptive transfer model.

83 of NLRX1 specifically in T cells, we used an adoptive-transfer model of colitis.

84 llowing in vitro BCR stimulation and in vivo adoptive transfer models confirmed that Ahr(-/-) B cells

85 eneic graft-versus-host disease model and in adoptive transfer models of experimental colitis.

86 row chimeras, conditional knockout mice, and adoptive transfer models were also used.

87 sessed the role of T cell-derived CD70 using adoptive-transfer models, including autoimmune inflammat

88 Similarly, in vivo, after adoptive transfer, Nr4a1-deficient MPPS contribute more

89 Moreover, adoptive transfer of 6-ECDCA- or CDCA-treated donor cell

90 as resist curative immunotherapy with either adoptive transfer of activated anti-OVA OT1 CTLs or agon

91 Treatment of hematological malignancies by adoptive transfer of activated natural killer (NK) cells

92 Furthermore, adoptive transfer of activated Tregs in rag(-/-) gammac(

93 Adoptive transfer of adipose tissue B2 cells (ATB2) from

94 s reduced B-cell lymphopoiesis is rescued by adoptive transfer of affected HSCs or bone marrow cells

95 Thus, adoptive transfer of allogeneic T9IL-33 cells offers an

96 Adoptive transfer of allospecific transgenic CD4 T cells

97 ata from animal models has demonstrated that adoptive transfer of allospecific Tregs offers greater p

98 Adoptive transfer of AMs pretreated with MSC-derived EVs

99 Using adoptive transfer of anergic B cells with subsequent acu

100 inflammatory to anti-inflammatory ATMs, and adoptive transfer of AT1-ILCs exacerbated metabolic diso

101 We further found that adoptive transfer of Atg5(-/-), but not wild-type, bone

102 The adoptive transfer of autologous T cells engineered to ex

103 owledge, this is the first report describing adoptive transfer of autologous TILs to mediate objectiv

104 Although adoptive transfer of autologous tumor antigen-specific T

105 Thus, we sought to determine if adoptive transfer of autologous tumour-infiltrating lymp

106 While adoptive transfer of B cells in Apoe (-/-) /Baffr (-/-)

107 nsulin resistance, which is recapitulated by adoptive transfer of B cells, but not purified immunoglo

108 Adoptive transfer of B-1a cells into septic mice signifi

109 tion with B. fragilis polysaccharides, or by adoptive transfer of B. fragilis-specific T cells.

110 This study indicated that the adoptive transfer of B10 cells alleviated periodontal in

111 pendent manner in response to S. aureus, and adoptive transfer of B1a cells was protective during acu

112 Adoptive transfer of B220(+)CD5(-) B cells from MOG-psig

113 Adoptive transfer of BM and spleen cells from allergic d

114 Adoptive transfer of BM, but not peripheral, granulocyte

115 ced acute allergic airway inflammation after adoptive transfer of BMDCs was examined by means of micr

116 Conversely, adoptive transfer of bone marrow-derived CD11c(+) cells

117 Furthermore, adoptive transfer of c-Src-silenced DCs in mouse tumors

118 In a human skin xenograft transplant model, adoptive transfer of CAR Tregs alleviated the alloimmune

119 Adoptive transfer of CB1R(-/-) bone marrow to ZDF rats a

120 Adoptive transfer of CD11b(+) pulmonary dendritic cells

121 Moreover, adoptive transfer of CD11b(+)Gr-1(hi) cells, after IL-17

122 Adoptive transfer of CD153+PD-1+CD44hiCD4+ T cells from

123 ncy analgesia, which can be rescued with the adoptive transfer of CD4(+) or CD8(+) T cells from late-

124 Adoptive transfer of CD4(+) T cells from MPO409-428- but

125 In addition, adoptive transfer of CD8(+) T cells from wild-type (wt)

126 Adoptive transfer of cells from mice immunized with DNA-

127 ggest that protection from colitis following adoptive transfer of CerS6-deficient splenocytes maybe r

128 Adoptive transfer of CerS6-deficient splenocytes, which

129 Adoptive transfer of chimeric antigen receptor (CAR)-red

130 Adoptive transfer of Chlamydia-specific CD4 TCR-Tg T cel

131 NGR) or IL10, and Rag1-/- mice that received adoptive transfer of control or Ifng-/- CD4+ T cells.

132 Adoptive transfer of conventional DCs, in particular CD1

133 Adoptive transfer of CRTC2/3m BM conferred the splenomeg

134 himurium was significantly reduced after the adoptive transfer of CX3CR1(+) cells directly into the i

135 himurium was significantly reduced after the adoptive transfer of CX3CR1(+) cells directly into the i

136 Adoptive transfer of Cx3cr1-proficient monocyte-enriched

137 epithelial migration of neutrophils, we used adoptive transfer of Cxcr2(-/-) neutrophils and chemokin

138 Adoptive transfer of DCs primed with wt RABV did not act

139 However, adoptive transfer of diabetes was not prevented when mic

140 osis and bactericidal activity in vitro, and adoptive transfer of DJ-1(-/-) bone marrow-derived monon

141 The adoptive transfer of donor-derived viral-specific cytoto

142 Adoptive transfer of donor-derived virus-specific cytoto

143 Early clinical trials demonstrate that adoptive transfer of donor-derived virus-specific T cell

144 Adoptive transfer of either CD3(+) or CD8(+), but not CD

145 The adoptive transfer of engineered T cells for the treatmen

146 Here, we have examined the adoptive transfer of ex vivo expanded human cord blood-d

147 Adoptive transfer of fluorescently labeled wild-type and

148 Adoptive transfer of forkhead box protein (FOX)3 regulat

149 aused minimal effects in wild-type mice, and adoptive transfer of gammadelta T cells prevented sensit

150 Purpose Adoptive transfer of genetically modified T cells is bei

151 In addition, adoptive transfer of HDAC11KO T cells resulted in signif

152 Adoptive transfer of Hdac3-deficient Tregs, unlike WT Tr

153 11c(+) cells (Lrp1(fl/fl); CD11c-Cre) and by adoptive transfer of HDM-pulsed CD11b(+) DCs from Lrp1(f

154 The adoptive transfer of HDM-pulsed LRP-1-deficient CD11b(+)

155 Adoptive transfer of HDM/HBCD-exposed BMDCs into naive m

156 ulation of eosinophils in the liver, whereas adoptive transfer of hepatic ILC2s aggravated liver infl

157 Adoptive transfer of high-affinity chimeric antigen rece

158 odel of allergic asthma, we demonstrate that adoptive transfer of human act-A-iTr1 cells, both in pre

159 Responses to adoptive transfer of human Tsp cells into immune-deficie

160 analysis of endogenous T cell responses and adoptive transfer of IAV-specific memory T cell populati

161 Adoptive transfer of Ifnar(-/-) NK cells into NK cell-de

162 gnancy loss, which could be abrogated by the adoptive transfer of IL-10(+/+) NK cells and not by IL-1

163 Finally, adoptive transfer of IL-36R-expressing T cells to IL-36R

164 phoid cells (ILC2) in blood and kidneys, and adoptive transfer of ILC2 also protected mice from IRI.

165 Adoptive transfer of ILC2s from wild-type mice was perfo

166 Importantly, adoptive transfer of ILC2s restored eosinophil influx an

167 Adoptive transfer of immune cells from IYIY-I2-BODIPY-tr

168 allergic airway inflammation, we found that adoptive transfer of IMs isolated from CpG-treated mice

169 Adoptive transfer of in vitro differentiated MCs restore

170 ), and IL-4-deficient (Il4(-/-)) mice and by adoptive transfer of in vitro-expanded ILC2s.

171 umulation in apoE(-/-) mice, we performed an adoptive transfer of iNKT cells and found that only wild

172 Adoptive transfer of iNKT cells from p47(phox-/-) or NOX

173 with GM-CSF increased MDSC accumulation, and adoptive transfer of IRF8-deficient T cells, but not GM-

174 Adoptive transfer of LN cells of sensitized mice into re

175 Moreover, adoptive transfer of lung CD4 TRM cells conferred protec

176 Adoptive transfer of Ly6C(+) monocytes gave rise to PD-L

177 Cell tracking and adoptive transfer of Ly6c(hi) monocytes showed Bmal1 def

178 e-induced mouse periodontitis model in which adoptive transfer of M1 macrophages showed a significant

179 Adoptive transfer of M2-like macrophages conferred contr

180 y the enteric pathogen Citrobacter rodentium Adoptive transfer of macrophage-rich peritoneal cells fr

181 Moreover, adoptive transfer of mature allogeneic NK cells in the n

182 In a BALB/c --> B6 lethal GVHD model, adoptive transfer of MDSCs from TLI/ATS/CTX-conditioned

183 Adoptive transfer of Mo-DCs to MAIT cell-deficient mice

184 AE mice did not resolve disease, whereas the adoptive transfer of MOG-psigma1-induced B220(+)CD5(+) B

185 re pronounced EAE with fewer Tregs, but upon adoptive transfer of MOG-psigma1-induced BTLA(+) Bregs,

186 Adoptive transfer of monocytes increased the induction o

187 etely resistant to EAE development following adoptive transfer of myelin-specific T cells and show su

188 In contrast, adoptive transfer of neonatal CD71(+) cells into adult r

189 Furthermore, adoptive transfer of NFAT1-deficient CD4(+) T cells into

190 hed mouse xenograft model of ovarian cancer, adoptive transfer of NK cells conditioned in the same wa

191 Particularly, the adoptive transfer of NK cells has garnered attention due

192 d on phenotypic and genotypic properties, by adoptive transfer of NK cells with ex vivo or in vivo cy

193 inflammation-associated tumors in mice, and adoptive transfer of Nod1(-/-) or IFNgamma(-/-) T cells

194 functional analyses performed in vivo using adoptive transfer of OVA-specific OT-II cells into wild-

195 utaneously established murine melanoma after adoptive transfer of p53-KO T cells.

196 Furthermore, adoptive transfer of PD-L1(+)/PD-L2(+) AAMvarphis into E

197 Adoptive transfer of peripheral blood-derived, melanoma-

198 Adoptive transfer of peripheral wild-type DCs rescued th

199 ts with P2X7(-/-) bone marrow chimeric mice, adoptive transfer of peritoneal macrophages, and myeloid

200 Adoptive transfer of PKCdelta-suppressed Mvarphi recapit

201 nocytes are the minimal requirements for the adoptive transfer of PNA.

202 he AIH could be treated with prednisolone or adoptive transfer of polyspecific Tregs.

203 Additionally, the adoptive transfer of pre-pubertal peritoneal cells impro

204 ancer, based on oncogenic transformation and adoptive transfer of primary precursor cells (hepatoblas

205 lammation in an atopic asthma model, whereas adoptive transfer of proangiogenic progenitor cells from

206 Adoptive transfer of pTregs from mice at low risk of sub

207 Adoptive transfer of purified B cells from MenC- or GBS-

208 hodepleting preparative regimen, followed by adoptive transfer of purified CD4(+) T cells, retroviral

209 Flow cytometry and adoptive transfer of purified cells show that antibiotic

210 Adoptive transfer of purified IVIg-generated pTreg prior

211 Adoptive transfer of receptor-engineered T cells has pro

212 plantation, recent advances were made by the adoptive transfer of regulatory and conventional T cells

213 Studies have demonstrated that the adoptive transfer of regulatory T cells (Tregs) can medi

214 umonitis, but not the dermatitis, induced by adoptive transfer of scurfy lymphocytes.

215 Adoptive transfer of Sema4c(-/-) CD19(+)CD138(+) cells i

216 Adoptive transfer of serum and T-cell depletion experime

217 Moreover, adoptive transfer of Sphk2(-/-) (but not Sphk2(-/-)Ifng(

218 Adoptive transfer of splenic B cells into B cell-deficie

219 tricular dilatation and hypertrophy, whereas adoptive transfer of splenic CD4(+) T cells (and, to a l

220 Adoptive transfer of splenic CD8(+) T cells from OVA-sen

221 Adoptive transfer of splenic DN cells gives rise to CD8a

222 Importantly, results from adoptive transfer of splenocytes from immunized animals

223 Adoptive transfer of splenocytes from ultrasound-treated

224 vivo Notch signaling, and demonstrated that adoptive transfer of such Tregs dramatically suppressed

225 Adoptive transfer of T cells engineered to express a hep

226 Adoptive transfer of T cells from irradiated PDA to tumo

227 Adoptive transfer of T cells from W7-791-immunized mice

228 Adoptive transfer of T cells genetically modified to exp

229 Adoptive transfer of T cells genetically modified to exp

230 enal dysfunction, and hypertension; however, adoptive transfer of T cells restored these processes.

231 The adoptive transfer of T cells that have been genetically

232 Finally, the adoptive transfer of T cells treated ex vivo with a GSK-

233 Treatment of B cell malignancies with adoptive transfer of T cells with a CD19-specific chimer

234 NOD-Idd22 mice were highly protected against adoptive transfer of T1D.

235 Adoptive transfer of TCR-transduced T cells significantl

236 Adoptive transfer of TEM8 CAR T cells induced regression

237 ed TGFbeta-induced inactivation ex vivo, and adoptive transfer of TGFBR-deficient CD8(+) T cells led

238 drive CF both in vitro and in vivo, whereas adoptive transfer of Th1 cells, opposite to activated IF

239 Adoptive transfer of Th17/1, but not Th1, cells confers

240 Adoptive transfer of the CD103(+)alpha4beta7(high) subse

241 Adoptive transfer of these CCR5Teff cells significantly

242 , we showed that they are not regulatory and adoptive transfer of these cells exacerbates atheroscler

243 Monitoring, selection, expansion, and adoptive transfer of these NK cells may allow monitoring

244 Importantly, adoptive transfer of these stabilized iTregs to HSV-1-in

245 2-deficient mice with normal bone marrow, or adoptive transfer of TNFR2-expressing MDSC into these mi

246 Adoptive transfer of Treg cells from vaccinated/ppins-pr

247 rocyte differentiation, which was rescued by adoptive transfer of Treg.

248 Tregs after BMT also induced cGVHD, whereas adoptive transfer of Tregs ameliorated it.

249 Confirming our observations, adoptive transfer of tumor-derived mMDSC reversed the ab

250 valuated the importance of adding TBI to the adoptive transfer of tumor-infiltrating lymphocytes (TIL

251 Adoptive transfer of tumor-reactive T cells can successf

252 yte infusion to dendritic cell vaccines, and adoptive transfer of tumor-specific cytotoxic T cells an

253 Consistently, adoptive transfer of Vgamma2Vdelta2 T cells attenuated T

254 Conversely, adoptive transfer of VNS-conditioned alpha7nAChR splenoc

255 eatment, platelet inhibition by aspirin, and adoptive transfer of wild-type (WT) platelets to CD40-KO

256 Adoptive transfer of wild-type and Il13(-/-) but not Il4

257 Adoptive transfer of wild-type BMDM normalized infection

258 alveolar lavage fluid IL-4 and IL-5, whereas adoptive transfer of wild-type CD19(+)CD138(+)IL-10(+) c

259 In contrast, adoptive transfer of wild-type MDSCs to hypertensive mic

260 Adoptive transfer of wild-type or p110delta(D910A) Tregs

261 Adoptive transfer of wild-type T cells, but not Ccr5-def

262 Macrophage depletion had no effect, whereas adoptive transfer of WT bone marrow improved wound heali

263 Adoptive transfer of WT bone marrow-derived hematopoieti

264 AI(-/-) mice following hepatic infection and adoptive transfer of WT bone-marrow-derived Mvarphi conf

265 Adoptive transfer of WT but not BLT1(-/-) or CXCR3(-/-)

266 on, but can be rescued from mortality by the adoptive transfer of WT CD4(+) T cells.

267 Adoptive transfer of WT IMs increases the reduced number

268 The adoptive transfer of WT mast cells restored allergic sym

269 e lack of an effect on parasite replication, adoptive transfer of WT platelets to CD40-KO mice, which

270 Adoptive transfer of ZIKV-immune CD8(+) T cells reduced

271 We performed adoptive transfers of both nontransgenic and TCR-transge

272 Using adoptive transfers of spleen and lung NK cells, we found

273 Adoptive transfer or an Ab-mediated reduction in neonata

274 ubsets occurred in Pdcd1(-/-) mice and, upon adoptive transfer, Pdcd1(-/-) KLRG1(+) ILC-2s significan

275 y, we use genetic lineage-tracing models and adoptive transfer protocols to address this question.

276 Abrogation of GM-CSF receptor signaling in adoptive transfer recipients of MOG35-55-specific T cell

277 MPECs deficient in HVEM failed to survive in adoptive transfer recipients.

278 In vivo depletion and adoptive transfer studies identified CD300b-expressing m

279 Using mixed bone marrow chimeras and adoptive transfer studies in which CD8 T cells either do

280 istribution was disrupted in the spleen, but adoptive transfer studies indicated that these cells wer

281 Genetic loss of function in mice and adoptive transfer studies revealed that bone marrow-deri

282 in Treg cells was further dissected through adoptive transfer studies using CCR8(-/-) mice.

283 Adoptive transfer studies with young T cells demonstrate

284 monkeys also conferred passive protection in adoptive transfer studies.

285 Using an adoptive transfer system and plasticity-prone Mir146a(-/

286 ns to suppress the autoimmune response after adoptive transfer, thereby avoiding potential overall im

287 KIR3DL1(+) NK cells gained reactivity after adoptive transfer to HLA-B( *)27:05(+) mice or bone marr

288 vo with/without human MSC-derived EVs before adoptive transfer to LPS-injured mice.

289 erived DC subsets was determined by means of adoptive transfer to naive mice.

290 TCR-transduced TIL1383I T cells prepared for adoptive transfer to patients as part of a clinical tria

291 toxicity against tumor cells and safety upon adoptive transfer to patients.

292 myc were more likely to persist longer after adoptive transfer to patients.

293 their T cells failed to induce colitis after adoptive transfer to Rag(-/-) mice.

294 Despite the ability of adoptive transfer to restore allergic airways inflammati

295 n vitro and reduced their ability, following adoptive transfer, to prime the expansion of Ag-specific

296 ne controlled cortical impact model, we used adoptive transfer, transgenic, and bone marrow chimera a

297 In ROCK2(+/-) mice, adoptive transfer with CD4(+) cells from OT-II mice rest

298 tor beta knockout mice were reconstituted by adoptive transfer with CD4+ or CD8+ T-cells subsets were

299 Combining natural killer (NK) cell adoptive transfer with hypomethylating agents (HMAs) is

300 nerated irradiation chimeras, or carried out adoptive transfers, with wild-type (WT) and/or MHC I-def