1 n sulfate sodium, Mdr1a(-/-), and CD45RB(hi)
adoptive transfer).
2 and attenuated Con A-induced hepatitis upon
adoptive transfer.
3 (TCR) may achieve cure of HBV infection upon
adoptive transfer.
4 t promoted curative antitumor immunity after
adoptive transfer.
5 n of functional CAR effector cells following
adoptive transfer.
6 triggering robust antitumor responses after
adoptive transfer.
7 ry and remodeling, and retain this memory on
adoptive transfer.
8 mained detectable from 6 h through 7 d after
adoptive transfer.
9 c cells from DNFB-fed mice to inhibit ACD on
adoptive transfer.
10 he pathogenesis of Pneumocystis pneumonia by
adoptive transfer.
11 protection against Francisella novicida upon
adoptive transfer.
12 134.5 mutant in vivo mediate protection upon
adoptive transfer.
13 bonucleoprotein immediately prior to in vivo
adoptive transfer.
14 ific B and T lymphocytes were analyzed in an
adoptive transfer airway inflammation mouse model in res
15 Adoptive transfer and cell depletion studies demonstrate
16 izing the source of therapeutic NK cells for
adoptive transfer and enhancing NK cell cytotoxicity and
17 Using
adoptive transfer and islet transplantation models, we d
18 ted in T-cell receptor beta knockout mice by
adoptive transfer,
and bone turnover, bone mineral densi
19 muridarum and Chlamydia trachomatis Using an
adoptive-transfer approach, we show that naive Tg CD4 T
20 genetically modified (beta2-AR-/-) mice, and
adoptive transfer approaches, we found that the degree o
21 Increases in the number of Eo-MDSC by
adoptive transfer caused a significant exacerbation of i
22 Through
adoptive transfer,
CD8(+) lung T cells but not CD4(+) T
23 Vgamma2Vdelta2 T cells for
adoptive transfer displayed central/effector memory and
24 1 population in Prkdc(-/-)IL2rg(-/-) mice by
adoptive transfer drives adipose fibrogenesis through ac
25 Adoptive transfer EAE studies linked this EAE phenotype
26 ta inhibition in CD8(+) T cells destined for
adoptive transfer,
enhancing their survival and also the
27 trophils were found to express SAP; however,
adoptive transfer experiment supported a neutrophil-extr
28 ability of isolated Tregs to inhibit IRI in
adoptive transfer experiments and protected mice from ci
29 We used
adoptive transfer experiments and studies in reporter mi
30 Adoptive transfer experiments and transcriptome analyses
31 Results from
adoptive transfer experiments between WT and CD73(-/-) m
32 Adoptive transfer experiments confirmed that iNKT cells
33 increased mortality after LPS challenge, and
adoptive transfer experiments confirmed that neutrophil-
34 Consistent with cell-based data,
adoptive transfer experiments demonstrated that the anti
35 Adoptive transfer experiments demonstrated that the geno
36 In vivo
adoptive transfer experiments further indicated the impo
37 Adoptive transfer experiments in mice show that modified
38 In
adoptive transfer experiments into tumor-bearing immunod
39 Adoptive transfer experiments of T(RM) cells corroborate
40 Adoptive transfer experiments revealed that intrahepatic
41 Transcriptome analyses and sequential
adoptive transfer experiments revealed that while Notch-
42 Adoptive transfer experiments show that antibiotic admin
43 A series of
adoptive transfer experiments with genetically engineere
44 ergy and anaphylaxis, various knockout mice,
adoptive transfer experiments, and in vitro assays to id
45 In
adoptive transfer experiments, converting apoB(+) T(regs
46 ng lymphocyte-deficient mice and a series of
adoptive transfer experiments, we demonstrate that genet
47 In
adoptive transfer experiments, wild type, but not Tnfa(-
48 already expressed in thymus, as confirmed by
adoptive transfer experiments.
49 thrc1-expressing fibroblasts in in vitro and
adoptive transfer experiments.
50 +) mice are pathogenic and cause ILD through
adoptive transfer experiments.
51 Using
adoptive-transfer experiments and ovariectomized mice, w
52 After
adoptive transfer in colorectal and breast mouse tumor m
53 , and biological activity of autologous Treg
adoptive transfer in humans, we conducted an open-label,
54 in response to TPO, and persist longer after
adoptive transfer in immunodeficient human TPO-transgeni
55 immunospots, cytotoxicity assays as well as
adoptive transfer in NOD/SCID/IL2Rgamma mice were used t
56 These T cells induced diabetes after
adoptive transfer,
indicating their pathogenicity.
57 In conclusion, the BMDC
adoptive transfer-
induced immunogenic tolerance in OVA-s
58 we discovered a new B-cell subset that, upon
adoptive transfer into B cell-deficient mice, was suffic
59 ed proliferation of B6 T cells in vitro, and
adoptive transfer into B6 recipients 2 weeks before hete
60 it in vivo alloantibody production following
adoptive transfer into C57BL/6 or high alloantibody-prod
61 Upon
adoptive transfer into hematopoietic stem cell transplan
62 and initiate heart allograft rejection upon
adoptive transfer into mATG treated B cell deficient rec
63 airway inflammatory cell infiltration after
adoptive transfer into mice; they also increased interle
64 d in mouse Nlrp6-deficient T cells following
adoptive transfer into Rag2-deficient mice, indicating t
65 nt from naive NK cells, we performed NK cell
adoptive transfer into RAG2/cgamma-chain(-/-) mice, NK c
66 BMDC
adoptive transfer may be developed into a new approach t
67 Thus, regulatory T cell
adoptive transfer may be useful as a cell-based therapy
68 Their selection, expansion, and/or
adoptive transfer may support strategies to eradicate HI
69 uberculosis-infected lungs using competitive
adoptive transfer migration assays and mathematical mode
70 PLG NPs was found to prevent diabetes in an
adoptive transfer model by impairing the ability of BDC-
71 ion and less disease severity, whereas in an
adoptive transfer model of inflammatory bowel disease, t
72 functionality of tolDCs was confirmed in the
adoptive transfer model of NOD-SCID mice where tolDCs de
73 We used an
adoptive transfer model to elucidate the kinetics of the
74 In a lymphopaenic mouse
adoptive transfer model, naive Mettl3-deficient T cells
75 er EAU was abrogated by BET inhibitors in an
adoptive transfer model.
76 of NLRX1 specifically in T cells, we used an
adoptive-transfer model of colitis.
77 Using
adoptive transfer models to compare infection-experience
78 row chimeras, conditional knockout mice, and
adoptive transfer models were also used.
79 Using
adoptive transfer models, we find that KO T regulatory c
80 sessed the role of T cell-derived CD70 using
adoptive-transfer models, including autoimmune inflammat
81 Using an
adoptive transfer mouse model of IIM, we show that sarco
82 restores their ability to induce colitis in
adoptive transfer mouse models.
83 In an
adoptive-transfer mouse model of type-1 diabetes, treatm
84 ial equation model of tumor regression after
adoptive transfer of a population of CTLs.
85 cell-directed enhancement of resolution, and
adoptive transfer of additional Tregs was sufficient to
86 ematopoietic stem cell transplantation, with
adoptive transfer of adenovirus-specific T cells being a
87 Adoptive transfer of adipose tissue B2 cells (ATB2) from
88 Adoptive transfer of allogeneic NK cells holds great pro
89 Thus,
adoptive transfer of allogeneic T9IL-33 cells offers an
90 Adoptive transfer of allospecific transgenic CD4 T cells
91 ata from animal models has demonstrated that
adoptive transfer of allospecific Tregs offers greater p
92 Adoptive transfer of AMs pretreated with MSC-derived EVs
93 ls of autoimmunity and transplant rejection,
adoptive transfer of antigen-specific 3C-iTregs prevente
94 n can be effectively targeted and ablated by
adoptive transfer of antigen-specific CD8(+) T cells.
95 Thus, we sought to determine if
adoptive transfer of autologous tumour-infiltrating lymp
96 We show that the
adoptive transfer of B(regs) dramatically decreased the
97 Remarkably,
adoptive transfer of B-1a cells, but not splenic B cells
98 This study indicated that the
adoptive transfer of B10 cells alleviated periodontal in
99 pendent manner in response to S. aureus, and
adoptive transfer of B1a cells was protective during acu
100 Adoptive transfer of BM, but not peripheral, granulocyte
101 ced acute allergic airway inflammation after
adoptive transfer of BMDCs was examined by means of micr
102 Experiments involving
adoptive transfer of bone marrow demonstrated that the m
103 Adoptive transfer of bone marrow ILC2 precursors confirm
104 Adoptive transfer of c-KIT(+) ECs into the neonatal circ
105 he combination of mild hyperthermia with the
adoptive transfer of CAR T cells can potentially increas
106 In a human skin xenograft transplant model,
adoptive transfer of CAR Tregs alleviated the alloimmune
107 Adoptive transfer of CB1R(-/-) bone marrow to ZDF rats a
108 ransplantation with head shielding; and (ii)
adoptive transfer of CD115+-ACE10/GFP+ monocytes to the
109 Adoptive transfer of CD11b(+) pulmonary dendritic cells
110 ncy analgesia, which can be rescued with the
adoptive transfer of CD4(+) or CD8(+) T cells from late-
111 ) animals as recipients, we demonstrate that
adoptive transfer of CD4(+) T cells alone confers marked
112 Adoptive transfer of CD4(+) T cells from PIV-vaccinated
113 2.5(mim)/calcitriol liposome administration,
adoptive transfer of CD4(+) T cells suppressed the devel
114 Survival was partially restored by
adoptive transfer of CD4(+), CD8(+), or total T cells.
115 Moreover,
adoptive transfer of CD4(+)CD45RB(high) T cells from CD8
116 Second,
adoptive transfer of CD8(+) T cells from OT1 mice to CD8
117 Furthermore, the
adoptive transfer of CD8(+) T cells from Valpha14(Tg) NC
118 validated screen hits by demonstrating that
adoptive transfer of CD8(+) T cells with Pdia3, Mgat5, E
119 Adoptive transfer of CerS6-deficient splenocytes, which
120 Adoptive transfer of Chlamydia-specific CD4 TCR-Tg T cel
121 Adoptive transfer of CRTC2/3m BM conferred the splenomeg
122 Evidently,
adoptive transfer of CTLs pre-cultured with TMPs from ir
123 himurium was significantly reduced after the
adoptive transfer of CX3CR1(+) cells directly into the i
124 Adoptive transfer of DCs to mucosal sites has been limit
125 osis and bactericidal activity in vitro, and
adoptive transfer of DJ-1(-/-) bone marrow-derived monon
126 Results presented from the
adoptive transfer of encephalitogenic T cells between wi
127 Adoptive transfer of engineered T cells into patients re
128 Individualized
adoptive transfer of ex vivo expanded CMV-specific CD8+
129 Here, we have examined the
adoptive transfer of ex vivo expanded human cord blood-d
130 In contrast,
adoptive transfer of ex vivo generated MDSC from cytokin
131 Adoptive transfer of fluorescently labeled wild-type and
132 Adoptive transfer of forkhead box protein (FOX)3 regulat
133 aused minimal effects in wild-type mice, and
adoptive transfer of gammadelta T cells prevented sensit
134 Adoptive transfer of Gas6-depleted BMM s failed to clear
135 Adoptive transfer of genetically engineered T cells expr
136 Adoptive transfer of genetically modified immune cells h
137 Purpose
Adoptive transfer of genetically modified T cells is bei
138 Furthermore, recombinant G-CSF or
adoptive transfer of granulocytic-MDSCs isolated from 4T
139 In addition,
adoptive transfer of HDAC11KO T cells resulted in signif
140 11c(+) cells (Lrp1(fl/fl); CD11c-Cre) and by
adoptive transfer of HDM-pulsed CD11b(+) DCs from Lrp1(f
141 The
adoptive transfer of HDM-pulsed LRP-1-deficient CD11b(+)
142 ulation of eosinophils in the liver, whereas
adoptive transfer of hepatic ILC2s aggravated liver infl
143 Adoptive transfer of high-affinity chimeric antigen rece
144 Importantly,
adoptive transfer of highly purified T(NLM) alone, from
145 ere transplanted with human skin followed by
adoptive transfer of human allogeneic splenocytes.
146 Adoptive transfer of human immunocytes from dual treated
147 Upon
adoptive transfer of human PBMC, this reductionist syste
148 cephalomyelitis (EAE), a murine model of MS,
adoptive transfer of IL-10(+) regulatory B cells (B(regs
149 gnancy loss, which could be abrogated by the
adoptive transfer of IL-10(+/+) NK cells and not by IL-1
150 Adoptive transfer of IL-10-proficient but not IL-10-defi
151 Finally,
adoptive transfer of IL-36R-expressing T cells to IL-36R
152 phoid cells (ILC2) in blood and kidneys, and
adoptive transfer of ILC2 also protected mice from IRI.
153 Adoptive transfer of ILC2s from wild-type mice was perfo
154 Importantly,
adoptive transfer of ILC2s restored eosinophil influx an
155 allergic airway inflammation, we found that
adoptive transfer of IMs isolated from CpG-treated mice
156 Finally, we demonstrate that
adoptive transfer of in vitro differentiated M-LECPs, bu
157 Adoptive transfer of in vitro differentiated MCs restore
158 An
adoptive transfer of in vitro-generated MDSCs before or
159 sm, a phenotype that can be recapitulated by
adoptive transfer of intestinal-associated pan-B cells.
160 EAU was induced in C57BL/6 mice by
adoptive transfer of IRBP1-20-specific T cells.
161 Adoptive transfer of labeled bone marrow-derived cells v
162 Adoptive transfer of LM-MDSC into LuM resulted in a shif
163 Moreover,
adoptive transfer of lung CD4 TRM cells conferred protec
164 Adoptive transfer of Ly6C(+) monocytes gave rise to PD-L
165 Cell tracking and
adoptive transfer of Ly6c(hi) monocytes showed Bmal1 def
166 Adoptive transfer of M2-like macrophages conferred contr
167 Here, we show that
adoptive transfer of macrophages containing antimicrobia
168 Adoptive transfer of macrophages, from either collagen-t
169 Adoptive transfer of mature DCs (lipopolysaccharide [LPS
170 Adoptive transfer of mature NK cells is sufficient to de
171 Due to their strong antimicrobial activity,
adoptive transfer of MDSCs generated by in vitro culture
172 Moreover, the
adoptive transfer of memory CD8 T cells from the livers
173 Adoptive transfer of miR-214(-/-) T cells into RAG1(-/-)
174 Importantly,
adoptive transfer of mixtures of CCR2(-/-) and CCR2(+/+)
175 Importantly,
adoptive transfer of monocyte/macrophages from wild-type
176 etely resistant to EAE development following
adoptive transfer of myelin-specific T cells and show su
177 Adoptive transfer of myeloid cells demonstrated that abe
178 We used mixed bone marrow chimeras and
adoptive transfer of naive CD4(+) T cells and Treg cells
179 te-stable gastrointestinal (GI) cancers, and
adoptive transfer of neoantigen-specific lymphocytes has
180 Adoptive transfer of neutrophils bearing LdCen(-/-) para
181 Adoptive transfer of neutrophils from beta-glucan-traine
182 Furthermore,
adoptive transfer of NFAT1-deficient CD4(+) T cells into
183 Adoptive transfer of NGAL-deficient CD4(+) T cells from
184 hed mouse xenograft model of ovarian cancer,
adoptive transfer of NK cells conditioned in the same wa
185 Particularly, the
adoptive transfer of NK cells has garnered attention due
186 Adoptive transfer of NK cells into NFIL3(-/-) mice befor
187 In support,
adoptive transfer of old CD4(+) T cells that were transf
188 In these mice,
adoptive transfer of ovalbumin-specific OT-I CD8 T cells
189 Intraplantar
adoptive transfer of paclitaxel-activated macrophages ev
190 wth in humanized mice generated by the human
adoptive transfer of PBMCs or the cotransplantation of h
191 Furthermore,
adoptive transfer of PD-L1(+)/PD-L2(+) AAMvarphis into E
192 ial infection (cecal ligature and puncture),
adoptive transfer of Pink1-deficient bone marrow or phar
193 Adoptive transfer of Pmel-1 x SLAMF6 -/- T cells to mela
194 Additionally, the
adoptive transfer of pre-pubertal peritoneal cells impro
195 ancer, based on oncogenic transformation and
adoptive transfer of primary precursor cells (hepatoblas
196 unction of individual T cell clones, and the
adoptive transfer of protective effector or regulatory T
197 Adoptive transfer of PTPN2-deficient CD8(+) T cells mark
198 hodepleting preparative regimen, followed by
adoptive transfer of purified CD4(+) T cells, retroviral
199 Flow cytometry and
adoptive transfer of purified cells show that antibiotic
200 Here we show that the
adoptive transfer of purified IgG from convalescent rhes
201 Adoptive transfer of purified immunoglobulin G (IgG) fro
202 Adoptive transfer of purified IVIg-generated pTreg prior
203 Adoptive transfer of recoverin-stimulated cells into nai
204 mental and preclinical evidence suggest that
adoptive transfer of regulatory T (Treg) cells could be
205 Studies have demonstrated that the
adoptive transfer of regulatory T cells (Tregs) can medi
206 Adoptive transfer of Sema4c(-/-) CD19(+)CD138(+) cells i
207 Adoptive transfer of sera containing anti-donor MHC clas
208 Adoptive transfer of splenic B cells into B cell-deficie
209 tricular dilatation and hypertrophy, whereas
adoptive transfer of splenic CD4(+) T cells (and, to a l
210 Adoptive transfer of splenic CD8(+) T cells from OVA-sen
211 Adoptive transfer of splenic DN cells gives rise to CD8a
212 Adoptive transfer of splenic T cells into NOD.Rag1(-/-)
213 As a result,
adoptive transfer of such IL-15-addicted NK cells is ass
214 Adoptive transfer of T cell expressing this public alpha
215 In comparison to
adoptive transfer of T cell progenitors, BMCs increased
216 Adoptive transfer of T cell receptor-engineered (TCR-eng
217 Finally,
adoptive transfer of T cells containing IL-6Ra(-/-) Treg
218 Adoptive transfer of T cells engineered to express a hep
219 The
adoptive transfer of T cells expressing chimeric antigen
220 Adoptive transfer of T cells genetically modified to exp
221 Immunotherapy with the
adoptive transfer of T cells redirected with CD19-specif
222 Adoptive transfer of T cells that express a chimeric ant
223 Adoptive transfer of T cells that express a chimeric ant
224 Finally, the
adoptive transfer of T cells treated ex vivo with a GSK-
225 Adoptive transfer of T(C)2 cells differentiated under hy
226 NOD-Idd22 mice were highly protected against
adoptive transfer of T1D.
227 Adoptive transfer of TCR-transduced T cells significantl
228 drive CF both in vitro and in vivo, whereas
adoptive transfer of Th1 cells, opposite to activated IF
229 Adoptive transfer of Th17 cells to naive mice is suffici
230 Adoptive transfer of Th17/1, but not Th1, cells confers
231 Adoptive transfer of the CD103(+)alpha4beta7(high) subse
232 Monitoring, selection, expansion, and
adoptive transfer of these NK cells may allow monitoring
233 Importantly,
adoptive transfer of these stabilized iTregs to HSV-1-in
234 Adoptive transfer of these three MDSCs led to differenti
235 Adoptive transfer of these tumor-specific cells signific
236 The effects of
adoptive transfer of transplant (tx), tumor (tm), and gr
237 bound after withdrawal of treatments, and by
adoptive transfer of treated lymphocytes into uninfected
238 In EAE-induced female mice,
adoptive transfer of Treg cells and spinal delivery of t
239 rocyte differentiation, which was rescued by
adoptive transfer of Treg.
240 Adoptive transfer of Tregs enhanced this CL activity.
241 Adoptive transfer of TSG6- or IL-4-primed BMM s i.t.
242 Adoptive transfer of tumor antigen-experienced T cells e
243 Adoptive transfer of tumor epitope-reactive T cells has
244 al to the success of checkpoint blockade and
adoptive transfer of tumor-infiltrating lymphocyte (TIL)
245 ng an immune response against cancer through
adoptive transfer of tumor-targeting lymphocytes has sho
246 lated autologous tumor cells followed by the
adoptive transfer of vaccine-primed lymphocytes after AS
247 vation, in vivo pre clinical PAD models, and
adoptive transfer of VEGF(165)b-expressing bone marrow-d
248 Consistently,
adoptive transfer of Vgamma2Vdelta2 T cells attenuated T
249 Moreover,
adoptive transfer of virus-specific effector CD8(+) T ce
250 Adoptive transfer of virus-specific T cells has proven t
251 eatment, platelet inhibition by aspirin, and
adoptive transfer of wild-type (WT) platelets to CD40-KO
252 hat in the wild-type mice and was rescued by
adoptive transfer of wild-type B-1 cells.
253 alveolar lavage fluid IL-4 and IL-5, whereas
adoptive transfer of wild-type CD19(+)CD138(+)IL-10(+) c
254 Adoptive transfer of wild-type or p110delta(D910A) Tregs
255 Adoptive transfer of wild-type T cells did not alter sur
256 lymphoid organs, and this can be restored by
adoptive transfer of wild-type T cells or administration
257 Adoptive transfer of WT bone marrow-derived hematopoieti
258 AI(-/-) mice following hepatic infection and
adoptive transfer of WT bone-marrow-derived Mvarphi conf
259 on, but can be rescued from mortality by the
adoptive transfer of WT CD4(+) T cells.
260 In parallel,
adoptive transfer of WT neutrophils into Par4(-/-) mice
261 CD4(+) T-cell depletion studies or the
adoptive transfer of WT OVA-specific CD4(+) T cells to W
262 Adoptive transfer of ZIKV-immune CD8(+) T cells reduced
263 Conversely,
adoptive transfer or purified donor-strain nT-regs inhib
264 dition of the LAG-3-blocking antibody to the
adoptive transfer protocol improved the SLAMF6 -/- T cel
265 y, we use genetic lineage-tracing models and
adoptive transfer protocols to address this question.
266 Abrogation of GM-CSF receptor signaling in
adoptive transfer recipients of MOG35-55-specific T cell
267 MPECs deficient in HVEM failed to survive in
adoptive transfer recipients.
268 male mice with pre-established obesity, Treg
adoptive transfer reduced the gWAT weight in 2 weeks.
269 Together with CL treatment, Treg
adoptive transfer reduced the SAT weight and further imp
270 ivity of these cells both in vitro and in an
adoptive transfer SCID model of pulmonary fibrosis.
271 We applied cell depletion and
adoptive transfer strategies using lymphocyte-deficient
272 Adoptive transfer studies demonstrated T cell intrinsic
273 dies has not previously been demonstrated in
adoptive transfer studies in nonhuman primates.
274 Bone marrow chimera and
adoptive transfer studies indicate that these memory T c
275 istribution was disrupted in the spleen, but
adoptive transfer studies indicated that these cells wer
276 Genetic loss of function in mice and
adoptive transfer studies revealed that bone marrow-deri
277 Rather, data from
adoptive transfer studies suggested that defective accum
278 in Treg cells was further dissected through
adoptive transfer studies using CCR8(-/-) mice.
279 Adoptive transfer studies using mice lacking beta2AR (be
280 Adoptive transfer studies were performed with Tc1 clones
281 ed through depletion (anti-CD4 antibody) and
adoptive transfer studies.
282 oduction by T cells and exacerbated EAE upon
adoptive transfer than did wild-type DCs.
283 ta) T cells exhibit longer persistence after
adoptive transfer than do CD28-costimulated CAR (28zeta)
284 G-3+/TNF-alphalow CD8 T cells and, following
adoptive transfer,
the rapid expression of exhaustion ma
285 preclinical and clinical development include
adoptive transfer therapies, direct stimulation, recruit
286 vo with/without human MSC-derived EVs before
adoptive transfer to LPS-injured mice.
287 B cell
adoptive transfer to mice reduced infarct volumes 3 and
288 ry, ELISA, RNA sequencing, quantitative PCR,
adoptive transfer to mice, and measurement of airway hyp
289 erived DC subsets was determined by means of
adoptive transfer to naive mice.
290 toxicity against tumor cells and safety upon
adoptive transfer to patients.
291 of allergic airway inflammation, and T-cell
adoptive transfer to recombination-activating gene 1 (Ra
292 Despite the ability of
adoptive transfer to restore allergic airways inflammati
293 ne controlled cortical impact model, we used
adoptive transfer,
transgenic, and bone marrow chimera a
294 Using
adoptive transfer,
we demonstrate that PI3Kgamma is impo
295 Using a genetic approach complemented by
adoptive transfer,
we found that neutrophils are essenti
296 nd conditional deletion of TSLP receptor and
adoptive transfer were used to identify the cellular sub
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 Adoptive transfers with several types of immune cells or