ライフサイエンスコーパス: xenogeneic

1 accomplished by grafting only the SDRs of a xenogeneic Ab onto human Ab frameworks.

2 In a xenogeneic adoptive transfer model, we have compared the

3 term metabolic function of microencapsulated xenogeneic adult porcine islets (API) was assessed in a

4 ing improved regression of human cancer in a xenogeneic allograft model.

5 When rejection occurred on days 4 and 8 in xenogeneic and allogeneic recipients, 60% (57-68) and 55

6 human regulatory T cells (Tregs) to suppress xenogeneic and allogeneic responses in vitro.

7 hESC(siRNA+IB) was strongly reduced in both xenogeneic and allogeneic settings.

8 exhibit compromised rejection of allogeneic, xenogeneic and missing self bone-marrow grafts.

9 At 2 days, injection sites of xenogeneic and syngeneic cells (cardiac-derived stem cel

10 at are capable of killing a large variety of xenogeneic and syngeneic cells.

11 possibility of imaging inflammation in both xenogeneic and syngeneic tumor models, which resulted in

12 find that cardiac fibroblasts that express a xenogeneic antigen can be effectively targeted and ablat

13 We estimated the decrease in expression of a xenogeneic antigen, Galalpha1-3Gal, which might be neede

14 ced in xenograft recipients against multiple xenogeneic antigens.

15 ursor experiments have been carried out in a xenogeneic background in order to utilize species-specif

16 licited immune response of healthy dogs to a xenogeneic BAL was blocked and BAL performance significa

17 o induce tolerance across a highly disparate xenogeneic barrier has not yet been demonstrated.

18 wo strategies to induce tolerance across the xenogeneic barrier, namely thymus transplantation and mi

19 survival across the discordant pig-to-baboon xenogeneic barrier.

20 olerance across a discordant (pig-to-baboon) xenogeneic barrier.

21 ial, but also to understanding the nature of xenogeneic barriers and mechanisms of heterochronicity,

22 nsplantation because immune responses across xenogeneic barriers are vigorous.

23 e transplant tolerance across allogeneic and xenogeneic barriers, and to support long-term thymopoies

24 ucing T cell tolerance across allogeneic and xenogeneic barriers.

25 mouse) and highly disparate (pig to rodent) xenogeneic barriers.

26 ion across allogeneic and potentially across xenogeneic barriers.

27 success of transplants across allogeneic and xenogeneic barriers.

28 nts of antigenicity in a clinically relevant xenogeneic biomaterial (i.e. BP) and further validates a

29 Xenogeneic biomaterials contain biologically relevant ex

30 nction has important implications for use of xenogeneic biomaterials, particularly in vascular applic

31 onstrate that anti-CD40L in combination with xenogeneic BMT can tolerize preexisting peripheral and i

32 Mixed xenogeneic bone marrow chimeras resulting from the trans

33 We have previously demonstrated that xenogeneic bone marrow engraftment and donor-specific to

34 on and in the facilitation of allogeneic and xenogeneic bone marrow engraftment.

35 and/or gammaDelta cell-mediated rejection of xenogeneic bone marrow.

36 increases the rapidity of PDLF attachment to xenogeneic bone replacement materials.

37 une response against the therapeutic and the xenogeneic carbohydrate galactose-alpha1-3-galactose, an

38 cellular responses that lead to rejection of xenogeneic cartilage are not well understood.

39 and may therefore contribute to rejection of xenogeneic cartilage.

40 on of KO mice with pig kidney membranes (ie, xenogeneic cell membranes expressing an abundance of alp

41 s play an important role in the rejection of xenogeneic cells and therefore represent a major obstacl

42 type; and improved survival of donor-derived xenogeneic cells at 2 and 4 wk in vivo.

43 contributes significantly to phagocytosis of xenogeneic cells by macrophages and suggest that genetic

44 y of CD47 may contribute to the rejection of xenogeneic cells by macrophages.

45 recent years, hepatic support systems using xenogeneic cells have been developed to support patients

46 nsplantation of a bioartificial adrenal with xenogeneic cells may be a treatment option for patients

47 on of coagulation pathways after exposure to xenogeneic cells or a vascularized xenograft.

48 The use of xenogeneic cells or tissues for tissue engineering appli

49 n the animals transplanted with syngeneic or xenogeneic cells, respectively.

50 served after injection of both syngeneic and xenogeneic cells.

51 ly high precursor frequency was detected for xenogeneic cellular responses in the rat anti-mouse comb

52 Furthermore, compared with fully xenogeneic chimeras (rat --> mouse), mixed xenogeneic ch

53 Mixed xenogeneic chimeras exhibit donor-specific humoral toler

54 y xenogeneic chimeras (rat --> mouse), mixed xenogeneic chimeras exhibit superior immunocompetence fo

55 In xenogeneic chimeras, T cell repertoire selection plays a

56 We have previously demonstrated that mixed xenogeneic chimerism and donor-specific T-cell tolerance

57 e ability of anti-CD40L mAb to promote mixed xenogeneic chimerism and donor-specific tolerance in B6

58 These results demonstrate that mixed xenogeneic chimerism establishes donor-specific humoral

59 Mixed allogeneic or xenogeneic chimerism indeed tolerizes both preexisting a

60 lability of human adrenal glands, sources of xenogeneic chromaffin cells will need to be identified i

61 Xenogeneic CM combined with tunnel technique leads to sa

62 were treated with the tunnel technique using xenogeneic CM.

63 +, CD8+, and CD4+CD8+ T cells in a rat/mouse xenogeneic co-culture.

64 Both xenogeneic collagen matrices combined with FDBA were eff

65 Considering xenogeneic collagen matrix (CM) and enamel matrix deriva

66 e purpose of this study is to determine if a xenogeneic collagen matrix (CM) might be as effective as

67 it-mouth design with CAF procedures or CAF + xenogeneic collagen matrix (CMX).

68 of inducing tolerance in a highly disparate xenogeneic combination and may have clinical potential t

69 lity has not been demonstrated in discordant xenogeneic combinations because of the difficulty in ach

70 ion in a pig-to-human model also reduces the xenogeneic consumption of human platelets by the porcine

71 the effect that these modifications have on xenogeneic consumption of human platelets in the absence

72 human CD19(+) B-lineage cells purified from xenogeneic cord blood stem cell/MS-5 murine stromal cell

73 We wished to determine the extent to which xenogeneic cornea fragments placed in the eyes of normal

74 Xenogeneic corneal fragments (guinea pig) are highly res

75 Xenogeneic corneal fragments implanted in the anterior c

76 By contrast, xenogeneic corneal fragments implanted in the anterior c

77 Neutralization of IL-7 in xenogeneic cultures led to an increase in Ig light-chain

78 man CD19(+) cells developing in human/murine xenogeneic cultures show differential expression of the

79 Prime requirements for allogeneic, or xenogeneic, decellularized scaffolds are biocompatibilit

80 In this model of xenogeneic DNA immunization, the presence of an hgp100 h

81 stems, ubiquitous defense mechanisms against xenogeneic DNA that hinder the use of genetic approaches

82 ght to improve on this strategy by combining xenogeneic DNA vaccination with an agonist anti-glucocor

83 In contrast to allogeneic donor ECDI-SPs, xenogeneic donor ECDI-SPs induced production of xenodono

84 Xenogeneic donor-specific tolerance can be induced by tr

85 T cells and render recipients tolerant of a xenogeneic donor.

86 porcine endogenous retroviruses (PERV) from xenogeneic donors into humans has been widely debated.

87 he bacterial ClpCP protease is the target of xenogeneic (dys)regulation by a SPO1 phage-derived facto

88 d by human CTL (huCTL) vs allogeneic and pig xenogeneic EC targets.

89 re of immune-competent mice to injections of xenogeneic EC-TCPS induced vigorous host immunity.

90 Matrix-embedding protects xenogeneic ECs against immune reaction in naive mice and

91 tolerance in allogeneic and closely related xenogeneic (eg, rat-to-mouse) combinations, the ability

92 nse and the subsequent activation invoked by xenogeneic encounter.

93 c, nude rats injected intraperitoneally with xenogeneic endothelial cells (ECs) produce antibodies ag

94 redox systems may provide a means to protect xenogeneic endothelial cells from NK cell-mediated cytot

95 erated from monocytes under the influence of xenogeneic endothelial cells in the absence of exogenous

96 cells after co-culturing with allogeneic and xenogeneic endothelial cells, respectively.

97 An in vitro model of xenogeneic engraftment was established to identify inhib

98 f specific T cell receptor-Vbeta occurs in a xenogeneic environment in a predictable fashion parallel

99 rtoire selection in tolerance induction in a xenogeneic environment.

100 d receptor in innate cellular recognition of xenogeneic epitopes.

101 Although a vigorous immune response to xenogeneic extracellular matrix biomaterials is expected

102 l biological scaffolds made of allogeneic or xenogeneic extracellular matrix derived from non-autolog

103 ival 3 weeks after injection of syngeneic or xenogeneic ferumoxides-labeled stem cells (cardiac-deriv

104 r tumorigenesis, we selectively targeted the xenogeneic form of survivin, a survival protein overexpr

105 induced by DEC205 targeting of the Ag in its xenogeneic form to maturing DCs.

106 an embryonic stem (hES) cells in defined and xenogeneic-free conditions will contribute substantially

107 ents a key step toward the fully defined and xenogeneic-free culture of hES cells.

108 C57BL/6 mice immunized with xenogeneic full-length hgp100 DNA were protected against

109 ight serve as a target for limiting unwanted xenogeneic fusion in the future.

110 om biomolecules induced smaller and necrotic xenogeneic GB; spider venom activated the innate immune

111 om autoimmune destruction and allogeneic and xenogeneic graft rejection.

112 s, and can instill long-lived allogeneic and xenogeneic graft tolerance.

113 of PBMC engraftment is development of acute xenogeneic graft- versus-host disease (GVHD) due to huma

114 Lack of acute xenogeneic graft- versus-host disease, but retention of

115 t, in a preclinical humanized mouse model of xenogeneic graft-versus-host disease (GVHD), sGARP preve

116 onstrate that IL-15 but not IL-2 exacerbates xenogeneic graft-versus-host disease (X-GVHD) in severe

117 a-treated Treg in a humanized mouse model of xenogeneic graft-versus-host disease confirmed IFN-alpha

118 e induction of IFNgamma-secreting Tregs in a xenogeneic graft-versus-host disease model and in adopti

119 T cells and complete rescue from hyperacute xenogeneic graft-versus-host disease modeling early and

120 ls mediated tumor rejection without inducing xenogeneic graft-versus-host disease, thus resulting in

121 generated Tregs that consistently suppressed xenogeneic graft-vs-host disease in immunodeficient mice

122 munosuppression by human Tregs in a model of xenogeneic graft-vs.-host disease induced by the transfe

123 ntal health using autogenous, allogenic, and xenogeneic grafting approaches.

124 ns to ABO-incompatible allogeneic grafts and xenogeneic grafts from other species.

125 d could influence the findings; for example, xenogeneic grafts may not recognize host inhibitory sign

126 nd residual host immune function against the xenogeneic grafts results in defective development and m

127 to enhance the recruitment of host huTreg to xenogeneic grafts to regulate cell-mediated xenograft re

128 hat were capable of rejecting allogeneic and xenogeneic grafts.

129 Here, we report a novel, optimized NHP xenogeneic GVHD (xeno-GVHD) small animal model that reca

130 s expressing an irrelevant CAR at preventing xenogeneic GVHD caused by HLA-A2+ T cells.

131 R gene also conferred resistance to DEX in a xenogeneic GVHD model in sublethally irradiated NOD-scid

132 In a human xenogeneic GVHD model, human IL-21-secreting cells were

133 d prolonged time to fatal GVHD in an in vivo xenogeneic GVHD model.

134 ed Tconvs, and provide durable prevention of xenogeneic GVHD.

135 D83 CAR T cells are also capable of treating xenogeneic GVHD.

136 iate into effectors able to mediate a potent xenogeneic GVHD.

137 Murine complement is capable of resisting xenogeneic hematopoietic engraftment through an antibody

138 A1CMAH knockout pigs were compared for their xenogeneic hepatic consumption of human platelets.

139 osuppression allows long-term functioning of xenogeneic hepatocyte retransplants and suggests that he

140 tocytes might address this problem; however, xenogeneic hepatocytes are thought to be functionally in

141 Following a single infusion, xenogeneic hepatocytes functioned for more than 80 days

142 Transplants consisting of xenogeneic hepatocytes might overcome these problems, an

143 Conserved pathway activation following xenogeneic, heterotypic fusion.

144 e-specific autoimmunity was seen only when a xenogeneic homolog of PAP was used as the immunogen.

145 generated by blastocyst complementation in a xenogeneic host.

146 ry considerably in their transmissibility to xenogeneic hosts.

147 s, and, as a result, are rapidly rejected in xenogeneic hosts.

148 d ~6-fold in mouse HSCT and ~2-fold in human xenogeneic HSCT.

149 hibiting allogeneic pig T cell responses and xenogeneic human anti-pig T cell responses in vitro.

150 4IgG4 on allogeneic pig T cell responses and xenogeneic human anti-pig T cell responses.

151 We used a xenogeneic human cord blood stem cell/murine stromal cel

152 ostimulatory pathways block the rejection of xenogeneic human embryonic-stem-cell-derived pancreatic

153 equivalents or normoglycemic rats with 5000 xenogeneic human islet equivalents.

154 Finally, huTreg partially suppressed xenogeneic human NK cell adhesion, NK cytotoxicity and d

155 fficient zygote genome editing technologies, xenogeneic human pluripotent stem cells may also open ne

156 We conclude that porcine Kupffer cells bind xenogeneic human RBC by recognition of a carbohydrate ep

157 Using xenogeneic (human) cells in immunosuppressed animals wit

158 is a murine T cell clone that recognizes the xenogeneic (human) class I MHC HLA-A2.1 molecule (A2) an

159 f primary GalT-KO skin grafts led to an anti-xenogeneic humoral response with no evidence for sensiti

160 , we explore the transcriptome of individual xenogeneic hybrids of human mesenchymal stem cells and m

161 between cells of different organisms (i.e., xenogeneic hybrids) can occur, and for humans this may o

162 shows that conferred advantages are rare in xenogeneic hybrids, whereas risks of cellular dysregulat

163 ve-type CD4 cells (CD4/CD45RA ) and in vitro xenogeneic hyporesponsiveness were observed.

164 Porcine thymic tissue is able to induce xenogeneic hyporesponsiveness.

165 endothelial-mediated activation of allo- and xenogeneic immune cells.

166 not appear to differ in the nature of their xenogeneic immune response to the administered rabbit se

167 and exhibited similar levels of anti-rabbit xenogeneic immune response, the NZW mice had significant

168 Xenogeneic immunization with orthologous Ags induces can

169 occurred, and no evidence of transmission of xenogeneic infections was found.

170 tested this hypothesis in a human-into-mouse xenogeneic islet transplant model and validated the conc

171 In a rat-to-mouse xenogeneic islet transplant model, we show that rat ECDI

172 nal requirements for tolerance induction for xenogeneic islet transplantation using donor ECDI-SPs.

173 trategy for tolerance induction for clinical xenogeneic islet transplantation.

174 Xenogeneic islets are susceptible to complement-mediated

175 nologic challenges facing transplantation of xenogeneic islets, and the concerns regarding transmissi

176 ical advantage of IUCT was demonstrated with xenogeneic IUCT.

177 mechanisms of post-transplant proteinuria in xenogeneic kidney transplantation and a potential strate

178 d the early development of proteinuria after xenogeneic kidney transplantation in baboons.

179 s combinations, its role in the rejection of xenogeneic marrow engraftment is unknown.

180 is to investigate the effect of filling with xenogeneic material the postextractive sockets of two su

181 results suggest that indirect recognition of xenogeneic MHC antigen plays a predominant role in graft

182 cells elicit a vigorous response to allo- or xenogeneic MHC class I molecules.

183 At present, it is not clear whether xenogeneic MHC molecules are recognized by T cells direc

184 survival of T cells positively selected by a xenogeneic MHC, as well as incomplete intrathymic deleti

185 ed decreased signal intensity not only for a xenogeneic mismatch in species but, surprisingly, also f

186 vitro, as well as engraftment potential in a xenogeneic model after partial myeloablation.

187 ited antileukemic activity in vivo against a xenogeneic model of disseminated AML.

188 t efficiency have been explored in a primate xenogeneic model of in utero hematopoietic stem cell tra

189 the induction of tolerance in the discordant xenogeneic model of pig-to-rodent thymic transplantation

190 ferent cellular mechanisms in allogeneic and xenogeneic model systems.

191 ive at impairing tumor development in murine xenogeneic model, activating the innate immune response

192 In the xenogeneic model, we quantified islet transplant exosome

193 development were established in vivo using a xenogeneic model.

194 profile of human HSC engraftment in a living xenogeneic model.

195 Moreover, in a xenogeneic mouse model of breast carcinoma, in vivo trea

196 ablished from EBV-infected B-cell lines in a xenogeneic mouse model of PTLD.

197 f HER2/neu-positive human breast tumors in a xenogeneic mouse model.

198 on in the presence of immunosuppression in a xenogeneic mouse model.

199 Xenogeneic mouse models are broadly used to study human

200 Two xenogeneic mouse models bearing intracranial human GBMs

201 his study reports the establishment of fully xenogeneic mouse-->rat multilineage chimeras and evaluat

202 Fully xenogeneic multilineage bone marrow chimerism was produc

203 sus-leukemia (GVL) effects in allogeneic and xenogeneic murine GVHD models.

204 T-cell function is severely impaired in the xenogeneic murine microenvironment.

205 inocytes was developed four decades ago, the xenogeneic nature of that conventional CEA culture syste

206 further genetic modification of the pig, and xenogeneic NK cell recognition and activation may be inh

207 irus (EBV)-driven human B-cell lymphoma in a xenogeneic NOD/SCID/IL2rg(null) mouse model.

208 of JAM-C in homing of human B cells, using a xenogeneic nonobese diabetic/severe combined immunodefic

209 of T cells (and T cell subsets) after either xenogeneic or allogeneic activation in vitro or in vivo.

210 ornea upon grafting to LSC-deficient mice in xenogeneic or syngeneic transplantation models.

211 Immunization of mice with plasmids encoding xenogeneic orthologues of tumor differentiation antigens

212 a developmental regulatory gene can generate xenogeneic pancreas and kidney(1,2).

213 uch as eptifibatide, interfere directly with xenogeneic PBPC-platelet interactions and may further am

214 bile acids in patient serum increases during xenogeneic perfusion for unknown reasons.

215 Xenogeneic peripheral blood chimerism was assessed after

216 methods for induction of immune tolerance to xenogeneic pig antigens.

217 prolong allogeneic islet graft survival and xenogeneic pig islet graft survival in diabetic NOD mice

218 prolongs allogeneic islet graft survival and xenogeneic pig islet graft survival in diabetic NOD mice

219 Highly disparate xenogeneic pig skin graft tolerance and efficient repopu

220 Highly disparate xenogeneic pig skin graft tolerance can be achieved by g

221 een with either allogeneic (rat-into-rat) or xenogeneic (pig-into-rat) transplants over 28 days, comp

222 A maternal immune response to the xenogeneic placental antigen was shown by the presence o

223 d ASGR1 expression as well as ASGR1-mediated xenogeneic platelet phagocytosis in vitro and ex vivo on

224 This xenogeneic platform provided explanted human lungs a sup

225 tiated cell lines are capable of recognizing xenogeneic porcine aortic endothelial cells in a calcium

226 rge-animal model raises the possibility that xenogeneic porcine islet tissue will also survive in hum

227 is potent enough to prevent the rejection of xenogeneic porcine islets in a large-animal model.

228 CD4 T cells are specifically tolerant of the xenogeneic porcine thymus donor and the recipient, but a

229 ll-depleted, thymectomized mice grafted with xenogeneic porcine thymus tissue.

230 However, in the xenogeneic rat-to-mouse combination, additional anti-Thy

231 he hypothesis that porcine sialoadhesin is a xenogeneic receptor that mediates porcine macrophage bin

232 poietic cell engraftment in highly disparate xenogeneic recipients remains unclear.

233 ouse embryonic ovarian somatic cells to form xenogeneic reconstituted ovaries, which are cultured und

234 -like cells (T1LCs) using long-term cultured xenogeneic reconstituted testes.

235 The xenogeneic regulation of bacterial cell function is a po

236 sed regimen was not effective for preventing xenogeneic rejection.

237 l ignorance and experience largely mitigated xenogeneic rejection.

238 ever, the immunogenicity of cells expressing xenogeneic reporter constructs limits their survival and

239 egs may be required to suppress the stronger xenogeneic response.

240 CD4 T cells and the indirect pathway in the xenogeneic response.

241 Both discordant and concordant xenogeneic responses are dominated by humoral immunity.

242 uTreg) suppress CD4+ T cell-mediated antipig xenogeneic responses in vitro and might therefore be use

243 fference between human T cell allogeneic and xenogeneic responses in vivo.

244 Xenogeneic responses were unique in the continued expres

245 ccommodation has been widely investigated in xenogeneic responses.

246 repared from monocytes ex vivo without using xenogeneic serum and may be used for immunotherapy.

247 As a consequence, thymopoiesis in this xenogeneic setting began by weeks 4-6, peaked at mo 3, a

248 derstanding the biochemistry of H-NS and how xenogeneic silencing affects bacterial evolution.

249 standing of the mechanisms and importance of xenogeneic silencing and counter-silencing in the succes

250 Xenogeneic silencing of horizontally-acquired genes by H

251 Most notably, xenogeneic silencing proteins bind incoming DNA that has

252 ession of foreign DNA in a process known as 'xenogeneic silencing.' Counter-silencing by a variety of

253 kin did not lead to accelerated rejection of xenogeneic skin.

254 opoietic engraftment across highly disparate xenogeneic species barriers poses a major obstacle to ex

255 ing T cell tolerance across highly disparate xenogeneic species barriers.

256 ant in the rejection of solid organs in some xenogeneic species combinations, its role in the rejecti

257 orcine donor responses in a highly disparate xenogeneic species.

258 This could present major limitations to xenogeneic stem cell transplantation as an approach to t

259 use of homologous stem cells, allogeneic or xenogeneic stem cells have been studied extensively in e

260 ated inflammatory reaction to allogeneic and xenogeneic stem cells may elicit a spectrum of effects,

261 response that is exaggerated with the use of xenogeneic stem cells.

262 ming comparing activation with allogeneic or xenogeneic stimulators.

263 fluence T cell repertoire in response to the xenogeneic stimulus.

264 n leukocyte antigen (HLA) antibodies against xenogeneic swine leukocyte antigen (SLA) antigens.

265 Using a xenogeneic system, here we define the bioenergetic chang

266 However, the xenogeneic T cell precursor frequency was found to be ma

267 litates metastasis in both the syngeneic and xenogeneic (T and B lymphocyte deficient) systems.

268 ted with an increased spontaneous killing of xenogeneic target cells.

269 ive selection is mediated exclusively by the xenogeneic thymic MHC.

270 Our results support the interpretation that xenogeneic thymic transplantation is a feasible strategy

271 normal mice usually remain healthy following xenogeneic thymic transplantation, thymus-grafted congen

272 Transplantation of xenogeneic thymus tissue allows xenograft tolerance indu

273 Xenogeneic thymus transplantation is an effective approa

274 f the uterus has been demonstrated only with xenogeneic tissue grafts.

275 The survival of xenogeneic tissue in the absence of immunosuppression in

276 t include alternative sources of islets (eg, xenogeneic tissue or human stem cells), extrahepatic sit

277 Mice were implanted s.c. with xenogeneic tissue, syngeneic tissue, or SIS, and the gra

278 ra-abdominal testis supports the survival of xenogeneic tissue.

279 Because xenogeneic tissues are subject to vigorous immune reject

280 Xenogeneic tissues induce vigorous T cell immunity, refl

281 haracterize further the cellular response to xenogeneic tissues, we used the intracellular fluorescen

282 CD4 T-cell reconstitution and xenogeneic tolerance is achieved in T cell-depleted, thy

283 LIV in the mediastinum, suggesting that full xenogeneic tolerance was not achieved in euthymic mice.

284 t before syngeneic, suboptimal syngeneic, or xenogeneic transplant exhibited superior function compar

285 ma and ascites formation in an athymic mouse xenogeneic transplant model of ovarian cancer.

286 rent research efforts in both allogeneic and xenogeneic transplantation are presented and discussed.

287 ed from the islets of the pancreas can cross xenogeneic transplantation immune barriers, induce tissu

288 In conclusion, xenogeneic transplantation of human PBSCs into NOD/SCID

289 and 3) models of syngeneic, allogeneic, and xenogeneic transplantation.

290 t preservation in syngeneic, allogeneic, and xenogeneic transplantation.

291 lls, tissues, and organs after allogeneic or xenogeneic transplantation.

292 The expression of xenogeneic TRIM5alpha proteins can restrict infection in

293 The results showed that the xenogeneic tumors can grow and metastasize.

294 The eradication of xenogeneic tumors in a murine environment shows that the

295 Rejection of xenogeneic tumors was also T-cell dependent as demonstra

296 peutic efficacy in mice with RL cell-derived xenogeneic tumors.

297 luenza virus type 1 (Sendai virus [SV]) as a xenogeneic vector to deliver the G glycoprotein of RSV.

298 Differences in xenogeneic versus allogeneic activation profiles exist t

299 linical efficacy of synthetic, allogeneic or xenogeneic vessels has been limited by thrombosis, rejec

300 llogeneic BALB/c or phylogenetically related xenogeneic WF rat stimulator cells while having undetect