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1 infects bovine mammary epithelial cells (MAC-T cell line).
2 cleic acid (DNA) from an HIV-infected Jurkat T cell line.
3 onotype found in the poly(F,Y,A,K)n-specific T cell line.
4 and proliferation by an epitope-specific CD4 T cell line.
5 essed in primary cells and an IL-2-dependent T cell line.
6  of the Notch target gene Hes1 in a leukemia T cell line.
7 ncrease in transfer of HIV-1(BaL) to a human T cell line.
8 from a peptide-independent alloreactive CD8+ T cell line.
9  active Cre recombinase into a loxP-reporter T cell line.
10 on factors indicated that this is a CD4-1(+) T cell line.
11 establishment of an IL-15-dependent CD4-1(+) T cell line.
12 ncorporation in HeLa cells and in the Jurkat T-cell line.
13 mma interferon (IFN-gamma) production by the T-cell line.
14 ng to the GATA3 promoter in the human Jurkat T-cell line.
15 n that against the Cdt-hypersensitive Jurkat T-cell line.
16 e occupancy of three ETS proteins in a human T-cell line.
17 (mac239)) replication in a transformed human T-cell line.
18 apoptotic cell death of the Tax2-established T cell lines.
19 ion in latently infected primary T cells and T cell lines.
20 ppaB kinase and JNK activation in both B and T cell lines.
21  that human GIMAP6 is expressed primarily in T cell lines.
22 primary human T cells but not in transformed T cell lines.
23 through luciferase reporter assays in Jurkat T cell lines.
24  CYLD silencing increases HIV replication in T cell lines.
25 CD4(+) T lymphocytes, but not in some CD4(+) T cell lines.
26  peptide specificity of the in vitro induced T cell lines.
27 ress membrane TRAIL, and induce apoptosis of T-cell lines.
28 n purified CD4+ T cells and Jurkat and HSB-2 T-cell lines.
29 ral blood mononuclear cells and EBV-specific T-cell lines.
30  of both integrins in murine lymphocytes and T-cell lines.
31 orylated in a panel of HTLV-1-infected human T-cell lines.
32 s infectious, yet it spreads poorly in other T-cell lines.
33 compared to the other five SIV-specific CD8+ T-cell lines.
34 o a small number of allergic subject-derived T-cell lines.
35 eases and their functional targets in B- and T-cell lines.
36  in a manner comparable to established mouse TS cell lines.
37 ells, and failure to yield trophoblast stem (TS) cell lines.
38 174 cells and the immortalized rhesus monkey T-cell line 221.
39 more limited neutralizing capacity against a T-cell line-adapted SIV compared to those of the milk Ig
40 positive and -negative clones of the WEHI7.2 T cell line after T cell receptor (TCR) activation by an
41 tosis in primary mouse T cells and in the H9 T cell line after TCR cross-linking.
42 tiation, specificity, or clonal diversity of T cell lines after ex vivo production.
43 ns decreased the survival of HTLV-1-infected T-cell lines, although no cell death was observed after
44 ing RNA in a VEGF receptor-expressing Jurkat T cell line and by SU5416, a pharmacological KDR inhibit
45 ll chemoattractant (CxCL13), both in a model T cell line and in primary human CD4(+) T cells.
46 lock proliferation of an IL-1alpha-dependent T cell line and inhibit production of TNF-alpha by activ
47                           Seventeen of these T cell lines and clones reacted to a broad range of stud
48  with IgE to both allergens, Amb a 1-induced T cell lines and clones responded weakly to Art v 6.
49 proliferation of intestinal gliadin-specific T cell lines and clones were measured as evidence of T c
50 ent for ARF-6 was observed in Nef-expressing T cell lines and in HIV-infected primary T cells.
51 gical inhibition reactivated latent HIV-1 in T cell lines and in primary CD4(+) T cells.
52  drugs that primed latent HIV-1 infection in T cell lines and in primary T cells for reactivation and
53 t SAMHD1 expression varies among four CD4(+) T cell lines and is transcriptionally regulated.
54  assays, both in terms of number of specific T cell lines and number of responding donors.
55 0-induced apoptosis was further confirmed in T cell lines and peripheral blood mononuclear cells usin
56 is indeed required for HIV-1 reactivation in T cell lines and primary CD4 T cells.
57 from infecting multiple human macrophage and T cell lines and primary cells by hT5Cyp, as were HIV-2R
58 letion or overexpression of hnRNPLL in B and T cell lines and primary T cells resulted in reciprocal
59 lowed the quantitative comparison of the two T cell lines and provided predictions for the conversion
60              USP9X silencing in both a human T-cell line and mouse primary T cells reduced T-cell rec
61 of Bim partially protected an IL-7-dependent T-cell line and peripheral T cells, especially cells wit
62 udy, we expressed HDAC7 mutant proteins in a T-cell line and use DNA microarrays to identify transcri
63 ects on the functional phenotype of specific T-cell lines and clones by means of flow cytometry, real
64                      We generated intestinal T-cell lines and clones from 7 patients with HLA-DQ2.2 (
65                The existing paradigm is that T-cell lines and clones from children differ from those
66  with myeloma and generated peptide-specific T-cell lines and clones from HLA-A*0201-positive (HLA-A*
67 s their recognition by EphA2-specific CD8(+) T-cell lines and clones in vitro via a mechanism that is
68   A panel of human GAD (hGAD65)-specific CD4 T-cell lines and hybridomas was generated to serve as de
69 miRNA expression in HTLV-1-transformed human T-cell lines and primary peripheral blood mononuclear ce
70 oduced robust cytotoxicity against malignant T-cell lines and primary tumors and were protective in a
71 uced the rapid degradation of MCPIP1 in both T-cell lines and quiescent human CD4+ T cells.
72 -cell responses against gluten by generating T-cell lines and T-cell clones from intestinal biopsies
73 l-2 family, is restricted to HTLV-1-infected T-cell lines and to T-cells expressing both Tax and HBZ
74 oth resting T cells and the nonactivated EL4 T cell line, and was up-regulated in both types of T cel
75 ding HIV-1 infection was also normal in most T cell lines, and flap mutant viruses replicated equival
76  cytokines produced by IFX-specific T cells, T cell lines, and T cell clones were evaluated at the mR
77 n increased Rac1 activity in both B-cell and T-cell lines, and its suppression was able to abrogate p
78                          Feline fibroblasts, T-cell lines, and primary peripheral blood mononuclear c
79 9 induced the greatest proliferation in CD4+ T-cell lines, and VirB9-specific CD4+ T-cell clones resp
80 n activation, however, some of the malignant T-cell lines are able to coexpress IL-17A and IL-17F, le
81  assays were performed using the Jurkat E6.1 T cell line as a model of T lymphocytes and Caco2-BBE mo
82 s associated with Tam resistance in the MCF7-T cell line as opposed to the Tam-sensitive MCF7 cell li
83 rosis factor alpha and interferon-gamma in a T cell line as well as in thymocytes.
84 rong promoter activity in mature NK cell and T cell lines as well as in immature NK cells.
85 ncing increases HIV infection in transformed T cell lines as well as primary CD4(+) T cells.
86         We observed that myelin-reactive CD4 T cell lines, as well as short-term PHA-activated CD4 T
87 ltivars Ayacuchana and Pasankalla stimulated T cell lines at levels similar to those for gliadin and
88 cassette with flanking loxP sites in a human T-cell line at the precise location of vector integratio
89 rived from rabbits immunized with the Jurkat T-cell line (ATG-Fresenius) or thymus cells (Thymoglobul
90 ify the APOBEC3 repertoire in multiple human T-cell lines, bulk leukocytes and leukocyte subsets, and
91 ecent phosphoproteomic studies of the Jurkat T cell line but difficult to reconcile with former bioch
92 were measured in an HIV-1-inducible reporter T cell line by flow cytometry.
93      SAMHD1 expression was induced in CD4(+) T cell lines by blocking DNA methyltransferase activity,
94 the CD4 T cell response to CCNB1, we derived T cell lines by multiple weekly rounds of stimulation wi
95 by hamster kidney)-21 and an HTLV-1-infected T cell line, C8166, physiologically relevant to HTLV-1-i
96 m, we show that autologous BK virus-specific T cell lines can be reliably generated from viremic KTR.
97       Cell encapsulation studies using an H9 T-cell line (CD4+) were conducted to evaluate feasibilit
98            We show that in an IL-7-dependent T cell line, cells protected from apoptosis nevertheless
99  mRNAs indicated that, compared to the human T-cell lines CEM and H9, prostate cell lines LNCaP and D
100  parental Jurkat cells or an unrelated human T cell line (CEM391) inhibited SOCE and led to sensitiza
101 ral blood mononuclear cells (PBMC) and a CD4 T-cell line compared to monocyte-derived macrophages, or
102 NF expression is elevated in HTLV-1-infected T-cell lines compared to uninfected T cells.
103                  The pathogenic C3Bir CD4(+) T-cell line contained more cells producing IL-17 than th
104 ased in a single round of replication from a T cell line containing A3G complexes (CEM cells) after i
105 ipid C-stimulated mouse iNKT cells and human T-cell lines containing NKTs primed with CD1d+C1R transf
106 re autoantigen-nonspecific, in that the same T cell line could suppress autoimmunity induced by three
107 28-35)SL8- and Gag(181-189)CM9-specific CD8+ T-cell lines could suppress the replication of an escape
108                  Using mutants of the Jurkat T-cell line deficient for key components of the T-cell r
109  of mutant CARD11 expression constructs into T cell lines demonstrated both loss-of-function and domi
110 n experiments using latently infected Jurkat T-cell lines demonstrated that the HKMT enhancer of Zest
111                                              T-cell lines derived from lung biopsy specimens of asthm
112                                        Human T-cell lines derived from nut-allergic patients produced
113 ix mutant replicated efficiently in the MT-4 T-cell line despite maintaining an MVB-targeting phenoty
114 d therefore these findings and the new model T cell line developed will contribute to a greater under
115 viral efficacies of 26 epitope-specific CD8+ T-cell lines directed against seven SIV epitopes in Tat,
116 processed A. fumigatus and the multispecific T-cell lines, directed against all 3 proteins, especiall
117                               Using a CD8(+) T-cell line displaying potent noncytotoxic HIV-1 suppres
118                        Using a CD1c-reactive T cell line (DN6) to complete an organism-wide survey of
119 ly, silencing of MOV10 expression in a human T cell line enhanced HIV-1 replication.
120                                       CD4(+) T-cell lines enriched for VZV specificity were generated
121        Here, we show that a set of malignant T-cell lines established from patients with cutaneous T-
122              Tax-positive HTLV-1-transformed T-cell lines express elevated levels of p21(CIP1/WAF1),
123                        Interestingly, stable T cell lines expressing dominant-negative RhoA mimicked
124                            We also show that T cell lines expressing modified U1 snRNAs exhibit reduc
125 NS5 protein inhibits HIV replication, CD4(+) T cell lines expressing this protein were generated.
126                          We generated CD4(+) T cell lines expressing varying levels of CCR5 on the ce
127 , in contrast to its parental virus, infects T-cell lines expressing low levels of cell surface CCR5.
128  was highlighted by data showing that CEM-SS T-cell lines expressing near-physiologic levels of APOBE
129 fers the possibility to generate BK-specific T cell lines for adoptive immunotherapy.
130 senting cells to an M1 epitope-specific CD8+ T-cell line for specific lysis.
131                 Furthermore, when generating T-cell lines for adoptive T-cell therapy, it avoids the
132 itopes, establishing antigen-specific memory T-cell lines for identifying CD8(+) and CD4(+) T-cell ep
133 ated a large number of MAGE-A3-specific CD4+ T cell lines from all individuals tested, enabling full
134 oted that all bronchoalveolar lavage-derived T cell lines from HLA-DP2-expressing CBD patients contai
135                                              T cell lines from KTR and healthy control showed similar
136 tion and CTL activity of PBMCs and of CD8(+) T cell lines from patients with MS.
137 ved through addition of IL-2 to HPV-specific T cell lines from RRP patients.
138 nical-scale protocol to generate BK-specific T cell lines from viremic KTR.
139 esent study, we established cytotoxic CD4(+) T cell lines from VV-immune donors, which recognize epit
140 us (HTLV; now known as HTLV-1) produced by a T-cell line from a lymphoma patient.
141                                              T-cell lines from all donors, vaccinated from 1 month to
142 ng was observed in mice injected with CD4(+) T-cell lines from diabetic donors.
143                    MBC4 was able to activate T-cell lines from donors with birch pollen allergy and f
144  significantly less frequent in EBV-specific T-cell lines from patients with EBV-associated nasophary
145            We developed a method to generate Ts cell lines from freshly isolated lamina propria lymph
146           In contrast to previous reports in T-cell lines, FTY720-induced toxicity in the Raji cell l
147                            In addition, CD8+ T cell lines generated by gD53-61, gD70-78, and gD278-28
148 peripheral blood mononuclear cell (PBMC) and T cell lines generated from healthy donors.
149 is of 50 of a total of 236 CD4(+) and CD8(+) T cell lines grown from individual handpicked islets or
150                          The majority of the T cell lines had high Foxp3 expression and secreted both
151              The resulting CD4(+) regulatory T cell lines had marked inhibition on autologous myelin
152                            Studies with CD8+ T cell lines have suggested that Mtb Ags gain access to
153     These findings demonstrate that in human T cell lines, HIV-1 and simian immunodeficiency virus ca
154 ll as a TCR derived from a CD1b-autoreactive T-cell line (HJ1Tg).
155 oth kill thymocytes, peripheral T cells, and T cell lines; however, we have found that galectin-9 and
156                       In primary T cells and T-cell lines, HRF triggered a high but nonsustained peak
157 stimulation in PBMCs, CD4(+) T cells, or the T cell line HuT78 activates the Notch pathway by nuclear
158                  We report that in the human T cell line HuT78 and in primary murine T lymphocytes, s
159               Using a previously established T-cell line immortalized with an HTLV-1 molecular clone
160 ectrometry was performed on the human Jurkat T cell line in the presence of U0126, an inhibitor of ER
161 imed in vitro a large number of specific CD4 T cell lines in all the donors.
162 , we analyzed the dynamics of the two CD4(+) T cell lines in mice during infection with L. monocytoge
163 enuate the proliferation of disease-specific T cell lines in response to gluten antigens and, therefo
164 ng DSBs, in benign Barrett's epithelial (BAR-T) cell lines in vitro and in patients with Barrett's es
165 t and in response to signaling in a cultured T-cell line in a manner which temporally correlates with
166  HDR donors in hESCs to generate an isogenic TS cell line in a scarless manner and to model the 16p11
167 issue-derived stem cells, and a human Jurkat T cell line) in vitro.
168 cific overexpression of either SOD in Jurkat T cell lines increases intracellular production of H2O2
169 eceptors from the regulatory IL-10-secreting T cell line induced by the random amino acid copolymers
170             We enumerated the Lipo5-specific T cell lines induced in vitro by weekly rounds of specif
171 OCS1 and SOCS3, but not SOCS2, in the Jurkat T cell line inhibited IFN-alpha-induced phosphorylated S
172 -tRNA(Val) observed in the homoplasmic 1624C>T-cell lines is caused by a rapid degradation of the dea
173 driving IL-17 secretion in short-term CD4(+) T cell lines isolated from human peripheral blood, altho
174 ramer(+) cells and cloned them from uncloned T cell lines isolated from spleen and lymph nodes of dia
175 nes were derived from HIV-reactive CD28+CD8+ T-cell lines isolated from 7 HIV+ HAART-treated patients
176                                    In Jurkat T-cell lines, it has been shown that TAC, in addition to
177 replication in a latently HIV-infected human T-cell line (J1.1).
178 on of endogenous c-Myc by Runx1 in the human T cell line Jurkat and murine primary hematopoietic cell
179 s increased after restimulation in the human T cell line Jurkat, in human memory and Th2 cells, and i
180                                          The T-cell line Jurkat ceased proliferation and died shortly
181       Our earlier work showed that a somatic T-cell line Jurkat mutant H123 bearing a defect in Ca(2+
182 GBV-C NS5A proteins were expressed in a CD4+ T cell line (Jurkat), and both induced a potent, dose-de
183 ent with SS, an acute lymphoblastic leukemia T-cell line (Jurkat), and JFL (a FAS-low variant of Jurk
184 (LBRM-33), similar to its effects on a human T-cell line (Jurkat), but did not inhibit IL-2 productio
185 en analyzed in physiologically more relevant T-cell lines (Jurkat and CEM), NC mutant viruses remaine
186 nfection of peripheral blood lymphocytes and T-cell lines (Jurkat and CEMX174).
187 f the herpesvirus saimiri-transformed CD8(+) T-cell line, K#1 50K, has potent HIV-1-inhibitory activi
188  interleukin-2 (IL-2) production by a murine T-cell line (LBRM-33), similar to its effects on a human
189 , two different murine CD4(+) TCR transgenic T cell lines, LLO118 and LLO56, both specific for the sa
190                                   The CD4(+) T cell lines lysed VV-infected, Ag- and peptide-pulsed t
191              Based on studies with activated T cell lines maintained in vitro, IL-2 is known to activ
192 d Ag-specific cytotoxic activity of a CD8(+) T cell line manifested in a 4-h assay (10-20% increase),
193                             Here, by using a T cell line model, we demonstrate that Id1 expression st
194 ant process, p101 was overexpressed in human T-cell lines Molt-4 and Jurkat.
195 B-HCV") has been shown to infect established T cell lines (Molt-4 and Jurkat) and primary human naive
196 sociation with DRMs in 293T cells and in the T-cell line, MOLT 4.
197 at we cloned from the MDV-transformed CD4(+) T-cell line MSB-1.
198 ell lymphotrophic virus (HTLV)-1-transformed T cell lines, MT-2, MT-4, SLB-1, and ATL-2.
199  and irradiated cells of an HTLV-1-producing T-cell line, MT2 was used to determine the permissivity
200                                 HIV-specific T cell lines obtained from vaccine recipients confirmed
201 e also analyzed A3 editing of HTLV-1 in five T-cell lines obtained from HTLV-1-infected patients.
202 44 internalization varied among cultured CD8 T cell lines of different specificities, and correlated
203  using HLA-A2 matched effector cells (CD8(+) T cell line or clone) and target cells supporting full H
204 al strains in pairwise competition assays in T-cell lines, primary cells, and the ecotropic human imm
205                                 Furthermore, T-cell lines primed in vitro from the blood of melanoma
206                              Other malignant T-cell lines produce IL-17A but not IL-17F.
207 AK kinase inhibitors have depressed leukemic T cell line proliferation.
208                                  Most of the T cell lines reacted with the peptides 9-23 and 14-28, l
209 we demonstrate that M. leprae-specific mouse T-cell lines recognize several of these antigens, with t
210  exogenous NY-ESO-1 protein, only one CD4(+) T cell line recognized NY-ESO-1(+) HLA class II-expressi
211        However, we found that virus-specific T cell lines recognized up to 10% of a panel of 44 HLA d
212                                  This CD4(+) T cell line recognizes target cells infected with influe
213 e, we showed that silencing IFN-lambda1 in T/T cell line reduced basal ISG expression and improved an
214 te more potently activated a CD1b-restricted T cell line relative to Mo-DCs pulsed with free lipid Ag
215                                    These rat TS cell lines represent valuable new in vitro models for
216                    Moreover, Art v 6-induced T cell lines responded stronger to Amb a 1.
217 xt to an "optimal" Kozak sequence in a human T cell line resulted in enhanced translation of a single
218 of complete STLV genome sequences from these T cell lines revealed them to be closely related but dis
219 dhesive properties of the human mature B and T cell lines RPMI 8866, Daudi and Jurkats.
220                               These CD4+CD25+T cell lines secrete high levels of IL-10 and IL-13 but
221          Analysis of expanded Vgamma2Vdelta2 T-cell lines showed the abundant presence of TLR2 mRNA,
222             In this study, we isolated a CD4 T cell line specific for CF that produces inflammatory c
223 e of A/Japan/305/1957 (H2N2), we generated a T cell line specific to this epitope.
224 nalyzed two naturally occurring human CD4(+) T cell lines specific for different peptides from cytoso
225 A-DR-typed healthy donors, we derived CD4(+) T cell lines specific for eight MDK peptides.
226                     In contrast, most of the T cell lines specific for Lipo5 reacted with G2, reveali
227                   IL-10-secreting regulatory T cell lines specific to glatiramer acetate [poly(Y,E,A,
228 were characterized in vitro by using a human T-cell line specific for the immunodominant epitope of B
229  T-cell receptor (TCR) cDNAs from murine CD8 T-cell lines specific for either pIRS-21097-1105 or pCDC
230                                          CD8 T-cell lines specific for NS3-1073 and NS5-2594 were exp
231  with collagen-induced arthritis (CIA), this T cell line specifically enhanced the severity of autoim
232 ed a CpG island that is methylated in CD4(+) T cell lines (such as Jurkat and Sup-T1), resulting in t
233 timulation of the Fas receptor in the Jurkat T-cell line, suggesting that Hip is a substrate unique t
234 ty of interactions are common to both B- and T-cell lines, suggesting interactions may be highly cell
235 xposed IKpDC induced apoptosis of the CD4(+) T cell line SupT1 via the TRAIL pathway.
236 xamined the fine specificity of VSG-specific T-cell lines, T-cell hybridomas, and Th cells activated
237                             Dau c 1-specific T-cell lines (TCL) and clones (TCC) established from PBM
238 re detected in 83% of Art v 125-36 -reactive T-cell lines (TCL) from mugwort-allergic individuals, bu
239             Can f 4-specific CD4(+)CD45RO(+) T-cell lines (TCLs) from allergic and healthy subjects w
240       In primary tumors and TCL1-transfected T-cell lines, TCR engagement leads to rapid recruitment
241 on of TrkB is also higher in HTLV-1-infected T-cell lines than in uninfected T cells.
242 rt hairpin RNA in both primary T cells and a T cell line that recapitulates the stability phase of re
243 ical to those recently found in a regulatory T cell line that secretes both IL-4 and IL-10 induced in
244 This approach identified several independent T cell lines that proliferated robustly in response to I
245 s among the drug, HLA, and TCR, we generated T cell lines that react to ALP or its metabolite oxypuri
246 sion with either HSV or VZV enriches for CD4 T cell lines that recognize the other agent at the whole
247 ild-type virus replication, a Tet-off Jurkat T-cell line that expressed approximately 15-fold-higher
248 t express human or macaque CD16 and a CD4(+) T-cell line that expresses luciferase from a Tat-inducib
249 cell carcinoma (RCC), we identified a CD4(+) T-cell line that showed TCR-mediated recognition and lys
250                        H5N1 peptide-specific T-cell lines that did not cross-react with H1 or H3 infl
251 lus fumigatus proteins, Aspergillus-specific T-cell lines that have a broad specificity and favorable
252 at it is possible to establish clonal CD8(+) T-cell lines that represent the most abundant specificit
253 spleen and lymph node cells in vitro yielded T-cell lines that specifically produced interferon-gamma
254 1) vif compromise virus replication in human T-cell lines that stably express APOBEC3F (A3F) or APOBE
255 by ELF5 will be instrumental to derive human TS cell lines that truly reflect early placental trophob
256  and enables derivation of trophoblast stem (TS) cell lines that, when injected into blastocysts, chi
257 epared M. tuberculosis-specific gamma9delta2 T cell lines to study their direct protective effects an
258 l antigen-specific C3H/HeJBir (C3Bir) CD4(+) T-cell line to C3H/HeSnJ SCID mice.
259  have used an IA(b)/OMP-19(107-122)-specific T-cell line to monitor antigen display ex vivo during ac
260 abilities of different epitope-specific CD8+ T-cell lines to control simian immunodeficiency virus (S
261 tor Vbeta genes in expanded microbe-reactive T-cell lines to determine their clonal diversity.
262 firmed the responsiveness of these cytotoxic T-cell lines to seven peptides described previously and
263 re examined in parallel with mouse and human T cell lines transfected with CD40.
264 ate the effect: an anti-myelin basic protein T-cell line treated with cefuroxime or penicillin was mo
265 s the major coreceptor for cellular entry of T-cell line-tropic (X4) HIV-1 strains.
266 olyclonal vaccinia virus-polyspecific CD8(+) T cell line, two conserved vaccinia-derived TAP-independ
267 D147-dependent phosphoproteome in the Jurkat T cell line upon treatment with T cell stimulating agent
268 cytosis in the adherent cell 293T and Jurkat T cell lines using a fusion protein of extracellular CD4
269 ects, allowing the isolation of HPV-specific T cell lines using tetramers.
270 f a beryllium-responsive, HLA-DP2-restricted T cell line was seen after the induction of 4-1BB ligand
271                                          One T cell line was stimulated by HLA-compatible MDK-transfe
272 strated that forced expression of GRAIL in a T cell line was sufficient for conversion of these cells
273 n of food allergen-reactive Bet v 1-specific T-cell lines was assessed.
274 +), OT-II CD4+ T cells, and the human Jurkat T cell line, we show that physiological levels of H(2)S
275 human T cells and a reporter assay in Jurkat T cell lines, we dissected the regulation of TLR10, a TL
276 ted CD4(+) T cells from spleen and lung, and T cell lines, we found that the majority of these T cell
277                               Using an early T-cell line, we describe two branches of this network.
278 a/beta pairs cloned from single cells of the T cell line were inserted into a retrovirus vector linke
279                                          The T cell lines were antigen-specific and showed no nonspec
280                               CD4-expressing T cell lines were constructed to constitutively express
281                         Continuously growing T cell lines were established from two baboons, animals
282                                   Polyclonal T cell lines were generated from either normal mice or m
283             In this study, CD4(+) regulatory T cell lines were generated from patients with multiple
284      By contrast, the peptide 14-28-specific T cell lines were not stimulated in any of these conditi
285                                       CD4(+) T cell lines were rendered virtually uninfectable, with
286                                              T cell lines were specific for 15 immunodominant peptide
287                    The peptide 9-23-specific T cell lines were specifically stimulated by autologous
288                            Allergen-specific T-cell lines were analyzed for epitope recognition.
289 28-35)SL8- and Gag(181-189)CM9-specific CD8+ T-cell lines were consistently superior at suppressing v
290        For epitope mapping, Mal d 1-specific T-cell lines were stimulated with overlapping synthetic
291  chemical genetic inhibitor system in Jurkat T cell lines, where the inhibitor blocked ZAP-70-depende
292     This 9-mer serves to direct cytolysis by T cell lines, whereas a related 10-mer (E7(11-20)), prev
293 Unexpectedly, IL-27 did not inhibit HIV-1 in T cell lines, whereas IL-2 inhibited HIV-1 replication i
294 ired for proliferation and survival of these T cell lines whether or not JAKs or STATs were mutated.
295  gIIFPLA(2) inhibited the proliferation of a T cell line, which was not seen with group IIA PLA(2).
296  interrogated vaccinia-reactive CD4 in vitro T cell lines with vaccinia protein fragments expressed f
297 age is observed upon infection of the Jurkat T-cell line with vesicular stomatitis virus G glycoprote
298               We screened 25 human cytotoxic T-cell lines with adenovirus specificity to extensively
299          In addition, treatment of malignant T-cell lines with peg-Arg I significantly impaired their
300 CR-alpha LCR-linked transgenes into existing T cell lines yields incomplete LCR activity.

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