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1 after the treatment course, as determined by enzyme-linked immunospot.
2 by IFN-gamma-specific immunofluorescence and enzyme-linked immunospot.
3  vigorous cytotoxic T lymphocyte response by enzyme-linked immunospot.
4 ononuclear cells (PBMCs), were studied using enzyme-linked immunospot.
5 from 12/12 donors released IFN-gamma (50-300 enzyme-linked immunospots/200,000 T cells) and prolifera
6                                 Furthermore, enzyme-linked immunospot analyses demonstrated prominent
7 D4 T-cell epitopes within OMPs, we performed enzyme-linked immunospot analyses for gamma interferon (
8    Immunohistochemical, flow cytometric, and enzyme-linked immunospot analyses of the spleen, kidney,
9                                        Using enzyme-linked immunospot analysis (ELISPOT) assays, we f
10 of 32 HDV-infected patients were analyzed by enzyme-linked immunospot analysis and intracellular cyto
11 responses against A20 cells, as assessed via enzyme-linked immunospot analysis in vitro and immune pr
12                                              Enzyme-linked immunospot analysis reveals that these CTL
13  of IFN-gamma-secreting cytotoxic T cells by enzyme-linked immunospot analysis that may have also fac
14  cells were not detected by immunoglobulin M enzyme-linked immunospot analysis until day 7.
15 ell epitopes were mapped by gamma interferon enzyme-linked immunospot analysis using five overlapping
16 ed subjects not on antiretroviral therapy by enzyme-linked immunospot analysis with 53 peptide pools
17  cancer patients and 18 healthy donors using enzyme-linked immunospot analysis.
18 onor, as determined by tetramer staining and enzyme-linked immunospot analysis.
19 ic CD8(+) T cells were detected by IFN-gamma enzyme-linked immunospot and (51)Cr release assay in loc
20 l responses, as detected by interferon-gamma enzyme-linked immunospot and allo-antibody production, r
21 in BALB/c mice revealed that the DNA induced enzyme-linked immunospot and antigen-specific proliferat
22 A27, B5, L1, and A33, using gamma interferon enzyme-linked immunospot and cytokine flow cytometry ass
23 nd assessed HBV-specific T-cell responses by enzyme-linked immunospot and cytometric bead array.
24 r +/- tumor lysates were tested in gamma-IFN enzyme-linked immunospot and cytotoxicity assays.
25 P. falciparum by performing standardized MBC enzyme-linked immunospot and enzyme-linked immunosorbent
26        However, gamma interferon (IFN-gamma) enzyme-linked immunospot and IFN-gamma/tumor necrosis fa
27                       Further, the IFN-gamma enzyme-linked ImmunoSPOT and in vitro 51Cr release assay
28 ses measured principally by gamma interferon enzyme-linked immunospot and neutralization assays were
29 ll responses were characterized by IFN-gamma enzyme-linked immunospot and whole blood intracellular c
30                    Preliminary studies using enzyme-linked immunospot and Winn assays suggested that
31 esponder cell frequency and interferon-gamma enzyme-linked immunospot, and antibodies were measured b
32 (as measured by interferon gamma production, enzyme-linked immunospot, and CD137 upregulation assays)
33 IAP, as revealed by proliferation, tetramer, enzyme-linked immunospot, and cytotoxicity analysis.
34     Results from functional analyses by DTH, enzyme-linked immunospot, and immunohistofluorescence as
35 ukin 2, 4, 5, and 6 were counted by means of enzyme-linked immunospot, and SFC counts were compared b
36  response to HCV antigens were enumerated by Enzyme Linked Immunospot Assay.
37 ysis), and more IFN-gamma-secreting cells by enzyme-linked immunospot assay (1460 vs 280 IFN-gamma sp
38 ls developed neutralizing antibodies and low enzyme-linked immunospot assay (E-SPOT) titers against S
39                                              Enzyme-linked immunospot assay (ELISPOT) analysis of pso
40 ssed by ex vivo gamma interferon (IFN-gamma) enzyme-linked immunospot assay (ELISPOT) and antibody as
41 LSA-1 and TRAP peptides were assessed by the enzyme-linked immunospot assay (ELISPOT) and enzyme-link
42  to detect autoreactive responses when using enzyme-linked immunospot assay (ELISPOT) and enzyme-link
43 ere detected by interferon-gamma (IFN-gamma) enzyme-linked immunospot assay (ELISPOT) assays using th
44     Gamma interferon (IFN-gamma) measured by enzyme-linked immunospot assay (ELISPOT) at multiple tim
45                   We used flow cytometry and enzyme-linked immunospot assay (ELISPOT) to examine B-ce
46                We used the ex vivo IFN-gamma enzyme-linked immunospot assay (ELISpot) to track T cell
47  antigen-specific IFN-gamma production in an enzyme-linked immunospot assay (ELISPOT).
48  after allogeneic BMT using gamma-interferon enzyme-linked immunospot assay (ELISPOT).
49 tion, and measured antibody-secreting cells (enzyme-linked immunospot assay [ELISPOT]) as an early ma
50 phisms with cellular (interferon [IFN] gamma enzyme-linked immunospot assay [ELISPOT]) immune respons
51 ted in these animals by the gamma interferon enzyme-linked immunospot assay against pools of short ov
52 specific CD8+ CTL responses were detected by enzyme-linked immunospot assay against several NY-BR-1 p
53 lobulin M antibody-secreting cells (ASCs) by enzyme-linked immunospot assay allowed for differentiati
54                                     Cultured enzyme-linked immunospot assay analysis demonstrated tha
55 lar sensitization was detected by performing enzyme-linked immunospot assay analysis for cytokines in
56 ce data of specific genes were combined with enzyme-linked immunospot assay analysis of critical epit
57                                              Enzyme-linked immunospot assay analysis of peripheral T-
58 rus-specific T-cell responses by means of an enzyme-linked immunospot assay and antibody responses by
59 A antibody-secreting B cells was analyzed by enzyme-linked immunospot assay and by analysis of Epstei
60                                              Enzyme-linked immunospot assay and ELISA analysis were r
61 (+) T cells, as detected by interferon gamma enzyme-linked immunospot assay and flow cytometry, were
62 he vaccine and drifted A(H3N2) viruses by an enzyme-linked immunospot assay and flow cytometry.
63                          By gamma interferon enzyme-linked immunospot assay and intracellular cytokin
64 ion assay) and T cell responses (measured by enzyme-linked immunospot assay and intracellular cytokin
65 ain SCC-derived antigens using the IFN-gamma enzyme-linked immunospot assay and intratumor (IT) and c
66  at multiple time points by interferon-gamma enzyme-linked immunospot assay and was correlated to the
67 tified memory responses measured by cultured enzyme-linked immunospot assay as well as in vitro inter
68 e measured in 9 patients by interferon-gamma enzyme-linked immunospot assay at 3 time points within 1
69 in the blood by gamma interferon (IFN-gamma) enzyme-linked immunospot assay at select time points; ho
70 re likely to have a positive response to ASC enzyme-linked immunospot assay at the late time point th
71  T-cell responses were analyzed using T-cell enzyme-linked immunospot assay before convalescent plasm
72 a virus were detected by an interferon gamma enzyme-linked immunospot assay but had no clear relation
73 analyzed in the gamma interferon (IFN-gamma)-enzyme-linked immunospot assay by using synthetic overla
74                        An Ag-specific B cell enzyme-linked immunospot assay confirmed these results a
75       FITC/DNFB skin painting and subsequent enzyme-linked immunospot assay demonstrated that flow-so
76 1 subject, antigen-specific interferon-gamma enzyme-linked immunospot assay detected an immunogenic d
77 e further confirmed by the results of CD4(+) enzyme-linked immunospot assay for interferon (IFN)-gamm
78 ng was performed using a CEA peptide and the enzyme-linked immunospot assay for interferon gamma prod
79 , and GAD65 peptides) were measured by IL-17 enzyme-linked immunospot assay in patients with new-onse
80 berculosis strain H37Rv as a stimulant in an enzyme-linked immunospot assay in sensitized individuals
81 ), and in healthy control subjects (n=10) by enzyme-linked immunospot assay in the presence and absen
82 validation cohort were measured by IFN-gamma enzyme-linked immunospot assay or intracellular cytokine
83 ed a 10- to 40-fold increase in HIV-specific enzyme-linked immunospot assay responses compared to tho
84 mmunosorbent assay titers, and EnvA-specific enzyme-linked immunospot assay responses, and these resp
85                                              Enzyme-linked immunospot assay results indicated that th
86 y higher numbers of spot-forming cells in an enzyme-linked immunospot assay than did T cells primed w
87 t gamma interferon production, determined by enzyme-linked immunospot assay to at least one of the th
88 1 transgenic NOD mice in an interferon-gamma enzyme-linked immunospot assay to identify autoantigenic
89 D8 T cell responses were quantified using an enzyme-linked immunospot assay to measure interferon-gam
90 MI responses by interferon gamma (IFN-gamma) enzyme-linked immunospot assay using 3 recombinant HCV p
91 eens of immunized mice by a gamma interferon enzyme-linked immunospot assay using peptides derived fr
92 gamma interferon-producing cells detected by enzyme-linked immunospot assay was increased (P < 0.01 f
93                                        Using enzyme-linked immunospot assay we found higher frequenci
94       Mycoplasma pneumoniae ASCs measured by enzyme-linked immunospot assay were assessed alongside M
95 asured by gamma interferon and interleukin 2 enzyme-linked immunospot assay were significantly higher
96      MPO-specific T cells were quantified by enzyme-linked immunospot assay with additional Treg cell
97 mined by intracellular cytokine staining and enzyme-linked immunospot assay) and produced anti-PR8 an
98 ss I Gag-tetramer staining, gamma interferon-enzyme-linked immunospot assay, and cytotoxic T-cell ass
99 ays, antigen-specific interferon (IFN)-gamma enzyme-linked immunospot assay, and enzyme-linked immuno
100 ern blot, delayed type hypersensitivity, and enzyme-linked immunospot assay, and reduced the number o
101 d multiparameter flow cytometric sorting and enzyme-linked immunospot assay, demonstrate that anti-Ga
102 ific T cells, enumerated by gamma interferon enzyme-linked immunospot assay, did not appear until 2 w
103 y-secreting cells (ASC) in blood measured by enzyme-linked immunospot assay, the antibody in lymphocy
104 s-specific CD4 responses by gamma interferon enzyme-linked immunospot assay, using 410 overlapping pe
105                          An interferon-gamma enzyme-linked immunospot assay, using peptide pools span
106  assay and/or ex vivo interferon (IFN)-gamma enzyme-linked immunospot assay, was documented in 45.5%
107                                     Using an enzyme-linked immunospot assay, we evaluated immunoglobu
108           Using flow cytometric analysis and enzyme-linked immunospot assay, we examined peripheral n
109 a interferon-secreting cells, as detected by enzyme-linked immunospot assay, were obtained in respons
110 cing CD4(+) T cell responses, as assessed by enzyme-linked immunospot assay, were significantly more
111 )-4-secreting cells were determined using an enzyme-linked immunospot assay, which demonstrated that
112       Viral loads, CD4(+) T-cell counts, and enzyme-linked immunospot assay-determined anti-HIV-1 CD8
113 e assessed using an ex-vivo interferon-gamma enzyme-linked immunospot assay.
114 s were detected by gamma interferon-specific enzyme-linked immunospot assay.
115  B cell Ig isotype switching was measured by enzyme-linked immunospot assay.
116 tibody-secreting cells were enumerated using enzyme-linked immunospot assay.
117  assays, intracelluar cytokine staining, and enzyme-linked immunospot assay.
118 l responses were assayed by interferon-gamma enzyme-linked immunospot assay.
119 ymphocyte proliferation and interferon gamma enzyme-linked immunospot assay.
120 racheobronchial lymph nodes as determined by enzyme-linked immunospot assay.
121  and in 22 (73%) of 30 vaccine recipients by enzyme-linked immunospot assay.
122 emory responses were evaluated by IFN- gamma enzyme-linked immunospot assay.
123 ulated memory B cells were detected using an enzyme-linked immunospot assay.
124 , and IL-6 cytokines as measured by cytokine enzyme-linked immunospot assay.
125  producing gamma interferon when analyzed by enzyme-linked immunospot assay.
126 producing B cells could still be detected by enzyme-linked immunospot assay.
127 5, 7, and 14 postgrafting, as measured by an enzyme-linked immunospot assay.
128 +) T lymphocytes were induced as analyzed by enzyme-linked immunospot assay.
129 h nodes, lungs, and Peyer's patches using an enzyme-linked immunospot assay.
130 -positive, HLA A2-positive individuals in an enzyme-linked immunospot assay.
131 pond to HIV-1 peptides in a gamma interferon enzyme-linked immunospot assay.
132 T-cell responses by using a gamma interferon enzyme-linked immunospot assay.
133 ed in the various tissues of GalT-/- mice by enzyme-linked immunospot assay.
134 us peptides via interferon-gamma (IFN-gamma) enzyme-linked immunospot assay.
135 mic lymphoid tissues were evaluated using an enzyme-linked immunospot assay.
136 red in peripheral blood mononuclear cells by enzyme-linked immunospot assay.
137 body assay, and an interferon gamma-specific enzyme-linked immunospot assay.
138 ses were assessed using an ex-vivo IFN-gamma enzyme-linked immunospot assay.
139 body- forming cells were determined using an enzyme-linked immunospot assay.
140  cells measured before challenge by cultured enzyme-linked immunospot assay.
141 and dsDNA antibody-secreting cells (ASCs) by enzyme-linked immunospot assay.
142 ral suppression assay (VSA) and an IFN-gamma enzyme-linked immunospot assay.
143 red by enzyme-linked immunosorbent assay and enzyme-linked immunospot assay.
144 mmunity to SHIV89.6 peptides was measured by enzyme-linked immunospot assay; strong responses to Gag
145 ent assays (ELISA) titers, and EnvA-specific enzyme-linked immunospot assays (ELISPOT) responses.
146 mune responses were measured by tetramer and enzyme-linked immunospot assays against gp100 and MART-1
147 e compared by standardized interferon- gamma enzyme-linked immunospot assays among 250 unvaccinated i
148                                              Enzyme-linked immunospot assays confirmed this high freq
149            Spleen cells were phenotyped, and enzyme-linked immunospot assays for autoantibody-produci
150 cluding MHC class I tetramer binding assays, enzyme-linked immunospot assays for IFN-gamma production
151  cells that recognize EBV-latent antigens in enzyme-linked immunospot assays for interferon gamma sec
152 BL/6 beta-gal transgenic skin were tested in enzyme-linked immunospot assays for recall responses to
153 c CD8(+)-T-cell responses were determined by enzyme-linked immunospot assays in 150 HIV-infected indi
154 s shown by cytotoxicity and interferon gamma enzyme-linked immunospot assays in six of nine patients.
155  immune-sensitization using the B and T-cell enzyme-linked immunospot assays may identify CMV-sensiti
156 eins were used to screen 15 normal donors in enzyme-linked immunospot assays of gamma interferon rele
157 pping peptides and gamma interferon-specific enzyme-linked immunospot assays of peripheral blood mono
158                                   Results of enzyme-linked immunospot assays of the immunized mice re
159  were assessed using interferon (IFN)- gamma enzyme-linked immunospot assays on peripheral blood mono
160                 Interferon-gamma (IFN-gamma) enzyme-linked immunospot assays on peripheral blood mono
161 s of Candida-specific T-cell responses using enzyme-linked immunospot assays revealed higher numbers
162           Proliferation and gamma interferon enzyme-linked immunospot assays using peripheral blood l
163                 Interferon gamma (IFN-gamma) enzyme-linked immunospot assays were performed before an
164                                              Enzyme-linked immunospot assays were performed to confir
165                                              Enzyme-Linked ImmunoSpot assays yielded parallel results
166  production in mixed lymphocyte reaction and enzyme-linked immunospot assays, respectively.
167 nterferon (IFN)-gamma and interleukin (IL)-5 enzyme-linked immunospot assays, respectively.
168                                    By use of enzyme-linked immunospot assays, the percentages of memo
169 s, trans-vivo delayed-type hypersensitivity, enzyme-linked immunospot assays, the use of antigen rece
170 ic T cells were measured by interferon-gamma enzyme-linked immunospot assays, using recombinant vacci
171  wild-type sequence was also demonstrated by enzyme-linked immunospot assays.
172 A-matched peptides by using gamma interferon enzyme-linked immunospot assays.
173 pol regimen, as measured by gamma interferon enzyme-linked immunospot assays.
174 T-cell responses as measured using IFN-gamma enzyme-linked immunospot assays.
175 DNA cells by IFN-gamma-secretion measured in enzyme-linked immunospot assays.
176 ls in both cytotoxicity assays and IFN-gamma enzyme-linked immunospot assays.
177 the lamina propria of the small intestine by enzyme-linked immunospot assays.
178 d mononuclear cells using flow cytometry and enzyme-linked immunospot assays.
179 aining, and fine mapping in interferon-gamma enzyme-linked immunospot assays.
180 cell responses, measured by interferon gamma enzyme-linked immunospot assays.
181 ld in-tube test (ELISA), and T-SPOT.TB test (enzyme-linked immunospot) at 17 centers in 11 European c
182                                              Enzyme-linked immunospots, cytotoxicity assays as well a
183 phore linked immunosorbent assay (FLISA) and enzyme linked immunospotting (ELISPOT).
184                 This result was supported by enzyme-linked immunospot (ELISPOT) analyses indicating c
185 erferon (IFN-gamma) and interleukin-5 (IL-5) enzyme-linked immunospot (ELISPOT) analyses were used to
186                        Using high resolution enzyme-linked immunospot (ELISPOT) analysis, we have rev
187 )-producing CD8(+) T cells, as determined by enzyme-linked immunospot (ELISPOT) analysis.
188 isease, CMV-specific interferon (IFN)- gamma enzyme-linked immunospot (ELISPOT) and CD8(+) and CD4(+)
189  the same protein following RSV infection by enzyme-linked immunospot (ELISPOT) and intracellular cyt
190 tricted epitope using interferon (IFN)-gamma enzyme-linked immunospot (ELISPOT) and intracellular cyt
191 Acute Hepatitis C (ATAHC), using HCV peptide enzyme-linked immunospot (ELISPOT) and multiplex in vitr
192 ctly ex vivo by gamma interferon (IFN-gamma) enzyme-linked immunospot (ELISPOT) assay (P = 2 x 10(-10
193 cific IgM antibody-secreting cells (ASCs) by enzyme-linked immunospot (ELISpot) assay allowed for dif
194 tive allo-HCT recipients with a CMV-specific enzyme-linked immunospot (ELISPOT) assay and for CMV inf
195  epitopes measured by interferon (IFN)-gamma enzyme-linked immunospot (ELISPOT) assay and HLA/peptide
196 nd lytic antigens by interferon (IFN)- gamma enzyme-linked immunospot (ELISPOT) assay and interleukin
197  responses, as indicated by gamma interferon enzyme-linked immunospot (ELISPOT) assay and intracellul
198 zed mice as determined by using quantitative enzyme-linked immunospot (ELISpot) assay and intracellul
199                             Interferon-gamma enzyme-linked immunospot (ELISPOT) assay and tetramer an
200         We have developed a gamma interferon enzyme-linked immunospot (ELISPOT) assay for evaluation
201 ere screened by gamma interferon (IFN-gamma) enzyme-linked immunospot (ELISPOT) assay for HLA class I
202                                      With an enzyme-linked immunospot (ELISPOT) assay for interferon
203                           A highly sensitive enzyme-linked immunospot (ELISPOT) assay for single cell
204 ned using a sensitive interferon (IFN)-gamma enzyme-linked immunospot (ELISPOT) assay in 187 Caucasia
205         IgG-secreting cells were detected by enzyme-linked immunospot (ELISPOT) assay in cell suspens
206  Quantification of interferon (IFN)-gamma by enzyme-linked immunospot (ELISPOT) assay is currently us
207  compared the HIV-specific ex vivo IFN-gamma enzyme-linked immunospot (ELISPOT) assay responses of 19
208                 Gamma interferon (IFN-gamma) enzyme-linked immunospot (ELISPOT) assay responses targe
209 nstrated VV-specific interferon (IFN)- gamma enzyme-linked immunospot (ELISPOT) assay responses; 21 (
210  to HSV-2 directly, ex vivo, we developed an enzyme-linked immunospot (ELISPOT) assay that utilized p
211 common cold coronaviruses.METHODSWe used the enzyme-linked immunospot (ELISPOT) assay to characterize
212        We developed and assessed a sensitive enzyme-linked immunospot (ELISPOT) assay to detect T cel
213 nized NZB/NZW mice were analyzed in vitro by enzyme-linked immunospot (ELISpot) assay to determine T
214 ecific responses in the vaccinia virus-based enzyme-linked immunospot (Elispot) assay using a panel o
215                                          The enzyme-linked Immunospot (ELISPOT) assay was used to det
216 y full-proteome gamma interferon (IFN-gamma) enzyme-linked immunospot (ELISPOT) assay were restricted
217 hort-term T-lymphocyte cell lines, IFN-gamma enzyme-linked immunospot (ELISPOT) assay with peripheral
218 responses were detected by use of a modified enzyme-linked immunospot (ELISpot) assay with recombinan
219 body-secreting cells (ASCs) were measured by enzyme-linked immunospot (ELISPOT) assay, and antibody r
220                           Tetramer staining, enzyme-linked immunospot (ELISPOT) assay, and cytotoxici
221                                     Here the enzyme-linked immunospot (ELISPOT) assay, intracellular
222  as assessed by gamma interferon (IFN-gamma) enzyme-linked immunospot (ELISPOT) assay.
223 mulation and assessed IFN-gamma secretion by enzyme-linked immunospot (Elispot) assay.
224 ed Env-specific immunoglobulin G (IgG) in an enzyme-linked immunospot (ELISPOT) assay.
225 were determined by using an interferon-gamma enzyme-linked immunospot (ELISpot) assay.
226 recombinant vaccinia vectors was measured by enzyme-linked immunospot (ELISPOT) assay.
227 rs with the same peptide pools in a cultured enzyme-linked immunospot (ELISPOT) assay.
228 pressed HIV-1 proteins in a gamma interferon-enzyme-linked immunospot (Elispot) assay.
229 and in vitro by mixed leukocyte reaction and enzyme-linked immunospot (ELISPOT) assay.
230 creting T cells in the hosts was measured by enzyme-linked immunospot (ELISPOT) assay.
231  quantified for all subjects in an IFN-gamma enzyme-linked immunospot (ELISpot) assay.
232 r flow cytometry, flow antibody binding, and enzyme-linked immunospot (ELISpot) assay.
233 8-27) pentamer staining and CD8(+) IFN-gamma enzyme-linked immunospot (ELISPOT) assay.
234  using peripheral blood mononuclear cells in enzyme-linked immunospot (Elispot) assays and using CTL
235                     In this study, sensitive enzyme-linked immunospot (elispot) assays have been util
236  detected by interferon (IFN) gamma and IL-2 enzyme-linked immunospot (ELISPOT) assays in 50% and 40%
237 pecific IFN-gamma responses were detected by enzyme-linked immunospot (ELISPOT) assays in all subject
238                           However, validated enzyme-linked immunospot (ELISpot) assays of influenza-s
239 ivity to escape variant peptides in standard enzyme-linked immunospot (ELISPOT) assays predicts the r
240 tantial CD8(+) T cell responses by IFN-gamma enzyme-linked immunospot (ELISPOT) assays to all 11 of t
241     In this study, we performed quantitative enzyme-linked immunospot (ELISPOT) assays to measure loc
242   CMV immunoglobulin G (IgG) avidity and CMV enzyme-linked immunospot (ELISpot) assays were employed
243              In interferon-gamma (IFN-gamma) enzyme-linked immunospot (ELISPOT) assays, antiviral res
244       Using IFN-gamma and interleukin (IL)-2 enzyme-linked immunospot (ELISpot) assays, we analyzed t
245                           Using tetramer and enzyme-linked immunospot (ELISPOT) assays, we have obser
246 es in enzyme immunoassay, proliferation, and enzyme-linked immunospot (ELISpot) assays.
247 um-release and confirmatory interferon-gamma enzyme-linked immunospot (ELISPOT) assays.
248 N-gamma) responses to the peptide epitope in enzyme-linked immunospot (ELISPOT) assays.
249 (MHC) tetramer staining and gamma interferon enzyme-linked immunospot (ELISPOT) assays.
250 unique to the seasonal or pandemic strain by enzyme-linked immunospot (ELISpot) assays.
251  interferon-gamma (IFN-gamma) release by CD4 enzyme-linked immunospot (ELISPOT) at one or more time p
252 lass II cellular immunity was analyzed using enzyme-linked immunospot (ELISPOT) by testing recipient
253 rferon gamma (IFN-gamma) production using an enzyme-linked immunospot (ELISPOT) CMV assay (T-SPOT.CMV
254 y (CMV-CMI) as determined by a peptide-based enzyme-linked immunospot (ELISPOT) CMV assay may identif
255                                          The enzyme-linked immunospot (Elispot) gamma interferon assa
256 ysaccharide cellular immunity, measured with enzyme-linked immunospot (ELISPOT) interferon gamma rele
257 tionated HIV-1 gag-specific interferon gamma enzyme-linked immunospot (ELISpot) response 4 weeks afte
258                                              Enzyme-linked immunospot (ELISpot) showed no interferon-
259                                 By contrast, enzyme-linked immunospot (ELISPOT), flow cytometry, time
260 ll responses were assessed in proliferation, enzyme-linked immunospot (ELISPOT), interferon (IFN)-gam
261 pping HCV peptides and 6 proteins by ex vivo enzyme-linked immunospot (ELISpot), intracellular cytoki
262                  Analyses included IFN-gamma enzyme-linked immunospot (ELISPOT), reverse transcriptio
263  T-cell responses as determined by IFN-gamma enzyme-linked immunospot (ELISPOT), tetramer, and cytoto
264 peripheral blood lymphocyte gamma interferon enzyme-linked immunospot (ELISPOT), tetramer, and intrac
265 r tissues and analyzed by flow cytometry and enzyme-linked ImmunoSpot (ELISpot).
266 unoglobulin (Ig) A antibody-secreting cells (enzyme-linked immunospot [ELISPOT] assay), IgG serologic
267 alpha, or CD40L), and more ex vivo IFN-gamma enzyme-linked immunospots (ELISPOTs) than did the RTS,S/
268 of 500 to 1,000 gamma interferon (IFN-gamma) enzyme-linked immunospots (ELISPOTS)/10(6) peripheral bl
269             T-cell responses were studied by enzyme-linked immunospot for interferon-gamma.
270 change between pre-study and postvaccination enzyme-linked immunospot frequency of purified CD8 T-cel
271  parameters, cell-mediated immunogenicity by enzyme-linked immunospot, functional neutralizing antibo
272 s (VZV) T-cell responses by interferon-gamma enzyme-linked immunospot (IFN-gamma ELISPOT) and VZV ant
273 sorbent assay (gpELISA) and interferon-gamma enzyme-linked immunospot (IFN-gamma ELISPOT), blood samp
274 cell proliferative responses, and cytokines (enzyme-linked immunospot) in 48 subjects with unresolved
275                                              Enzyme-linked immunospot, intracellular cytokine stainin
276 ce was assessed by skin and heart grafts and enzyme-linked immunospot, intracellular cytokine, and mi
277  flow cytometry for cell surface markers and enzyme-linked immunospot methods to assess the subset di
278 llograft recipients was evaluated ex vivo by enzyme-linked immunospot, mixed lymphocytes reaction, cy
279                       Using interferon-gamma enzyme-linked immunospot, Mtb39-specific CD8+ T lymphocy
280 ers and T-cell immunity to AAV, validated by enzyme-linked immunospot on the second day after gene in
281  = 0.0043), IFN-gamma production measured by enzyme-linked immunospot (P < 0.0001), and multiplex cyt
282 sed by enzyme-linked immunosorbent assay and enzyme-linked immunospot performed at baseline and from
283                        Furthermore, positive enzyme-linked immunospot reactions to belagenpumatucel-L
284 gnitude of the SIV-specific gamma interferon enzyme-linked immunospot response.
285                  A hierarchy was observed in enzyme-linked immunospot responses (with the strongest r
286 ys developed high-frequency gamma interferon enzyme-linked immunospot responses against BCG purified
287  animals developed vigorous gamma interferon enzyme-linked immunospot responses and moderate prolifer
288  We assessed KSHV-specific interferon- gamma enzyme-linked immunospot responses in a cohort of 154 in
289 pment of neutralizing antibody and IFN-gamma enzyme-linked immunospot responses to AAV1 capsid at day
290 gnitude and the breadth of interferon- gamma enzyme-linked immunospot responses were inversely correl
291                                   IFN- gamma enzyme-linked immunospot responses were significantly di
292  interferon (IFN)-gamma secretion, IFN-gamma enzyme-linked immunospot responses, and direct ex vivo i
293 strong ex vivo tetramer and interferon gamma enzyme-linked immunospot responses, and endogenous expre
294 d II were used to stimulate interferon-gamma enzyme-linked immunospot responses.
295 e ELISA (1.31 cases per 100 person-years) or enzyme-linked immunospot result (1.78 cases per 100 pers
296 ated cell sorter, mixed lymphocyte reaction, enzyme-linked immunospot, signaling studies, and a rat m
297                  We previously introduced an enzyme-linked immunospot spot (ELISpot)-based assay to m
298  anti-Salmonella mucosal immune responses by enzyme-linked immunospot studies.
299 ear cells were tested using interferon-gamma enzyme-linked immunospot T assays measuring the response
300                                Postchallenge enzyme-linked immunospot values for Gag and Env as well

 
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