ライフサイエンスコーパス: gamma-interferon

1 tor, monocyte chemoattractant protein 1, and gamma interferon.

2 e I interferons (IFN-I), interleukin 12, and gamma interferon.

3 reas C4 synthesis occurred on treatment with gamma interferon.

4 by 28 dpi except interleukin 12 (IL-12) and gamma interferon.

5 ved coma scores, as well as higher levels of gamma interferon.

6 in vitro when chlamydiae are incubated with gamma interferon.

7 se and cationic amino acid transporter 2 via gamma interferon.

8 MCP-1, MCP-2, MCP-3, and monokine induced by gamma-interferon.

9 n 17 and tumor necrosis factor-alpha but not gamma-interferon.

10 ursting during transcriptional activation by gamma-interferon.

11 induction of CD25, CD69, interleukin-2, and gamma-interferon.

12 By contrast, activity of the diverse gamma-interferon-activated inhibitor of translation (GAI

13 The GAIT (gamma-interferon-activated inhibitor of translation) com

14 ecruitment to a region containing a putative gamma-interferon activation sequence (GAS) element at -4

15 both burst size and frequency in response to gamma-interferon activation.

16 t CTLs failed to upregulate FasL and produce gamma interferon after engagement with target cells and

17 ad elevated splenic CD4(+) T cells producing gamma interferon and interleukin-17A, indicating that PN

18 boratory HIV database (1,300 peptides) using gamma interferon and interleukin-2 (IFN-gamma/IL-2) Fluo

19 e, suggesting Th1 polarization, and produced gamma interferon and other cytokines after reactivation

20 These cells are able to produce gamma interferon and remain metabolically active but hav

21 Individual baboons expressed more gamma interferon and tumor necrosis factor alpha in resp

22 The frequency of CD8 T cells producing gamma interferon and tumor necrosis factor in response t

23 L)-17A secretion by Th17 cells, 2) inhibited gamma-interferon and tumor necrosis factor alpha secreti

24 ) produced less tumor necrosis factor alpha, gamma interferon, and granzyme B.

25 tein 2, RANTES, tumor necrosis factor alpha, gamma interferon, and interleukin-10 were upregulated in

26 L10 [gamma interferon-inducible protein 10], gamma interferon, and lambda interferon) in association

27 ach of these strains was also used to infect gamma interferon- and lipopolysaccharide-activated murin

28 erium avium complex (DMAC) disease with anti-gamma interferon autoantibodies.

29 cing T cells that antagonized the release of gamma-interferon by spontaneously arising GAD65 autoimmu

30 actic protein-1/CCL2 and monokine induced by gamma interferon/CXCL9 in the hypotensive and normotensi

31 WT, interleukin-4-deficient (IL-4(-/-)), and gamma interferon-deficient (IFN-gamma(-/-)) C57BL/6 mice

32 Moreover, vaccinated gamma interferon-deficient (IFN-gamma(-/-)) mice also sh

33 inal wash antibodies and an antigen-specific gamma interferon-dominated Th1-biased T cell response.

34 By measuring gamma interferon enzyme-linked immunosorbent spot (ELISP

35 eptides from rDEN2Delta30 and used them in a gamma interferon enzyme-linked immunosorbent spot assay

36 As measured by a gamma interferon enzyme-linked immunosorbent spot assay

37 etermined via a newly established guinea pig gamma interferon enzyme-linked immunosorbent spot assay.

38 Gamma interferon enzyme-linked immunosorbent spot assays

39 ear cells from these donors were screened in gamma interferon enzyme-linked immunosorbent spot assays

40 tibility complex (MHC) tetramer staining and gamma interferon enzyme-linked immunospot (ELISPOT) assa

41 or cytokines/chemokines (IL-2, IL-12, IL-17, gamma interferon, granulocyte-macrophage colony-stimulat

42 Resistance to Toxoplasma is dependent on gamma interferon (IFN-gamma) activation of both hematopo

43 Neutralization of gamma interferon (IFN-gamma) ameliorated the enhancement

44 Affymetrix microarray analysis revealed that gamma interferon (IFN-gamma) and 16 antiviral interferon

45 hat Brucella-specific CD8(+) T cells express gamma interferon (IFN-gamma) and can transition to long-

46 Gamma interferon (IFN-gamma) and CCL5 were induced in lu

47 Plasma levels of gamma interferon (IFN-gamma) and CXCL9 (monokine induced

48 function, defined by increased production of gamma interferon (IFN-gamma) and granzyme B and expressi

49 CNS CD4 T cells was associated with reduced gamma interferon (IFN-gamma) and granzyme B expression b

50 e show that activated CD8(+) T cells express gamma interferon (IFN-gamma) and granzymes but that gran

51 splenic T cells secreted significantly more gamma interferon (IFN-gamma) and had significantly more

52 -alpha) in the draining lymph node (DLN) and gamma interferon (IFN-gamma) and IL-10 in the lung.

53 require eosinophils, and was independent of gamma interferon (IFN-gamma) and IL-17.

54 elper-1 (Th1), Th2, and Th17 cells, elevated gamma interferon (IFN-gamma) and interleukin (IL)-17 pro

55 enged with HHV-6 preparations indicated that gamma interferon (IFN-gamma) and interleukin-10 (IL-10)

56 Although gamma interferon (IFN-gamma) and interleukin-10 (IL-10)

57 We screened the gamma interferon (IFN-gamma) and interleukin-10 (IL-10)

58 nity to acute infection is the production of gamma interferon (IFN-gamma) and interleukin-12 (IL-12),

59 xpression of inflammatory markers, including gamma interferon (IFN-gamma) and interleukin-12p40 (IL-1

60 e to that provoked by LVS but with increased gamma interferon (IFN-gamma) and interleukin-17A (IL-17A

61 from the mutant-immunized mice produced more gamma interferon (IFN-gamma) and interleukin-4.

62 Gamma interferon (IFN-gamma) and interleukin-5 (IL-5) en

63 associated with NK cells and DCs, including gamma interferon (IFN-gamma) and RANTES, were increased

64 Induction of gamma interferon (IFN-gamma) and T-bet was observed with

65 tumor necrosis factor alpha (TNF-alpha), and gamma interferon (IFN-gamma) and the memory markers CD27

66 ting a cytokine storm by their production of gamma interferon (IFN-gamma) and tumor necrosis factor a

67 ociated with increased production of mucosal gamma interferon (IFN-gamma) and tumor necrosis factor a

68 sion is induced by proinflammatory cytokines gamma interferon (IFN-gamma) and tumor necrosis factor a

69 YopE69-77-specific CD8(+) T cells producing gamma interferon (IFN-gamma) and tumor necrosis factor a

70 Th1, Th2, and Th17 cytokines; however, early gamma interferon (IFN-gamma) and tumor necrosis factor a

71 Increases in gamma interferon (IFN-gamma) and tumor necrosis factor a

72 dged by low cytotoxic function and decreased gamma interferon (IFN-gamma) and tumor necrosis factor a

73 ic CD8(+) T lymphocytes capable of producing gamma interferon (IFN-gamma) and tumor necrosis factor a

74 SC subjects produce less gamma interferon (IFN-gamma) and tumor necrosis factor a

75 ory CD8(+) T cells that were able to secrete gamma interferon (IFN-gamma) and tumor necrosis factor a

76 tion of interleukin-17A (IL-17A), IL-22, and gamma interferon (IFN-gamma) as well as the antimicrobia

77 mice were also completely unable to produce gamma interferon (IFN-gamma) at any time points followin

78 ty of NK cells to proliferate and to produce gamma interferon (IFN-gamma) but positively associated w

79 monstrated that the functional production of gamma interferon (IFN-gamma) by antigen-specific CD4(+)

80 h was associated with enhanced production of gamma interferon (IFN-gamma) by NK cells.

81 to amplified T cell activation, higher serum gamma interferon (IFN-gamma) concentrations, enhanced in

82 In the livers of C57BL/6 mice, gamma interferon (IFN-gamma) controls intracellular Leis

83 s in vivo, wild-type mice were injected with gamma interferon (IFN-gamma) DNA or colony-stimulating f

84 SIV-specific T cells producing gamma interferon (IFN-gamma) dominated these responses.

85 Gamma interferon (IFN-gamma) drives antiparasite respons

86 on in BALB/c mice, whereas neutralization of gamma interferon (IFN-gamma) enhanced protection in C57B

87 ested for responses against HERV peptides in gamma interferon (IFN-gamma) enzyme immunospot (ELISPOT)

88 saic immunogens induced significantly higher gamma interferon (IFN-gamma) enzyme-linked immunosorbent

89 m HIV-1 Gag and Env were used as antigens in gamma interferon (IFN-gamma) enzyme-linked immunosorbent

90 y enzyme-linked immunosorbent assay (ELISA), gamma interferon (IFN-gamma) enzyme-linked immunosorbent

91 e transcriptases (RT), were identified using gamma interferon (IFN-gamma) enzyme-linked immunosorbent

92 e-specific T-cell activation was measured by gamma interferon (IFN-gamma) enzyme-linked immunosorbent

93 ial epitope targeting rates, as confirmed by gamma interferon (IFN-gamma) enzyme-linked immunosorbent

94 ith primary HIV-1 infection were screened by gamma interferon (IFN-gamma) enzyme-linked immunospot (E

95 topes targeted, measured directly ex vivo by gamma interferon (IFN-gamma) enzyme-linked immunospot (E

96 +) T cell responses defined by full-proteome gamma interferon (IFN-gamma) enzyme-linked immunospot (E

97 22 did not worsen abscesses but did increase gamma interferon (IFN-gamma) expression at these sites.

98 osuppressive anthrax lethal toxin impairs NK gamma interferon (IFN-gamma) expression, but neither let

99 mice show the importance of both T cells and gamma interferon (IFN-gamma) for survival of a measles v

100 ation of STAg led to increased production of gamma interferon (IFN-gamma) from natural killer (NK) ce

101 tions of interleukin 1ra (IL-1ra), IL-6, and gamma interferon (IFN-gamma) increased markedly.

102 Gamma interferon (IFN-gamma) induces expression of the t

103 Gamma interferon (IFN-gamma) is an important driver of i

104 Gamma interferon (IFN-gamma) is an inflammatory cytokine

105 vo approaches reveals that the expression of gamma interferon (IFN-gamma) is epigenetically silenced

106 We confirmed that gamma interferon (IFN-gamma) is essential for induction

107 n reported that the proinflammatory cytokine gamma interferon (IFN-gamma) is responsible.

108 restingly, IgA(-/-) mice had lower pulmonary gamma interferon (IFN-gamma) levels and decreased number

109 Despite substantial in vivo gamma interferon (IFN-gamma) levels, T-bet-knockout (KO)

110 centages of CD4(+)Tbet(+) cells and elevated gamma interferon (IFN-gamma) mRNA in PBMCs.

111 of the biofilm, even when prestimulated with gamma interferon (IFN-gamma) or TNF-alpha or cocultured

112 eukin-17A/F (IL-17A/F) and CXCL10 but not of gamma interferon (IFN-gamma) or tumor necrosis factor (T

113 KT) cells from coexposed mice expressed less gamma interferon (IFN-gamma) per cell than did those fro

114 -derived macrophages (MDM) requires NOX2 and gamma interferon (IFN-gamma) pretreatment.

115 to 18 h postinfection, and was unaffected by gamma interferon (IFN-gamma) pretreatment.

116 rease P. falciparum-specific in vitro recall gamma interferon (IFN-gamma) production after CHMI, and

117 Further studies have shown that gamma interferon (IFN-gamma) production and activation o

118 T-bet, but not its tyrosine mutant, rescues gamma interferon (IFN-gamma) production and inhibits Th2

119 s of cognate antigen-specific T cell clones: gamma interferon (IFN-gamma) production and mobilization

120 reatment with anti-CXCL10 antibodies reduced gamma interferon (IFN-gamma) production and Th17 cell in

121 Innate gamma interferon (IFN-gamma) production by CD8(+) T cell

122 (MHCII) and CD80 on CD11c-positive cells and gamma interferon (IFN-gamma) production by NK cells afte

123 iters and increased numbers of and increased gamma interferon (IFN-gamma) production by several diffe

124 servation of CD4(+) T cells and an increased gamma interferon (IFN-gamma) production from stimulated

125 ureus and greatly promoted proliferation and gamma interferon (IFN-gamma) production in CD4 and CD8 T

126 ost potent combinations capable of eliciting gamma interferon (IFN-gamma) production in NK cells.

127 evident, while decreased mitogen-stimulated gamma interferon (IFN-gamma) production suggested immuno

128 ciency prevents proper T cell activation and gamma interferon (IFN-gamma) production, which are criti

129 role in CD4+ Th1 lineage differentiation and gamma interferon (IFN-gamma) protein expression by CD4+

130 IL-10)/tumor necrosis factor alpha and IL-12/gamma interferon (IFN-gamma) ratios, and higher antibody

131 vants correlated better with enhanced T-cell gamma interferon (IFN-gamma) recall responses rather tha

132 Gamma interferon (IFN-gamma) release assays (IGRAs) are

133 ssing target cells, including stimulation of gamma interferon (IFN-gamma) release, specific target ce

134 enes might mediate the greater virulence and gamma interferon (IFN-gamma) resistance of C. muridarum

135 tion inflammatory syndrome (IRIS), we tested gamma interferon (IFN-gamma) response by enzyme-linked i

136 mune response to malaria by initiating a CD4 gamma interferon (IFN-gamma) response early in a blood-s

137 The gamma interferon (IFN-gamma) response, mediated by the S

138 n in rhesus macaques, SC-Ad generated higher gamma interferon (IFN-gamma) responses and higher transg

139 berculosis (TB) vaccine candidates, elicited gamma interferon (IFN-gamma) responses from both TB and

140 /-) mice display organ burdens and pulmonary gamma interferon (IFN-gamma) responses similar to those

141 This strain also resulted in better gamma interferon (IFN-gamma) responses than the strain w

142 pitope and found individuals who had ex vivo gamma interferon (IFN-gamma) responses to the peptide ep

143 The majority of gamma interferon (IFN-gamma) responses were associated w

144 Lung gamma interferon (IFN-gamma) responses were blunted and

145 of HIV-1-specific CD4 T cell proliferation, gamma interferon (IFN-gamma) secretion, and, to a lesser

146 ion of MDMs by lipopolysaccharide (LPS) plus gamma interferon (IFN-gamma) stimulation caused no effec

147 In this study, we report that gamma interferon (IFN-gamma) treatment, but not IFN-alph

148 Gamma interferon (IFN-gamma) was detected in serum betwe

149 esponse to viral antigen, while secretion of gamma interferon (IFN-gamma) was more limited in compari

150 Gamma interferon (IFN-gamma) was recently shown to inhib

151 er of CD4 T cells and CD8 T cells expressing gamma interferon (IFN-gamma) were observed in IL-17A(-/-

152 hese activated effector CD8 T cells produced gamma interferon (IFN-gamma) when stimulated with dengue

153 activated T cells with the respective CD4(+) gamma interferon (IFN-gamma)(+), CD4(+) interleukin-5 (I

154 This was further validated by depleting gamma interferon (IFN-gamma), a cytokine known to contro

155 pon MAIT cell selection by MR1, secretion of gamma interferon (IFN-gamma), and an innate interleukin

156 tion, secretion of the inflammatory cytokine gamma interferon (IFN-gamma), and host defense against t

157 chose TLR7, transcription factor p65 (RelA), gamma interferon (IFN-gamma), and IFN-gamma-inducible pr

158 ctor alpha (TNF-alpha), IL-1alpha, IL-1beta, gamma interferon (IFN-gamma), and IL-9.

159 ression of mRNAs for CD3delta, CD4, CD8beta, gamma interferon (IFN-gamma), and inducible nitric oxide

160 Levels of BALF leukocytes, gamma interferon (IFN-gamma), and interleukin 10 (IL-10)

161 ent on CD8(+) T cells, involves perforin and gamma interferon (IFN-gamma), and is correlated with the

162 tumor necrosis factor alpha (TNF-alpha) and gamma interferon (IFN-gamma), and previous studies have

163 lammatory cytokines IL-22, IL-17a, IL-1beta, gamma interferon (IFN-gamma), and TNF-alpha, as well as

164 in interleukin 1beta (IL-1beta), IL-6, IL-8, gamma interferon (IFN-gamma), and tumor necrosis factor

165 simultaneously produce interleukin-2 (IL-2), gamma interferon (IFN-gamma), and tumor necrosis factor

166 mory phenotype and usually expressed CD107a, gamma interferon (IFN-gamma), and tumor necrosis factor

167 ing tumor necrosis factor alpha (TNF-alpha), gamma interferon (IFN-gamma), CCL2, CCL3, and interleuki

168 reased production of interleukin 17 (IL-17), gamma interferon (IFN-gamma), CCL4, and granulocyte-macr

169 train of C. neoformans engineered to produce gamma interferon (IFN-gamma), denoted H99gamma, demonstr

170 production of interleukin 15 (IL-15), IL-18, gamma interferon (IFN-gamma), granulocyte colony-stimula

171 6), tumor necrosis factor alpha (TNF-alpha), gamma interferon (IFN-gamma), IL-1beta, and inducible ni

172 PD-L1 blockade leads to balanced increase in gamma interferon (IFN-gamma), IL-2, and IL-13 secretion,

173 myristate acetate and ionomycin, we examined gamma interferon (IFN-gamma), IL-4, IL-5, and IL-17 prod

174 oduced significantly higher amounts of IL-2, gamma interferon (IFN-gamma), IL-4, IL-6, and IL-17A in

175 )17 cells could develop in mice deficient in gamma interferon (IFN-gamma), IL-4, or IL-10.

176 er, we also observed increased production of gamma interferon (IFN-gamma), IL-5, IL-9, IL-17, and IL-

177 ing tumor necrosis factor alpha (TNF-alpha), gamma interferon (IFN-gamma), IL-6, and IL-1beta were hi

178 n of the proinflammatory cytokines IL-1beta, gamma interferon (IFN-gamma), IL-6, or IL-10.

179 The T(h)1 and T(h)17 cytokines gamma interferon (IFN-gamma), interleukin-12 (IL-12) p70

180 wed significantly lower expression levels of gamma interferon (IFN-gamma), interleukin-6 (IL-6), and

181 by DH82 cells (P < 0.01), while secretion of gamma interferon (IFN-gamma), interleukin-6 (IL-6), inte

182 of CD4(+) Th1 cells and NKT cells producing gamma interferon (IFN-gamma), it increased the ratio of

183 Treatment with gamma interferon (IFN-gamma), l-arginine, and tetrahydro

184 iver, infected TLR4(-/-) mice showed reduced gamma interferon (IFN-gamma), tumor necrosis factor (TNF

185 0057(pYA5199) produced significant levels of gamma interferon (IFN-gamma), tumor necrosis factor alph

186 igher in DeltaTgPL1-infected mice, including gamma interferon (IFN-gamma), tumor necrosis factor alph

187 the DLNs soon after immunization, including gamma interferon (IFN-gamma), tumor necrosis factor alph

188 1 response, and specifically, high levels of gamma interferon (IFN-gamma), tumor necrosis factor alph

189 Gene expression of gamma interferon (IFN-gamma), tumor necrosis factor alph

190 R. typhi(GFPuv)-infected BALB/c mice elicits gamma interferon (IFN-gamma), tumor necrosis factor alph

191 mokine (C-X-C motif) ligand 10 (CXCL10), and gamma interferon (IFN-gamma), was also significantly upr

192 by treatment with E2, but the proportion of gamma interferon (IFN-gamma)- and tumor necrosis factor

193 ween cytokine-producing T cell subsets with, gamma interferon (IFN-gamma)- and tumor necrosis factor

194 vium subsp. paratuberculosis survival inside gamma interferon (IFN-gamma)-activated bovine macrophage

195 The gamma interferon (IFN-gamma)-activated inhibitor of tran

196 lex that promoted translational silencing in gamma interferon (IFN-gamma)-activated myeloid cells.

197 11c(high) dendritic cell populations and the gamma interferon (IFN-gamma)-dependent CD4(+) T cell res

198 Experimental cerebral malaria (ECM) is a gamma interferon (IFN-gamma)-dependent syndrome.

199 Gamma interferon (IFN-gamma)-induced C4 promoter activat

200 ranscription factor CEBP-beta, regulates the gamma interferon (IFN-gamma)-induced expression of Dapk1

201 ss I (MHC-I) or CD4(+) T lymphocytes through gamma interferon (IFN-gamma)-induced MHC-II.

202 nfection is dependent on the activity of the gamma interferon (IFN-gamma)-inducible nitric oxide synt

203 ls are the primary effector cells regulating gamma interferon (IFN-gamma)-mediated host resistance.

204 to be perforin (Prf)-mediated cell lysis and gamma interferon (IFN-gamma)-mediated induction of an an

205 umenting a cell-autonomous role for IRF-1 in gamma interferon (IFN-gamma)-mediated inhibition of MNV

206 otein FopC, which is required for evasion of gamma interferon (IFN-gamma)-mediated signaling, is able

207 4-depleted mice also increased the number of gamma interferon (IFN-gamma)-positive CD8(+) central mem

208 ve demonstrated that antigen-specific CD8(+) gamma interferon (IFN-gamma)-positive T-cell responses a

209 ith virus-specific circulating ASFV-specific gamma interferon (IFN-gamma)-producing cells.

210 ted killing, and decreases the proportion of gamma interferon (IFN-gamma)-producing NK cells that had

211 in response to C. rodentium was dependent on gamma interferon (IFN-gamma)-producing NK1.1(+) cells an

212 Gamma interferon (IFN-gamma)-producing T cells were indu

213 p of LANA and STAT1 binding sites in several gamma interferon (IFN-gamma)-regulated genes.

214 and production of ESAT-6- or CFP-10-specific gamma interferon (IFN-gamma)-secreting and tumor necrosi

215 of activated CD8(+) T cells and Gag-specific gamma interferon (IFN-gamma)-secreting CD8(+) cells, low

216 In addition, the frequency and number of gamma interferon (IFN-gamma)-secreting effector memory (

217 lper type 1 isotype-switched antibodies, and gamma interferon (IFN-gamma)-secreting T cell responses.

218 The inflammatory reaction is orchestrated by gamma interferon (IFN-gamma)-secreting Th1 cells, and re

219 Furthermore, gamma interferon (IFN-gamma)-stimulated primary peritone

220 Furthermore, P. gingivalis suppressed gamma interferon (IFN-gamma)-stimulated release of IP-10

221 and upstream stimulatory factor 1 (USF-1) in gamma interferon (IFN-gamma)-treated hepatocytes.

222 In this study, using dual gamma interferon (IFN-gamma)-yellow fluorescent protein

223 induced miR-155 and proinflammatory cytokine gamma interferon (IFN-gamma).

224 n serum levels of interleukin 12 (IL-12) and gamma interferon (IFN-gamma).

225 ell as the ability of the T cells to secrete gamma interferon (IFN-gamma).

226 receptor superfamily member 9 (TNFRSF9); and gamma interferon (IFN-gamma).

227 ulmonary CD4(+) T cells capable of secreting gamma interferon (IFN-gamma).

228 more interleukin-4 (IL-4) and IL-10 and less gamma interferon (IFN-gamma).

229 fection requires type I (alpha/beta) and II (gamma) interferon (IFN) production.

230 Infected mice mounted innate (gamma interferon [IFN-gamma] and soluble interleukin 2 r

231 ressing genes involved in cellular immunity (gamma interferon [IFN-gamma] and the IFN-gamma-inducible

232 (interleukin-17 [IL-17] and IL-6) and liver (gamma interferon [IFN-gamma] and tumor necrosis factor a

233 terleukin 2 [IL-2], IL-4, IL-10, IL-17A, and gamma interferon [IFN-gamma]) and rendered T cells refra

234 ed substantially higher levels of antiviral (gamma interferon [IFN-gamma], 10-kDa gamma interferon-in

235 r alpha [TNF-alpha], interleukin-12 [IL-12], gamma interferon [IFN-gamma], and IL-6), chemokines (mon

236 flammatory Th1 (interlukin-1beta [Il-1beta], gamma interferon [Ifn-gamma], and tumor necrosis factor-

237 expressed latency-specific genes (e.g., the gamma interferon [IFN-gamma], Cxcl9, and Ccl5 genes) are

238 cell-mediated immune cytokine and chemokine (gamma interferon [IFN-gamma], interleukin 10 [IL-10], IL

239 udies with protection from clinical malaria (gamma interferon [IFN-gamma], interleukin-10 [IL-10], an

240 espite having no impact on mucosal cytokine (gamma interferon [IFN-gamma], tumor necrosis factor [TNF

241 iently produced multiple effector cytokines (gamma interferon [IFN-gamma], tumor necrosis factor alph

242 f systemic and TB antigen-stimulated type 1 (gamma interferon [IFN-gamma], tumor necrosis factor alph

243 evels of degranulation, cytokine expression (gamma interferon [IFN-gamma], tumor necrosis factor alph

244 ulating levels of proinflammatory cytokines (gamma interferon [IFN-gamma], tumor necrosis factor alph

245 whereas recombinant viruses expressing IL-4, gamma interferon, IL-12p35, IL-12p40, or IL-12p70 do not

246 of natural killer (NK) cells, which produce gamma interferon in an IFN-I-dependent fashion, and is i

247 le nitric oxide synthase, interleukin-6, and gamma interferon in kidney tissue.

248 tigen-independent activation and produce IFN-gamma (interferon) in situ.

249 eased interleukin-6 secretion, and decreased gamma interferon-induced protein 10 secretion.

250 increased the production of IL-6 and CXCL10/gamma interferon-induced protein 10, which are implicate

251 iviral (gamma interferon [IFN-gamma], 10-kDa gamma interferon-induced protein [IP-10]) and proinflamm

252 ors (interferon regulatory factor 7, CXCL10 [gamma interferon-inducible protein 10], gamma interferon

253 g as a nuclear pattern recognition receptor, gamma interferon-inducible protein 16 (IFI16) colocalize

254 IFN-gamma, interferon-inducible protein-10 (IP-10), tumor ne

255 gamma-Interferon-inducible lysosomal thiol reductase (GI

256 Gamma-interferon-inducible lysosomal thiol reductase (GI

257 Gamma-interferon-inducible lysosomal thiol reductase (GI

258 H2-M molecular chaperone, the proteasome and gamma-interferon-inducible lysosomal thiol reductase rev

259 ng the AIM2 (absent in myeloma 2) and IFI16 (gamma-interferon-inducible protein 16) inflammasomes.

260 PAN RNA expression decreased expression of gamma interferon, interleukin-18, alpha interferon 16, a

261 T-cell responses were screened by gamma interferon/interleukin-2 (IFN-gamma/IL-2) FluoroSp

262 Mphis incubated with lipopolysaccharide and gamma interferon (LPS/IFN-gamma) and with interleukin-4

263 HCV-specific CD8 T-cell activation (CD107a, gamma interferon, macrophage inflammatory protein 1beta,

264 4, also known as LIGHT), monokine induced by gamma interferon (MIG), and granzyme B (P <0.00001).

265 and of the CXCR3 ligand monokine induced by gamma interferon (MIG).

266 [GRO-alpha], IP-10, and monokine induced by gamma interferon [MIG]), were upregulated in Campylobact

267 ors in BBB disruption, the administration of gamma interferon-neutralizing antibody ameliorated the e

268 ls were found in FI-RSV immune mice, whereas gamma interferon-positive (IFN-gamma(+)) and TNF-alpha(+

269 gher among Th17 cells than among IL-17(-) or gamma interferon-positive (IFN-gamma(+)) cells, even upo

270 Furthermore, a greater proportion of gamma interferon-positive (IFN-gamma(+)) effector CD8 an

271 er the first MVA-CMDR boost, vaccine-induced gamma interferon-positive (IFN-gamma(+)) Gag-specific T-

272 tion correlated with high numbers of CD4(+), gamma interferon-positive (IFN-gamma(+)), tumor necrosis

273 crosis factor alpha-positive [TNF-alpha(+)], gamma interferon-positive [IFN-gamma(+)]) CD4(+) effecto

274 The levels of anti-SIV gamma interferon-positive, CD4(+), and CD8(+) T cells at

275 The levels of specific gamma interferon-positive, interleukin-10-positive T cel

276 rs of activated CD4+ T cells in all tissues, gamma interferon-producing (IFN-gamma+) CD8+ T cells in

277 okine production, leukocyte infiltrates, and gamma interferon-producing CD4(+) T cells, as well as an

278 ally, there was a marked reduction of CD4(+) gamma interferon-producing effector T cells responsible

279 e the function of CD8(+) T cells in terms of gamma interferon production or prevent their apoptosis t

280 cells exhibited high functional avidity for gamma interferon production, whereas VP3(173-181)-specif

281 crophage markers, and increased the level of gamma interferon production, while it decreased the leve

282 NLuc infection of AG129 mice (alpha/beta and gamma interferon receptor deficient) showed rapid spread

283 imilar disease development in alpha/beta and gamma interferon receptor knockout mice, including neuro

284 However, the trpB mutant remains virulent in gamma interferon receptor-deficient (IFN-gammaR(-/-)) mi

285 ly reported that mice lacking alpha/beta and gamma interferon receptors (IFN-alpha/betaR and -gammaR)

286 ly reported that mice lacking alpha/beta and gamma interferon receptors permit high levels of DENV re

287 acid hybridization probe, a M. tuberculosis gamma interferon release assay, and is closely related t

288 s have correlated the results of interferon (gamma interferon) release assays (IGRAs) with known mark

289 RSV infection induced an RSV-specific human gamma interferon response in HIS mouse splenocytes.

290 were screened for the ability to stimulate a gamma interferon response in vitro using whole blood fro

291 and TssM produced high-titer IgG and robust gamma interferon-secreting T cell responses against the

292 of Af5517-aspirated mice displayed decreased gamma interferon secretion and increased interleukin-4 t

293 ptibility within tumor necrosis factor alpha/gamma interferon-stimulated macrophages in a STAT3/6-ind

294 g regimen resulted in significantly elevated gamma interferon T cell responses and high-avidity antig

295 are more responsive to induction of MHC-I by gamma-interferon than other neuronal populations.

296 and CAAT mutant promoters were activated by gamma interferon, the Sp1 and Inr mutants were repressed

297 larly, increased levels of STAT-1 induced by gamma interferon treatment inhibited HPV genome amplific

298 levels of granzyme B, granzyme K, perforin, gamma interferon, tumor necrosis factor alpha, and inter

299 ointestinal tract, but a slight reduction of gamma interferon was observed in the ceca of mice infect

300 roteins, intracellular cytokine staining for gamma interferon was utilized to identify novel RSV-spec