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1 ation whether it was evaluated by humoral or cellular immunity.
2 expression, including many genes involved in cellular immunity.
3 erized vector for inducing both antibody and cellular immunity.
4 ials, likely due to inefficient induction of cellular immunity.
5 ing cell 'spreading', an initiating event in cellular immunity.
6 ing CD40 failed to produce either humoral or cellular immunity.
7 elopment of vaccines that efficiently target cellular immunity.
8 tion of balanced Th-1 polarization and Th-17 cellular immunity.
9 hrough chromatinization as part of intrinsic cellular immunity.
10 vant dose for inducing potent and long-lived cellular immunity.
11 esponses but are more limited for generating cellular immunity.
12 conserved receptor that limits and redirects cellular immunity.
13 ensively explored concept aimed at improving cellular immunity.
14 ly therapeutic approach to enhance antiviral cellular immunity.
15 nt (allo-BMT) is controlled by donor-derived cellular immunity.
16 dow of time for the generation of protective cellular immunity.
17 on with heterologous vaccines elicits potent cellular immunity.
18 icity, cross-reactivity, and antigenicity in cellular immunity.
19 chanisms of these drugs and their effects on cellular immunity.
20 by the paucity of information on targets of cellular immunity.
21 spected to protect HIV-1-infected cells from cellular immunity.
22 calcium bursts as an important aspect of fly cellular immunity.
23 vor epigenetic reprogramming and escape from cellular immunity.
24 ox vaccine recipients with severely impaired cellular immunity.
25 valuate kidney damage, humoral immunity, and cellular immunity.
26 activation of Ab-induced innate or adaptive cellular immunity.
27 m which to identify correlates of protective cellular immunity.
28 nd adjuvant followed by NYVAC elicits potent cellular immunity.
29 be an effective vaccine formula in inducing cellular immunity.
30 oute in induction of systemic HIV-1-specific cellular immunity.
31 er therapeutic strategy via up-regulation of cellular immunity.
32 s with concomitant engagement of humoral and cellular immunity.
33 yield greater IL-27 production and sustained cellular immunity.
34 rAd)-based vectors can induce potent mucosal cellular immunity.
35 may benefit parasite escape from humoral and cellular immunity.
36 e overcome through the induction of enhanced cellular immunity.
37 d animals, suggesting an effect of rEV576 on cellular immunity.
38 up, activates NF-kappaB-mediated humoral and cellular immunity.
39 important link between humoral immunity and cellular immunity.
40 eptors (FcR) on APCs can enhance humoral and cellular immunity.
41 athways of innate immunity and induce strong cellular immunity.
42 cterial peritonitis, known to have defective cellular immunity.
43 resulting in enhanced and prolonged effector cellular immunity.
44 se interactions are important in humoral and cellular immunity.
45 icipatory role for this unique population in cellular immunity.
46 cant part of transferred immunity is passive cellular immunity.
47 tes with strong pretransplant donor-reactive cellular immunity.
48 , therefore providing a potential target for cellular immunity.
49 d cell surface to escape recognition by host cellular immunity.
50 as a means to induce Ag-specific humoral and cellular immunity.
51 e that favors development of skin-associated cellular immunity.
52 nstitute a powerful platform for stimulating cellular immunity.
53 PA axis, which modulate spleen shrinkage and cellular immunity.
54 ferentiation and maintenance, of humoral and cellular immunity.
55 ues will facilitate research into protective cellular immunity.
56 role in the regulation of various stages of cellular immunity.
57 ey regulators of measles vaccine humoral and cellular immunity.
58 iferation and plant growth at the expense of cellular immunity.
59 IV B clade fusion protein designed to induce cellular immunity.
60 e development will augment either humoral or cellular immunity.
61 nal immunity" to distinguish it from passive cellular immunity.
62 , who championed the role of phagocytosis in cellular immunity.
63 tibodies, but with no detectable GP-directed cellular immunity.
64 T cell dichotomy is essential for effective cellular immunity.
65 echanism for fine-tuning and optimization of cellular immunity.
66 be used to elicit human anti-RSV humoral and cellular immunity.
67 ovel function for nonhuman TRIM5 variants in cellular immunity.
68 nts a potent vaccine adjuvant of humoral and cellular immunity.
69 Toll-like receptor 9 agonist, which augments cellular immunity.
70 sign HIV-1 vaccines that stimulate effective cellular immunity.
71 s that contain important targets of anti-HIV cellular immunity.
72 comitantly to effector Th cells that support cellular immunity.
73 ent on DCs to stimulate long-term anti-tumor cellular immunity.
74 erving sufficient normal T cells to maintain cellular immunity.
75 responses, and 1V270 potently generates Th1 cellular immunity.
76 stemic corticosteroid therapy, which impairs cellular immunity.
78 ponses are valuable tools to shape and drive cellular immunity against cancer and intracellular infec
81 esponses and suggest that enhancing adaptive cellular immunity against HEV might prevent persistent H
83 ) reaction, and induction of serological and cellular immunity against HPV16/18 E7 and KLH were monit
84 ontribute to the induction and activation of cellular immunity against intracellular pathogens, such
86 , indicating that MV-NIS treatment triggered cellular immunity against the patients' tumor and sugges
90 the unique potential to activate humoral and cellular immunity, an actual challenge is to increase pl
91 both a novel strategy of virus evasion from cellular immunity and a novel role for a cellular protei
92 es with the polyfunctionality and potency of cellular immunity and are a prime example of the potenti
93 dendritic cells (DCs) are key components of cellular immunity and are thought to originate and renew
96 um suggested that POLR3A mutations triggered cellular immunity and cross-reactive humoral immune resp
97 The microbiome plays an important role in cellular immunity and energy metabolism and has been imp
98 tein boosting, elicited systemic and mucosal cellular immunity and exhibited equivalent, significant
99 e activation, in combination with suppressed cellular immunity and failed cytotoxic T cell anti-tumor
102 Mtb) results in the generation of protective cellular immunity and formation of granulomatous structu
103 by envelope protein boosting, elicits broad cellular immunity and functional, envelope-specific seru
104 de that MCP-1 plays a key role in regulating cellular immunity and IFN-gamma production following pne
105 n of the same HLA alleles in vaccine-induced cellular immunity and in natural immune control is of re
106 e association with progressive impairment of cellular immunity and increasing susceptibility to oppor
107 osteopontin (OPN), an important component of cellular immunity and inflammation, showed higher expres
108 he early stage of HIV infection, humoral and cellular immunity and innate immune functions in oral mu
110 of autologous transfer strategies to explore cellular immunity and potential therapeutic applications
111 (LdCen(-/-) and Ldp27(-/-)) induce a strong cellular immunity and provide protection against viscera
112 his may prove useful in monitoring patients' cellular immunity and recovery from active BKV infection
113 The recognition events that mediate adaptive cellular immunity and regulate antibody responses depend
114 M and Mycobacterium tuberculosis is based on cellular immunity and relies on the type-1 cytokine path
115 de evidence for transplacental regulation of cellular immunity and suggest that IL-10 may influence T
116 hat vaccine-induced MDSCs inhibit protective cellular immunity and suggest that preventing MDSC induc
117 boosting elicits enhanced intestinal mucosal cellular immunity and that oral or ileal vector delivery
118 animals provide a unique model for exploring cellular immunity and the control of SIV infection and f
119 a detailed characterization of SIV-specific cellular immunity and viral control in the first 6 mo fo
120 immunodominance is crucial to understanding cellular immunity and viral evasion mechanisms and will
121 an the other two strains in both humoral and cellular immunities, and their tumor growth was signific
122 orally coinciding with onset of SIV-specific cellular immunity, and elevated plasma Th1 cytokine and
123 for infectious agents boost humoral but not cellular immunity, and have poorly-understood mechanisms
125 genesis, preceding and outweighing antitumor cellular immunity, and likely contribute to disease prog
126 dy pTreg, the cross-talk between humoral and cellular immunity, and regulation of the inflammatory re
127 s suggest that the acute phase and activated cellular immunity are associated with increased cellular
129 novel and dominant targets of KSHV-specific cellular immunity are identified and compared to T cells
130 supporting the notion that both humoral and cellular immunity are important for development of prote
133 didate providing broad antiviral humoral and cellular immunity as a foundation for future development
135 lso exhibits adjuvant effects on humoral and cellular immunity as well as an enhancement of polyinosi
136 ill and vaccinated subjects retained strong cellular immunity, as indicated by high levels of mucosa
139 will inform the development of an effective cellular immunity-based human immunodeficiency virus vac
140 .p. infection with ORF31STOP elicited strong cellular immunity but a non-neutralizing Ab response.
142 particle (VRP) boost, increasing humoral and cellular immunity by at least 1 order of magnitude compa
143 the evidence that triggering of TA-specific cellular immunity by TA-targeted mAb, in conjunction wit
144 macrophage death, as well as, activation of cellular immunity by the TA, causing increased T-cell ac
145 stinal nematodes is associated with impaired cellular immunity, characterized by reduced lymphocyte p
147 could induce the durable, robust humoral and cellular immunity commonly seen in CMV seropositive subj
148 munodeficiency virus type 1 (HIV-1)-specific cellular immunity contributes to the control of HIV-1 re
149 IFN-gamma plays a central role in activating cellular immunity, controlling cell proliferation, and i
153 s infection has been regarded as inferior to cellular immunity directed to the intracellular pathogen
155 skin cells via the NK1R promotes humoral and cellular immunity during skin genetic immunizations.
157 this prime-boost strategy can induce strong cellular immunity, especially in vaginal tissues, and mi
159 contribution of FcgammaR in the induction of cellular immunity, FcgammaR single- and double-knockout
160 e show that PrfA*(G155S) enhanced functional cellular immunity following an intravenous or intramuscu
161 of innate immunity and HER2/neu humoral and cellular immunity following cryoablation with or without
162 tanding the relationship between humoral and cellular immunity following immunization with conjugate
164 , and current efforts focus on understanding cellular immunity for targeted vaccine development.
165 hydrates while suppressing genes involved in cellular immunity (gamma interferon [IFN-gamma] and the
166 umab, PD-1-antibody, can enhance antimyeloma cellular immunity generated by pomalidomide, leading to
167 udy was initiated to evaluate the breadth of cellular immunity generated through immunization of rhes
169 though the contribution of TRIM5 proteins to cellular immunity has not yet been studied, their intera
171 roperties of stem cells to maintain lifelong cellular immunity have been hypothesized for many years,
172 dies; however, vaccines exclusively inducing cellular immunity have not been studied to formally test
173 ected hosts despite CMV-specific humoral and cellular immunity; however, how it does so remains undef
174 oad occurrence of CD40L(+) CD8(+) T cells in cellular immunity implicates that helper functions are n
175 mechanism couples innate viral sensing with cellular immunity in a single protein and could be explo
177 ly, whereas the kinetics of the SIV-specific cellular immunity in breast milk mirrored that of the bl
182 blish the level of L. monocytogenes-specific cellular immunity in healthy adults, and, together with
186 ut to investigate the role of humoral versus cellular immunity in rVSV vaccine-mediated protection ag
189 SNPs in cytokine/cytokine receptor genes and cellular immunity in subjects following primary smallpox
190 ctive comparison of M. tuberculosis-specific cellular immunity in subjects with active tuberculosis a
191 aerosol rAd immunization to generate potent cellular immunity in the lung suggests that using differ
193 rets, all vaccinated ferrets showed improved cellular immunity in the lungs and peripheral blood.
195 e required for optimal T cell activation and cellular immunity in this in vivo nonlymphoid tumor mode
196 y adults with Ty21a and assessed humoral and cellular immunity in vaccinated volunteers and controls
197 e, a differential requirement for humoral vs cellular immunity in vaccine-induced protection against
198 ultiple-route DNA vaccinations induce strong cellular immunity, in addition to potent and high-avidit
199 ders have revealed that states of suppressed cellular immunity, in combination with enhanced humoral
200 IVIG has a much broader ability to regulate cellular immunity including innate and adaptive componen
202 nical testing of vaccines designed to induce cellular immunity, including those against influenza vir
203 infectious challenge, research in pursuit of cellular immunity-inducing vaccine adjuvants should no l
205 of CMV infection is largely accounted for by cellular immunity, involving various T-cell and B-cell s
208 cells (DC) to mediate CD4(+) T cell help for cellular immunity is guided by instructive signals recei
214 ngle adjuvant that enhances both humoral and cellular immunity is rare and thus underlines the import
215 ong-standing notion that humoral rather than cellular immunity is sufficient to facilitate Lyme disea
219 adjuvant for enhancing antiviral humoral and cellular immunity, leading to enhanced protection agains
220 lar immune responses in eukaryotes, and this cellular immunity likely involves changes in subcellular
221 tion induced both HA-specific antibodies and cellular immunity likely to provide heterotypic immunity
222 xperiment to determine whether crossreactive cellular immunity limits symptomatic illness in antibody
223 lar rAd5-Env boosting increased Env-specific cellular immunity markedly in mucosal as well as systemi
224 tective immunity, and there is evidence that cellular immunity may also be important in related arena
225 d suggest that crosstalk between the CNS and cellular immunity may be a general mechanism by which in
228 agglutination-inhibiting (HI) antibodies and cellular immunity measured by ex vivo leukocyte response
229 S) serotype-specific capsular polysaccharide cellular immunity, measured with enzyme-linked immunospo
231 gens; however, the impact of vector-specific cellular immunity on subsequent insert-specific T cell r
232 -gamma, TNF-alpha, and NOS2, key elements of cellular immunity, perform critical protective functions
234 of neutralizing antibodies, indicating that cellular immunity plays a primary role in viral clearanc
235 Finally, pretransplant assays of anti-CMV cellular immunity predicted post-transplant CMV replicat
236 sponses in the lungs explains why protective cellular immunity quickly declines following influenza v
237 ose of the control monkeys while MV-directed cellular immunity reached levels at least as high as in
240 pectives for differential shaping of desired cellular immunity required to fight the wide range of co
243 to selection pressures from both humoral and cellular immunity, resulting in the continuous generatio
244 nation strategies designed to elicit durable cellular immunity should target the generation of TSCM c
246 ast Asia, especially for those with impaired cellular immunity such as human immunodeficiency virus-i
247 h emphasis on the tumor microenvironment and cellular immunity, taking into account novel nanotechnol
249 ork of Elie Metchnikoff and the discovery of cellular immunity, the phagocytic clearance of cellular
250 ral protection against pathogens and promote cellular immunity through diverse nonclassical effector
251 tibodies have important roles in controlling cellular immunity through interaction with activating or
254 virus (EBV) provides a useful model to study cellular immunity to a genetically stable, persistent hu
256 CD154 mediates key facets of humoral and cellular immunity to alloantigens, and is tolerogenic to
257 is overlapping, and preexisting humoral and cellular immunity to both are exhibited in human populat
258 cPLA(2) in the induction of cell autonomous cellular immunity to Chlamydia and highlight the many no
259 s a major barrier limiting the capability of cellular immunity to contain infection and the ability o
260 This study investigates the contribution of cellular immunity to cross-protection using mouse models
262 may be required toward mechanisms that boost cellular immunity to gH and gL within future subunit vac
263 ntigen (HBsAg) sometimes develop humoral and cellular immunity to HBV proteins such as core and polym
264 the effects of TIV and LAIV immunization on cellular immunity to live influenza A virus in children
266 difference in the development of humoral or cellular immunity to pneumococcal colonization between w
268 vaccines should elicit effective humoral and cellular immunity to protect an individual from infectio
269 r data suggest that eosinophils promote host cellular immunity to reduce influenza virus replication
270 are thought to have a function in intrinsic cellular immunity to several viruses including human imm
273 e products often mediate opposing effects on cellular immunity to tumor cells, pathogens, and autoant
275 inants of the AAVrh32.33 capsid that augment cellular immunity to vector-encoded proteins or those of
276 esults indicate that after infection durable cellular immunity to WHV is essential for the long-term
278 bination antiretroviral therapy, recovery of cellular immunity triggers inflammation to a preexisting
280 a key autoantigen driving the Th17-dependent cellular immunity underlying another chronic inflammator
283 rP18tri vector can induce strong humoral and cellular immunity via different immunization routes and
284 dherence to host cells, and modulating human cellular immunity via interactions with T cells and neut
285 rotection was mainly antibody dependent, but cellular immunity was also beneficial in protecting agai
290 ical anergy and other evidence of diminished cellular immunity, we hypothesized that decreased skin d
291 mechanisms underlying wasp virulence and fly cellular immunity, we used a joint transcriptomic/proteo
292 protection for DENV vaccines on the basis of cellular immunity, we wanted to compare the cellular imm
295 ate a multifaceted immune response including cellular immunity, which may provide protection against
297 ntibodies and Th1-predominant donor-specific cellular immunity with high frequency of IFN-gamma and l
298 1 vaccine is devising a strategy to generate cellular immunity with sufficient breadth to deal with t
300 an emerging technology to induce therapeutic cellular immunity without the need for autologous antige
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