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1 provide a new insight for the development of passive immunotherapy.
2 r therapeutic intervention through augmented passive immunotherapy.
3 east cancer, a number of concerns exist with passive immunotherapy.
4 sition to evaluate the effects of anti-Abeta passive immunotherapy.
5 roles against malignancy in both active and passive immunotherapy.
6 nous IgG or monoclonal antibody cocktail for passive immunotherapy.
7 ent with conventional active vaccination and passive immunotherapy.
8 their levels, such as secretase inhibitors, passive immunotherapy against Abeta and mGluR5 antagonis
9 K should be further explored as a target for passive immunotherapy against complicated S. aureus infe
11 NA represents a viable delivery platform for passive immunotherapy against HIV-1 with expansion to a
12 e is an urgent need for the development of a passive immunotherapy against the category B select agen
13 monoclonals can be potential candidates for passive immunotherapy and for guiding immunogen design.
14 ding mutations in the hE16 epitope to resist passive immunotherapy and for the selection of neutraliz
15 More than ten new approaches to active and passive immunotherapy are under investigation in clinica
19 rulence factor for R. oryzae, and anti-Ftr1p passive immunotherapy deserves further evaluation as a s
21 e greatest promise for generating active and passive immunotherapies for treating overdose or addicti
24 orum quenching vaccines for use in active or passive immunotherapy for prevention or treatment of S.
26 hese data cast further doubt on the value of passive immunotherapy for the treatment of EBOV infectio
28 complex class I and II molecules, active and passive immunotherapy has moved to center stage once aga
35 mmune plasma demonstrates the feasibility of passive immunotherapy, it is limited in quantity, variab
36 lso show that targeting these oligomers with passive immunotherapy leads to some improvement in motor
39 study, an ovine antibody-based platform for passive immunotherapy of C. difficile infection is descr
40 17-1A and GA733, has been a useful target in passive immunotherapy of CRC patients with mAb and in ac
44 y have important implications for active and passive immunotherapy of prostate and other cancers.
45 ssociated micro-hemorrhages, i.c.v.-targeted passive immunotherapy offers a promising therapeutic app
46 imaging was employed to study the effects of passive immunotherapies on lethality and viral dissemina
49 a possible explanation of why adoptive (i.e. passive) immunotherapy protocols can sometimes actually
50 evaluate the potential efficacy of active or passive immunotherapy regimens as adjunctive treatments.
51 clinical trials are ongoing using active and passive immunotherapy targeting the amyloid-beta (Abeta)
52 ently, ~16% of participants in an anti-Abeta passive immunotherapy trial for mild-to-moderate Alzheim
54 logical tau oligomers in aged Tg2576 mice by passive immunotherapy using tau oligomer-specific monocl
55 F4 can be used to identify AL candidates for passive immunotherapy using the chimeric form of the ant
56 ing through the B-cell and T-cell receptors; passive immunotherapies utilizing these receptors, such
59 Alzheimer's disease (AD) patients treated by passive immunotherapy with humanized anti-amyloid beta m
63 fied as being farthest along in development; passive immunotherapy with monoclonal antibodies, postex
66 vide "proof of principle" for the ability of passive immunotherapy with rituximab to elicit an active
68 MAbs may provide the most effective form of passive immunotherapy, with the caveat that these may de
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