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1 r the responses to pertactin and serotype 6B pneumococcal polysaccharide.
2 Four of the antibodies cross-reacted with pneumococcal polysaccharide.
3 f IgM memory cells in the immune response to pneumococcal polysaccharides.
4 pendent Ag LPS, and type II T-independent Ag pneumococcal polysaccharides.
7 pendent humoral immune responses to isolated pneumococcal polysaccharide Ags and highlight the potent
8 d uninfected control subjects with 23-valent pneumococcal polysaccharide and tetanus toxoid vaccines.
9 ride standards were used for quantitation of pneumococcal polysaccharides and conjugates with confirm
10 or tetanus diphtheria combination, 23-valent pneumococcal polysaccharide, and for all vaccines combin
12 s formed on immunization with thyroglobulin, pneumococcal polysaccharide, and ssDNA-methylated BSA.
13 normal concentrations of antibodies against pneumococcal polysaccharides, and better renal function
14 ter, two sets of latex particles coated with pneumococcal polysaccharides, and serotype-specific anti
15 but not those of anti-tetanus toxoid or anti-pneumococcal polysaccharide antibodies, fell significant
18 ss may reflect immune paralysis due to large pneumococcal polysaccharide antigen loads and/or a poten
19 generated antigen-specific IgM responses to pneumococcal polysaccharide antigens, whereas PC1(hi) ce
20 nce typing and a microarray for detection of pneumococcal polysaccharide capsule biosynthesis genes t
22 100 serotypes were initially included in the pneumococcal polysaccharide conjugate vaccine (PCV) in 2
25 ococcal vaccine in the elderly, we evaluated pneumococcal polysaccharide-derived oligosaccharides con
26 ependent type 2 antigens (TI-2 Ags), such as pneumococcal polysaccharides, elicit weak immunoglobulin
27 ed IgG Ab production after immunization with pneumococcal polysaccharides in mice with disruptions in
28 nd immune response in neonatal mice, using a pneumococcal polysaccharide of serotype 1 conjugated to
30 fection or intraperitoneal immunization with pneumococcal polysaccharide or 4-hydroxy-3-nitrophenyl-a
32 hat respond to vaccination with the purified pneumococcal polysaccharide (PPS) has been a topic of de
37 viduals that respond poorly to the 23-valent pneumococcal polysaccharide (PPS) vaccine, Pneumovax, su
39 fference in levels of IgG antibodies against pneumococcal polysaccharide (PPS), older adults had lowe
40 sed combinatorial library cloning to isolate pneumococcal polysaccharide (PPS)-specific Fab fragments
42 her mice were naive or immunized with native pneumococcal polysaccharide (PPS; Pneumovax23) or protei
43 independent Ig isotype responses to isolated pneumococcal polysaccharides (PPS) required TLR signalin
45 ine (T-dependent) and Pneumovax23 (23-valent pneumococcal polysaccharide [PPV23], T-independent).
51 CD40 monoclonal antibody to mice, along with pneumococcal polysaccharide, provides a substitute for T
54 have a receptor that interacts with capsular pneumococcal polysaccharides, setting the stage for furt
55 enabled even greater boosting of protective pneumococcal polysaccharide-specific IgG responses when
56 lly, late recovering patients displayed less pneumococcal polysaccharide-specific immunoglobin M-prod
57 neumococcus cells are impaired in generating pneumococcal polysaccharide-specific responses and succu
58 ore they had developed antibody responses to pneumococcal polysaccharide, still failed to show a resp
59 GBS-III, biochemically identical to capsular pneumococcal polysaccharide type 14 (PPS14) of Streptoco
61 sis of human observational data suggest that pneumococcal polysaccharide vaccination (PPV) could be p
65 in antigens were normal, but the response to pneumococcal polysaccharide vaccination was moderately i
68 7; Prevnar) in infancy followed by 23-valent pneumococcal polysaccharide vaccine (23vPPV; Pneumovax)
69 -treated patients had decreased responses to pneumococcal polysaccharide vaccine (57% of patients had
70 rted that the 7-valent diphtheria-conjugated pneumococcal polysaccharide vaccine (PCV7) is safe and i
71 administration of the heptavalent conjugated pneumococcal polysaccharide vaccine (PCV7) were also ass
74 ther passive immunization with the 23-valent pneumococcal polysaccharide vaccine (Pneumovax(R) 23; PP
77 dose 6 months later, and 1 dose of 23-valent pneumococcal polysaccharide vaccine (PPSV23) 1 month lat
78 jugate vaccine (PCV13) followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 2 months la
79 15-valent PCV (PCV15) followed by 23-valent pneumococcal polysaccharide vaccine (PPSV23) 8 weeks lat
80 gate vaccine (PCV13) compared with 23-valent pneumococcal polysaccharide vaccine (PPSV23) among US ad
81 ortions and incidence matching the 23-valent pneumococcal polysaccharide vaccine (PPSV23) and 13-vale
82 usly vaccinated with >/= 1 dose of 23-valent pneumococcal polysaccharide vaccine (PPSV23) and had CD4
83 rt 1 (n = 350) previously received 23-valent pneumococcal polysaccharide vaccine (PPSV23) and were ra
84 tion Practices has recommended the 23-valent pneumococcal polysaccharide vaccine (PPSV23) for nonelde
85 PD), with the effectiveness of the 23-valent pneumococcal polysaccharide vaccine (PPSV23) for prevent
87 te vaccine (PCV13) followed by the 23-valent pneumococcal polysaccharide vaccine (PPSV23) remains unc
88 Controversy persists over the benefits of pneumococcal polysaccharide vaccine (PPV) for adults at
92 (PCV13) concurrently, followed by 23-valent pneumococcal polysaccharide vaccine (PPV23) 2 months lat
93 determine the effectiveness of the 23-valent pneumococcal polysaccharide vaccine (PPV23) among Navajo
95 grouped serotypes contained in the 23-valent pneumococcal polysaccharide vaccine (PPV23) decreased at
99 >/= 200 randomized to receive the 23-valent pneumococcal polysaccharide vaccine (PPV23) or placebo a
100 V (PCV13) vs regions that used the 23-valent pneumococcal polysaccharide vaccine (PPV23) was also ana
101 65 years or older; previously only 23-valent pneumococcal polysaccharide vaccine (PPV23) was recommen
103 umonia (n = 16) and healthy volunteers given pneumococcal polysaccharide vaccine (PPV; n = 14) or pne
104 (PCV) followed by either a dose of 23-valent pneumococcal polysaccharide vaccine (PSV23) or a fourth
107 althy human adults with Pneumovax (23-valent pneumococcal polysaccharide vaccine [PPV23]), IgG anti-c
108 s, but it remains unclear whether use of the pneumococcal polysaccharide vaccine alters the overall r
112 Four of 16 patients in group 1 responded to pneumococcal polysaccharide vaccine compared with 14 of
115 se findings support the effectiveness of the pneumococcal polysaccharide vaccine for the prevention o
118 e vaccine (PCV) followed by either a dose of pneumococcal polysaccharide vaccine or a fourth PCV dose
119 gate vaccine followed by 1 dose of 23-valent pneumococcal polysaccharide vaccine or a single dose of
120 udy murine immune responses to the 23-valent pneumococcal polysaccharide vaccine Pnu-Imune, both in v
123 rs after transplantation and the response to pneumococcal polysaccharide vaccine was significantly lo
124 eritoneal B1b compartment, immunization with pneumococcal polysaccharide vaccine yielded comparable a
125 stem activation using the standard 23-valent pneumococcal polysaccharide vaccine, (3) daily sampling
126 rgeting high-risk groups was undertaken with pneumococcal polysaccharide vaccine, and subsequently ra
127 sera of people immunized with the 23-valent pneumococcal polysaccharide vaccine, we confirmed that h
128 ne response to that induced by the 23-valent pneumococcal polysaccharide vaccine, which has been the
138 uded in the 7-valent conjugate and 23-valent pneumococcal polysaccharide vaccines accounted for 78 pe
142 of the UAD-2 assay was achieved by capturing pneumococcal polysaccharides with serotype-specific mono