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1                                              Hib antibody levels were protective in >99% of those sur
2                                              Hib conjugated to the carrier proteins CRM(197) and teta
3                                              Hib disease can be almost completely eliminated through
4                                              Hib IgG was associated with age at third immunization (P
5                                              Hib immunization was introduced in Kenyan infants in 200
6                                              Hib PS binding of the recombinant Fabs was evaluated qua
7                                              Hib-CRM(197) induced a rapid increase in CRM(197)-specif
8                                              Hib-CRM(197) induced PS and CRM(197) antibodies, vigorou
9                                              Hib-meningococcal outer membrane protein complex (OMPC)
10                                              Hib-OMPC is unique among glycoconjugate vaccines by enga
11                                              Hib-OMPC was significantly less immunogenic in TLR2 KO m
12  effect on Hib immunogenicity of combining 2 Hib vaccines (Hib-tetanus toxoid [TT]-A and Hib-TT-B) wi
13 ifBC genes were detected in 109 of 170 (64%) Hib strains and in 46 of 162 (28%) NTHi isolates (P = 0.
14 TP/Hib and 7VPnC (group 2), or DTP and 7VPnC/Hib (group 3) at ages 2, 3 and 4 months.
15 ng either A2 or A18 L chains isolated from a Hib PS-vaccinated adult.
16 dually with an Fd region known to generate a Hib PS-combining site when paired with an A2-Arg(95a)-Jk
17  B cells were measured before a booster of a Hib-serogroup C meningococcal (MenC) conjugate vaccine a
18 ion against Hib disease wane over time after Hib vaccination at 2, 3, and 4 months of age without a b
19 ibody levels and clinical protection against Hib disease wane over time after Hib vaccination at 2, 3
20 introduction of an efficient vaccine against Hib.
21            In children aged <5 years of age, Hib incidence was 0.06 per 100 000 (2 cases), compared w
22  Hib vaccines (Hib-tetanus toxoid [TT]-A and Hib-TT-B) with diphtheria-TT-acellular pertussis (DTaP)(
23  degradation mediated by both Slimb-Cul1 and Hib-Cul3 E3 ligases.
24 n immunodeficiency virus (HIV) infection and Hib vaccination status were determined for children with
25 nt serum antibody responses against MenC and Hib could be elicited by inl immunization in combination
26 umoniae, nontyphoidal salmonellae (NTS), and Hib were the most frequently isolated pathogens, and hav
27                       We found that OMPC and Hib-OMPC engaged human Toll-like receptor 2 (TLR2) expre
28         With the success of pneumococcal and Hib conjugate vaccines in reducing the risk of meningiti
29  zone for N. meningitidis, S. pneumoniae and Hib were achieved within 1h.
30       Polyribitolribosyl phosphate (PRP) and Hib conjugate (PRP-T) vaccine given as a booster during
31 psule typing was more accurate than SAST and Hib-minus variants were rare.
32 ective thresholds; antibodies to tetanus and Hib were higher.
33 tibody levels in children aged <5 years, and Hib vaccine coverage and timing in children aged 1 to <2
34  compared with two or three doses of another Hib vaccine (conditional odds ratio 6.77 [95% CI 3.26-14
35                                  All A2 anti-Hib PS Abs sequenced to date possess a 10-amino acid L c
36 Abs, and these are the highest affinity anti-Hib Abs.
37                            Low affinity anti-Hib PS mAbs of infants are encoded by a heterogeneous gr
38                        The low affinity anti-Hib PS mAbs of infants immunized with Hib oligosaccharid
39                     Higher-titer baboon anti-Hib PRP did not express two previously defined cross-rea
40                            In contrast, anti-Hib IgG2 and anti-PC IgG2 were not affected in either G-
41 variable region gene sequences encoding anti-Hib PS mAbs of infants immunized with Hib oligosaccharid
42                                     For anti-Hib antibodies, 4 of 14 (29%) and 5 of 6 (83%), respecti
43 previously defined cross-reactive human anti-Hib PRP idiotypes and was biased towards lambda light-ch
44 tand these age-related changes in human anti-Hib PS immune responses we determined the variable regio
45                                     IgA anti-Hib antibody was also lower in the asplenic group, as wa
46 en exposure even in those with very low anti-Hib-PS antibody.
47        For infants with <1 microgram/mL anti-Hib-PS IgG antibody, mean AI rose by the time of preboos
48 ne A2 is used to encode the majority of anti-Hib Abs, and these are the highest affinity anti-Hib Abs
49 ination were followed by high postboost anti-Hib-PS IgG antibody levels and avidity.
50  ages 2, 3, and 4 months showed reduced anti-Hib polysaccharide IgG (geometric mean concentration [GM
51                                     The anti-Hib avidity index postvaccination strongly correlated wi
52                                     The anti-Hib PS repertoire of children differs from that of adult
53 inct immunologic characteristics of the anti-Hib PS responses in young children immunized with other
54 wer in the asplenic group, as was total anti-Hib antibody measured by RIA.
55 ne or with Hib and DTaP-based vaccines; anti-Hib capsular polysaccharide IgG, poly-ribosyl-ribitol-ph
56                        In a cohort with anti-Hib IgG <1.0 microg/mL following primary immunization, a
57   Avidity differed between infants with anti-Hib-PS IgG antibody <1 or >1 microg/mL postprimary serie
58 philus influenzae b oligosaccharide antigen (Hib) and the Streptococcus pneumoniae antigen phosphocho
59  of TLR2 by Hib-OMPC was MyD88 dependent, as Hib-OMPC-induced TNF production was ablated in MyD88 kno
60  repertoire to the Haemophilus influenzae b (Hib) polysaccharide (PS).
61 zed with DTaP5/IPV/Haemophilus influenzae b (Hib-TT) vaccine at 2-3-4 months, 13-valent pneumococcal
62 mophilus influenzae strains, one serotype b (Hib) and two nonencapsulated b capsule-negative variants
63 on of the Haemophilus influenzae serotype b (Hib) conjugate vaccine into national immunization has le
64 he introduction of H. influenzae serotype b (Hib) conjugate vaccines.
65 ne containing Haemophilus influenzae type b (Hib) and group C meningococcal polysaccharides, as well
66 ng clinical isolates of encapsulated type b (Hib) and nonencapsulated (NTHi) H. influenzae.
67           Encapsulated H. influenzae type b (Hib) and type f (Hif) are the most common serotypes asso
68 oliferated to Haemophilus influenzae type b (Hib) antigen.
69 umoniae), and Haemophilus influenzae type b (Hib) are three most common pathogens accounting for most
70               Haemophilus influenzae type b (Hib) capsular polysaccharide (PS) induces protective ant
71 ponses to the Haemophilus influenzae type b (Hib) component of acellular pertussis-containing combina
72 us (IPV), and Haemophilus influenzae type b (Hib) conjugate vaccine (DTaP-IPV-Hib) among children wit
73 90s, when the Haemophilus influenzae type b (Hib) conjugate vaccine for infants was introduced.
74               Haemophilus influenzae type b (Hib) conjugate vaccine is not perceived as a public heal
75 October 1992, Haemophilus influenzae type b (Hib) conjugate vaccine was introduced to infants in the
76               Haemophilus influenzae type b (Hib) conjugate vaccine, delivered as a three-dose series
77 nogenicity of Haemophilus influenzae type b (Hib) conjugate vaccines and the effect on Hib immunogeni
78 spread use of Haemophilus influenzae type b (Hib) conjugate vaccines has nearly eradicated invasive H
79 aride (PS) of Haemophilus influenzae type b (Hib) covalently linked to carrier proteins, unlike pure
80 s of invasive Haemophilus influenzae type b (Hib) disease and carriage.
81  incidence of Haemophilus influenzae type b (Hib) disease compared with control populations.
82 e of invasive Haemophilus influenzae type b (Hib) disease has significantly decreased since the intro
83 r of cases of Haemophilus influenzae type b (Hib) disease in the UK has risen.
84 ement of anti-Haemophilus influenzae type b (Hib) IgG avidity.
85               Haemophilus influenzae type b (Hib) invasive disease and oropharyngeal carriage continu
86               Haemophilus influenzae type b (Hib) is a leading cause of childhood bacterial meningiti
87 dy avidity to Haemophilus influenzae type b (Hib) polysaccharide (PS) was assessed in infants vaccina
88 ve shown that Haemophilus influenzae type b (Hib) polysaccharide conjugate vaccines can reduce nasoph
89 mmunized with Haemophilus influenzae type b (Hib) PS conjugate vaccine varies with age and Ag formula
90  to compare the genome of a virulent type b (Hib) strain with that of the laboratory-passaged Rd KW20
91 troduction of Haemophilus influenzae type b (Hib) vaccination and the rollout of antiretroviral thera
92 troduction of Haemophilus influenzae type b (Hib) vaccination of children has led to a decline in inc
93  schedule for Haemophilus influenzae type b (Hib) vaccination of infants in the United Kingdom consis
94 icacy of the conjugate H. influenzae type b (Hib) vaccine was the misidentification of isolates as se
95 uce conjugate Haemophilus influenzae type b (Hib) vaccine, which, as in other developing countries bu
96 accharide and Haemophilus influenzae type b (Hib) vaccines in ITP patients.
97 ction against Haemophilus influenzae type b (Hib), a rapidly invading encapsulated bacteria, is depen
98 me), invasive Haemophilus influenzae type b (Hib), acute hepatitis B, hepatitis A, varicella, Strepto
99 pneumococcal, Haemophilus influenzae type b (Hib), and meningococcal vaccines.
100 xtracted from Haemophilus influenzae type b (Hib), and the corresponding glycoconjugate made by conju
101  C (MenC) and Haemophilus influenzae type B (Hib), both of which are conjugated to the nontoxic mutan
102 haride (LOS), Haemophilus influenzae type b (Hib), or Listeria monocytogenes.
103 otect against Haemophilus influenzae type b (Hib), serogroup C Neisseria meningitidis, and multiple c
104 ive bacterium Haemophilus influenzae type b (Hib).
105 80 including hepatitis A, acute hepatitis B, Hib, and varicella.
106               Structural differences between Hib pili and P-pili suggest a difference in the strategi
107                          The ability to bind Hib PS resided exclusively with those Fab fragments havi
108 n following infant (with or without booster) Hib vaccination.
109 for the burden of invasive disease caused by Hib and other H. influenzae serotypes.
110 eumonia cases and pneumonia deaths caused by Hib.
111 b to the human nasopharynx is facilitated by Hib pili, filaments expressed on the bacterial surface.
112                        Engagement of TLR2 by Hib-OMPC was MyD88 dependent, as Hib-OMPC-induced TNF pr
113 nd A18, only A2 contributes to the canonical Hib PS paratope.
114         Twenty-four invasive and 42 carriage Hib isolates, collected during 1992-1997, were character
115 ncentration and the frequency of circulating Hib-specific memory B cells were measured before a boost
116 urface exposed and was found in all clinical Hib and Hif isolates tested.
117                           However, combining Hib-TT-B with DTaP(5)/IPV did not reduce the anti-PRP an
118 ical characteristics of laboratory-confirmed Hib cases diagnosed during 2009-2012.
119 on was obtained for all laboratory-confirmed Hib cases diagnosed during 2009-2012.
120                                    Conjugate Hib vaccine was delivered on time in a 3-dose primary se
121 in older children; and coverage of conjugate Hib vaccination was high (91% having 3 doses at 1-2 year
122 ion immunity after introduction of conjugate Hib vaccine in infancy without a booster dose in Kenya.
123                    Introduction of conjugate Hib vaccine within the routine childhood immunization pr
124 he vaccine is made by chemically conjugating Hib capsular polysaccharide to the outer membrane protei
125                           In many countries, Hib vaccine booster doses have been implemented after in
126 econd year of life on the basis of declining Hib antibody concentrations after the primary series.
127 t Hib vaccine program, perhaps by decreasing Hib carriage in child reservoirs.
128  encapsulated by SAST were capsule-deficient Hib variants (Hib-minus).
129 patients in the rituximab group demonstrated Hib killing (2 of 14 [14%], 5 of 6 [83%], P < .05).
130 or this conserved Arg residue in determining Hib PS-binding affinity.
131 kappa usage and CDR-3 length, in determining Hib PS-binding affinity.
132      In 1996, after switching to a different Hib conjugate vaccine, DTP-HbOC (which combines diphther
133                                       A DTaP-Hib vaccine evaluated in infants vaccinated at ages 2, 3
134 doses of their infant primary course as DTaP-Hib, compared with two or three doses of another Hib vac
135 ertussis-Haemophilus influenzae type b (DTaP-Hib) conjugate vaccines, 105 infants born at <32 weeks'
136         Despite reduced immunogenicity, DTaP-Hib combination vaccines appear to prime for immunologic
137 cines that contain acellular pertussis (DTaP-Hib).
138 tussis-containing combination vaccines (DTaP-Hib) is unclear.
139 us influenzae type b (DTP/Hib; group 1), DTP/Hib and 7VPnC (group 2), or DTP and 7VPnC/Hib (group 3)
140 pertussis/Haemophilus influenzae type b (DTP/Hib; group 1), DTP/Hib and 7VPnC (group 2), or DTP and 7
141 In industrialized countries with established Hib vaccination programs, however, little is known about
142 es of pneumonia cases and deaths to estimate Hib pneumonia burden.
143 to contribute to the repertoire, we examined Hib PS binding to a series of recombinant Fab fragments
144                   Abs with high affinity for Hib PS from infants, like most mAbs from adults, react o
145 of mAbs from children have high affinity for Hib PS, and the overall variable region gene repertoire
146   As with the recently published finding for Hib-TT complexes, it is the carbohydrate component that
147 pecific BCR sequences have been reported for Hib and TT, which made a vaccine containing these two Ag
148  or had not, respectively, received a fourth Hib conjugate vaccine dose (mean age, 3.9 years).
149 ldren and in those who had received a fourth Hib dose.
150 against the C terminus of HifD and HifE from Hib strain Eagan bound to HifD and HifE proteins, respec
151  Amino acid sequence analysis of pilins from Hib pili and from P-pili expressed on uropathogenic Esch
152 105 infants born at <32 weeks' gestation had Hib IgG geometric mean concentrations (GMCs) and MCC ser
153                        Premature infants had Hib GMCs of 0.27 microg/mL, with 21% achieving GMCs >1.0
154 nus-whole cell pertussis vaccines with HbOC [Hib oligosaccharide CRM197]), cases of invasive Hib dise
155 rn immunoblot analysis of immunoprecipitated Hib pili demonstrated that HifD and HifE copurified with
156                                 Importantly, Hib and Hif resistance against the bactericidal effect o
157 2A, hmwC, and hia genes were not detected in Hib strains.
158 cal studies of mechanisms of interference in Hib/DTaP vaccines.
159 eletion of the gene encoding for PH (lph) in Hib and Hif significantly reduced the interaction betwee
160  decreased after the initiation of an infant Hib vaccine program, perhaps by decreasing Hib carriage
161 (P=.03) after initiation of statewide infant Hib vaccination programs in 1991.
162 e pilus subunits among type b H. influenzae (Hib) and nontypeable H. influenzae (NTHI) strains.
163                                     Invasive Hib disease in England and Wales has been declining sinc
164                                     Invasive Hib disease is no longer a major cause of acute bacteria
165 known about individuals who develop invasive Hib disease.
166 gate vaccines has nearly eradicated invasive Hib disease where the vaccines are used.
167 nd microbiological surveillance for invasive Hib disease (primarily meningitis) in the Western Region
168 NTS: Culture-based surveillance for invasive Hib disease at Kilifi District Hospital from 2000 throug
169  to rapid and sustained declines in invasive Hib disease incidence across all age groups.
170                      An increase in invasive Hib disease incidence in the UK has coincided with the d
171 an 5 years, the annual incidence of invasive Hib disease 1 year before and 1 and 3 years after vaccin
172              Initially, the rate of invasive Hib disease decreased dramatically but has been increasi
173 study describes the epidemiology of invasive Hib disease in England and Wales during 2000-2012 and th
174 s enhanced national surveillance of invasive Hib disease in England and Wales.
175  oligosaccharide CRM197]), cases of invasive Hib disease increased, suggesting ongoing Hib transmissi
176 ylaxis, Guillain-Barre syndrome, or invasive Hib disease.
177 e extremely effective in preventing invasive Hib disease in infants and young children.
178  the carriers and caused 80% of the invasive Hib disease that occurred during April 1996-March 1997.
179  person-years) vs the third dose of DTaP-IPV-Hib (rate, 12.4 per 100 person-years) as the most recent
180 equently received the third dose of DTaP-IPV-Hib (rate, 12.8 per 100 person-years) after MMR, the IRR
181 son-years) after the second dose of DTaP-IPV-Hib (rate, 15.1 per 100 person-years).
182  receipt of live MMR vs inactivated DTaP-IPV-Hib as the most recent vaccine was associated with a low
183 ection, comparing receipt of MMR vs DTaP-IPV-Hib as the most recent vaccine.
184 the alternating limb group received DTaP-IPV-Hib in the left leg at 2 months and in the right leg at
185                                     DTaP-IPV-Hib vaccination was associated with an increased risk of
186 mong 1- to 2-year-olds who received DTaP-IPV-Hib vaccine versus historical comparators (relative risk
187 sed risk was detected among 149,337 DTaP-IPV-Hib vaccinees versus historical comparators for any outc
188 tember 2008-January 2011 to compare DTaP-IPV-Hib vaccinees with historical recipients of other DTaP-c
189                    Vaccination with DTaP-IPV-Hib was not associated with an increased risk of epileps
190  and Haemophilus influenzae type b (DTaP-IPV-Hib) administered at ages 3, 5, and 12 months and MMR at
191 zae type b (Hib) conjugate vaccine (DTaP-IPV-Hib) among children within the Vaccine Safety Datalink p
192 influenzae type b combined vaccine (DTaP-IPV-Hib) at 2, 3, and 4 months of age, and the pneumococcal
193 irus-Haemophilus influenzae type b (DTaP-IPV-Hib) vaccine since September 2002.
194 eceived MMR after the third dose of DTaP-IPV-Hib, MMR (rate, 8.9 per 100 person-years) vs the third d
195 cine repertoire identified a number of known Hib-specific sequences but only one previously described
196  immunogenic in TLR2 KO mice, inducing lower Hib PS IgG and IgM titers compared with those in wild-ty
197 e every year from 2009 to 2012, and measured Hib antibody concentrations in five cross-sectional samp
198 th no junctional residue showed little or no Hib PS binding.
199 ted more to piliated Hib than to nonpiliated Hib or to a mutant containing a hifE gene insertion.
200 accines by engaging TLR2, and the ability of Hib-OMPC to elicit protective levels of Abs after one do
201 ict the effect of combined administration of Hib and DTaP vaccines on Hib immunogenicity and would be
202 ifE of strain Eagan inhibited the binding of Hib to human erythrocytes but did not inhibit the bindin
203 countries include a fourth dose (booster) of Hib vaccine in the second year of life on the basis of d
204                             Global burden of Hib disease is substantial and almost entirely vaccine p
205 3 and December 2001, a total of 443 cases of Hib infection occurred in children eligible for vaccinat
206                                   Control of Hib disease in England and Wales is currently the best t
207  vaccination program enhanced the control of Hib infection in England and Wales.
208 , however, suggesting that a booster dose of Hib vaccine following infant vaccination is not essentia
209 ars following infant priming with 3 doses of Hib conjugate vaccine, anti-PRP IgG geometric mean conce
210 bution, syndrome distribution, and effect of Hib vaccine.
211 sons for this increase, the effectiveness of Hib conjugate vaccine was estimated by use of the screen
212 ity data were used for national estimates of Hib meningitis and non-pneumonia, non-meningitis disease
213 ly correlated with the relative frequency of Hib-specific sequences, indicating that the postvaccinat
214 hildren has led to a decline in incidence of Hib disease in young Alaskan children.
215                             The incidence of Hib meningitis remained low (averaging 1.3 per 100 000 c
216  adults, coinciding with the introduction of Hib vaccination.
217 .001) and coincided with the introduction of Hib vaccination.
218                    In Kenya, introduction of Hib vaccine into the routine childhood immunization prog
219                      Continued monitoring of Hib carriage may provide insights into the epidemiology
220 elop estimates of incidence and mortality of Hib meningitis and serious non-pneumonia, non-meningitis
221 haryngeal carriage is low and the profile of Hib antibodies suggests that protection wanes only after
222 cines have contributed to increased rates of Hib infection.
223 Kenya, use of a three-dose primary series of Hib vaccine without a booster dose has resulted in a sig
224 007 to 2010 was complemented with studies of Hib carriage in children aged 1 to <2 years, Hib antibod
225 omprehensive literature search of studies of Hib disease incidence, case-fatality ratios, age distrib
226                              Expanded use of Hib vaccine could reduce childhood pneumonia and meningi
227                        Conjugate vaccines of Hib PS linked to proteins, such as CRM(197), increase th
228          Widespread vaccination with PRP-OMP Hib conjugate vaccine did not eliminate carriage in this
229                 Phage were selected based on Hib PS binding.
230 ic health priority in Africa because data on Hib disease burden and vaccine effectiveness are scarce.
231 b (Hib) conjugate vaccines and the effect on Hib immunogenicity of combining 2 Hib vaccines (Hib-teta
232 d administration of Hib and DTaP vaccines on Hib immunogenicity and would be suitable for preclinical
233 ve Hib disease increased, suggesting ongoing Hib transmission despite widespread vaccination.
234  either PsA-TT, one-fifth dose of PsACWY, or Hib-TT.
235 ge, a cross-sectional study of oropharyngeal Hib carriage was conducted among Alaska Native children
236 HifE proteins, respectively, of all piliated Hib and NTHI strains tested.
237 E of strain Eagan also bound to all piliated Hib strains but did not bind to the piliated NTHI strain
238  the mature protein reacted more to piliated Hib than to nonpiliated Hib or to a mutant containing a
239 nti-Haemophilus influenzae b polysaccharide (Hib PS) antibodies elicited in elderly subjects followin
240 aemophilus influenzae type b polysaccharide (Hib PS).
241 s influenzae type b capsular polysaccharide (Hib PS) could be studied at the molecular level with pha
242                     Higher baseline and post-Hib-MenC booster responses (anti-PRP IgG and memory B ce
243 utine childhood immunization program reduced Hib disease incidence among children younger than 5 year
244 ic in infants and have significantly reduced Hib infections in the United States, but require multipl
245 n achieved since the introduction of routine Hib vaccination in 1992.
246        After the introduction of the routine Hib conjugate vaccination programme for infants, median
247 pared with 35.5 per 100 000 prior to routine Hib vaccination.
248                                  Spontaneous Hib-PS antibody rises after primary series DTaP-PRP-T-HB
249 to the nasopharynx, where the three-stranded Hib pilus filaments provide a robust tether to withstand
250                                    Sustained Hib conjugate vaccine-induced immunity in children is de
251  fimbriae 2 + 3 (FIMs), diphtheria, tetanus, Hib, MCC and PCV13 serotypes were compared to responses
252                           We calculated that Hib caused about 8.13 million serious illnesses worldwid
253                            We estimated that Hib caused 371,000 deaths (247,000-527,000) in children
254  of electron micrograph images, we show that Hib pili comprise a helix 70 A in diameter with threefol
255                                          The Hib pilus filament has 3.0 subunits per turn, with each
256                                          The Hib-associated case fatality rate was 9.4% (10/106 cases
257 logically and structurally similar among the Hib strains but vary among the NTHI strains.
258 children aged <5 years annually), as did the Hib oropharyngeal carriage rate (0.9%).
259 to 1086327) and found to be the same for the Hib and two Hib(-) strains as well as some other encapsu
260  immunogenic region of the HifA pilin in the Hib pilus structure.
261 ssociated with reduced immunogenicity of the Hib component, although there is little agreement on the
262 d by shifts in the major VL component of the Hib PS-specific repertoire or by diminution of the prote
263 ith the DTaP vaccine used in this study, the Hib GMC of premature infants was extremely low.
264                                         This Hib population was highly clonal, since only 2 strains,
265 pa1 gave equivalent and strongest binding to Hib PS.
266                   Antibody concentrations to Hib and pneumococcal serotypes 14 and 18C were measured
267                      However, in contrast to Hib, infections caused by H. influenzae serotype f (Hif)
268 times their original length, while damage to Hib pili occurs by slight shearing of subunits with resp
269 odies than unexposed infants (n = 54) did to Hib (0.37 [interquartile range {IQR}, 0.22-0.67] mg/L vs
270 le for CD1-restricted T cells in immunity to Hib.
271  = 46) had lower specific antibody levels to Hib (0.67 [IQR, 0.16-1.54] mg/L vs 1.34 [IQR, 0.15-4.82]
272 ntly lower IgM concentrations in response to Hib (P<.05) and to both pneumococcal serotypes 14 (P<.00
273 ociated with the increased susceptibility to Hib disease among individuals carrying the A2b allele.
274 on also proliferated to proteinase K-treated Hib antigen, suggesting that it recognized a nonpeptide.
275 and found to be the same for the Hib and two Hib(-) strains as well as some other encapsulated divisi
276 ccine formulations given to fully vaccinated Hib cases with those administered to fully immunised age
277 ningitidis tetanus toxoid conjugate vaccine (Hib-MenC-TT), administered in the left leg at 12 months.
278 ophilus influenzae type b conjugate vaccine (Hib-TT).
279  immunogenicity of combining 2 Hib vaccines (Hib-tetanus toxoid [TT]-A and Hib-TT-B) with diphtheria-
280 by SAST were capsule-deficient Hib variants (Hib-minus).
281                                         When Hib and Hif PH variants were separately expressed in non
282 duction in the antibody response to PRP when Hib-TT-A was administered in combination with DTaP(3) an
283 vaccinated at 2, 3, and 4 months of age with Hib conjugate vaccine and followed up to 43 and 72 month
284 vaccinated at 2, 3, and 4 months of age with Hib conjugate vaccines, avidity increased in the period
285                 Crowding was associated with Hib carriage.
286                          Of 53 children with Hib admitted during 2002-2005, 29 (55%) were age-ineligi
287 ion status were determined for children with Hib disease admitted 2002-2005.
288 ntroduction, the median age of children with Hib was 8 months; case fatality was 23%.
289 h swabs taken, 46 (9.3%) were colonized with Hib.
290 nus-acellular pertussis (DTaP) combined with Hib-PS conjugated to tetanus toxoid (PRP-T) and hepatiti
291 y anti-Hib PS mAbs of infants immunized with Hib oligosaccharide-diphtheria toxin vaccine vaccine are
292 g anti-Hib PS mAbs of infants immunized with Hib oligosaccharide-diphtheria toxin vaccine.
293 cell response, 19 adults were immunized with Hib-CRM(197), and antibody titers, carrier protein-speci
294  like most mAbs from adults, react only with Hib PS and the structurally similar PS of Escherichia co
295 unized subcutaneously with Hib alone or with Hib and DTaP-based vaccines; anti-Hib capsular polysacch
296  influenzae (NTHi) isolates were probed with Hib cap-gene-containing plasmid pUO38 and with IS1016; a
297      Rats were immunized subcutaneously with Hib alone or with Hib and DTaP-based vaccines; anti-Hib
298                             Vaccination with Hib conjugate vaccine PRP-OMP (polyribosylribitol phosph
299 mentation of routine infant vaccination with Hib polysaccharide-tetanus protein conjugate (PRP-T) vac
300 Hib carriage in children aged 1 to <2 years, Hib antibody levels in children aged <5 years, and Hib v

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