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1 CoV-2 infection after vaccination (so-called breakthrough infection).
2 -CoV-2-specific antibody response had a mild breakthrough infection.
3 d increase and 3.1-fold decrease for Omicron breakthrough infection.
4 lter booster administration in response to a breakthrough infection.
5 neutralizing-antibody response after Omicron breakthrough infection.
6 vaccination, natural protection, and vaccine breakthrough infection.
7 including vaccination, primary infection and breakthrough infection.
8 nity is the most likely explanation for this breakthrough infection.
9 s following vaccination and possible risk of breakthrough infection.
10 was seen only among HTx recipients with CMV breakthrough infection.
11 eviously, we identified 2 women with vaccine breakthrough infection.
12 atly reduced in fully vaccinated people with breakthrough infection.
13 vely in vaccinees who experienced SARS-CoV-2 breakthrough infection.
14 er diagnosis, and 39 109 (14.8%) developed a breakthrough infection.
15 doses of mRNA vaccine with or without alpha breakthrough infection.
16 of 5.9 months, 68 (2.5%) participants had a breakthrough infection.
17 sed to low-level replication as the cause of breakthrough infection.
18 .16; 95% CI, 1.96-2.38) had a higher rate of breakthrough infection.
19 RS-CoV-2-specific antibodies and experienced breakthrough infection.
20 an efficacious HIV/AIDS vaccine, even after breakthrough infection.
21 was seen only among HTx recipients with CMV breakthrough infection.
22 immune responses in vaccinated hosts during breakthrough infection.
23 will be crucial to identify the mechanism of breakthrough infections.
24 -CoV and WIV-1 challenge in mice resulted in breakthrough infections.
25 ferring varying levels of protection against breakthrough infections.
26 hallenge with a higher dose, however, led to breakthrough infections.
27 dented transmissibility and ability to cause breakthrough infections.
28 iants of concern have emerged that can cause breakthrough infections.
29 S-CoV-2 are needed to anticipate the risk of breakthrough infections.
30 2 variants, may account for reinfections and breakthrough infections.
31 f multiple innate immune cell subsets during breakthrough infections.
32 June 2021, of which 125 (9.1%) were vaccine breakthrough infections.
33 kthrough infections, and mRNA-1273 (Moderna) breakthrough infections.
34 tant and thus more likely to lead to vaccine breakthrough infections.
35 pose to higher acute viremia in the event of breakthrough infections.
36 n, similar to results with 2022 CP from BA.1 breakthrough infections.
37 COVID-19 vaccine-induced seropositivity and breakthrough infections.
38 ffectiveness of two-dose vaccination against breakthrough infections.
39 cluding for most patients who had SARS-CoV-2 breakthrough infections.
40 ur results may help to improve prediction of breakthrough infections.
41 a combination of widespread vaccination and breakthrough infections.
42 ralizing antibody titers, suggesting ongoing breakthrough infections.
43 bly explaining suppressed viremia in vaccine breakthrough infections.
44 cination were at markedly decreased risk for breakthrough infections.
45 uced immune responses and protection against breakthrough infections.
46 ults in improved early disease parameters in breakthrough infections.
47 well as durably control viral replication in breakthrough infections.
48 y of the gamma -spz could explain occasional breakthrough infections.
49 alysed; only three were classified as "true" breakthrough infections.
50 -2.06) across the range of uncertainty about breakthrough infections.
51 t who cannot be vaccinated or who experience breakthrough infections.
52 .88]) were associated with increased risk of breakthrough infections.
53 generally higher than those against BA.1 in breakthrough infections.
54 humans to antibody-dependent enhanced (ADE) breakthrough infections?
56 ed in all ages and were marginally lower for breakthrough infections, 2.33 (95% CI [1.96, 2.76]; p <
58 similar total anti-FLS IgG levels following breakthrough infection, 4-fold higher plasma concentrati
59 a higher proportion of asymptomatic or mild breakthrough infections (55.0% versus 28.6%, respectivel
62 r thrice vaccinated individuals with omicron breakthrough infection; a 46-fold increase in plasma neu
64 n was associated with a 28% reduced risk for breakthrough infection (adjusted IRR [AIRR], 0.72; 95% C
65 ogic malignancies were at increased risk for breakthrough infections (adjusted OR ranged from 2.07 fo
67 ction IgG levels in the 40 participants with breakthrough infection after dose 2 were similar to leve
69 ased awakening frequency was associated with breakthrough infection after the 1st booster with 3.01 +
72 BNT162b2 COVID-19 vaccine had a low risk of breakthrough infection after up to 8 months of follow-up
73 ciated with an increased risk for SARS-CoV-2 breakthrough infection after vaccination, but no studies
75 reduction in risk of all-cause mortality for breakthrough infection among CLD patients with cirrhosis
76 a statistically significantly lower risk for breakthrough infection among individuals receiving the B
77 ociation of BA.4/BA.5 with increased risk of breakthrough infection among previously vaccinated or in
78 avirus 2 (SARS-CoV-2) Omicron variant causes breakthrough infections among convalescent patients and
79 immune responses, and the high incidence of breakthrough infections among vaccinated individuals hig
80 red in 13 patients (4%), including 1 case of breakthrough infection and 12 relapses, and was associat
83 the success of Omicron subvariants to cause breakthrough infection and reinfection may in part be du
85 mune suppression had a higher risk of severe breakthrough infection and should be included in groups
86 memory T cell populations occurs early after breakthrough infection and suggests that CD8(+) T cells
87 NT162b2 vaccine, examining their relation to breakthrough infections and immune imprinting in the con
90 acute seronegative HIV infection and in PrEP breakthrough infections and that FTC is associated with
91 l lenacapavir resistance given the rarity of breakthrough infections and the reduced replication capa
92 inst emerging variants and the prevention of breakthrough infections and transmission remain elusive.
94 2799 (69%) were unvaccinated, 475 (12%) were breakthrough infections, and 782 (19%) had unknown vacci
95 ns, reinfections, BNT162b2 (Pfizer-BioNTech) breakthrough infections, and mRNA-1273 (Moderna) breakth
97 ing immunity from infection and vaccination, breakthrough infections are becoming increasingly common
99 ections, variant viruses continue to emerge, breakthrough infections are frequent, and vaccine hesita
100 is connected to people who are unvaccinated, breakthrough infections are increasingly frequent for in
106 r was associated with increased incidence of breakthrough infection, both in models adjusted for pote
107 oV-2 variants and whether vaccination and/or breakthrough infection (BTI) can elicit antibodies capab
109 V-2 Delta variant was weakly associated with breakthrough infection, but several potential nonlineage
110 gest medical center in Israel, we identified breakthrough infections by performing extensive evaluati
112 duals and the later clinical consequences of breakthrough infection can provide insight into strategi
114 , we identified 1728 vaccinated persons with breakthrough infection (cases) and 1728 propensity score
117 show higher mean Ct value in all cohorts of breakthrough infections compared to the cohort of primar
118 he 150-150 mg dose had a higher incidence of breakthrough infections compared to those who received t
120 d evasion of humoral immunity from BA.1/BA.2 breakthrough-infection convalescent plasma but greater e
122 low-frequency alleles) were associated with breakthrough infection, defined as SARS-CoV-2 infection
127 were less likely to experience PCR-confirmed breakthrough infection during the ancestral SARS-CoV-2 v
128 wer among participants who later experienced breakthrough infection during the Delta surge (median, 2
129 h lower antibody levels were associated with breakthrough infection during the Delta surge, no signif
130 5% CI, 3.7-11.1) compared with those without breakthrough infection during the Omicron surge (median,
133 ination followed by viral infection, such as breakthrough infection, eosinophils have been linked to
135 Importantly, sera from people who had XBB breakthrough infection exhibited robust neutralizing act
136 ctories after a third/booster vaccination or breakthrough infection following second vaccination in 1
137 booster were contrasted against 9824 vaccine-breakthrough infections following a bivalent mRNA booste
138 x, and previous infection, hazard ratios for breakthrough infection for having twice the immunologica
139 cinated hosts, key features that distinguish breakthrough infection from both Type 1- and Type 2-skew
141 methods and tools applicable to analysis of breakthrough infection genomes in general vaccine effica
142 continued gel dosing postinfection, neither breakthrough infection had evidence of drug resistance b
143 accinated patients, vaccinated patients with breakthrough infections had a higher percentage of antig
144 vaccinated patients with confirmed COVID-19 breakthrough infections had lower rates of true-positive
147 ry syndrome coronavirus 2 (SARS-CoV-2), rare breakthrough infections have been reported, including in
148 lution of new variants and the occurrence of breakthrough infections highlight the need for new and e
151 nfections, vs 6.7% and 1.3% in those without breakthrough infections (HR for hospitalization: 13.48;
152 ion against infection, leaving the extent of breakthrough infections (i.e., disease ameliorated but i
153 y towards vaccines and common occurrence of "breakthrough" infections (i.e., infections of vaccinated
155 host are consistent with clinical reports on breakthrough infection in anti-HBs-positive patients inf
157 trends, outcomes and disparities of COVID-19 breakthrough infection in fully vaccinated SUD patients
158 unted serologic reactivity; investigation of breakthrough infection in PrEP users; and potentially fo
159 nses up to six months following Omicron BA.1 breakthrough infection in six mRNA-vaccinated individual
164 S-CoV-2 vaccine-induced immune responses and breakthrough infections in patients with inflammatory bo
165 or vaccination to monitor formerly unnoticed breakthrough infections in the population as well as to
166 of the first complete-genome analysis of the breakthrough infections in the RV144 trial, this work de
167 unvaccinated persons, there were 2332 (0.5%) breakthrough infections in the vaccinated group and 40 5
168 (HCWs) in Israel, a high rate of SARS-CoV-2 breakthrough infections in this group was observed durin
171 s the importance of comprehensive studies of breakthrough infections in vaccine trials to determine w
176 examine if sleep metrics predicted COVID-19 breakthrough infection independent of age and gender.
179 g immunocompetent, unboosted patients, Delta breakthrough infections induced 10.8-fold higher titers
180 investigated through sieve analysis of HIV-1 breakthrough infections (infected vaccine and placebo re
181 at eosinophilic recruitment during influenza breakthrough infection is non-pathological and represent
183 etroviral resistance selected by PrEP during breakthrough infections is important because of the risk
184 Prior vaccination followed by Delta or BA.1 breakthrough infections led to a high degree of cross-re
187 mmunity against SARS-CoV-2 following Omicron breakthrough infection manifests significantly less ADCC
189 yield lower, shorter-term protection against breakthrough infection (median 22.4 mo and 5 to 95% quan
190 95% CI, 1.8-2.9) compared with those without breakthrough infection (median, 5.8; 95% CI, 5.5-6.1) (P
191 ically yield more durable protection against breakthrough infections (median 29.6 mo; 5 to 95% quanti
192 e we studied six AMP trial participants with breakthrough infections mediated by multiple viral linea
194 utrophil extracellular traps in the lungs of breakthrough infection mice, in contrast with allergic s
196 orbid conditions, and those with vaccination breakthrough infections must be interpreted in the conte
197 going uncertainties about virus variants and breakthrough infections necessitate continued vigilance
199 Although multiple vaccines are available, breakthrough infections occur especially by emerging var
201 high-risk hematological disorders; however, breakthrough infections occur, and the reasons for treat
203 nsights into the potential mechanisms behind breakthrough infections occurred even after the vaccinat
206 ce indexes was observed in participants with breakthrough infections occurring after specimen collect
207 nse were at much greater risk for SARS-CoV-2 breakthrough infection (odds ratio [OR], 3.05; 95% CI, 1
208 ry to ensure persistent immunity to minimize breakthrough infections of COVID-19, due to newly emergi
212 variant-specific epitopes induced following breakthrough infection or bivalent vaccination can bridg
213 ation monitoring may be required to minimize breakthrough infection or relapsing mucormycosis associa
214 ata suggest that two vaccine doses and delta breakthrough infection or three vaccine doses and option
217 otherapy (aOR, 2.71; CI, 2.27-3.24) prior to breakthrough infection, or leukemias or lymphomas (aOR,
218 increased hospitalization and mortality from breakthrough infections, our findings have implications
219 durability of immunity and the likelihood of breakthrough infections over time following vaccination
220 er and frail males may be more vulnerable to breakthrough infections owing to low antibody responses
222 spite high vaccine coverage with evidence of breakthrough infections, posing significant challenges t
225 cine type (OR, 0.72; 95% CI, .51-.99), while breakthrough infection prior to the fourth dose (OR, 3.6
226 SARS-CoV-2 vaccination, whether boosters or breakthrough infections provide greater protection again
229 ys, which could account for the high vaccine breakthrough infection rates and limited duration of vac
230 cine breakthrough infections and showed >15% breakthrough infection rates during the Omicron wave sta
234 Decreased antibody responses in Omicron breakthrough infections relative to Delta were potential
238 antify the extent to which uncertainty about breakthrough infections results in uncertainty about vac
242 ination dose: primary outcome was SARS-CoV-2 breakthrough infection; secondary outcomes were emergenc
245 dentified 10 genomic regions associated with breakthrough infection (SLC6A20, ST6GAL1, MUC16, FUT6, M
246 ion from severe disease and hospitalization, breakthrough infections still occur, most likely due to
247 n had substantially higher risk for COVID-19 breakthrough infection than those without such a conditi
248 cer within the past year had higher risk for breakthrough infections than those who did not (HR, 1.24
249 the COVID-19 pandemic, most infections are "breakthrough" infections that occur in individuals with
250 rthermore, using the serum from BA.1 vaccine breakthrough infections, there are, likewise, significan
252 a symptomatic fully vaccinated patient with breakthrough infection to household contacts was suspect
254 vaccines and subsequently increased risk for breakthrough infections, underscoring the need for addit
258 cancer had significantly increased risk for breakthrough infections vs patients without cancer (HR,
259 .6% and 3.9%, respectively, in patients with breakthrough infections, vs 6.7% and 1.3% in those witho
262 Overall, the incidence rate for COVID-19 breakthrough infection was 5.0 per 1000 person-months am
264 -19 breakthrough illness within 28 days of a breakthrough infection was low among vaccinated PWH and
267 icant age, gender and ethnic disparities for breakthrough infection were observed in vaccinated SUD p
268 tection against Omicron BA.4/5 infection and breakthrough infections were associated with higher leve
272 ved between the two vaccines, although fewer breakthrough infections were detected in the BA.5-vaccin
273 type and BA.5 vaccine-boosted animals, fewer breakthrough infections were detected in the BA.5-vaccin
276 Antibody level trajectories and frequency of breakthrough infections were evaluated by tumor type and
277 es available for serologic analyses, vaccine breakthrough infections were found to be associated with
278 e followed up through 14 months, and vaccine breakthrough infections were identified by increasing le
281 ccine no longer offered good protection, and breakthrough infections were observed in all animals and
282 on of Wuhan-Hu-1 persisted following Omicron breakthrough infection, which increased IgG avidity agai
283 larpGAP was completely attenuated showing no breakthrough infections while efficiently inducing high-
284 ose with COVID-19 before vaccination or with breakthrough infections who had blood samples and sympto
285 mia while receiving ganciclovir; 3 (20%) had breakthrough infection with all three methods, including
287 tudy, rhesus macaques, after vaccination and breakthrough infection with homologous simian-human immu
288 days of follow-up (adjusted hazard ratio for breakthrough infection with prior infection, 0.18 [95% C
289 39%) of 36 volunteers subsequently developed breakthrough infection with the omicron variant after di
291 n status was known, a substantial number had breakthrough infections with Delta or Omicron variants (
294 nated health care workers, the occurrence of breakthrough infections with SARS-CoV-2 was correlated w
297 ID-19) vaccine antibody response and risk of breakthrough infection, with implications for future vac
298 re associated with an increased incidence of breakthrough infection, with the highest relative risk o