A recombinant prime, peptide boost vaccination strategy can focus the immune response on to more than one epitope even though these may not be immunodominant in the complex immunogen

Vaccine ◽  
1997 ◽  
Vol 15 (15) ◽  
pp. 1661-1669 ◽  
Author(s):  
David Davis ◽  
Bror Morein ◽  
Lennart Åkerblom ◽  
Karin Lövgren-Bengtsson ◽  
Mariëlle E. van Gils ◽  
...  
2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Yuan Gu ◽  
Bin Zhan ◽  
Yaping Yang ◽  
Xiaodi Yang ◽  
Xi Zhao ◽  
...  

Trichinellosis is a widespread zoonosis primarily caused byTrichinella spiralis. Mucosal immunity is crucial for preventingTrichinella spiralisinfection. In our previous study, a DNA vaccine with theTrichinellaantigen Ts87 delivered by an attenuatedSalmonella typhimuriumelicited partial protection againstTrichinella spiralisinfection in mice. In the current study, to elicit a more robust immune response and develop a potent vaccination strategy against trichinellosis, a heterologous prime-boost vaccination regimen for Ts87 was used in mice and the protective efficacy was evaluated compared to the homologous DNA prime-boost or protein prime-boost immunization alone. The results revealed that the DNA-prime/protein-boost vaccination with Ts87 induced higher levels of both humoral and cellular immune responses. The challenge results showed that mice with the DNA-prime/protein-boost vaccination displayed higher muscle larval reduction than those immunized with DNA prime-boost or protein prime-boost. The results demonstrated that mice vaccinated with Ts87 in a DNA-prime/protein-boost strategy effectively elicited a local IgA response and mixed Th1/Th2 immune response that might be responsible for improved protection againstTrichinella spiralisinfection.


2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Ernesta Cavalcanti ◽  
Maria Antonietta Isgrò ◽  
Domenica Rea ◽  
Lucia Di Capua ◽  
Giusy Trillò ◽  
...  

Abstract Background Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection and the resulting disease, coronavirus disease 2019 (COVID-19), have spread to millions of people globally, requiring the development of billions of different vaccine doses. The SARS-CoV-2 spike mRNA vaccine (named BNT162b2/Pfizer), authorized by the FDA, has shown high efficacy in preventing SARS-CoV-2 infection after administration of two doses in individuals 16 years of age and older. In the present study, we retrospectively evaluated the differences in the SARS-CoV-2 humoral immune response after vaccine administration in the two different cohorts of workers at the INT - IRCCS “Fondazione Pascale” Cancer Center (Naples, Italy): previously infected to SARS-CoV-2 subjects and not infected to SARS-CoV-2 subjects. Methods We determined specific anti-RBD (receptor-binding domain) titers against trimeric spike glycoprotein (S) of SARS-CoV-2 by Roche Elecsys Anti-SARS-CoV-2 S immunoassay in serum samples of 35 healthcare workers with a previous documented history of SARS-CoV-2 infection and 158 healthcare workers without, after 1 and 2 doses of vaccine, respectively. Moreover, geometric mean titers and relative fold changes (FC) were calculated. Results Both previously infected and not infected to SARS-CoV-2 subjects developed significant immune responses to SARS-CoV-2 after the administration of 1 and 2 doses of vaccine, respectively. Anti-S antibody responses to the first dose of vaccine were significantly higher in previously SARS-CoV-2-infected subjects in comparison to titers of not infected subjects after the first as well as the second dose of vaccine. Fold changes for subjects previously infected to SARS-CoV-2 was very modest, given the high basal antibody titer, as well as the upper limit of 2500.0 BAU/mL imposed by the Roche methods. Conversely, for naïve subjects, mean fold change following the first dose was low ($$ \overline{x} $$ x ¯ =1.6), reaching 3.8 FC in 72 subjects (45.6%) following the second dose. Conclusions The results showed that, as early as the first dose, SARS-CoV-2-infected individuals developed a remarkable and statistically significant immune response in comparison to those who did not contract the virus previously, suggesting the possibility of administering only one dose in previously SARS-CoV-2-infected subjects. FC for previously infected subjects should not be taken into account for the generally high pre-vaccination values. Conversely, FC for not infected subjects, after the second dose, were = 3.8 in > 45.0% of vaccinees, and ≤ 3.1 in 19.0%, the latter showing a potential susceptibility to further SARS-CoV-2 infection.


Vaccine ◽  
2006 ◽  
Vol 24 (31-32) ◽  
pp. 5852-5861 ◽  
Author(s):  
Wen-Tssann Liu ◽  
Wei-Ting Lin ◽  
Chung-Chin Tsai ◽  
Chuan-Chang Chuang ◽  
Chin-Len Liao ◽  
...  

Vaccine ◽  
2004 ◽  
Vol 23 (6) ◽  
pp. 819-826 ◽  
Author(s):  
Ghislaine Gallez-Hawkins ◽  
Xiuli Li ◽  
Anne E. Franck ◽  
Lia Thao ◽  
Simon F. Lacey ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (9) ◽  
pp. e74820 ◽  
Author(s):  
Rachel Buglione-Corbett ◽  
Kimberly Pouliot ◽  
Robyn Marty-Roix ◽  
Kim West ◽  
Shixia Wang ◽  
...  

2004 ◽  
Vol 85 (2) ◽  
pp. 409-413 ◽  
Author(s):  
Ann Jaffray ◽  
Enid Shephard ◽  
Joanne van Harmelen ◽  
Carolyn Williamson ◽  
Anna-Lise Williamson ◽  
...  

Human immunodeficiency virus type 1 (HIV-1) subtype C is the predominant HIV in southern Africa, and is the target of a number of recent vaccine candidates. It has been proposed that a heterologous prime/boost vaccination strategy may result in stronger, broader and more prolonged immune responses. Since HIV-1 Gag Pr55 polyprotein can assemble into virus-like particles (VLPs) which have been shown to induce a strong cellular immune response in animals, we showed that a typical southern African subtype C Pr55 protein expressed in insect cells via recombinant baculovirus could form VLPs. We then used the baculovirus-produced VLPs as a boost to a subtype C HIV-1 gag DNA prime vaccination in mice. This study shows that a low dose of HIV-1 subtype C Gag VLPs can significantly boost the immune response to a single subtype C gag DNA inoculation in mice. These results suggest a possible vaccination regimen for humans.


2021 ◽  
Author(s):  
Francisco Raposo ◽  
Giuseppe Lippi

Abstract Objectives The main purpose of this study was to evaluate the anti-SARS-CoV-2 RBD Ig G antibody response in BNT162b2 vaccine recipients who erroneously received vaccine overdose. Methods Measurement of antibody levels at different time-points was performed to define the dynamics of immunization after a wrongly vaccination schedule. Three recipients had no previous evidence of infection and received the first shot of Oxford/AstraZeneca before the Pfizer/BioNTech vaccine. Another patient, formerly infected by SARS-CoV-2, received one shot of BNT162b2 vaccine. Results At day 6 after the second vaccine dose the serum increase of anti-SARS-CoV-2 RBD Ig G antibodies was analogous for the three SARS-CoV-2 naïve recipients. At 14 days the antibody level increased and reached a peak, though displaying a different pattern among the three recipients. At 21 days the serum antibody level started to decrease from its maximum value. The data for the previously infected recipient were in agreement with values found in COVID-19 positive receivers. Thus, after the single prime-dose of vaccine, the elicited antibody response was similar to prime-boost vaccination in naïve recipients. Conclusions This study confirms the efficiency of the BNT162b vaccine in eliciting a sustained antibody response as heterologous boost-vaccine in previously Oxford/AstraZeneca vaccinated recipients, as well as, prime-vaccine in COVID-19 infected receivers. Importantly, the humoral immunity response of recipients was not proportional to the vaccine overdose. Nonetheless, we cannot portray a univocal effect of vaccine overdose concerning anti-SARS-CoV-2 antibody response because the values found especially in the three SARS-CoV-2 naïve subjects were highly heterogeneous.


2002 ◽  
Vol 76 (15) ◽  
pp. 7910-7912 ◽  
Author(s):  
Diane E. Webster ◽  
Michelle L. Cooney ◽  
Zhongjun Huang ◽  
Damien R. Drew ◽  
Ian A. Ramshaw ◽  
...  

ABSTRACT Despite eradication attempts, measles remains a global health concern. Here we report results that demonstrate that a single-dose DNA immunization followed by multiple boosters, delivered orally as a plant-derived vaccine, can induce significantly greater quantities of measles virus-neutralizing antibodies than immunization with either DNA or plant-derived vaccines alone. This represents the first demonstration of an enhanced immune response to a prime-boost vaccination strategy combining a DNA vaccine with edible plant technology.


PLoS ONE ◽  
2012 ◽  
Vol 7 (4) ◽  
pp. e34735 ◽  
Author(s):  
Eva Calvo-Pinilla ◽  
Nicolás Navasa ◽  
Juan Anguita ◽  
Javier Ortego

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