Selection and Monitoring of Patients for Immunotherapy (Peptide Vaccines)

2015 ◽  
pp. 63-84
Author(s):  
Xiao Liu ◽  
Justin Kline
Keyword(s):  
2020 ◽  
Vol 17 ◽  
Author(s):  
Anam Naz ◽  
Tahreem Zaheer ◽  
Hamza Arshad Dar ◽  
Faryal Mehwish Awan ◽  
Ayesha Obaid ◽  
...  

Background: Helicobacter pylori infection and its treatment still remains a challenge to human health worldwide. A variety of antibiotics and combination therapies are currently used to treat H. pylori induced ulcers and carcinoma; however, no effective treatment is available to eliminate the pathogen from the body. Additionally, antibiotic resistance is also one of the main reasons for prolonged and persistent infection. Aim of the study: Until new drugs are available for this infection, vaccinology seems the only alternative opportunity to exploit against H. pylori induced diseases. Methods: Multiple epitopes prioritized in our previous study have been tested for their possible antigenic combinations, and results in 169-mer and 183-mer peptide vaccines containing the amino acid sequences of 3 and 4 epitopes respectively, along with adjuvant (Cholera Toxin Subunit B adjuvant at 5’ end) and linkers (GPGPG and EAAAK). Results: Poly-epitope proteins proposed as potential vaccine candidates against H. pylori include SabAHP0289-Omp16-VacA (SHOV), VacA-Omp16-HP0289-FecA (VOHF), VacA-Omp16-HP0289-SabA (VOHS), VacA-Omp16-HP0289-BabA (VOHB), VacA-Omp16-HP0289-SabA-FecA (VOHSF), VacAOmp16-HP0289-SabA-BabA (VOHSB) and VacA-Omp16-HP0289-BabA-SabA (VOHBS). Structures of these poly-epitope peptide vaccines have been modelled and checked for their affinity with HLA alleles and receptors. These proposed poly-epitope vaccine candidates bind efficiently with A2, A3, B7 and DR1 superfamilies of HLA alleles. They can also form stable and significant interactions with Toll-like receptor 2 and Toll-like receptor 4. Conclusion: Results suggest that these multi-epitopic vaccines can elicit a significant immune response against H. pylori and can be tested further for efficient vaccine development.


Vaccine ◽  
1994 ◽  
Vol 12 (9) ◽  
pp. 776-782 ◽  
Author(s):  
H NARUSE ◽  
K OGASAWARA ◽  
K TAKAMI ◽  
K KAJINO ◽  
T GOTOHDA ◽  
...  

2014 ◽  
Vol 123 (3) ◽  
pp. 433-440 ◽  
Author(s):  
Adam M. Swartz ◽  
Kristen A. Batich ◽  
Peter E. Fecci ◽  
John H. Sampson
Keyword(s):  

2017 ◽  
Vol 5 (3) ◽  
pp. 222-233 ◽  
Author(s):  
Eleni Maria Varypataki ◽  
Naomi Benne ◽  
Joke Bouwstra ◽  
Wim Jiskoot ◽  
Ferry Ossendorp

2017 ◽  
Vol 13 (8) ◽  
pp. 2463-2474 ◽  
Author(s):  
Kai Schulze ◽  
Thomas Ebensen ◽  
Saranya Chandrudu ◽  
Mariusz Skwarczynski ◽  
Istvan Toth ◽  
...  

Author(s):  
Anurag Singh ◽  
Anand Maurya ◽  
Gaurav Mishra ◽  
Rajendra Awasthi ◽  
Kamal Dua ◽  
...  

Background: The novel coronavirus 2019 (COVID-19) infection has caused the global emergence of coronavirus in humans during the last 12 months. Till May 11, 2021, the confirmed global COVID-19 cases and deaths reached 158551526 and 3296855, respectively. Methods: Goblet cells and ciliated cells in the nose act as the initial infection site of SARS-CoV-2. Thus, mucus immunity is important to protect from infection. The outburst of SARS-CoV-2 infection can be halted only when an effective vaccine will be developed. Results: Globally, over 100 different vaccines are under investigation, including DNA vaccines, RNA vaccines, inactivated virus vaccines, adenovirus-based vaccines, recombinant/ subunit protein vaccines, peptide vaccines, and virus-like particles etc. Inactivated virus vaccines and mRNA, and adenovirus-based vaccines have moved fast into clinical trials. Conclusion: : Vaccines containing spike protein of SARS-CoV as subunit could effectively prevent binding of coronavirus to the host cell and membrane fusion. Thus, spike protein can be used as a major target for subunit vaccine preparation.


Hepatitis B ◽  
1984 ◽  
pp. 215-224 ◽  
Author(s):  
G. R. Dreesman ◽  
I. Ionescu-Matiu ◽  
Y. Sanchez ◽  
R. C. Kennedy ◽  
J. T. Sparrow ◽  
...  

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