» Articles » PMID: 27272940

Protective Effects of a Modified Vaccinia Ankara-based Vaccine Candidate Against Crimean-Congo Haemorrhagic Fever Virus Require Both Cellular and Humoral Responses

Overview
Journal PLoS One
Date 2016 Jun 9
PMID 27272940
Citations 46
Authors
Affiliations
Soon will be listed here.
Abstract

Crimean-Congo Haemorrhagic Fever (CCHF) is a severe tick-borne disease, endemic in many countries in Africa, the Middle East, Eastern Europe and Asia. There is no approved vaccine currently available against CCHF. The most promising candidate, which has previously been shown to confer protection in the small animal model, is a modified Vaccinia Ankara virus vector expressing the CCHF viral glycoprotein (MVA-GP). It has been shown that MVA-GP induces both humoral and cellular immunogenicity. In the present study, sera and T-lymphocytes were passively and adoptively transferred into recipient mice prior to challenge with CCHF virus. Results demonstrated that mediators from both arms of the immune system were required to demonstrate protective effects against lethal challenge.

Citing Articles

Recombinant Vaccine Production: Production of a Recombinant CCHF MVA Vaccine.

Kennedy E, Hewson R, Dowall S Methods Mol Biol. 2024; 2893:257-272.

PMID: 39671043 DOI: 10.1007/978-1-0716-4338-9_19.


The Role of Nucleocapsid Protein (NP) in the Immunology of Crimean-Congo Hemorrhagic Fever Virus (CCHFV).

Pirincal A, Doymaz M Viruses. 2024; 16(10).

PMID: 39459881 PMC: 11512346. DOI: 10.3390/v16101547.


Interventions for the control of Crimean-Congo hemorrhagic fever and tick vectors.

de la Fuente J, Ghosh S, Lempereur L, Garrison A, Sprong H, Lopez-Camacho C NPJ Vaccines. 2024; 9(1):181.

PMID: 39353956 PMC: 11445411. DOI: 10.1038/s41541-024-00970-5.


Cellular immunity to nucleoproteins (NP) of Crimean-Congo hemorrhagic fever virus (CCHFV) and Hazara Virus (HAZV).

Kalkan-Yazici M, Karaaslan E, Guler-Cetin N, Doymaz M Med Microbiol Immunol. 2024; 213(1):20.

PMID: 39320473 DOI: 10.1007/s00430-024-00802-2.


Vaccine approaches and treatment aspects against Crimean Congo hemorrhagic fever.

Sarmadi S, Ghalyanchilangeroudi A, Najafi H Virusdisease. 2024; 35(2):377-383.

PMID: 39071873 PMC: 11269551. DOI: 10.1007/s13337-024-00868-9.


References
1.
Arda B, Aciduman A, Johnston J . A randomised controlled trial of ribavirin in Crimean Congo haemorrhagic fever: ethical considerations. J Med Ethics. 2011; 38(2):117-20. DOI: 10.1136/medethics-2011-100107. View

2.
Ascioglu S, Leblebicioglu H, Vahaboglu H, Chan K . Ribavirin for patients with Crimean-Congo haemorrhagic fever: a systematic review and meta-analysis. J Antimicrob Chemother. 2011; 66(6):1215-22. DOI: 10.1093/jac/dkr136. View

3.
Schmaljohn C, Parker M, Ennis W, Dalrymple J, Collett M, Suzich J . Baculovirus expression of the M genome segment of Rift Valley fever virus and examination of antigenic and immunogenic properties of the expressed proteins. Virology. 1989; 170(1):184-92. DOI: 10.1016/0042-6822(89)90365-6. View

4.
Buttigieg K, Dowall S, Findlay-Wilson S, Miloszewska A, Rayner E, Hewson R . A novel vaccine against Crimean-Congo Haemorrhagic Fever protects 100% of animals against lethal challenge in a mouse model. PLoS One. 2014; 9(3):e91516. PMC: 3951450. DOI: 10.1371/journal.pone.0091516. View

5.
Du X, Jin R, Ning N, Li L, Wang Q, Liang W . In vivo distribution and antitumor effect of infused immune cells in a gastric cancer model. Oncol Rep. 2012; 28(5):1743-9. DOI: 10.3892/or.2012.2013. View