» Articles » PMID: 31368828

Immunological Considerations in the Development of Vaccines

Overview
Date 2019 Aug 2
PMID 31368828
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

is an opportunistic human pathogen capable of causing a wide range of potentially life-threatening infections. With multidrug-resistant infections on the rise, the need for a rationally-designed vaccine against this pathogen is critical. A number of vaccine platforms have shown promising results in pre-clinical studies, but no vaccine has successfully advanced to licensure. Growing evidence suggests that an effective vaccine may require Th17-type CD4 T cells to prevent infection. In this review, we summarize recent pre-clinical studies of vaccines, specifically focusing on those that induce Th17-type cellular immunity. We also highlight the importance of adjuvant selection and immunization route in vaccine design in order to target vaccine-induced immunity to infected tissues. Advances in cellular immunology and adjuvant biology may ultimately influence better vaccine platforms that can protect targeted human populations.

Citing Articles

Proteomic approach to identify host cell attachment proteins provides protective Pseudomonas aeruginosa vaccine antigen FtsZ.

Jurado-Martin I, Tomas-Cortazar J, Hou Y, Sainz-Mejias M, Mysior M, Sadones O NPJ Vaccines. 2024; 9(1):204.

PMID: 39468053 PMC: 11519640. DOI: 10.1038/s41541-024-00994-x.


A multiantigenic antibacterial nanovaccine utilizing hybrid membrane vesicles for combating Pseudomonas aeruginosa infections.

Peng X, Luo Y, Yang L, Yang Y, Yuan P, Chen X J Extracell Vesicles. 2024; 13(10):e12524.

PMID: 39400457 PMC: 11472236. DOI: 10.1002/jev2.12524.


Exploiting immunopotential PAPI-1 encoded type IVb major pilin targeting .

Arefian Jazi M, Hajikhani B, Goudarzi M, Ebrahimipour G Heliyon. 2024; 10(17):e36859.

PMID: 39281519 PMC: 11401190. DOI: 10.1016/j.heliyon.2024.e36859.


A computational approach to developing a multi-epitope vaccine for combating Pseudomonas aeruginosa-induced pneumonia and sepsis.

Roy S, Biswas M, Foyzur Raman M, Hasan R, Rahmann Z, Uddin P K M Brief Bioinform. 2024; 25(5).

PMID: 39133098 PMC: 11318047. DOI: 10.1093/bib/bbae401.


Development of a nano-emulsion based multivalent protein subunit vaccine against .

Howlader D, Mandal R, Lu T, Maiti S, Dietz Z, Das S Front Immunol. 2024; 15:1372349.

PMID: 38698863 PMC: 11063228. DOI: 10.3389/fimmu.2024.1372349.


References
1.
Muranski P, Borman Z, Kerkar S, Klebanoff C, Ji Y, Sanchez-Perez L . Th17 cells are long lived and retain a stem cell-like molecular signature. Immunity. 2011; 35(6):972-85. PMC: 3246082. DOI: 10.1016/j.immuni.2011.09.019. View

2.
Pier G . Promises and pitfalls of Pseudomonas aeruginosa lipopolysaccharide as a vaccine antigen. Carbohydr Res. 2003; 338(23):2549-56. DOI: 10.1016/s0008-6215(03)00312-4. View

3.
Kolls J, Linden A . Interleukin-17 family members and inflammation. Immunity. 2004; 21(4):467-76. DOI: 10.1016/j.immuni.2004.08.018. View

4.
Doring G, Pier G . Vaccines and immunotherapy against Pseudomonas aeruginosa. Vaccine. 2008; 26(8):1011-24. DOI: 10.1016/j.vaccine.2007.12.007. View

5.
Manni M, Ding W, Stohl L, Granstein R . Muramyl dipeptide induces Th17 polarization through activation of endothelial cells. J Immunol. 2011; 186(6):3356-63. PMC: 3048901. DOI: 10.4049/jimmunol.1000847. View