outer membrane vesicle
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2022 ◽  
Vol 11 (1) ◽  
Author(s):  
Chanel A. Mosby ◽  
Sutonuka Bhar ◽  
Matthew B. Phillips ◽  
Mariola J. Edelmann ◽  
Melissa K. Jones

2021 ◽  
pp. 2106307
Author(s):  
Jingmei Pan ◽  
Xilin Li ◽  
Binfen Shao ◽  
Funeng Xu ◽  
Xuehui Huang ◽  
...  

2021 ◽  
Vol 2 ◽  
pp. 100009
Author(s):  
Eline F. de Jonge ◽  
Melanie D. Balhuizen ◽  
Ria van Boxtel ◽  
Jianjun Wu ◽  
Henk P. Haagsman ◽  
...  

2021 ◽  
pp. 2101180
Author(s):  
Robert Richter ◽  
Mohamed A. M. Kamal ◽  
Marcus Koch ◽  
Bart‐Jan Niebuur ◽  
Anna‐Lena Huber ◽  
...  

Author(s):  
Kathryn A Matthias ◽  
Kristie L Connolly ◽  
Afrin A Begum ◽  
Ann E Jerse ◽  
Andrew N Macintyre ◽  
...  

Abstract Background Despite decades of research efforts, development of a gonorrhea vaccine has remained elusive. Epidemiological studies suggest that detoxified outer membrane vesicle (dOMV) vaccines from Neisseria meningitidis (Nm) may protect against infection with Neisseria gonorrhoeae (Ng). We recently reported that Nm dOMVs lacking the major outer membrane proteins (OMPs) PorA, PorB, and RmpM induced greater antibody cross-reactivity against heterologous Nm strains than wild-type (WT) dOMVs and may represent an improved vaccine against gonorrhea. Methods We prepared dOMV vaccines from meningococcal strains that were sufficient or deleted for PorA, PorB, and RmpM. Vaccines were tested in a murine genital tract infection model and antisera were used to identify vaccine targets. Results Immunization with Nm dOMVs significantly and reproducibly enhanced gonococcal clearance for mice immunized with OMP-deficient dOMVs; significant clearance for WT dOMV-immunized mice was observed in one of two experiments. Clearance was associated with serum and vaginal anti-Nm dOMV IgG antibodies that cross-reacted with Ng. Serum IgG was used to identify putative Ng vaccine targets, including PilQ, MtrE, NlpD, and GuaB. Conclusions Meningococcal dOMVs elicited a protective effect against experimental gonococcal infection. Recognition and identification of Ng vaccine targets by Nm dOMV-induced antibodies supports the development of a cross-protective Neisseria vaccine.


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