Whole-cell vaccine candidates induce a protective response against virulent Acinetobacter baumannii

被引:7
|
作者
Dollery, Stephen J. [1 ]
Zurawski, Daniel V. [2 ]
Bushnell, Ruth V. [1 ]
Tobin, John K. [1 ]
Wiggins, Taralyn J. [1 ]
MacLeod, David A. [1 ]
Tasker, Naomi J. P. E. R. [1 ]
Alamneh, Yonas A. [2 ]
Abu-Taleb, Rania [2 ]
Czintos, Christine M. [2 ]
Su, Wanwen [2 ]
Escatte, Mariel G. [2 ]
Meeks, Heather N. [3 ]
Daly, Michael J. [4 ]
Tobin, Gregory J. [1 ]
机构
[1] Biol Mimet Inc, Frederick, MD 21702 USA
[2] Walter Reed Army Inst Res, Ctr Infect Dis Res, Wound Infect Dept, Bacterial Dis Branch, Silver Spring, MD USA
[3] Def Threat Reduct Agcy, Ft Belvoir, VA USA
[4] Uniformed Serv Univ Hlth Sci, Dept Pathol, Bethesda, MD USA
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
pulmonary; protection; A; baumannii; humoral; vaccine; whole-cell; UVC; MDP; MN2+-PEPTIDE COMPLEX; RADIATION-RESISTANCE; IMMUNIZATION;
D O I
10.3389/fimmu.2022.941010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acinetobacter baumannii causes multi-system diseases in both nosocomial settings and a pre-disposed general population. The bacterium is not only desiccation-resistant but also notoriously resistant to multiple antibiotics and drugs of last resort including carbapenem, colistin, and sulbactam. The World Health Organization has categorized carbapenem-resistant A. baumannii at the top of its critical pathogen list in a bid to direct urgent countermeasure development. Several early-stage vaccines have shown a range of efficacies in healthy mice, but no vaccine candidates have advanced into clinical trials. Herein, we report our findings that both an ionizing gamma-radiation-inactivated and a non-ionizing ultraviolet C-inactivated whole-cell vaccine candidate protects neutropenic mice from pulmonary challenge with virulent AB5075, a particularly pathogenic isolate. In addition, we demonstrate that a humoral response is sufficient for this protection via the passive immunization of neutropenic mice.
引用
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页数:11
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