T Cell Immunity and the Quest for Protective Vaccines against Staphylococcus aureus Infection

被引:22
作者
Armentrout, Erin I. [1 ,2 ]
Liu, George Y. [3 ,4 ]
Martins, Gislaine A. [5 ,6 ,7 ]
机构
[1] Cedars Sinai Med Ctr CSMC, Lung Inst, Los Angeles, CA 90048 USA
[2] CSMC, Div Pulm & Crit Care Med, Los Angeles, CA 90048 USA
[3] Univ Calif San Diego, Collaborat Halt Antibiot Resistant Microbes, La Jolla, CA 92161 USA
[4] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[5] CSMC, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USA
[6] CSMC, Res Div Immunol, Dept Biomed Sci, Los Angeles, CA 90048 USA
[7] CSMC, Dept Med, Div Gastroenterol, Los Angeles, CA 90048 USA
关键词
Staphylococcus aureus; vaccine; antibodies; T cell-mediated immunity; tissue-resident memory T cells; PYOGENIC BACTERIAL-INFECTIONS; SURGICAL SITE INFECTION; LABORATORY MICE; NASAL CARRIAGE; CUTTING EDGE; DOUBLE-BLIND; WHOLE-BLOOD; IFN-GAMMA; PHASE-II; TGF-BETA;
D O I
10.3390/microorganisms8121936
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus aureus is a wide-spread human pathogen, and one of the top causative agents of nosocomial infections. The prevalence of antibiotic-resistant S. aureus strains, which are associated with higher mortality and morbidity rates than antibiotic-susceptible strains, is increasing around the world. Vaccination would be an effective preventive measure against S. aureus infection, but to date, every vaccine developed has failed in clinical trials, despite inducing robust antibody responses. These results suggest that induction of humoral immunity does not suffice to confer protection against the infection. Evidence from studies in murine models and in patients with immune defects support a role of T cell-mediated immunity in protective responses against S. aureus. Here, we review the current understanding of the mechanisms underlying adaptive immunity to S. aureus infections and discuss these findings in light of the recent S. aureus vaccine trial failures. We make the case for the need to develop anti-S. aureus vaccines that can specifically elicit robust and durable protective memory T cell subsets.
引用
收藏
页码:1 / 20
页数:20
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