is a leading cause of diarrhea among children globally and of diarrheal deaths among children under 5 years of age in low- and middle-income countries. To date, no licensed vaccine exists. We review evidence that serum IgG antibodies to LPS represent a good correlate of protection against shigellosis; this could support the process of development and evaluation of vaccine candidates. Case-control and cohort studies conducted among Israeli soldiers serving under field conditions showed significant serotype-specific inverse associations between pre-exposure serum IgG antibodies to LPS and shigellosis incidence. The same serum IgG fraction showed a dose-response relationship with the protective efficacy attained by vaccine candidates tested in phase III trials of young adults and children aged 1-4 years and in Controlled Human Infection Model studies and exhibited mechanistic protective capabilities. Identifying a threshold level of these antibodies associated with protection can promote the development of an efficacious vaccine for infants and young children.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6663123PMC
http://dx.doi.org/10.1080/21645515.2019.1606971DOI Listing

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