TY - JOUR
T1 - Status of paratyphoid fever vaccine research and development
AU - Martin, Laura B.
AU - Simon, Raphael
AU - MacLennan, Calman A.
AU - Tennant, Sharon M.
AU - Sahastrabuddhe, Sushant
AU - Khan, M. Imran
N1 - Publisher Copyright:
© 2016 World Health Organization.
PY - 2016/6/3
Y1 - 2016/6/3
N2 - Salmonella enterica serovars Typhi and Paratyphi (S. Paratyphi) A and B cause enteric fever in humans. Of the paratyphoid group, S. Paratyphi A is the most common serovar. In 2000, there were an estimated 5.4 million cases of S. Paratyphi A worldwide. More recently paratyphoid fever has accounted for an increasing fraction of all cases of enteric fever. Although vaccines for typhoid fever have been developed and in use for decades, vaccines for paratyphoid fever have not yet been licensed. Several S. Paratyphi A vaccines, however, are in development and based on either whole cell live-attenuated strains or repeating units of the lipopolysaccharide O-antigen (O:2) conjugated to different protein carriers. An O-specific polysaccharide (O:2) of S. Paratyphi A conjugated to tetanus toxoid (O:2-TT), for example, has been determined to be safe and immunogenic after one dose in Phase I and Phase II trials. Two other conjugated vaccine candidates linked to diphtheria toxin and a live-attenuated oral vaccine candidate are currently in preclinical development. As promising vaccine candidates are advanced along the development pipeline, an adequate supply of vaccines will need to be ensured to meet growing demand, particularly in the most affected countries.
AB - Salmonella enterica serovars Typhi and Paratyphi (S. Paratyphi) A and B cause enteric fever in humans. Of the paratyphoid group, S. Paratyphi A is the most common serovar. In 2000, there were an estimated 5.4 million cases of S. Paratyphi A worldwide. More recently paratyphoid fever has accounted for an increasing fraction of all cases of enteric fever. Although vaccines for typhoid fever have been developed and in use for decades, vaccines for paratyphoid fever have not yet been licensed. Several S. Paratyphi A vaccines, however, are in development and based on either whole cell live-attenuated strains or repeating units of the lipopolysaccharide O-antigen (O:2) conjugated to different protein carriers. An O-specific polysaccharide (O:2) of S. Paratyphi A conjugated to tetanus toxoid (O:2-TT), for example, has been determined to be safe and immunogenic after one dose in Phase I and Phase II trials. Two other conjugated vaccine candidates linked to diphtheria toxin and a live-attenuated oral vaccine candidate are currently in preclinical development. As promising vaccine candidates are advanced along the development pipeline, an adequate supply of vaccines will need to be ensured to meet growing demand, particularly in the most affected countries.
KW - Developing countries
KW - Enteric fever
KW - Paratyphoid fever
KW - Salmonella
KW - Salmonella paratyphi
KW - Salmonella paratyphi A
KW - Vaccine development
KW - Vaccine policy
KW - Vaccines
UR - http://www.scopus.com/inward/record.url?scp=84964689463&partnerID=8YFLogxK
U2 - 10.1016/j.vaccine.2016.03.106
DO - 10.1016/j.vaccine.2016.03.106
M3 - Article
C2 - 27083427
AN - SCOPUS:84964689463
SN - 0264-410X
VL - 34
SP - 2900
EP - 2902
JO - Vaccine
JF - Vaccine
IS - 26
ER -