TY - JOUR
T1 - Synthesis and Evaluation of QS-21-Based Immunoadjuvants with a Terminal-Functionalized Side Chain Incorporated in the West Wing Trisaccharide
AU - Wang, Pengfei
AU - Devalankar, Dattatray A.
AU - Dai, Qipu
AU - Zhang, Ping
AU - Michalek, Suzanne M.
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/10/21
Y1 - 2016/10/21
N2 - Three QS-21-based vaccine adjuvant candidates with a terminal-functionalized side chain incorporated in the west wing trisaccharide have been synthesized. The terminal polar functional group serves to increase the solubility of these analogues in water. Two of the synthetic analogues have been shown to have adjuvant activity comparable to that of GPI-0100. The stand-alone adjuvant activity of the new synthetic analogues again confirmed that it is a feasible way to develop new saponin-based vaccine adjuvants through derivatizing at the west wing branched trisaccharide domain. Inclusion of an additional polar functional group such as a carboxyl group (as in 3x) or a monosaccharide (as in 4x and 5x) is sufficient to increase the water solubility of the corresponding synthetic analogues to a level comparable to that of GPI-0100 and suitable for immunological studies and clinical application. The structure of the incorporated side chain has a significant impact on the adjuvant activity in terms of the magnitude and nature of the host's responses.
AB - Three QS-21-based vaccine adjuvant candidates with a terminal-functionalized side chain incorporated in the west wing trisaccharide have been synthesized. The terminal polar functional group serves to increase the solubility of these analogues in water. Two of the synthetic analogues have been shown to have adjuvant activity comparable to that of GPI-0100. The stand-alone adjuvant activity of the new synthetic analogues again confirmed that it is a feasible way to develop new saponin-based vaccine adjuvants through derivatizing at the west wing branched trisaccharide domain. Inclusion of an additional polar functional group such as a carboxyl group (as in 3x) or a monosaccharide (as in 4x and 5x) is sufficient to increase the water solubility of the corresponding synthetic analogues to a level comparable to that of GPI-0100 and suitable for immunological studies and clinical application. The structure of the incorporated side chain has a significant impact on the adjuvant activity in terms of the magnitude and nature of the host's responses.
UR - http://www.scopus.com/inward/record.url?scp=84992365356&partnerID=8YFLogxK
U2 - 10.1021/acs.joc.6b00922
DO - 10.1021/acs.joc.6b00922
M3 - Article
C2 - 27709937
AN - SCOPUS:84992365356
SN - 0022-3263
VL - 81
SP - 9560
EP - 9566
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 20
ER -