TY - JOUR
T1 - Plasmids encoding foot-and-mouth disease virus VP1 epitopes elicited immune responses in mice and swine and protected swine against viral infection
AU - Wong, H. T.
AU - Cheng, S. C.S.
AU - Chan, E. W.C.
AU - Sheng, Z. T.
AU - Yan, W. Y.
AU - Zheng, Z. X.
AU - Xie, Y.
PY - 2000/12/5
Y1 - 2000/12/5
N2 - VP1 is a capsid protein of foot-and-mouth disease virus (FMDV) and contains epitopes of the virus. Plasmids encoding two VP1 epitopes (amino acid residues 141-160 and 200-213) and a host-self immunoglobulin molecule were constructed to produce a new type of FMD DNA vaccine. Two plasmids, namely, pCEIM and pCEIS, containing mouse immunoglobulin (IgG) or swine IgG were subjected to immunogenicity testing in mice and swine, respectively. In mice administrated pCEIM in the abdomen using a genegun, both FMDV-specific T-cell proliferation and neutralizing antibodies were detected. In swine immunized with pCEIS at the back of the ear, immune responses were achieved after the second administration. Swine showed a T-cell proliferative response with a stimulation index (SI) of up to 8.1 and a neutralizing antibody response that was able to protect suckling mice from 102 LD50 (lethal dose 50) FMDV challenge. To compare the immunogenicity of the DNA-based vaccine candidate, versus the protein-based vaccine candidates, a second group of swine was immunized with the protein F1-sclgG, which was encoded by the plasmid pCEIS. Injection with F1-sclgG elicited a T-cell proliferative response of SI < 1.7 and a neutralizing antibody response that protected suckling mice from up to 105 LD50 FMDV challenge. In the challenge test, three of three swine immunized with pCEIS were fully protected from FMDV challenge. (C) 2000 Academic Press.
AB - VP1 is a capsid protein of foot-and-mouth disease virus (FMDV) and contains epitopes of the virus. Plasmids encoding two VP1 epitopes (amino acid residues 141-160 and 200-213) and a host-self immunoglobulin molecule were constructed to produce a new type of FMD DNA vaccine. Two plasmids, namely, pCEIM and pCEIS, containing mouse immunoglobulin (IgG) or swine IgG were subjected to immunogenicity testing in mice and swine, respectively. In mice administrated pCEIM in the abdomen using a genegun, both FMDV-specific T-cell proliferation and neutralizing antibodies were detected. In swine immunized with pCEIS at the back of the ear, immune responses were achieved after the second administration. Swine showed a T-cell proliferative response with a stimulation index (SI) of up to 8.1 and a neutralizing antibody response that was able to protect suckling mice from 102 LD50 (lethal dose 50) FMDV challenge. To compare the immunogenicity of the DNA-based vaccine candidate, versus the protein-based vaccine candidates, a second group of swine was immunized with the protein F1-sclgG, which was encoded by the plasmid pCEIS. Injection with F1-sclgG elicited a T-cell proliferative response of SI < 1.7 and a neutralizing antibody response that protected suckling mice from up to 105 LD50 FMDV challenge. In the challenge test, three of three swine immunized with pCEIS were fully protected from FMDV challenge. (C) 2000 Academic Press.
KW - DNA vaccine
KW - Foot-and-mouth disease
KW - IgG carrier
KW - VP1 epitopes
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000165894500004
UR - https://openalex.org/W2091423663
UR - https://www.scopus.com/pages/publications/0034610234
U2 - 10.1006/viro.2000.0607
DO - 10.1006/viro.2000.0607
M3 - Journal Article
SN - 0042-6822
VL - 278
SP - 27
EP - 35
JO - Virology
JF - Virology
IS - 1
ER -