The invention belongs to the field of
gene engineering, and particularly relates to application of
chikungunya virus structural protein in improvement of pseudovirus stability, a construction method of the
chikungunya virus structural protein and vaccines,
antibody evaluation and in-vivo
gene therapy products. The method comprises the following steps: constructing a human
codon optimized Asian strain CHIKV-E3 + E2 + 6K + E1
structural protein eukaryotic vector, and designing two types of binder expression plasmids of targeted T cells; the vector, a psPAX2 helper
plasmid and a
lentivirus target vector containing an SFFV
promoter and a ZsGreen
reporter gene (or a CAR therapeutic
gene) are co-transformed into a 293
T cell, and the
lentivirus is prepared through culture,
filtration and
centrifugation. The
lentivirus can efficiently infect
Jurkat cells and activate human T cells, obviously reduces the infection efficiency on 293T cells so as to reduce the off-target effect, has excellent stability in human serum, and provides a safe and efficient
gene delivery tool for in-vivo CAR-T therapy.