Common Recombinant subunit vaccine expressed in Pichia pastoris
Subunit vaccines often suffer from poor immunogenicity and require certain helper molecules known as adjuvants to induce or enhance an appropriate immune response to the antigen. T‐cell activation is crucial in inducing protective immune responses. Antigens mannosylated by P. pastoris have shown to have enhanced antigen presentation and T‐cell activation properties compared with their nonglycosylated counterparts. Therefore, glycoproteins derived from P. pastoris have the potential to function as adjuvants.
Construct name | Used strain | Used vector | Targeted disease |
---|---|---|---|
PIMP‐V1 and PIMP‐V2 | KM71 | pPICZαA | Malaria |
P1‐3CD | PichiaPink | pPink‐HC | Hand–foot–mouth disease |
DENV‐3 E | KM71 | pPICZ‐A | Dengue |
CHIKV‐C‐E3‐E2‐6K‐E1 | GS115 | pPIC9K | Chikungunya |
Gp350 | GS115 | pPICZαA | EBV infection |
RBD219‐N1 | X‐33 | pPICZαA | SARS |
VP2–VP5–Fc | GS115 | pPIC9K | Infectious bursal |
F protein | GS115 | pPICZαA | Newcastle |
OmpA | GS115 | pPIC9K | P. mirabilis infection |
BoNT Hc | X‐33 | pPICZ‐A | Botulism |
Tc52 | GS115 | pPICZαA | Chagas |
Apa | GS115 | pPIC9K | Tuberculosis |
HBHA | GS115 | pPIC9K | Tuberculosis |
CFP10‐Fcγ2a | GS115 | pPICZαA | Tuberculosis |
ESAT6‐CFP10‐Fcγ2a | GS115 | pPICZαA | Tuberculosis |
ESAT6‐Fcγ2a | GS115 | pPICZαA | Tuberculosis |
CFP10‐HspX‐Fcγ2a | GS115 | pPICZαA | Tuberculosis |
ESAT6‐HspX‐Fcγ2a | GS115 | pPICZαA | Tuberculosis |
Glycoprotein D | GS115 | pPIC9K | HSV‐2 infection |
OmpA‐Fc | GS115 | pPIC9K | Bordetellosis |
Table: Common Recombinant Subunit Vaccine Expressed In Pichia Pastoris
Ref: Pichia pastoris: A highly successful expression system for optimal synthesis of heterologous proteins