Table 2.
Examples of the current pipeline of pre-clinical AIDS vaccines being studied in Asia
| Vaccine vector | Immunity induced | Comment | Institution | References |
|---|---|---|---|---|
| Novel DNA vaccine vector | T and B cell immunity | Reduced DNA dose, enhanced immunogenicity | China CDC | [17] |
| Modified Tiantan vaccina | T-cell immunity, antibodies | Mucosal delivery with potentially less adverse effects compared to wild type Tiantan sp. | HK Univ., Tsinghua Univ., Chinese Academy of Medical Sciences, Peking Univ. Medical School, Chinese Academy of Sciences, China CDC | [18, 19] |
| CD40 ligand-expressing vaccines | Enhanced T- and B-cell immunity | Likely to improve durability of immunity. | University of Toronto | [20] |
| Envelope trimers | Neutralizing antibodies | Use of primary isolates may enhance antibody responses. | University of Melbourne | [21] |
| Peptides within particle-based vaccines | Durable T-cell immunity | Overlapping peptides induce broad T-cell immunity. Encapsulating peptides inside nanoparticles may permit durable immunity. | University of Melbourne | [22,23] |
| BCG vectors | T-cell and antibodies | Widely used vaccine vector with good safety record. | Osaka University | [24] |
| Influenza vectors | Mucosal T-cell immunity | Attenuated influenza strains with inserted HIV antigens could induce good pan-mucosal immunity. | University of Melbourne | [25] |
| Sendai virus vectors (alone or in prime-boost regimens) | Mucosal immunity | Attenuated parainfluenza virus vector could induce good pan-mucosal immunity. | The University of Tokyo/ DNAVEC Corporation/ China CDC | [26,27] |