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. Author manuscript; available in PMC: 2011 Sep 1.
Published in final edited form as: Curr Opin HIV AIDS. 2010 Sep;5(5):435–452. doi: 10.1097/COH.0b013e32833c95c1

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]