Review of preventative HIV vaccine clinical trials in South Africa

被引:25
作者
Laher, Fatima [1 ]
Bekker, Linda-Gail [2 ]
Garrett, Nigel [3 ,4 ]
Lazarus, Erica M. [1 ]
Gray, Glenda E. [1 ,5 ]
机构
[1] Univ Witwatersrand, Fac Hlth Sci, Perinatal HIV Res Unit, Johannesburg, South Africa
[2] Univ Cape Town, Desmond Tutu HIV Fdn, Cape Town, South Africa
[3] Ctr AIDS Programme Res South Africa, Durban, South Africa
[4] Univ KwaZulu Natal, Sch Nursing & Publ Hlth, Dept Publ Hlth Med, Durban, South Africa
[5] South African Med Res Council, Cape Town, South Africa
关键词
DOUBLE-BLIND; NEUTRALIZING ANTIBODIES; TYPE-1; VACCINE; EFFICACY TRIAL; AIDS VACCINE; SAFETY; IMMUNOGENICITY; RESPONSES; IMMUNITY; MVA;
D O I
10.1007/s00705-020-04777-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
New HIV infections continue relentlessly in southern Africa, demonstrating the need for a vaccine to prevent HIV subtype C. In South Africa, the country with the highest number of new infections annually, HIV vaccine research has been ongoing since 2003 with collaborative public-private-philanthropic partnerships. So far, 21 clinical trials have been conducted in South Africa, investigating seven viral vectors, three DNA plasmids, four envelope proteins, five adjuvants and three monoclonal antibodies. Active vaccine candidates have spanned subtypes A, B, C, E and multi-subtype mosaic sequences. All were well tolerated. Four concepts were investigated for efficacy: rAd5-gag/pol/nef showed increased HIV acquisition in males, subtype C ALVAC/gp120/MF59 showed no preventative efficacy, and the trials for the VRC01 monoclonal antibody and Ad26.Mos4.HIV/subtype C gp140/ aluminum phosphate are ongoing. Future trials are planned with DNA/viral vector plus protein combinations in concert with pre-exposure prophylaxis, and sequential immunization studies with transmitted/founder HIV envelope to induce broadly neutralizing antibodies. Finally, passive immunization trials are underway to build on the experience with VRC01, including single and combination antibody trials with an antibody derived from a subtype-C-infected South African donor. Future consideration should be given to the evaluation of novel strategies, for example, inactivated-whole-virus vaccines.
引用
收藏
页码:2439 / 2452
页数:14
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