# HIV Vaccine: Recent Advances, Current Roadblocks, and Future Directions

**Authors:** Muni Rubens, Venkataraghavan Ramamoorthy, Anshul Saxena, Nancy Shehadeh, Sandeep Appunni

PMC · DOI: 10.1155/2015/560347 · Journal of Immunology Research · 2015-10-22

## TL;DR

This paper reviews progress in HIV vaccine development, highlighting challenges and future strategies to create an effective vaccine.

## Contribution

The paper provides a comprehensive review of recent HIV vaccine trials and outlines novel approaches for future vaccine development.

## Key findings

- Recent trials have explored inducing broadly reactive neutralizing antibodies and CD8 T cell responses.
- Host and viral factors significantly influence the effectiveness of vaccine-induced immune responses.
- Combination approaches and DNA vaccines are promising for future HIV vaccine development.

## Abstract

HIV/AIDS is a leading cause of mortality and morbidity worldwide. In spite of successful interventions and treatment protocols, an HIV vaccine would be the ultimate prevention and control strategy. Ever since identification of HIV/AIDS, there have been meticulous efforts for vaccine development. The specific aim of this paper is to review recent vaccine efficacy trials and associated advancements and discuss the current challenges and future directions. Recombinant DNA technologies greatly facilitated development of many viral products which were later incorporated into vectors for effective vaccines. Over the years, a number of scientific approaches have gained popularity and include the induction of neutralizing antibodies in late 1980s, induction of CD8 T cell in early 1990s, and combination approaches currently. Scientists have hypothesized that stimulation of right sequences of somatic hypermutations could induce broadly reactive neutralizing antibodies (bnAbs) capable of effective neutralization and viral elimination. Studies have shown that a number of host and viral factors affect these processes. Similarly, eliciting specific CD8 T cells immune responses through DNA vaccines hold future promises. In summary, future studies should focus on the continuous fight between host immune responses and ever-evasive viral factors for effective vaccines.

## Full-text entities

- **Genes:** ITIH4 (inter-alpha-trypsin inhibitor heavy chain 4) [NCBI Gene 3700] {aka GP120, H4P, IHRP, ITI-HC4, ITIHL1, PK-120}, CCR5 (C-C motif chemokine receptor 5) [NCBI Gene 735311], CD4 (CD4 molecule) [NCBI Gene 713807], IGHG3 (immunoglobulin heavy constant gamma 3 (G3m marker)) [NCBI Gene 3502] {aka IgG3}, Nef [NCBI Gene 156110], Env [NCBI Gene 155971], IGHV1-2 (immunoglobulin heavy variable 1-2) [NCBI Gene 28474] {aka IGHV12, V35}, gag-pol (Gag-Pol) [NCBI Gene 155348], CXCR5 (C-X-C motif chemokine receptor 5) [NCBI Gene 643] {aka BLR1, CD185, MDR15}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CCR5 (C-C motif chemokine receptor 5) [NCBI Gene 1234] {aka CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, LOC102723407 (immunoglobulin heavy variable 4-38-2-like) [NCBI Gene 102723407] {aka IGHV4, IGHV4-30, IGHV4-38-2, IGHV4-39, IGHV4-b, IGVH4-39}, gag (Pr55(Gag)) [NCBI Gene 155030], NDUFB3 (NADH:ubiquinone oxidoreductase subunit B3) [NCBI Gene 4709] {aka B12, CI-B12, MC1DN25}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}
- **Diseases:** SIV infected (OMIM:270100), ADCVI (MESH:D014777), infected (MESH:D007239), AIDS (MESH:D000163), Cytotoxicity (MESH:D064420), Hepatitis B (MESH:D006509), HIV (MESH:D015658), viremia (MESH:D014766), CMV (MESH:D003586)
- **Chemicals:** glycan (MESH:D011134), -C (MESH:D002244), MF59 (MESH:C089950), CH103 (MESH:C014893), Asn (MESH:D001216), RV144 (MESH:C048498), 3BNC117 (-),  (MESH:D016915),  (MESH:D019444)
- **Species:** Macaca mulatta (rhesus macaque, species) [taxon 9544], Vesicular stomatitis virus (species) [taxon 11276], Adeno-associated virus (species) [taxon 272636], Human adenovirus 26 (no rank) [taxon 46928], Measles morbillivirus (no rank) [taxon 11234], Canarypox virus (no rank) [taxon 44088], Qubevirus faecium (species) [taxon 39804], macacine betaherpesvirus 3 (Rhesus cytomegalovirus, no rank) [taxon 47929], Semliki Forest virus (no rank) [taxon 11033], Human immunodeficiency virus 1 (no rank) [taxon 11676], Human immunodeficiency virus (species) [taxon 12721], Human adenovirus 5 (no rank) [taxon 28285], Homo sapiens (human, species) [taxon 9606], Modified Vaccinia Ankara virus (no rank) [taxon 467144], Simian-Human immunodeficiency virus (species) [taxon 57667], Mus musculus (house mouse, species) [taxon 10090], Orthopoxvirus vaccinia (species) [taxon 10245], HSV [taxon 39059], Sindbis virus (no rank) [taxon 11034], Adenoviridae (family) [taxon 10508], Venezuelan equine encephalitis virus (no rank) [taxon 11036]
- **Mutations:** -46G54W

## Full text

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## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC4633685/full.md

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Source: https://tomesphere.com/paper/PMC4633685