Abstract

During the extended clinically latent period associated with Human Immunodeficiency Virus (HIV) infection the virus itself is far from latent. This phase of infection generally comes to an end with the development of symptomatic illness. Understanding the factors affecting disease progression can aid treatment commencement and therapeutic monitoring decisions. An example of this is the clear utility of CD4+ T-cell count and HIV-RNA for disease stage and progression assessment.Elements of the immune response such as the diversity of HIV-specific cytotoxic lymphocyte responses and cell-surface CD38 expression correlate significantly with the control of viral replication. However, the relationship between soluble markers of immune activation and disease progression remains inconclusive. In patients on treatment, sustained virological rebound to >10 000 copies/mL is associated with poor clinical outcome. However, the same is not true of transient elevations of HIV RNA (blips). Another virological factor, drug resistance, is becoming a growing problem around the globe and monitoring must play a part in the surveillance and control of the epidemic worldwide. The links between chemokine receptor tropism and rate of disease progression remain uncertain and the clinical utility of monitoring viral strain is yet to be determined. The large number of confounding factors has made investigation of the roles of race and viral subtype difficult, and further research is needed to elucidate their significance.Host factors such as age, HLA and CYP polymorphisms and psychosocial factors remain important, though often unalterable, predictors of disease progression. Although gender and mode of transmission have a lesser role in disease progression, they may impact other markers such as viral load. Finally, readily measurable markers of disease such as total lymphocyte count, haemoglobin, body mass index and delayed type hypersensitivity may come into favour as ART becomes increasingly available in resource-limited parts of the world. The influence of these, and other factors, on the clinical progression of HIV infection are reviewed in detail, both preceding and following treatment initiation.

Highlights

  • Host factors such as age, Human Leukocyte Antigen (HLA) and CYP polymorphisms and psychosocial factors remain important, though often unalterable, predictors of disease progression

  • Readily measurable markers of disease such as total lymphocyte count, haemoglobin, body mass index and delayed type hypersensitivity may come into favour as ART becomes increasingly available in resource-limited parts of the world

  • The influence of these, and other factors, on the clinical progression of Human Immunodeficiency Virus (HIV) infection are reviewed in detail, both preceding and following treatment initiation

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Summary

Conclusion

The evolution of HIV infection from the fusion of the first virion with a CD4+ T-cell to AIDS and death is influenced by a multitude of interacting factors. In gaining an understanding of the prognostic significance of just a few of these elements it may be possible to improve the management and long-term outcome for individuals. Research into host-virus interactions has great potential to enhance the development of new therapeutic strategies. Immunological parameters such as levels of CD38 expression and the diversity of HIV-specific cytotoxic lymphocyte responses allow insight into the levels of autologous control of the virus. Virological monitoring, including drug resistance surveillance, will continue to play a considerable role in the management of HIV infection. As with any illness of such magnitude, it is clear that a multitude of factors must be taken into account in order to ensure optimum quality of life and treatment results

Osmond DH
10. CASCADE collaboration
56. Ledergerber B
Findings
84. Deeks SG
Full Text
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