Therapeutic Immune Recovery and Reduction of CXCR4-Tropic HIV-1.

Bader, Joëlle; Däumer, Martin; Schöni-Affolter, Franziska; Böni, Jürg; Gorgievski, Meri; Martinetti, Gladys; Thielen, Alexander; Klimkait, Thomas (2017). Therapeutic Immune Recovery and Reduction of CXCR4-Tropic HIV-1. Clinical infectious diseases, 64(3), pp. 295-300. Oxford University Press 10.1093/cid/ciw737

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BACKGROUND In the absence of therapy, CXCR4 (X4)-tropic human immunodeficiency virus type 1 (HIV-1) increases over time, associated with accelerated disease progression. In contrast, the majority of patients receiving long-term combination antiretroviral therapy (cART) present with CCR5 (R5)-tropic HIV-1 variants. It is unclear whether cART itself mediates the reduction of X4-tropic HIV-1. The current study aimed at assessing the tropism of viral integrates in patients' blood during fully suppressive cART. METHODS The relative frequencies of X4-tropic proviral HIV-1 variants were determined by means of next-generation sequencing (False Positive Rate (FPR), 3.5%; R5- or X4 tropic variants occurring at less than 2% of the total virus population) for 35 treated patients in the Swiss HIV Cohort Study and followed longitudinally over time. Full viral suppression and a continuous CD4 T-cell recovery during cART were documented for all patients. Viral phylogenetic changes and sequence evolution were analyzed. RESULTS The majority of patients (80%) experienced no frequency increase in X4-tropic proviruses during therapy. Although some proviral sequence evolution was demonstrable in >50% of these patients during therapy, this growing viral diversity was in no case paralleled by the emergence or expansion of X4-tropic provirus variants. In the remaining 20% of patients, the documented expansion of X4-tropic provirus was based on the outgrowth of single viral variants from minority populations already present before therapy initiation. CONCLUSION Our study demonstrates that X4-tropic HIV sharply declines in most patients during successful therapy, which indicates a preferential tropism-dependent provirus elimination in the immunocompetent host. The recently implemented World Health Organization strategies of immediate therapy initiation are fully in line with this gradual loss of X4 tropism during therapy. Moreover, the early use of coreceptor antagonists against the remaining CCR5-tropic viruses may be indicated.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Service Sector > Institute for Infectious Diseases

UniBE Contributor:

Gorgievski, Meri

Subjects:

500 Science > 570 Life sciences; biology
600 Technology > 610 Medicine & health

ISSN:

1058-4838

Publisher:

Oxford University Press

Language:

English

Submitter:

Siegfried Hektor Hapfelmeier-Balmer

Date Deposited:

19 Jul 2017 10:32

Last Modified:

19 Jul 2017 10:32

Publisher DOI:

10.1093/cid/ciw737

PubMed ID:

27838645

Uncontrolled Keywords:

CXCR4-tropic; HIV; immune system.; tropism

BORIS DOI:

10.7892/boris.95173

URI:

https://boris.unibe.ch/id/eprint/95173

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