Literature DB >> 29555018

Incomplete inhibition of HIV infection results in more HIV infected lymph node cells by reducing cell death.

Laurelle Jackson1,2, Jessica Hunter1,2, Sandile Cele1, Isabella Markham Ferreira1,2, Andrew C Young1,3, Farina Karim1, Rajhmun Madansein4,5, Kaylesh J Dullabh4, Chih-Yuan Chen4, Noel J Buckels4, Yashica Ganga1, Khadija Khan1, Mikael Boulle1, Gila Lustig1, Richard A Neher6,7, Alex Sigal1,2,8.   

Abstract

HIV has been reported to be cytotoxic in vitro and in lymph node infection models. Using a computational approach, we found that partial inhibition of transmissions of multiple virions per cell could lead to increased numbers of live infected cells. If the number of viral DNA copies remains above one after inhibition, then eliminating the surplus viral copies reduces cell death. Using a cell line, we observed increased numbers of live infected cells when infection was partially inhibited with the antiretroviral efavirenz or neutralizing antibody. We then used efavirenz at concentrations reported in lymph nodes to inhibit lymph node infection by partially resistant HIV mutants. We observed more live infected lymph node cells, but with fewer HIV DNA copies per cell, relative to no drug. Hence, counterintuitively, limited attenuation of HIV transmission per cell may increase live infected cell numbers in environments where the force of infection is high.
© 2018, Jackson et al.

Entities:  

Keywords:  HIV induced cell death; Lymph node; cell-to-cell spread; computational biology; human; infectious disease; microbiology; multiple Infections per cell; systems biology; viral fitness; virus

Mesh:

Substances:

Year:  2018        PMID: 29555018      PMCID: PMC5896883          DOI: 10.7554/eLife.30134

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


  68 in total

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