- Open Access
Persistent resistance to HIV-1 infection in CD4 T cells from exposed uninfected Vietnamese individuals is mediated by entry and post-entry blocks
© Sáez-Cirión et al; licensee BioMed Central Ltd. 2006
- Received: 03 August 2006
- Accepted: 08 November 2006
- Published: 08 November 2006
We have previously reported that CD4 T cells from some exposed uninfected (EU) Vietnamese intravenous drug users are relatively resistant to HIV infection in vitro. Here, we further characterized the restriction of viral replication in CD4 T cells from five EUs and assessed its persistence in serial samples.
CD4 T cells and/or PBMC sampled during a period of between 2 and 6 years were challenged with replication-competent HIV-1 and other retroviral particles pseudotyped with envelope proteins of various tropisms. CCR5 expression and function in resistant CD4 T cells was evaluated. The step at which HIV-1 replication is restricted was investigated by real-time PCR quantification of HIV-1 reverse transcripts.
We identified three patterns of durable HIV-1 restriction in EU CD4 T cells. CD4 T cells from four of the five EU subjects were resistant to HIV-1 R5 infection. In two cases this resistance was associated with low CCR5 surface expression, which was itself associated with heterozygous CCR5 mutations. In the other two cases, CD4 T cells were resistant to HIV-1 R5 infection despite normal CCR5 expression and signaling function, and normal β-chemokine secretion upon CD4 T cell activation. Instead, restriction appeared to be due to enhanced CD4 T cell sensitivity to β-chemokines in these two subjects. In the fifth EU subject the restriction involved post-entry steps of viral replication and affected not only HIV-1 but also other lentiviruses. The restriction was not overcome by a high viral inoculum, suggesting that it was not mediated by a saturable inhibitory factor.
Various constitutive mechanisms of CD4 T cell resistance to HIV-1 infection, affecting entry or post-entry steps of viral replication, are associated with resistance to HIV-1 in subjects who remain uninfected despite long-term high-risk behavior.
- Human Immunodeficiency Virus
- Human Immunodeficiency Virus Infection
- Mean Fluorescence Intensity
- CCR5 Expression
- W276 Cell
Cellular susceptibility to human immunodeficiency virus (HIV) infection in vitro varies widely among individuals [1, 2]. Both host genetic and acquired mechanisms regulate HIV-1 replication. HIV requires numerous host cell factors for efficient replication . The recent discovery of several molecules endowed with antiretroviral activity in mice and primates underlines the contribution of innate intracellular resistance to infection by HIV and other retroviruses . Some of these molecules, such as the cytidine deaminase APOBEC3G, have been implicated in the restriction of HIV-1 replication in resting human T cells [5, 6]. Resistance to HIV-1 infection in vivo has not so far been linked to the expression or genetic polymorphism of these restriction factors [7, 8], but the efficiency of viral replication is likely to be determined in large part by the balance between required factors and restrictive factors.
Some individuals who are highly exposed to HIV-1 and yet remain uninfected (exposed uninfected individuals, EU) are likely to be naturally resistant to infection. Relative resistance of CD4 T cells and/or macrophages to HIV-1 infection has been reported in selected EUs [9–11]. This resistance was usually restricted to HIV-1 isolates using the CCR5 chemokine receptor (R5 isolates) to enter target cells [12–14]. Invalidating mutations in the CCR5 gene confer resistance to HIV-1 R5 infection in vitro [15, 16], and the CCR5Δ32 homozygous genotype is associated with protection against HIV-1 acquisition in Caucasians . Reduced in vitro susceptibility to HIV-1 R5 of EU CD4 T cells bearing wild-type CCR5 has been linked to low CCR5 expression on the target cell surface and/or to increased secretion of natural CCR5 ligands – the β-chemokines RANTES/CCL5, MIP-1α/CCL3 and MIP-1β/CCL4  – by CD4 or CD8 T lymphocytes [18–20]. Infection of CD4 T cells may also be inhibited by unidentified soluble antiviral factors secreted by CD8 T lymphocytes . Nevertheless, CD8 T cell associated resistance to HIV-1 infection was reported to wane in EUs who reduced their high-risk behavior, suggesting that reduced exposure led to decreased CD8 T cell antiviral immunity [22, 23].
We have previously shown that some Vietnamese intravenous drug users who remained uninfected by HIV despite more than 15 years of drug use (resulting in a high prevalence of other blood-borne viral infections) have low CD4 T cell permissiveness to HIV infection in vitro . In order to identify the mechanisms of CD4 T cell resistance in this population, we investigated the characteristics of HIV-1 restriction in five Vietnamese EUs who were monitored for between 2 and 6 years. We identified three different patterns of restriction, affecting viral entry or post-entry steps. We also found that CD4 T cell resistance to HIV was stable over time.
CD4 T cell resistance to single-round HIV-1 infection in Vietnamese EUs
In a previous study of Vietnamese IDU EUs we identified some individuals whose CD4 T lymphocytes showed reduced susceptibility to in vitro infection by replicative strains of HIV-1 . HIV-1 replication in CD4 T cells from three EUs (W276, W278 and B195) was far less efficient than in CD4 T cells from healthy controls. Analysis of the CCR5 gene in the same population revealed heterozygous mutations in some subjects [24, 25]. In two cases (B184 and W336) the mutations in CCR5 were associated with reduced co-receptor function in transfected cell lines [24, 26], but the effect of these mutations in heterozygous primary cells was not assessed.
Characteristics of the study subjects.
Year of birth
Remarkably, CD4 T cells from subject W276 were resistant to both R5 and X4 HIV-1 pseudotypes and also to the HIV-VSVG pseudotype. These results indicated that the restriction was independent not only of HIV coreceptors, as previously shown , but also of the entry pathway used by the virus (fig. 1).
CCR5 expression and function in HIV-1 R5 restricted cells
As already mentioned, CCR5 heterozygous mutations had been detected in subjects B184 and W336 (G106R and C178R respectively) [24, 25]. These (or equivalent) mutations, when present in the homozygous state in transfected cell lines, affect the receptor conformation and both CCR5 membrane trafficking and function [24, 26]. However, CCR5 surface expression by these two EUs' primary CD4 T cells has not been evaluated before.
Therefore, the low surface expression of CCR5 on CD4 T cells from EUs B184 and W336 is likely linked to CCR5 mutations and appears to affect R5 virus entry into target cells. However, HIV R5 replication in CD4 T cells from subjects W278 and B195 was restricted despite normal CCR5 surface expression (fig. 2A). We therefore examined whether CCR5 function was impaired in the CD4 T cells of these two subjects, affecting signaling events potentially involved in HIV-1 replication [28, 29].
As actin cytoskeleton reorganization is a major characteristic of chemokine responses, we analyzed CCR5-mediated actin polymerization in CD4 T cells from subjects W278 and B195. RANTES stimulation of CD4 T cells induced a rapid increase in the F-actin content of cells from the two EUs and from four CCR5-wt controls (fig. 2B). The peak responses occurred 15–30 s after stimulation, in keeping with a fully functional chemoreceptor . Cell pretreatment with the CCR5 inhibitor TAK-779  abrogated actin polymerization.
The restriction in CD4 T cells from subjects W278 and B195 affected HIV-1 viruses pseudotyped with different R5 tropic envelopes (JRFL  and YU2 ) (fig. 2C). These results confirmed that the restriction in W278 and B195 CD4 T cells is specific for the CCR5 entry pathway and indicated that it is independent of CCR5 expression and function.
Abrogation of viral restriction in cells from subjects W278 and B195 with anti-β-chemokines
β-chemokines produced by mitogen-activated CD4 T cells.
To investigate the possibility of enhanced sensitivity to β-chemokines, we infected non-stimulated CD4 T cells from subject B195 (not enough cells from subject W278 were available) in the presence of a cocktail of recombinant RANTES, MIP1α and MIP1β added at increasing concentrations. In the presence of low levels (≤ 5 ng) of recombinant β-chemokines, HIV-1 replication was comparable in B195 and CCR5-wt control CD4 T cells (Fig. 3C), as already observed in the absence of added β-chemokines (Fig. 3B). In contrast, when the β-chemokine levels were increased, the efficiency of infection fell sharply in B195 CD4 T cells and far less markedly in control CD4 T cells (fig. 3C) (ID50 values were 8.12 ± 1.58 ng/ml and 59.34 ± 16.87 ng/ml for B195 and control respectively). CD4 T cell CCR5 surface expression was similar in the two individuals (data not shown). These results indicated that HIV infection of CD4 T cells from EU subject B195 was unusually susceptible to inhibition by β-chemokines.
Pantropic restriction of HIV replication in subject W276 affects several lentiviruses
The blockade of in vitro HIV infection in CD4 T cells from subject W276 was independent of viral tropism and of the entry pathway (fusion or endocytosis) (fig. 1). In a fluorimetric fusion assay with cells expressing HIV-1 envelope proteins , W276 CD4 T cells showed normal membrane fusion (not shown), further supporting post-entry restriction of viral replication in these cells.
To determine whether the restriction of viral replication in CD4 T cells from subject W276 was specific to HIV-1 or also affected other lentiviruses, we challenged the cells with SIVagm and SIVmac luciferase reporter viruses (fig. 4C) pseudotyped with VSV-G. Replication of both viruses was strongly inhibited in W276 CD4 T cells.
Persistence of HIV-1 restriction in primary cells from Vietnamese EUs
Restriction in infectivity assays.
PBMC samples tested for HIV-1 infectivitya
CD4 cell samples tested for HIV-1 infectivitya
1999 (1, 7)
1998 (1), 1999 (1, 7), 2004 (6)
1998 (1), 2000 (4)
1998 (1), 2000 (4, 8), 2004 (6)
1998 (1), 2001 (1, 4)
1998 (1, 11), 2004 (1)
1998 (1), 1999 (1)
1998 (11), 1999 (1, 7)
We have previously reported that CD4 T cells from some Vietnamese individuals who remain free of infection after several years of intravenous drug use show reduced susceptibility to HIV-1 infection . Here we extended our investigations of the mechanisms underlying HIV-1 restriction in CD4 T cells and found that both entry and post-entry steps of HIV-1 replication could be affected. Interestingly, the restriction in one of these subjects also affected other lentiviruses. In addition, the restriction mechanisms persisted for several years.
The same patterns of in vitro CD4 T cell resistance to HIV-1 infection were observed after alleged interruption of at-risk behaviors, suggesting that the mechanisms of resistance in these subjects do not depend on exposure to the virus but rather might be linked to constitutive factors. It is noteworthy in this respect that heterozygous CCR5 mutations in two of the five EUs studied here (B184 and W336) were associated with low CCR5 surface expression on their primary CD4 T cells and with resistance of these cells to HIV-1 R5 infection. CCR5Δ32 heterozygosity has been associated with decreases both in CCR5 surface expression and in susceptibility to in vitro infection by R5 viruses, although to a lesser extent than CCR5Δ32 homozygosity [35–37]. Low CCR5 expression in CCR5Δ32 heterozygous cells has been attributed to several mechanisms, including sequestration of the wild-type molecule by the mutant molecule in the endoplasmic reticulum, and reduced gene dosage [37–39]. The molecular mechanisms underlying the reduced CCR5 expression in the heterozygous Vietnamese EUs' CD4 T cells are under investigation.
CD4 T cells from subjects W278 and B195 were also resistant to infection by HIV-1 R5, even though these EUs had the wild-type CCR5 molecule. HIV restriction in these subjects' cells was abrogated by anti-β-chemokine Abs. Accordingly, PCR experiments suggested that the block in CD4 T cells from subjects W278 and B195 affected very early steps of viral replication , likely reflecting inhibition of viral entry by β-chemokine ligands of CCR5 . Partial resistance to HIV-1 R5 in cells from some CCR5-wt EUs has previously been linked to decreased CCR5 expression on the CD4 T cell surface and to increased β-chemokine secretion . CCR5 expression on CD4 T cells from subjects W278 and B195 was not subnormal. However, as CCR5 expression on thawed cells (including from controls) was too low for FACS analysis, our experiments were done 10 days after PHA stimulation and we cannot therefore formally exclude the possibility that CCR5 expression was reduced on W278 and B195 CD4 T cells at the time of infection (three days after PHA stimulation) and recovered rapidly thereafter. Nevertheless, β-chemokine secretion by CD4 T cells upon mitogen activation was not higher in the two EUs than in controls, suggesting that the inhibitory mechanism differs from those previously reported. Moreover, non-stimulated CD4 T cells from these two EUs expressed normal levels of CCR5 and allowed HIV-1 entry and replication. However, in these conditions, in which endogenous secretion of β-chemokines is very low, HIV-1 infection was inhibited by exogenous β-chemokines at lower concentrations than in experiments with control cells. Thus, HIV-1 inhibition in PHA-activated CD4 T cells appears to result from enhanced sensitivity to secreted β-chemokines. In the context of wild-type CCR5, this increased sensitivity might be governed by the chemoreceptor microenvironment, which has been shown to influence both CCR5 affinity for its agonists  and β-chemokine-induced CCR5 internalization .
CD4 T cells from subject W276 exhibited a pantropic restriction phenotype independent of the virus entry pathway. Viral replication was blocked at early post-entry steps, probably through impaired reverse transcription. The restriction pattern in W276 cells (i.e. non-saturable, blockade of several lentiviruses) differed from that attributed to TRIM5α and APOBEC family proteins – restriction factors that also target early post-entry steps of viral replication [43–45]. Preliminary analyses of heterokaryons obtained by fusion of W276 CD4 T cells with the HIV-susceptible cell line A2.01 (data not shown) suggest that the restriction in EU W276 cells might be due to missing or defective cell factor(s) necessary for viral replication, rather than to antiviral molecules.
Strong CD4 T cell resistance to HIV-1 infection is a highly unusual phenomenon and it is reportedly more frequent among EUs [9, 11]. These cells provide unique opportunities for identifying novel HIV-1 resistance mechanisms. For example, the CCR5Δ32 homozygous genotype was first identified in two EUs with reduced susceptibility to HIV-1 infection , but has since been associated with protection in Caucasians  and has led to the development of CCR5-targeting drugs . However, CCR5Δ32 homozygosity accounts for cell resistance in only a small fraction of Caucasian EUs.
Each of the in vitro resistance mechanisms described here may contribute to protection against HIV-1 infection in exposed uninfected Vietnamese individuals, possibly in conjunction with other innate or adaptive antiviral responses [47, 48]. Low CCR5 expression due to CCR5 mutations in target cells may limit the infection and spread of HIV-1 R5 viruses, which are preferentially transmitted and predominate in the early phases of the human infection [49, 50]. β-chemokine-mediated resistance to HIV-1 R5 infection of activated CCR5-wt CD4 T cells could limit HIV-1 transmission and spread at preferential sites of viral replication. Indeed, HIV-1 replication occurs mainly in activated CD4 T cells, which tend to be located in β-chemokine-rich environments such as lymph nodes and gut-associated lymphoid tissue [51, 52]. Finally, near-complete restriction of viral replication, as found in the cells of EU subject W276, probably protects against HIV-1 transmission, as in CCR5Δ32 homozygous individuals. Identification of the mechanisms and molecules involved in such broad lentivirus restriction may lead to new viral and/or cellular targets for anti-HIV therapy.
The five EUs studied here (Table 1) belonged to a population of intravenous drug users (IDU) who had been exposed to HIV-1 through needle sharing for many years [11, 53]. Subjects W276, W278, and B195 correspond to subjects EU1 to EU3 and subject B184 corresponds to subject EU13 in . W336 was first described in . When recruited, they had been using drugs for 17 to 26 years. All continued high-risk practices for several years despite medical counseling. Four subsequently said they had stopped at-risk drug use between 2000 and 2003 (Table 1). Subject B195 was lost to follow-up in July 1999. Controls were Vietnamese (20) and European (7) healthy blood donors with a low risk of HIV-1 infection (Red Cross, Vietnam and Centre de Transfusion Sanguine Ile-de-France, Rungis, France). All the infectivity assays with EU CD4 T cells were performed in parallel with susceptible CD4 T cells from at least three randomly selected controls. All participants gave their informed consent.
CD4 T cells
Peripheral blood mononuclear cells (PBMC) from EUs and controls were isolated from whole blood by Ficoll-Hypaque centrifugation. CD4 cells were purified from thawed PBMC by positive selection with antibody-coated immunomagnetic beads (Miltenyi Biotech, France). Activated CD4 T cells (>95% CD4+CD3+CD25+ as estimated by flow cytometry) were obtained after stimulation for three days with phytohemagglutinin (PHA, 1 μg/ml) and interleukin-2 (IL2) (Chiron, France, 100 IU/ml) and were maintained in RPMI 1640 medium containing 10% fetal calf serum, penicillin/streptomycin (100 U/ml) and IL2.
Production of reporter viral particles and infectious challenge
Pseudotyped reporter retroviral particles were produced by transiently co-transfecting 293T cells with the proviral constructs pNL-Luc-E-R+, pSIVmac-Luc-E-R+ or pSIVagm-Luc-E-R+ [43, 54] and the VSV-G, HxB2-Env, BaL-Env, JRFL-Env or YU2-Env expression vectors (7.5 μg each) using the lipofection reagent SuperFect (Qiagen, France). Supernatants were harvested 48 h after transfection, and 105 CD4 T cells were infected (m.o.i: 0.1–1.0) in triplicate in 96-well plates with a spinoculation protocol  (1 hour of centrifugation at room temperature at 1500 g, followed by 1 hour at 37°C). After challenge, cells were extensively washed and then cultured.
Quantification of luciferase activity in cell lysates
Three days after challenge the cells were harvested and lysed with 100 μl of luciferase lysis buffer (Promega, France). Luciferase activity was quantified in 10 μl of each lysate with the Promega Luciferase Assay System in a Veritas microplate luminometer (Turner BioSystems, CA, USA).
CCR5 genotypic characterization
DNA was extracted from PBMC with the DNeasy Tissue Kit (Qiagen, Courtaboeuf, France). The full-length coding region (exon 4) of the CCR5 gene was amplified with primers and in conditions described elsewhere .
PCR products were purified with the ExoSAP-IT® enzyme for PCR Product Clean-Up (Pharmacia-Amersham, USA) and were directly sequenced with the BigDye Terminator cycle sequencing kit (ver.3.1; Applera, France). Sequences were determined with an automatic sequencer (ABI-Prism 3100, Applied Biosystem, USA) and analyzed with SeqScape software version 2.5 (Applied Biosystem, USA).
Flow cytometry of CCR5 expression
Ten days after PHA activation, CD4 T cells were incubated for 30 minutes at room temperature with CCR5-FITC (clone 2D7) (BD Bioscience, France) and analyzed on a Cytomics FC500 flow cytometer (Beckman Coulter, Paris, France).
CCR5-mediated actin polymerisation
Actin polymerization in CD4 T cells was measured as described elsewhere . Briefly, ten days after PHA stimulation, cells (1 × 107 cells/mL) were incubated in RPMI medium containing 20 mM HEPES in the presence or absence of inhibitor. RANTES (30 nM) was then added to the cell suspension. At each indicated time point (15 s to 2 min), a 50-μL aliquot of cell suspension was mixed with 200 μL of labeling buffer consisting of 10-7 M FITC-phalloidin (Sigma), 0.125 mg/mL L-α-lysophosphatidylcholine palmitoyl (Sigma) and 4.5% PFA in PBS. The kinetics of actin polymerization was monitored by means of flow cytometry. Results are expressed as follows: [MFI after addition of ligand/MFI before addition of ligand] × 100]. MFI values before ligand addition were arbitrarily set at 100%. Owing to the large number of cells required, CD4 T cells were amplified on irradiated heterologous feeder PBMC for two weeks prior to testing. The pattern of HIV-1 restriction in amplified cells was similar to that found in the primary CD4 T cells (not shown). TAK-779 was obtained through the NIH AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH.
Quantification of secreted β-chemokines
Levels of β-chemokines, RANTES, MIP-1α and MIP-1β in the supernatants of CD4 T cells were measured after 72 h of culture with or without PHA stimulation, by using commercial ELISA kits (Quantikine, R&D systems, France).
Real-time PCR quantification of HIV-1 replication intermediates
Three days after PHA stimulation, CD4 T cells were challenged with DNase (Invitrogen, France)-pretreated viruses (1 h at room temperature). At the times indicated, 5 × 105 cells were washed in PBS and lysed, then total DNA was extracted with the DNeasy Tissue Kit (Qiagen, France). Early HIV-1 reverse transcription products were quantified with an ABI PRISM 7000 instrument (Applied Biosystems, France) using specific primers and probe as previously described . One hundred nanograms of template DNA was used per reaction, and the albumin gene was used as a housekeeping gene to normalize sample input. 8E5 cells containing one integrated copy of HIV-1 per cell  were used to construct standard curves.
We thank Luong Thu Tram and Nguyen Van Ngai for follow-up of the exposed uninfected individuals, Annie David for technical assistance, Nathaniel Landau and Jay Levy for the gift of plasmids and vectors, and Ioannis Theodorou for advice and help in CCR5 genotyping.
This work was supported by the French National Agency for AIDS Research (ANRS) (#1268 and 2005/194) and Sidaction (#50007-02-00/AO16-2). ASC was the recipient of postdoctoral fellowships from ANRS and Sidaction.
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