- Open Access
HTLV-1 drives vigorous clonal expansion of infected CD8+ T cells in natural infection
© Melamed et al. 2015
- Received: 7 August 2015
- Accepted: 2 November 2015
- Published: 9 November 2015
Human T-lymphotropic Virus Type I (HTLV-1) is a retrovirus that persistently infects 5–10 million individuals worldwide and causes disabling or fatal inflammatory and malignant diseases. The majority of the HTLV-1 proviral load is found in CD4+ T cells, and the phenotype of adult T cell leukemia (ATL) is typically CD4+. HTLV-1 also infects CD8+ cells in vivo, but the relative abundance and clonal composition of the two infected subpopulations have not been studied. We used a high-throughput DNA sequencing protocol to map and quantify HTLV-1 proviral integration sites in separated populations of CD4+ cells, CD8+ cells and unsorted peripheral blood mononuclear cells from 12 HTLV-1-infected individuals.
We show that the infected CD8+ cells constitute a median of 5 % of the HTLV-1 proviral load. However, HTLV-1-infected CD8+ clones undergo much greater oligoclonal proliferation than the infected CD4+ clones in infected individuals, regardless of disease manifestation. The CD8+ clones are over-represented among the most abundant clones in the blood and are redetected even after several years.
We conclude that although they make up only 5 % of the proviral load, the HTLV-1-infected CD8+ T-cells make a major impact on the clonal composition of HTLV-1-infected cells in the blood. The greater degree of oligoclonal expansion observed in the infected CD8+ T cells, contrasts with the CD4+ phenotype of ATL; cases of CD8+ adult T-cell leukaemia/lymphoma are rare. This work is consistent with growing evidence that oligoclonal expansion of HTLV-1-infected cells is not sufficient for malignant transformation.
- Human retroviral infection
- Cytotoxic T cells
The retrovirus Human T-Lymphotropic Virus Type I (HTLV-1) causes a life-long infection in an estimated 5–10 million individuals world-wide, resulting in disabling or fatal inflammatory and malignant diseases in ~10 % of infected people . It is not completely understood what determines an individual’s risk of these HTLV-1-associated diseases; however, a high proviral load (PVL; the number of proviral copies per 100 cells) in peripheral blood mononuclear cells (PBMCs) is correlated with the risk of both the central nervous system inflammatory disease known as HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) and the malignant disease adult T-cell leukemia/lymphoma (ATL) [2, 3].
HTLV-1 can infect most nucleated mammalian cells in vitro, including both CD4+ and CD8+ T cells, but in vivo the virus is predominantly found in CD4+ T cells [4, 5]. The reasons for this preferential carriage in CD4+ T cells in vivo are not clear; mechanisms related to the cell-type distribution of cellular receptors for HTLV-1  and to long-term selection in vivo  have been suggested. ATL is typically a malignancy of CD4+ cells [8, 9]. The standard model of HTLV-1-driven cell transformation focuses on life-long clonal expansion of HTLV-1-infected CD4+ cells as a precursor to malignancy .
HTLV-1-infected CD8+ cells may have great importance. Tax-specific CD8+ cells are themselves more likely than CD8+ cells specific to another virus to be infected with HTLV-1 . Virus-specific CD8+ cells can both exert a protective antiviral effect and contribute to the pathogenesis of viral diseases such as HAM/TSP. It is unknown which of the effects attributed to the Tax-specific CD8+ cells result from their infection status, and there are conflicting reports in the literature on their functionality [12–14].
High-throughput analysis of proviral integration sites  has given new insights into the integration site preferences and frequency distribution of HTLV-1- infected clones in asymptomatic carriers (AC) of the virus and in patients with the different disease manifestations [15–17]; the relationship between integration site, HTLV-1 clonality, proviral expression and the immune response [18, 19]; and the integration site and clonality in related retroviruses [20–22]. Since there is typically a single integrated HTLV-1 provirus per cell  the number of HTLV-1-infected clones can be quantified by the abundance of observed integration sites.
Previous analyses of HTLV-1 integration were carried out on populations of unsorted PBMCs, and so did not distinguish between the different cell populations, in particular CD8+ and CD4+ T cells. The objective of the current study was to analyse the clonality of HTLV-1-infected CD4+ and CD8+ cells in both unsorted PBMCs and purified CD4+ and CD8+ populations, and quantify the contribution to the HTLV-1 proviral load made by each respective population.
Five percent of the proviral load of HTLV-1 is carried by CD8+ cells
Subject samples used in this work
Absolute cell counts (cells/µl)
Populations within T cells (%)
Populations in PBMC (%)
CD3+CD4+ in total
CD3+CD8+ in total
The proviral load in the sorted and unsorted populations (Additional file 2: Table S1) was measured using qPCR. As expected in this cohort, unsorted cells had a high proviral load (median 5 copies, range 3.7 to 11.33 copies per 100 PBMCs). In the samples sorted for CD4+ or CD8+ cells, the median proviral load was 12.3 copies (6.0–30.2) and 2.0 (1.1–6.2) copies per 100 cells, respectively.
The contribution of CD8+ cells to the load was significantly correlated with the proviral load in unsorted cells and with the proviral load in CD8+ cells (p = 0.02 and p = 0.01 respectively, Spearman’s rank correlation, Fig. 1a). There was no correlation between the proviral load in CD4+ cells and the contribution of CD8+ cells to the load.
HTLV-1-infected CD8+ cells are highly oligoclonal
We wished to compare the degree of oligoclonality between the infected CD8+ cells and the infected CD4+ cells in each subject. The proviral load in PBMCs was strongly correlated with both the proviral load in CD8+ cells (p < 0.0001, Spearman’s rank correlation) and the proviral load in CD4+ cells (p = 0.004, Spearman’s rank correlation) (Fig. 1b).
The oligoclonality index  is a measure of non-uniformity in the clone frequency distribution. The median oligoclonality index of the CD8+ samples was 0.60 (range 0.53–0.83), significantly higher than that of the CD4+ samples (median 0.53, range 0.43–0.66) (p = 0.0005, Wilcoxon signed rank test, Fig. 2b). That is, there was a less uniform clone frequency distribution—a greater degree of oligoclonality—in the CD8+ clones than in CD4+ clones. Whereas the infected CD4+ cell population often consisted of one or few highly abundant clones and a large number of clones each of which was observed only once, the CD8+ population contained a significantly smaller total number of clones (p < 0.0001, Mann–Whitney); and a much smaller proportion of the load in CD8+ cells was made up by singletons (clones observed only once) than in the CD4+ population (Fig. 2c).
We found, as observed before , no correlation between oligoclonality index and proviral load either in the unsorted PBMCs or in the CD4+ cells. In the CD8+ cells, however, there was a significant positive correlation (p = 0.017, Spearman’s rank correlation) between the oligoclonality and proviral load in CD8+ cells (Fig. 2d).
The total number of clones observed in the CD4+ samples was significantly higher than in sorted CD8+ samples. However, it was also higher than the number in the unsorted PBMC samples. We hypothesize that this is due to enrichment of infected cells from small clones by cell sorting. We used the recently developed DivE method to estimate the total number of clones (clonal diversity)  in the blood. The estimated total number of CD8+ clones in the circulation was approximately tenfold less than that of CD4+ clones (Fig. 2e).
HTLV-1-infected CD8+ clones are over-represented among the most abundant clones in non-malignant HTLV-1 infection
To test whether CD8+ clones were more likely to be present among the most abundant clones than expected by chance, we compared the proportion of clones with an absolute abundance of more than 1 copy per 10,000 PBMCs between CD4+ and CD8+ clones (Fig. 3b). This proportion was significantly greater in CD8+ clones (~10 %) than in the CD4+ clones (~5 %; p < 0.0001, Fisher’s exact test). Ranking all clones in descending order of abundance (Fig. 3c), CD8+ clones were found more often among the 10 most abundant clones (clone 1–10) than in the next 10 (clones 11–20; p = 0.012, Fisher’s exact test).
The abundant CD4+ and CD8+ HTLV-1-infected T-cell clones are long-lived in vivo
HTLV-1 infection alters the frequency of CD8+ cells but not CD4+ cells in peripheral blood
HTLV-1 primarily infects CD4+ T-cells in vivo, and the great majority of ATL cases are CD4+ . The smaller, HTLV-1-infected CD8+ cell population has not been intensely studied. Small numbers of other cell types such as monocytes  may be infected. However, our data show that other cell types were unlikely to be present in the clonally expanded populations of HTLV-1-infected cells, because almost all (99.7 %) of the most highly abundant clones were identified as CD4+ or CD8+ cells. Small numbers of CD4+ monocytes might have been included in the sorted CD4+ fraction, but this number is likely to be very small because monocytes are not efficiently selected by magnetic bead sorting owing to their lower expression of CD4+ .
Our results show that HTLV-1-infected CD8+ cell clones make an unexpectedly large impact on the clone frequency distribution observed in the blood. While the CD8+ clones represent only a minority (median 5 %) of the proviral load, they are often highly represented among the most abundant clones in the blood, and among the most long-lived clones (across all clone abundances).
Comparison of the clone frequency distribution of proviruses between infected CD8+ and CD4+ cells revealed significant differences between the two populations. Whereas proviruses in infected CD4+ cells were present in a very large number of clones, each of which was often of low abundance, the clones observed in CD8+ T cells were often highly abundant. The oligoclonality index was significantly higher in CD8+ cell samples than in CD4+ cell samples and the proportion of the proviral load carried by low-abundance clones (clones observed only once) was significantly higher among CD4+ cell samples.
Previous investigations of HTLV-1 clonality showed no correlation between the HTLV-1 proviral load and the oligoclonality index in non-malignant HTLV-1 infection, but the correlation was significant in malignant HTLV-1 infection [15, 17, 20]. This observation was repeated here in the unsorted PBMCs; however, there was a significant positive correlation between the oligoclonality index in CD8+ cells and the proviral load in these cells. This observation suggests that the ratio of infectious spread (infection of new clones) to mitotic spread (proliferation of infected cells by increased mitotis or reduced apoptosis) differs between CD4+ and CD8+ cells during chronic HTLV-1 infection.
It is not known what mechanisms contribute to the difference in the degree of clonal expansion between the two cell types in HTLV-1 infection. We previously showed that the genomic integration site of the provirus plays a role in driving or silencing proviral gene expression, which in turn drives clonal expansion of CD4+ cells [15, 18]. However, infected CD8+ cells can express high levels of Tax and can then be killed by Tax-specific CD8+ cells [11, 28]. It is not known whether Tax-expressing CD4+ cells are killed as efficiently as Tax-expressing CD8+ cells. Proliferation of HTLV-1-infected CD8+ cells may be selectively enhanced by their response to specific antigen, such as those expressed by other persistent viruses or, perhaps most likely, antigens of HTLV-1 itself.
Oligoclonal expansion of Tax-specific CTLs has been reported , but it was not known whether these expanded clones are also infected by the virus. The notion that HTLV-1-infected, HTLV-1-specific CTLs grow to high abundance in the circulation is consistent with the previous observations that HTLV-1-specific CTLs are preferentially infected with HTLV-1  and that the frequency of HTLV-1-specific CTLs is correlated with the proviral load [30, 31].
Sibon et al.  cultured clones of HTLV-1-infected and uninfected CD4+ and CD8+ cells, and concluded that the more vigorous expansion observed in infected CD8+ cells in vitro was due to a reduction in apoptosis rather than increased proliferation. If this is also the case in vivo, it could explain how CD8+ clones proliferate and persist, with a low risk of generating the somatic mutations that contribute to malignant transformation . IL-15 has been shown to protect Tax-specific cells from apoptosis . HTLV-1 Tax upregulates both IL-15 and its receptor [35, 36], and an increase in IL-15 mRNA has been observed in HAM/TSP patients . Thus, HTLV-1 may exploit a normal IL-15-dependent pathway for the maintenance of memory CD8+ cells  to maintain its own infected CD8+ cell population. Cytokine-dependent proliferation of infected CD8+ cells could also explain the observation made in this study that the proportion of CD8+ T cells in the PBMCs was positively correlated with the viral burden in the CD8+ cells: abundant IL-15 secreted by infected cells could also drive proliferation of uninfected CD8+ T cells.
Previously  we reported the clone frequency distribution of HTLV-2, a virus closely related to HTLV-1; HTLV-2 is mainly found in CD8+ cells in infected individuals. Unlike HTLV-1, HTLV-2 does not cause leukemia or lymphoma. The findings here and those observed in HTLV-2 infection share several similarities. As we observed in HTLV-1-infected CD8+ cells, HTLV-2 infection was characterized by a high oligoclonality index due to a small number of abundant clones in the absence of malignancy. The oligoclonality index in HTLV-2 was significantly correlated with the proviral load, as observed here in HTLV-1-infected CD8+ (but not CD4+) cells. These observations suggest that physiological differences between CD8+ cells and CD4+ cells contribute to the observed differences in the clone frequency distribution between the two infected cell populations.
HTLV-1 infection is associated with a strong, constitutively active anti-HTLV-1 cytotoxic T-lymphocyte (CTL) response. Virtually all individuals with non-malignant HTLV-1-infection possess CTLs specific to Tax peptides [39, 40]. The most immunogenic peptide encoded by the virus is Tax11-19, which is efficiently presented in the context of HLA-A2 [41, 42]. Despite its high immunogenicity, this peptide is highly conserved. HTLV-2 encodes a nearly identical immunodominant peptide . It is possible that this highly immunogenic peptide provides a selective advantage to the virus by driving proliferation of infected, antigen-specific T cells.
We conclude that the combined mitotic and antigenic effects of Tax in maintaining proliferation of infected CD8+ T cells may outweigh the negative selection by Tax-specific CTL-mediated killing of the infected CD8+ T cells.
We recently showed that the HTLV-1 proviral load, the strongest predictor of the risk of both inflammatory disease (HAM/TSP) and malignant disease (ATL), does not correlate with the degree of clonal expansion (the oligoclonality index), but rather with the total number of HTLV-1-infected clones. We also found, in an analysis of the integration site preferences among ~200 ATL patients, that the malignant ATL clones resemble the low-abundance clones more closely than the intermediate-abundance clones that have undergone oligoclonal proliferation . ATL can arise by the rapid emergence (within 18 months) of a previously rare clone, outgrowing the pre-existing oligoclonally expanded clones . Finally, HTLV-2 was found in highly abundant clones in vivo, but this virus does not cause leukemia or lymphoma . However, malignant diseases of CD8+ T cells are generally rarer than those of CD4+ T cells , suggesting that the cell type determines the risk of malignancy. The viral mechanisms that cause clonal proliferation of HTLV-1-infected cells may be distinct from those that lead to malignant transformation.
The observation that HTLV-1 causes oligoclonal proliferation of infected cells led to a widespread assumption that the oligoclonal proliferation predisposes to leukemogenesis. Here we show that contrary to that assumption, the cells that undergo the greatest clonal expansion in HTLV-1 infection are the HTLV-1-infected CD8+ cells. However, cases of CD8+ ATL are very rare. The results of the present study therefore add further to the conclusion  that oligoclonal T-cell proliferation per se does not predispose to malignant disease in HTLV-1 infection. Further work is needed to determine the mechanisms involved with the selective expansion of certain CD8+ clones, and their potential role in HTLV-1-associated disease.
Blood samples and anonymized patient information were obtained through the Communicable Diseases Tissue Bank at Imperial College, approved by the UK National Research Ethics Service (NRES reference 09/H0606/106). Samples were donated by HTLV-1-infected subjects attending the National Centre for Human Retrovirology, St Mary’s Hospital, Imperial College Healthcare NHS Trust, London after giving written informed consent.
Cells and samples
PBMC samples from 12 HTLV-1-infected individuals were analysed. See Table 1 for details of samples used. The 12 subjects included 6 patients with HAM/TSP and 6 asymptomatic carriers. ACs with a high PVL were selected; if the PVL is less than 0.1 % the number of proviruses sampled does not give adequate statistical power. One of the ACs (HGL) was diagnosed with HAM/TSP approximately 1 year after the sample was taken.
PBMCs were isolated from blood using Histopaque-1077 (Sigma-Aldrich) and cryopreserved in fetal bovine serum (Gibco) containing 10 % dimethylsulfoxide (Sigma-Aldrich). DNA was extracted from sorted or unsorted cells using the DNeasy Blood and Tissue Kit (Qiagen) according to the manufacturer’s protocol, and eluted in Qiagen EB buffer.
Uncultured, unfixed, cryopreserved PBMCs were sorted sequentially on the basis of CD4 and CD8 expression, using magnetic beads (Miltenyi). First, CD4+ cells were positively selected, and CD8+ cells were then selected from the CD4− fraction. The cells were passed twice over sorting columns at each stage, to maximize purity and recovery.
Purity testing and analysis of cell population frequency in unsorted samples was carried out using flow cytometry, after fixation and staining for surface expression of CD3 (clone UCHT1, eBioscience), CD4 (clone RPA-T4, eBioscience) and CD8 (clone SFCI21Thy2D3, Beckman Coulter).
Genomic DNA was extracted from both the sorted and the unsorted cell populations, and from unsorted PBMCs at a second time point (median time difference 3.4 years) where available. Proviral integration sites were mapped and quantified as previously described . Sequencing of amplified integration sites was done using the Illumina GAII, HiSeq or MiSeq platforms, using 50-base paired-end reads and a 6-base barcode to allow multiplexing. Sequence data were aligned against a combined reference of the human genome (hg18) and the HTLV-1 genome sequence using an Eland implementation of CASAVA software (Illumina), then filtered and quantified for clone abundance using in-house software as previously described. See Additional file 2: Table S2 and Additional file 8 for details of the sequencing results.
Based on the assumption that HTLV-1 infects differentiated, mature CD4 or CD8 single-positive cells, we attributed any integration site found in both CD4+ and CD8+ cells to the cell subpopulation (CD4+ or CD8+) in which it was identified with a higher frequency (greater number of proviruses). The frequency of these putative contaminating clones was significantly inversely correlated with the measured purity of the sample, and significantly positively correlated with the frequency of the contaminating population and its share of the load (not shown).
Data analysis was carried out using R (http://www.R-project.org/ ). The oligoclonality index was calculated using the package reldist . Unless specified otherwise, non-parametric statistical tests were used. A result was considered statistically significant when p < 0.05 (two-tailed).
The total number of clones present in the circulation was estimated using the DivE estimator . DivE fits multiple mathematical models to individual-based rarefaction curves; such curves plot the expected number of clones against the number of infected cells sampled. Numerical criteria are then used to score models on their ability to accurately estimate additional data. The best-performing models are extrapolated to estimate the total number of clones in the blood, based on the proviral load in the respective subject.
AM, CRMB and GPT designed the experiments, AM and HAK carried out the experiments, AM, DJL and AGR analysed the data. AM and CRMB wrote the manuscript. All authors read and approved the final manuscript.
The authors wish to thank Maria-Antonietta Demontis (Section of Infectious Diseases, Imperial College London, London, UK) and the staff and donors at the National Centre for Human Retrovirology (Imperial College Healthcare NHS Trust, St Mary’s Hospital, London, UK). We thank Laurence Game, Adam Giess and Marian Dore (Genomics Laboratory, MRC Clinical Sciences Centre, Hammersmith Hospital, London, UK), and the High Performance Computing service staff at Imperial College (http://www.imperial.ac.uk/ict/services/teachingandresearchservices/highperformancecomputing). This work was supported by a Wellcome Trust Senior Investigator award 100291 to CRMB. GPT is supported by the NIHR Imperial Biomedical Research Centre. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors declare that they have no competing interests.
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