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Journal of Virology, October 2006, p. 9710-9719, Vol. 80, No. 19
0022-538X/06/$08.00+0     doi:10.1128/JVI.01022-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Peripheral Blood B-Cell Death Compensates for Excessive Proliferation in Lymphoid Tissues and Maintains Homeostasis in Bovine Leukemia Virus-Infected Sheep{dagger}

Christophe Debacq,1 Nicolas Gillet,1 Becca Asquith,2 Maria Teresa Sanchez-Alcaraz,3 Arnaud Florins,1 Mathieu Boxus,1 Isabelle Schwartz-Cornil,4 Michel Bonneau,4 Geneviève Jean,5 Pierre Kerkhofs,6 Jack Hay,7 André Théwis,5 Richard Kettmann,1 and Luc Willems1*

Molecular and Cellular Biology, FNRS-FUSAG, Gembloux, Belgium,1 Department of Immunology, Imperial College, London, United Kingdom,2 Department of Medical Genetics and Microbiology, University of Toronto, Toronto, Ontario, Canada,3 U892 INRA, Jouy-en-Josas, France,4 Zootechny Unit, FUSAG, Gembloux, Belgium,5 Department of Virology, Veterinary and Agrochemical Research Centre, Uccle, Belgium,6 Department of Immunology, University of Toronto, Toronto, Ontario, Canada7

Received 18 May 2006/ Accepted 7 July 2006


   ABSTRACT
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
The size of a lymphocyte population is primarily determined by a dynamic equilibrium between cell proliferation and death. Hence, lymphocyte recirculation between the peripheral blood and lymphoid tissues is a key determinant in the maintenance of cell homeostasis. Insights into these mechanisms can be gathered from large-animal models, where lymphatic cannulation from individual lymph nodes is possible. In this study, we assessed in vivo lymphocyte trafficking in bovine leukemia virus (BLV)-infected sheep. With a carboxyfluorescein diacetate succinimidyl ester labeling technique, we demonstrate that the dynamics of lymphocyte recirculation is unaltered but that accelerated proliferation in the lymphoid tissues is compensated for by increased death in the peripheral blood cell population. Lymphocyte homeostasis is thus maintained by biphasic kinetics in two distinct tissues, emphasizing a very dynamic process during BLV infection.


   INTRODUCTION
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
In vertebrates, continuous recirculation of lymphocytes from blood through tissues and lymph nodes is critical for protection of the host during pathological inflammatory processes, as well as physiological emigration of lymphocytes that participate in immune surveillance (1, 4, 6, 11, 16, 33). The network of exchange between blood and lymph through the lymph node is absolutely required to maintain normal cell homeostasis. The presence of homeostatic control of lymphocyte numbers ensures an equilibrium where cell production equals cell loss. In an immune system where lymphocyte production is continuous and the total number of cells is constant, each newly produced lymphocyte can only survive if another one dies; i.e., the rate of peripheral cell renewal depends on the life span of peripheral cells. However, the life expectancy of a lymphocyte is not an intrinsic property of the cell but is determined by factors such as the environment, viral infections, and the presence or absence of another, competing, cell population. We previously studied lymphocyte homeostasis, more particularly, lymphocyte proliferation and death, in different animal models of chronic leukemia, including sheep infected by the bovine leukemia virus (BLV) (7-9). In this model, proliferation was estimated by intravenous injection of bromodeoxyuridine (BrdU), a thymidine analog which is incorporated into the newly synthesized DNA via the pyrimidine salvage pathway. Although BrdU uptake by cells might occur in blood, its incorporation is thought to occur mainly, if not exclusively, in lymphoid tissues such as the lymph nodes, the spleen, or the bone marrow (7). By this approach, the estimated B-cell proliferation rates in infected and control sheep were 0.020 day–1 and 0.011 day–1, respectively, meaning that 2.0 and 1.1% of the cells were produced by proliferation in 1 day. In contrast, the death rates of BrdU-labeled cells were not significantly different between the two categories of animals (average death rate, 0.089 day–1 versus 0.094 day–1, respectively). The imbalance created by the net increase in proliferation in the absence of compensating cell death was estimated at 7% growth in a day (7), leading to a theoretical very fast doubling of the cell population. However, this considerable increase in lymphocyte numbers is, in fact, not observed in vivo. Therefore, other processes, including a reduction of cell recirculation through the lymph node, as well as massive elimination of cells in secondary lymphoid tissues (28, 29), could play a role in maintaining homeostasis.

The goal of this study was to test these hypotheses by tracking B cells from blood to lymph and back from lymph to blood. The strategy that we used was based on a single intravenous injection of carboxyfluorescein diacetate succinimidyl ester (CFSE) into BLV-infected sheep. In vivo administration of the dye has achieved a blood leukocyte labeling index of >95%, making it feasible to track lymphocyte migration through the lymph node in vivo (3, 27). While most studies of lymphocyte recirculation and homing have been done with rodents (12), sheep offer the opportunity to study recirculation of lymphocytes through tissues by direct cannulation of individual lymphatic vessel (15). Therefore, lymphatic cannulation of sheep, combined with CFSE injection, provided quantitative and qualitative physiological measurements of the recirculation and death of lymphocytes through lymph nodes for extended periods of time in normal and pathological situations.


   MATERIALS AND METHODS
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Cannulation of efferent lymphatics. Eleven sheep were kept under controlled conditions at the Veterinary and Agrochemical Research Centre (Machelen, Belgium). Five animals (2147, 2149, 2152, 4533, and 4534) were used as uninfected controls, whereas sheep 107, 1095, 2091, 2158, 4535, and 4536 were experimentally infected with a BLV wild-type cloned provirus (strain 344) as described previously (31). Table 1 illustrates the percentages of B cells in the blood and lymph, as well the type of cannulated lymph node (prescapular or mesenteric), in the experimental sheep. Total leukocyte counts were determined by using a Coulter counter ZN, and the number of lymphocytes was estimated under a microscope after staining with May-Grünwald-Giemsa. In parallel, the serum of each sheep was analyzed for BLV seropositivity by immunodiffusion and enzyme-linked immunosorbent assay techniques (25). Cannulae were surgically established in intestinal or prescapular efferent lymphatics to allow chronic sampling of lymph as previously described (34). Briefly, sheep were fasted for 24 h preceding surgery and anesthetized by intravenous injection of pentobarbital sodium (Nembutal; Abbott) or fluothane (Covely) with closed-circuit anesthetic equipment. Aseptic surgical techniques were used throughout the surgery. Silicone (Vygon) or vinyl (Scientific Commodities) catheters were filled with heparin (Sigma) and positioned in efferent lymphatic vessels. Following surgery, animals were allowed to recover for at least 24 h prior to cell collection. Lymph samplings were performed arbitrarily at short intervals of time in the beginning of the experiment in order to precisely define the best kinetics of CFSE-labeled cell migration. All animals were housed in metabolism cages during lymph collection and allowed free access to food and water during the experiment. Handling of animals and experimental procedures were conducted in accordance with institutional and national guidelines for animal care and use.


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  		TABLE 1. Overall design of the lymph node cannulation studya

 
In vivo CFSE cell labeling and immunophenotyping. Twenty-five milligrams of CFSE dissolved in 4 ml of dimethyl sulfoxide and 40 µl of heparin (1,000 U/ml) was directly injected into the peripheral blood via the jugular vein in order to label blood leukocytes (27). At regular intervals of time, blood was collected by jugular venipuncture and peripheral blood mononuclear cells (PBMCs) were isolated by Percoll gradient centrifugation (Sigma). Lymph was collected in sterile bottles attached to bottle holders pasted to the skin of animals and containing 1,000 U of heparin. Lymphocytes were harvested by low-speed centrifugation, and cell viability was estimated by trypan blue dye exclusion.

Cells were labeled with monoclonal antibodies directed against surface immunoglobulin M (anti-sIgMs, clone 1H4, mouse IgG1; Pig45A2, mouse IgG2b), CD4 (ST4, mouse IgG1), CD5 (CC17, mouse IgG1), CD8 (CC58, mouse IgG1), CD11b (CC125, mouse IgG1), {gamma}{delta} T cells (86D, mouse IgG1), CD21 (GB25A, mouse IgG1), and L-selectin (DU1-29, IgG1) provided by C. Howard (Institute for Animal Health, Compton, United Kingdom) and by one of us (I.S.-C.) or obtained from VMRD Inc. Cells were then labeled with a rat anti-mouse IgG1 phycoerythrin-conjugated antibody or with a rat anti-mouse IgG2a+b peridinin chlorophyll protein (PerCp) antibody (Becton Dickinson Immunocytometry Systems). For detection of the p24 major capsid antigen, PBMCs were cultivated at 37°C in a 5% CO2-air atmosphere in RPMI 1640 medium supplemented with 10% fetal calf serum, 2 mM L-glutamine, 100 U of penicillin, and 100 µg of streptomycin per ml (Sigma). After 24 h of culture, PBMCs were collected and washed once with phosphate-buffered saline-0.5% bovine serum albumin. The cells were fixed and permeabilized with the IntraStain reagent (DAKO). Internal detection of the p24 viral protein was performed by sequential incubation with 4'G9 monoclonal antibody and a rat anti-mouse IgG1 phycoerythrin conjugate (Becton Dickinson Immunocytometry Systems). Finally, cells were analyzed in combination with CFSE by flow cytometry on a Becton Dickinson FACScan flow cytometer. Ten thousand events were collected for each sample, and data were analyzed with the CellQuest software (Becton Dickinson Immunocytometry Systems).

Mathematical model. To estimate the proliferation and disappearance rates of different cell populations, a mathematical model was constructed (details were provided by Asquith et al. [2]). Briefly, the model uses two pieces of data from the flow cytometry analyses, i.e., the proportion of CFSE+ cells (P) and the ratio of the mean fluorescence intensity of the CFSE+ population to the CFSE– population (I), to estimate the rate of proliferation and the rate of death of CFSE-labeled B lymphocytes. To develop the model, we first estimated the number of divisions (halving of fluorescence) between an average CFSE+ cell and an average CFSE– cell at time zero. It was found to be five for sheep 2152, 4533, 4534, 2091, 2158, 4535, and 4536 and six for sheep 2147. The model for five divisions is x0 = –(p + d)x0, x1 = 2px0 – (p + d)x1, x2 = 2px1 – (p + d)x2, x3 = 2px2 – (p + d)x3, x4 = 2px3 – (p + d)x4, and x5 = 2px4 – (p + d)x5 + {lambda}, where xi is the proportion of B cells that have undergone i divisions since CFSE labeling. In the model, the cells in the x5 category are CFSE– (either because they have divided five times since labeling and therefore lost their fluorescence or because they were not labeled by the initial injection). The average proliferation rate of cells is p, the average disappearance rate is d, and the average replacement rate is {lambda}. These equations can be solved analytically and then used to find expressions for I, the ratio of the mean fluorescence intensity (MFI) of the CFSE+ population to the CFSE– population, and P, the proportion of CFSE+ cells, as follows:

Formula

Formula
Here, J is the MFI of the CFSE label in undivided cells and F is the proportion of peripheral blood B cells labeled by the initial injection. These formulas were fitted to the experimental data by nonlinear regression, and lymphocyte kinetics were estimated.


   RESULTS
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
B lymphocytes from BLV-infected and control sheep recirculate at similar rates. The kinetics of the whole peripheral blood population can be investigated by in vivo administration of CFSE (i) because cells are labeled regardless of their division state; (ii) because CFSE labels all of the cells in the whole peripheral blood; (iii) because of instability of the succinimidyl ester moiety, initial labeling by CFSE ends within a few minutes; and (iv) because insufficient CFSE reaches the lymph nodes to directly label cells in this compartment (27). Cell migration from the peripheral blood through individual lymph nodes can then be identified by placing indwelling catheters into the efferent lymphatic vessels and subsequent analysis by flow cytometry. We first verified that no CFSE-labeled cells were detectable in the efferent lymph immediately after CFSE injection (see Fig. S1 in the supplemental material).

Figure 1A illustrates an example of B-cell-CFSE dual flow cytometry analysis performed on lymph recovered from a BLV-infected sheep (4535) and a control (4534) sheep at 2, 22, and 94 h after CFSE injection. The percentages of B+ CFSE+ cells in the total B-cell population were low at 2 h post CFSE injection, increased at 22 h, and stabilized later on.


Figure 1
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  		FIG.1. B-cell trafficking through the lymph node. (A) The efferent lymphatic vessels from the prescapular lymph nodes of a BLV-infected (4535) and a control (4534) sheep were surgically cannulated, allowing chronic sampling of lymph. Animals were injected intravenously with 25 mg of CFSE. At regular intervals of time (2, 22, and 94 h), lymph was collected and B cells were labeled with the anti-IgM 1H4 monoclonal antibody in association with a phycoerythrin conjugate. Ten thousand cells were then analyzed by two-color flow cytometry (x axis = CFSE; y axis = B lymphocytes). The percentages of CFSE+ B cells within the total B-lymphocyte population are indicated in the upper right quadrants. (B) Lymph samples from four BLV-infected (107, 1095, 4535, and 4536) and four control (2149, 2152, 4533, and 4534) sheep were continuously collected at regular intervals of time (in hours) post CFSE injection, and the percentages of CFSE+ B cells within the total B-cell population were determined. A vertical line is placed at 24 h. (C) Graphic distribution of the percentages of CFSE+ B cells in efferent lymph recovered at 26 h after CFSE injection. Individual values (BLV-infected [{blacktriangleup}, 107; {blacklozenge}, 1095; {blacksquare}, 4535; •, 4536] and uninfected [{triangleup}, 2149;{diamond}, 2152; {square}, 4533; {circ}, 4534] sheep) and mean values (black lines) are represented. NS means no statistically significant difference by the Student t test. (D) Schematic representation of the change in label over time in the lymph. The model contains two parameters, i.e., the rate of increase in the label (a) and the equilibrium value of the label (k). Neither the rate of recirculation of labeled B cells to the lymph nor the equilibrium value of labeled cells in the lymph varied between BLV-infected and uninfected sheep (P = 0.39 and P = 0.57 for a and k, respectively, according to the Wilcoxon-Mann-Whitney two-tailed test).

 
To extend these observations, the recirculation kinetics of CFSE-labeled blood B cells was determined by this approach in four BLV-infected and four control sheep (Fig. 1B). The data shown for sheep 4533, 4534, 4535, and 4536 result from prescapular cannulation; the data for sheep 2149, 2152, and 107 were obtained with mesenteric lymph; and sheep 1095 was cannulated in both the prescapular and mesenteric lymph nodes. Although the appearance rate of CFSE+ B lymphocytes in the efferent lymph slightly varied in different animals, the percentage of labeled cells consistently reached an equilibrium level of approximately 3 to 7% after about 20 to 30 h. These recirculation kinetics in control sheep are thus in accordance with previous reports assuming that the maximum recovery of all subsets of lymphocytes in efferent lymph is about 24 h (27, 33). However, we could not observe a significant difference between the kinetics of CFSE-labeled cell exit from the lymph nodes independently of the cannulated lymph node. Importantly, the recirculation rates in BLV-infected sheep did not significantly differ from those in the controls (as determined by a two-tailed Student t test at 26 h; Fig. 1C). Furthermore, we analyzed the change in the label over time in the lymph by fitting a growth model with two parameters—the rate of increase of the label (a) and the equilibrium value of the label (k) (Fig. 1D). Finally, neither the rate of recirculation of labeled B cells to the lymph nor the equilibrium value of labeled cells in the lymph varied between BLV-infected and uninfected sheep (P = 0.39 and P = 0.57 for a and k, respectively, according to the Wilcoxon-Mann-Whitney two-tailed test).

Peripheral blood B cells from BLV-infected and control sheep exhibit different CFSE kinetics. If recirculation through lymph nodes is not involved, other regulatory processes, such as higher death rates of the peripheral blood B-lymphocyte population, might compensate for a global excess of proliferation in BLV-infected sheep. To test this hypothesis, CFSE kinetic profiles of peripheral blood B lymphocytes were compared in BLV-infected and control sheep. We first verified that CFSE injection indeed leads to very efficient fluorescent labeling of PBMCs in vivo (Fig. 2A), as reported in a previous paper (27). After reaching a labeling index of >95% 1 min after injection, the percentages of CFSE-labeled cells within the PBMC population rapidly dropped at 2 h (illustrated in panel A for a noninfected sheep). Flow cytometry analyses with PBMCs isolated from a BLV-infected (2091) and a control (2147) sheep at days 0, 1, 6, and 34 after CFSE injection are illustrated in Fig. 2B. At day 1, approximately half of the B cells were CFSE+ (51.6 and 46.0% in the control and BLV-infected sheep, respectively; Fig. 2B). The percentage of CFSE-labeled B cells in blood then decreased more quickly in the infected sheep than in the uninfected animal (4.6% and 15.8% at day 34 for the infected and uninfected sheep, respectively). A similar difference in kinetics was observed in two other BLV-infected sheep (4535 and 4536) and two controls (4533 and 4534) (Fig. 2C). Indeed, the percentages of CFSE-labeled B cells reached a level below 5% around days 27 to 42 for BLV-infected sheep (2091, 4535, and 4536), whereas the same value was obtained only after 83 days in the controls (2147, 4533, and 4534) (arrows in Fig. 2C). Interestingly, the decrease in CFSE+ peripheral blood B cells was thus consistently faster in BLV-infected animals than in controls.


Figure 2
Figure 2
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  		FIG.2. B-cell CFSE kinetics in peripheral blood. (A) CFSE was injected into the jugular vein of a control sheep (117), and blood was recovered at different times (before and 1 min, 2 h, and 6 days after injection) from the other jugular vein. PBMCs were isolated by Percoll gradient centrifugation, and fluorescence was measured by flow cytometry of 10,000 cells (x axis = CFSE; y axis = number of events). (B) One BLV-infected (2091) and one control (2147) sheep were injected intravenously with a bolus of CFSE, and an aliquot of blood was collected by jugular venipuncture before injection and at 1, 6, or 34 days postinjection. PBMCs were purified, and B cells were labeled with the anti-IgM 1H4 monoclonal antibody and stained with a phycoerythrin conjugate. Finally, 10,000 cells were analyzed by flow cytometry (x axis = CFSE; y axis = B lymphocytes). The percentages of CFSE+ B cells within the total B-lymphocyte population are indicated in the upper right quadrants. (C) Kinetics of the CFSE+ B-cell population in the peripheral blood of three BLV-infected (2091, 4535, and 4536; solid lines) and three control (2147, 4533, and 4534; dotted lines) sheep. The arrows indicate key times of CFSE kinetics (day 27 and day 83) at which the percentages of labeled B cells reached baseline levels in BLV-infected sheep and in the controls, respectively.

 
A CD11b subpopulation accounts for the difference in CFSE kinetics in BLV-infected sheep. To test whether this difference in kinetics was associated with a particular cell phenotype, CFSE labeling was evaluated in four subsets of B cells expressing L-selectin, CD21, CD5, or CD11b. These markers were selected primarily because the migration competence of B lymphocytes correlates with the surface expression of L-selectin and CD21 mediating subsequent integrin-dependent adherence (14, 35). Moreover, BLV preferentially replicates in CD5+ and CD11b+ B lymphocytes, although cells negative for these receptors are also less efficient targets for the virus (5, 22). After CFSE injection, PBMCs were isolated from BLV-infected or control sheep; labeled sequentially with an anti-IgM antiserum and with anti-L-selectin, anti-CD21, anti-CD5, or anti-CD11b monoclonal antibodies; and then analyzed by three-color flow cytometry. Importantly, all of the cell populations in the peripheral blood were CFSE labeled with efficiencies of >95% (data not shown). For three out of the four markers (i.e., L-selectin, CD21, and CD5), the CFSE profiles were the same for marker-positive and marker-negative cells and the difference between the CFSE profiles of uninfected and infected animals was maintained (Fig. 3). In contrast, the kinetics of CD11b– B lymphocytes was similar between BLV-infected and control samples (and particularly at day 26 [arrow]), indicating that the expression of the CD11b integrin accounted for the particular CFSE profile of infected sheep.


Figure 3
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  		FIG. 3. Kinetic analyses of B-cell subsets. At regular time intervals of the CFSE kinetic analysis of three BLV-infected sheep (2091, 4535, and 4536) and three controls (2147, 4333, and 4534) (Fig. 2), PBMCs were labeled with a B-lymphocyte-specific antibody and with a peridinin-chlorophyll-protein conjugate. The PBMCs were then incubated with monoclonal antibodies directed against L-selectin, CD21, CD5, or CD11b and with a phycoerythrin conjugate. Finally, 10,000 events of thrice-labeled cells were analyzed by flow cytometry. The percentages of CFSE+ B cells expressing L-selectin, CD21, CD5, or CD11b in the corresponding B-lymphocyte subsets were determined at different time intervals (in days). At day 26, the percentages of CFSE+ CD11b– B cells reached baseline levels in both infected sheep and controls (arrow).

 
The death rate of peripheral blood B cell is increased in BLV-infected sheep. A reduction in the proportion of CFSE+ lymphocytes can be due either to cell death or to label dilution below the threshold of detection due to proliferation. These parameters could be quantified assuming that the fluorescence intensity of the CFSE label is halved upon cell division. A mathematical model was designed by incorporating a relationship between I (the ratio of the mean fluorescence intensities of B+ CFSE+ and B+ CFSE– populations) and P (the proportion of CFSE+ B cells) (Asquith et al., unpublished data). By fitting this model to the CFSE data (theoretical fits, Fig. 4) from four BLV-infected and four control sheep, the average proliferation rate (p) and death rate (d) of the CFSE+ B-cell population could be estimated (Table 2). The proliferation rate is an estimate of the proportion of B cells that divide in 1 day (e.g., in sheep 2147, if p = 0.049 day–1 then approximately 4.9% of the CFSE+ B lymphocytes proliferate in 1 day). Similarly, the death rate (0.079 day–1) is the proportion of labeled B cells that disappear from the blood of the animal in 1 day. On the basis of the measured incorporation levels, the proliferation and death rates were calculated for all of the sheep studied (Table 2). The mean proliferation rates were not significantly different in the two categories of animals (0.029 ± 0.017 for the controls and 0.039 ± 0.003 for the BLV-infected sheep; no statistically significant difference by the Student t test). In contrast, a statistically significant difference (P < 0.01 by the two-tailed unpaired Student t test) was observed between the death rates of B lymphocytes from BLV-infected and control sheep.


Figure 4
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  		FIG. 4. Theoretical fit of the model to the CFSE data. The percentages of CFSE+ B cells (P [black squares]) and the ratio of the MFI of B+ CFSE+ cells to the MFI of B+ CFSE– cells (I [open triangles]) were determined by flow cytometry analyses. The data corresponding to the P and I values were fitted simultaneously to a mathematical model, yielding theoretical curves.

 

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  		TABLE 2. Minimal proliferation and death rates estimated from CFSE dataa

 
We thus conclude that in BLV-infected sheep, the peripheral blood B-lymphocyte population undergoes increased cell death. This conclusion is supported by the fact that very few cells labeled with CFSE in the blood and trafficking through the lymph node are able to express viral capsid antigen p24 (Fig. 5A). The most straightforward interpretation of this observation is that efficient immune selection is exerted toward cells spontaneously expressing BLV.


Figure 5
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  		FIG. 5. Model summarizing the dynamic parameters studied. (A) PBMCs from two BLV-infected sheep were isolated from total blood, and cells were collected in parallel from lymph. Cells were cultivated for 24 h in RPMI medium supplemented with 10% fetal calf serum, 2 mM glutamine, and penicillin-streptomycin. B cells and viral capsid protein p24 were then labeled with specific monoclonal antibodies and analyzed by flow cytometry. The percentages of CFSE+ B cells expressing p24 in blood are represented by black bars, and data from lymph are represented by gray bars. The data are mean values and standard deviations resulting from more than five samplings taken over a period of 46 h post CFSE injection. (B) Quantification of proliferation and death rates in BLV-infected sheep. Excessive proliferation in the lymphoid tissues measured by BrdU incorporation can be compensated for by an increase in cell death in the peripheral blood, as deduced from the CFSE kinetics. The percentages shown represent the proliferation or death rates determined in BLV-infected or control sheep. **, statistically significant difference (P < 0.01) by the two-tailed unpaired Student t test.

 

   DISCUSSION
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
Homeostatic regulation of lymphocyte numbers in the peripheral blood results from a series of physiological factors of which cell proliferation and death are only partial components. Indeed, the kinetics of a cell population is also influenced by recirculation to lymphoid organs, in which proliferation is thought to primarily occur, at least under normal or chronic conditions. Our initial experiments based on BrdU kinetics thus pertained mainly to cells in lymphoid tissues leading to an apparent discrepancy; i.e., the imbalance created by the net increase in proliferation in the absence of compensating cell death was estimated at 7% growth in a day (7). Since this considerable growth rate was not reflected by an increase in the corresponding lymphocyte numbers, other regulatory mechanisms, including a reduction of recirculation through the lymph node, as well as massive elimination of cells in other tissues, could play a role. On the basis of CFSE labeling of peripheral blood leukocytes, we demonstrate here that the latter mechanism is an important factor during chronic BLV infection. Collectively, observations deduced from BrdU and CFSE kinetics can tentatively be summarized in a global model (Fig. 5B). Quantification of the dynamic parameters by the two approaches shows that the excess proliferation in lymphoid organs can be compensated for by increased cell death in the peripheral blood. In fact, immunophenotyping of the cell populations involved adds another level of complexity. CD11b– B lymphocytes recirculate efficiently via the lymph nodes; cells lacking this marker are mostly restricted to the peripheral blood and spleen (14). This is consistent with previous reports showing that the recirculating subpopulation has the phenotype CD11b– CD21+ L-selectin+ CD5– and is detected in efferent lymph (23, 35). Interestingly, expression of CD11b also specifically correlates with the particular CFSE kinetics observed in BLV-infected sheep (Fig. 3). Since CD11b+ B lymphocytes preferentially accumulate while disease progresses (5), the increased death rate of this population could appear paradoxical. However, it should be noted that CFSE kinetics pertains to CD11b+ cells exclusively labeled within the peripheral blood but not in the white pulp of the spleen. Indeed, cells do not stain fluorescently in spleen biopsy material isolated at 30 min after CFSE injection (see Fig. S2 in the supplemental material). We therefore hypothesize that the CD11b+ B-cell death in the peripheral blood is compensated for by an excess in proliferation occurring in the spleen follicles, a parameter that remains to be precisely quantified in this particular organ.

Since 11.9% of the B cells from the peripheral blood pool disappear each day in BLV-infected sheep, compared to 5.2% in controls, the CFSE kinetics reveals a very dynamic process in a rather chronic disease lasting several months (if not years) before transformed lymphocytes finally accumulate at the final leukemic stage. Furthermore, there is also a clear trend toward excessive proliferation but this difference is not statistically significant (0.039 ± 0.003 versus 0.029 ± 0.017 in the controls). Among a series of plausible hypotheses that cannot be formally excluded, one of the possible models is that the increased turnover results from an activated immune response directed toward the virus. Continuous expression of viral antigens could indeed exacerbate proliferation of virus-reactive immune cells either directly or via cytokines and thus also potentially BLV-infected B lymphocytes. Excessive proliferation of uninfected B lymphocytes in response to BLV infection has recently been clearly documented (10). Whether a similar antiviral process is also responsible for expansion of BLV-infected B cells is unknown. Arguments against this hypothetical mechanism of indirect viral spread include the absence of a selective growth advantage conferred on infected cells. Why would a viral antigen-specific B cell be preferentially infected by the virus? We therefore favor a model in which the virus plays an active role by continuously expressing viral proteins, like that encoded by the tax oncogene, able to promote cell proliferation. The oncogenic potential of Tax, which has been extensively exemplified in numerous systems (13, 17, 26, 30, 32), would favor replication of the infected cell. Indirectly, permanent tax expression would also concomitantly stimulate the antiviral immune response, which in turn would clear the infected cells. Shutoff of viral expression by viral accessory proteins (24) would then allow a minority of these cells to escape the immune response. Since very few lymphocytes expressing viral proteins can be directly observed in vivo (18, 19), the frequency of infected cells surviving the host immune pressure is low. Also, this process would only marginally affect the very large majority of infected cells containing a silent virus (or a less frequently expressed virus). The net outcome of this model would be global stability of the proviral loads, with some fluctuations of individual clones, as revealed by long-term follow-up of proviral integration sites by ligation-mediated PCR (20, 21). Although still hypothetical, this model best reconciles all of the currently available evidence, i.e., the oncogenic potential of Tax (13, 17, 26, 30, 32), the permanent stimulation of the immune system, the low levels of detectable cells expressing viral proteins in vivo, the apparent stability of individual proviral clones, and the CFSE kinetics reported here.


   ACKNOWLEDGMENTS
 
We thank the Belgian Foundation against Cancer, the 6th framework program INCA project of the European Union (LSHC-CT-2005-018704), the Bekales Foundation, the Fortis Bank Assurance, the Fonds National de la Recherche Scientifique (FNRS), the Leverhulme Trust, and the Interuniversity Attraction Poles Programme—Belgian Science Policy P4/30 for financial support. C.D. (postdoctoral researcher), N.G. (Télévie fellow), A.F. (research fellow), M.B. (FRIA fellow), R.K., and L.W. (research directors) are members of the FNRS.

We are grateful to Patrice Urbain and Samy Ilunga Nyarusoke for experimental assistance. The antibodies were kindly provided by K. Walravens (CODA/CERVA, Uccle, Belgium), J. J. Letesson (FUNDP, Namur, Belgium), D. Portetelle (FSAGx, Gembloux, Belgium), and C. Howard (Institute for Animal Health, Compton, United Kingdom).


   FOOTNOTES
 
* Corresponding author. Mailing address: National Fund for Scientific Research, Molecular and Cellular Biology Laboratory, 13 avenue Maréchal Juin, 5030 Gembloux, Belgium. Phone: 32-81-622157. Fax: 32-81-613888. E-mail: willems.l{at}fsagx.ac.be. Back

{dagger} Supplemental material for this article may be found at http://jvi.asm.org/. Back


   REFERENCES
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

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Journal of Virology, October 2006, p. 9710-9719, Vol. 80, No. 19
0022-538X/06/$08.00+0     doi:10.1128/JVI.01022-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



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