INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

Bovine leukemia virus (BLV) is among the most widespread livestock pathogens in the United States. A recent comprehensive survey revealed that 89% of dairy operations in the United States, and 41 to 47% of all dairy cattle, are infected with BLV (25). Despite a continued effort to link immune responses against BLV and development of the nonbenign states of enzootic bovine leukosis (EBL) (i.e., persistent lymphocytic [PL] state and tumor development), the role of cell-mediated immunity remains enigmatic. Yet, the host must keep the number of BLV-positive (BLV⁺) cells from accumulating, as two-thirds of infected cattle remain in the benign alymphocytic (AL) state of infection. Due to the protracted pathology of EBL in cattle, most investigations of BLV pathogenesis have been done in sheep. In contrast, we chose to pursue the role of cellular cytotoxicity in the natural host, cattle. Consequently, the extended latency of BLV dictated the use of a cross-sectional study, comparing groups of cattle that had remained in their state of infection for an extended period of time. This study was designed to address whether the state of infection correlated with a specific immune response.

In BLV investigations using sheep, proviral integration and an increase in circulating CD8⁺ lymphocytes precede seroconversion (60). In the sheep model, identification of specific CD4 and CD8 T-cell epitopes (19) and protection against BLV challenge (38, 39, 42) have been demonstrated after rVVenv inoculation. Furthermore, peptide immunizations have also been shown protective against BLV infection in sheep (24). The picture is less defined in cattle. While several immunization studies in cattle have induced (2, 31) or failed to produce (6, 48) protection, none of these studies addressed the role of cellular cytotoxicity. Also, in cattle, class I and class II BoLA haplotypes show some correlation with state of infection (12, 32, 62, 64). However, an actual effector population of cellular cytotoxicity against components of BLV has not been identified in cattle.

A functional role of ⁺ T cells in response to pathogens in cattle is still poorly defined. ⁺ T lymphocytes in ruminants express a diverse repertoire of the T-cell receptor (TcR) (22, 23), and ruminants have an unusually high number of ⁺ cells in circulation as well as in certain tissues (9). The possible connection between a ⁺ T-cell response and the ability of most BLV-infected animals to avoid severe disease has not been addressed. ⁺ T cells have been shown to mount cytotoxic, cytokine, and proliferative responses in several other viral infections. Most relevant to the present study is herpes simplex virus infection, where ⁺ T cells have been shown to directly recognize the gI protein (51) and also correlate with protection (30, 51, 52). In addition, ⁺ T cells are notably activated in cytomegalovirus (14), influenza virus (26), and Sendai virus (37) infections and, importantly, in several bovine viral infections such as those caused by bovine respiratory syncytial virus (50), bovine herpesvirus 1 (47), and foot-and-mouth disease virus (3). Activated ⁺ T cells are also evident during simian and human immunodeficiency virus (SIV and HIV) infections, although their presence does not necessarily correlate with protection (63; reviewed in reference 41), and activated ⁺ T cells in SIV and HIV infections also react to certain cells lines (17, 57; reviewed in references 8 and 28).

Human T-lymphotropic virus type 1 (HTLV-1) is genetically and structurally closely related to BLV. However, the immune responses to these viruses may require separate consideration, as no report links (HTLV-1) and ⁺ T-cell responses. First, HTLV-1 infects T cells in humans, while BLV infects B cells in cattle. Inherently, the potential for affecting the immune system varies when a different lymphocyte population is the major target for infection. Second, the -TcR repertoire in cattle is much greater than in humans (23), allowing for a more diversified ⁺ T-cell response in cattle.

Here, we test the hypothesis that AL cattle possess lymphocytes capable of lysing cells expressing BLV antigen. The results demonstrate that cytotoxic ⁺ T lymphocytes of the natural host, cattle, recognize both autologous and xenogeneic target cells expressing BLV env but not irrelevant viral antigen (wild-type vaccinia virus). Additionally, this response is not seen in cattle that are BLV negative (BLV) or PL, suggesting that these ⁺ cytotoxic T lymphocytes (CTLs) are intimately connected to BLV pathogenesis.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Classification of BLV and AL animals. Delineation between infectious states of naturally BLV-infected cattle used previously established criteria (1) of total white blood cell (WBC) counts and agar gel immunodiffusion (AGID) analysis. Four BLV, five BLV⁺ AL, and five BLV⁺ PL adult cattle used in this investigation are listed in Table 1. Briefly, BLV cattle were free of serum antibody to BLV and had no integrated provirus as seen by PCR of the pol gene (4). AL cattle were seropositive and carried BLV provirus. In contrast to AL animals, which had WBC and B-cell counts similar to those of BLV animals, PL animals had elevated numbers of WBC and circulating B cells. All BLV⁺ cattle had remained unchanged in status for 5 to 8 years.

Flow cytometry for surface markers. Briefly, mouse monoclonal antibodies (MAbs) specific to bovine surface markers were incubated with 10⁶ cells for 90 min at room temperature. Cells were washed three times with phosphate-buffered saline (PBS) and incubated with fluorescein isothiocyanate-conjugated goat anti-mouse immunoglobulin G (IgG; heavy plus light chain) for 90 min at room temperature. Cells were washed three times with PBS, fixed in 1% paraformaldehyde in PBS, and analyzed on an EPICS Profile II (Coulter Corp., Miami, Fla.) within 5 days. Antibodies to CD2 (ILA42), CD4 (ILA11), CD8 (ILA51), and IgM (ILA30) (27), from the American Type Culture Collection (Manassas, Va.), and -TcR1 subset (86D) (33), from the European Collection of Animal Cell Culture (Salisbury, United Kingdom), were produced from purchased hybridomas, while the pan--TcR MAb GD3.8 (61) was kindly provided by the laboratory of Mark Jutila (Bozeman, Mont.). Both 86D, which recognizes an external epitope, and GD3.8 -specific antibodies immunoprecipitate 38- and 40-kDa peptides, supporting TcR1 specificity. Another CD8 MAb (38-65) from the First International Antibody Workshop (27) was available in our lab. Two-color flow cytometry was performed similarly, with the addition of a 20-min preincubation with Fc Block (PharMingen, San Diego, Calif.) to eliminate interference from Fc receptor expression. Biotinylated MAbs were added at preoptimized concentrations followed by strepavidin-phycoerythrin conjugate. Cells were analyzed the same day or fixed in 1% paraformaldehyde and analyzed within 5 days.

Cell culture of hybridomas, target cell lines, PBM cells, and autologous fibroblast lines. All cells were maintained in complete RPMI 1640 (cRPMI) supplemented with either 5% (cRPMI-5) or 10% (cRPMI-10) fetal calf serum (FBS; Sigma, St. Louis, Mo.). Before use, each lot of serum was verified free of detectable anti-BLV antibody by the AGID assay. Hybridomas were grown in cRPMI-5. Peripheral blood mononuclear (PBM) cells were isolated and cultured as described below ("Effector cell expansion protocol"). Primary autologous fibroblast cultures used for target cells were established from skin biopsies of each AL and BLV animal studied and were either used directly or frozen at 70°C in 10% dimethyl sulfoxide in FBS. Briefly, minced skin sections were cultured for 10 to 14 days, and outwardly migrating fibroblasts were collected for an initial expansion of three to four passages, at which point aliquots were frozen in liquid nitrogen to allow for retrieval of early passages. In general, fibroblasts could be passaged more than 30 times before senescence (approximately 100 generations). D17 cells (canine osteosarcoma; obtained from the lab of Howard Temin) were maintained in cRPMI-5.

Recombinant and wild-type vaccinia virus preparation. Wild-type vaccinia virus and recombinant vaccinia virus expressing the BLV env gene (rVVenv) were kindly provided by Misao Onuma (39) and Virogenetics, Inc. (Troy, N.Y.). New viral working stocks were produced by infecting a monolayer of Vero cells with the original virus preparations at a multiplicity of infection of 2 and culturing the cells in cRPMI-10 for 5 days. The infected cells were pelleted for 10 min at 250 × g in a preparative centrifuge, and the pellet was freeze-thawed three times. Prior to use, viral stocks were trypsinized for 30 min at 37°C. Viral titer was determined using a standard plaque assay. Tenfold dilutions of vaccinia virus were added to monolayers of either Vero cells or autologous fibroblasts in cRPMI without FBS for 2 h. An equal volume of cRPMI-10 was then added to each well, and the plates were incubated for 3 to 4 days; then the culture medium was removed, and the cells were stained with 1% crystal violet (Roboz Surgical Instrument Co., Washington, D.C.). Similar PFU for a given virus preparation were observed with Vero cells or autologous fibroblasts (data not shown). Viral stocks were kept at 4°C or frozen at 70°C, depending on length of storage before use.

Effector cell expansion protocol. Heparinized blood was obtained by jugular venipuncture from normal and infected adult Holstein females. PBM cells were isolated over IsoPrep (Robbins Scientific, Bloomington, N.J.) at 1,400 × g for 30 min, washed three times with PBS, resuspended in 25 ml of cRPMI-10, and incubated at 1 × 10⁶ to 2 × 10⁶/ml for 2 h in a 162-cm² tissue culture flask. Adherent cells were then discarded; nonadherent cells were transferred to a standing 75-cm² tissue culture flask and incubated for 3 days, after which 25 ml of cRPMI-10 with 50 U of recombinant human interleukin-2 (rhIL-2) per ml was added. Expansion was continued for 7 to 9 days; then viable cells were isolated over IsoPrep and used in cytotoxicity assays. Short-term cell lines were restimulated on a similar culture cycle. Briefly, viable cells were isolated from the expansion culture and combined with autologous irradiated PBM cells (3,500 rad) for 2 to 3 days; then rhIL-2 (25 U/ml; half the concentration used in the initial expansion) was added for another 7 to 9 days. Lines remained viable in sufficient numbers for use in assays for four to six cycles of restimulation. Although IL-12 can elicit ⁺ T cells, we have shown that macrophages from AL animals produce prostaglandin E₂, which can inhibit in vitro expansion of ⁺ T cells (46).

Cytotoxicity assays. Autologous fibroblasts, uninfected or infected with vaccinia virus vectors (multiplicity of infection of 5) for 12 to 18 h, were trypsinized, rinsed, and labeled with 1 µCi of Na⁵¹CrO₄ per 2,000 cells in cRPMI for 45 min. As target cells, autologous fibroblasts and D17 cells were >95 and 99% viable (by trypan blue exclusion), respectively, at 36 h of infection (data not shown). Using immunofluorescence, rVVenv-infected cells were approximately 80% positive for vaccinia virus antigen 12 h postinfection (data not shown). After labeling, targets were washed three times with PBS and resuspended in cRPMI-10; then 5,000 cells were added per well in 96-well plates for the assay. Gradient-purified effector cells were added at various effector-to-target (E:T) ratios, with a final volume of 200 µl. Plates were spun for 3 min at 150 × g before and after the 6-h assay. Supernatants were transferred to tubes and counted using a gamma counter.

Depletion of CD8⁺ and ⁺ T cells from the effector population. Using MAbs to CD8, CD4, and -TcR, specific subpopulations were depleted by complement lysis or two rounds of panning as adapted from previously published protocols (16, 34). Briefly, complement lysis was accomplished by incubating the population with a preoptimized amount of MAb on ice for 1 h in cRPMI. A final volume of 33% rabbit complement (Cedarlane, Hornby, Ontario, Canada) was added, and incubation continued with rotation for 1 h at 37°C; then cell debris was allowed to settle for 5 min on ice. Suspended cells were washed three times in cRPMI and adjusted to desired concentrations in cRPMI-10. Alternatively, plastic culture dishes were coated with MAb diluted in PBS with 1% bovine serum albumin at 4°C overnight and were washed five times with PBS before use. Cells were allowed to adhere to the plate for 1 h at room temperature. Nonadherent cells were transferred to a second plate, and the incubation was repeated. CD8 and CD4 depletions were done by complement lysis (MAb 38-65 [IgG2a] and ILA11 [IgG2a], respectively) and depletions by two rounds of panning (MAb 86D [IgG1]). Following depletions, the remaining cells were washed three times and resuspended to the original volume with cRPMI-10.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

⁺ T-lymphocyte expansion from PBM cells is unique to AL animals. Because the majority of BLV-infected cattle remain in the benign AL state of infection, BLV-specific T cells may limit viral infection. To address the hypothesis that antigen-reactive effector cells could be expanded from BLV⁺ but not BLV animals, PBM cells were cultured in vitro. T-cell proliferation is composed of two phases, antigen-specific activation resulting in up-regulated IL-2 receptor expression followed by IL-2-dependent expansion of activated cells (5). The distribution of phenotypes of freshly isolated and cultured populations from BLV, AL, and PL cattle is shown in Table 2. Preexpansion cell populations were similar in both AL and BLV animals, although AL animals had more CD4⁺ and CD2⁺ cells than either BLV or PL animals. Further analysis of these CD markers was not done. PL cattle showed the symptomatic increase in B cells. However, following the 10- to 12-day expansion in the presence of endogenously expressed BLV and rhIL-2, AL animals had a significantly higher proportion of ⁺ T lymphocytes than either BLV (P < 0.001) or PL (P < 0.001) animals, suggesting that activation of T cells by BLV followed by IL-2 expansion of antigen-specific T cells occurs preferentially in the cells from AL animals. The postexpansion cultures from BLV and PL cattle did not contain statistically different numbers of ⁺ T cells (P > 0.025). While the relative numbers of CD4⁺ cells also increased slightly in all groups, the proportion of CD8⁺ cells in AL animals decreased in contrast to both BLV (P < 0.001) and PL animals (P < 0.001). Typically, expansion of cells from BLV-free cattle yielded few viable cells, presumably due to the lack of antigen-specific stimulation during the first 3 days of in vitro culture.

View this table: [in this window] [in a new window]   TABLE 2.   Surface phenotypes of PBM cells from BLV, AL, and PL cattle

In vitro expansion of AL PBM cells yields an Env-reactive cytotoxic population. To examine the function of the expanded cell populations, autologous fibroblasts were used as targets to assess cytotoxic ability. Expression of rVVenv in target cells was confirmed by intracellular immunofluorescence and Western blot analysis using polyclonal anti-vaccinia virus serum and anti-gp51 MAbs, respectively (data not shown). Cytolytic activity against autologous fibroblasts infected with rVVenv but not against wild-type vaccinia virus was detected in expanded populations from AL animals (Fig. 1A). In seven different experiments with five different AL animals and three BLV animals, the Env-specific lysis by cells from AL animals ranged from 30 to 65%, while cells from uninfected animals failed to lyse the target cells (less than 5%). Despite the expansion of mainly CD8⁺ T cells from BLV animals on three occasions (Table 2), those effectors were not able to lyse rVVenv-expressing autologous fibroblasts (Fig. 1B).

View larger version (16K): [in this window] [in a new window]   FIG. 1.   Cytotolysis of rVVenv-expressing autologous fibroblasts by expanded PBM cells from AL animal 17 (A) and BLV animal 4205 (B). Targets were either infected with rVVenv (triangles) or wild-type vaccinia virus (circles) or uninfected (squares) in a 6-h 51Cr release assay. Spontaneous release was less than 30%, and all determinations were performed in triplicate. The data are representative of seven experiments with three different AL animals and two different BLV animals. Standard deviations were less than 5% for all data points.

Depletion of ⁺, but not CD8⁺ and CD4⁺, T lymphocytes reduces Env-specific lysis in AL animals. To determine the T-lymphocyte population responsible for the observed lysis, CD8⁺ and/or ⁺ T lymphocytes were depleted in the postexpansion effector populations. A reduction of cytotoxicity resulted when ⁺ cells were removed (Fig. 2). Treatment with MAb 86D, which recognizes 50 to 70% of ⁺ T cells in the expanded populations, caused an approximate 50% reduction in lysis of env-expressing target cells, suggesting the involvement of ⁺ T cells. Depletion of CD8⁺ T cells or CD4⁺ and CD8⁺ T cells, to remove the -TcR population and address the role of -TcR cells in BLV cytotoxicity, did not alter Env-specific lysis (Fig. 2). Thus, BLV-infected animals in the AL state of infection possess ⁺ T cells that lyse env-expressing target cells, while BLV animals did not have detectable cytotoxic ⁺ T cells.

View larger version (31K): [in this window] [in a new window]   FIG. 2.   Cytotolysis of rVVenv-expressing autologous fibroblasts by expanded PBM cell subsets from two AL animals, 17 (A) and 201 (B). The assay was performed as for Fig. 1, at E:T ratios of 50:1 (A) and 30:1 (B). Target cells were either infected with rVVenv (filled) or wild-type vaccinia virus (hatched) or uninfected (clear). Spontaneous release was less than 30%, and all determinations were performed in triplicate. The data are representative of two experiments with two different AL animals. See Materials and Methods for depletion protocols.

Expanded AL effectors are not classically MHC restricted. Previously, NK-like cell lines from cattle (40) were shown to lyse bovine herpesvirus 1-infected D17 cells (a canine osteosarcoma cell line). The vast majority of cells in that study were ⁺ T cells, which prompted us to test the cytolytic activity of the AL-derived effectors against several common target cell lines. Effectors expanded from AL animals would not kill K562, YAC-1, Daudi, Vero, NMU, or COLO cells (data not shown). However, similar to autologous fibroblasts (Fig. 1), D17 cells were also lysed by AL-derived effector cells when infected with rVVenv (Fig. 3). Minimal lysis of wild-type vaccinia virus-infected and uninfected D17 cells was noted at the highest E:T ratio (<10% specific lysis). The phenotypic distribution of the effector populations used in Fig. 3 are shown in Table 3. The use of D17 cells consequently allows comparison of animals in different states of infection using a single target population, while focusing the examination on major histocompatibility complex (MHC)-nonrestricted cytotoxicity. Thus, as expected, cytolytic ⁺ T cells from BLV-infected animals in the AL state are not classically MHC restricted. Interestingly, PL animals possess higher numbers of BLV-producing cells in vivo (18), and in vitro demonstration of BLV antigens is much enhanced using cells from PL animals compared to AL animals (15). Therefore, based on BLV antigen availability in culture, ⁺ T-cell expansion and cytotoxicity should be greater in cells from PL animals. This outcome was not observed in Table 2 and Fig. 3, suggesting only cytotoxic ⁺ T cells from AL animals recognize BLV Env.

View larger version (15K): [in this window] [in a new window]   FIG. 3.   Cytotolysis of rVVenv-expressing D17 cells by short-term cell lines (culture and one restimulation) from AL animal 17 (A), PL animal 2 (B), and BLV animal 602 (C). Targets were either uninfected (squares) or infected with wild-type vaccinia virus (circles) or rVVenv (triangles) and used in a 6-h 51Cr release assay. Spontaneous release was less than 30%, and all determinations were performed in triplicate. The data are representative of two experiments with two different AL animals, two different BLV animals, and three different PL animals. Standard deviations were less than 5% for all data points.

Restimulated AL cell lines retain their ability to lyse rVVenv-expressing targets. Since culture of PBM cells from AL animals evoked a cytotoxic effector population, the cultured cells were restimulated to assess continued antigen specificity and enrichment for cytotoxicity. Indeed, Fig. 4 shows that short-term cell lines were capable of substantial (50 to 100%) lysis after three to four rounds of restimulation. Although individual cultures varied in their relative lysis of rVVenv and wild-type vaccinia virus-infected targets, specific cytotoxicity remained high with continued in vitro culture (Fig. 4).

View larger version (23K): [in this window] [in a new window]   FIG. 4.   Env-specific lysis of rVVenv-infected D17 cells by short-term T-cell lines from animal 201. Lines were restimulated three to four times with irradiated PBM cells and 25 U of rhIL-2 per ml after initial expansion culture (nx). Independently derived 3-week cultures are given the letters A, B, and C. D17 cells were infected with either rVVenv (solid) or wild-type vaccinia virus (hatched). Spontaneous release was less than 35%, and determinations were done in triplicate at an E:T ratio of 20:1. The data are representative of two restimulation experiments for this animal.

Cell lines from AL animals are unique in their lysis of rVVenv-expressing targets. To test whether in vitro restimulation results in cytotoxic ⁺ T cells regardless of state of infection, cell lines from animals in all three categories were tested for cytotoxic ability. Figure 5 shows that restimulated AL-derived cell lines lysed rVVenv-expressing D17 cells, while cell lines from BLV and PL animals did not (Fig. 5). Cells from one AL animal (animal 4) rarely lysed rVVenv-expressing targets after initial PBM cell expansion. However, following repeated restimulation, cells from this AL animal also showed high env-specific lysis (Fig. 6). Therefore, cattle in the AL state of infection possess cells capable of lysing cells that express a BLV antigen; in contrast, animals in the PL state of infection, as well as uninfected animals, do not have cytotoxic cells specific for BLV antigens.

View larger version (21K): [in this window] [in a new window]   FIG. 5.   rVVenv-specific lysis of D17 target cells by restimulated lines from AL but not from BLV or PL animals. Lines were restimulated one to four times with irradiated PBM cells and 25 U of rhIL-2 per ml after initial expansion culture. D17 cells were infected with either rVVenv (solid) or wild-type vaccinia virus (hatched). Two BLV (A, 920-3x; B, 920-2x), seven AL (C, 4-4x; D, 17-4x; E, 17-3x; F, 17-2x; G, 201-2x; H, 201-1x; I, 234-1x), and seven PL (J, 019-3x; K, 019-2x; L, 019-1x; M, 2-3x; N, 2-1x; O, 191-3x; P, 191-1x) cell lines were used. The cell lines are representative of a larger pool tested, and sequential numbers do not necessarily refer to a continuous restimulation culture. Spontaneous release was less than 30%, and determinations were done in triplicate at an E:T ratio of 30:1. The data are representative of two restimulation experiments.

View larger version (20K): [in this window] [in a new window]   FIG. 6.   rVVenv-specific lysis of D17 target cells by restimulated lines from AL animal 4 despite insignificant lysis after first culture. Effector populations were either cultured once from PBM cells (cultured) or subsequently restimulated two (4-2x) or four (4-4x) times with irradiated PBM cells and 25 U of rhIL-2 per ml after initial culture. D17 cells were infected with either rVVenv (solid) or wild-type vaccinia virus (hatched). Spontaneous release was less than 25%, and determinations were done in triplicate at an E:T ratio of 20:1.

⁺ T cells in restimulated AL cell lines increase in relative number and correlate with cytotoxicity. Because others have observed an increase in CD2 ⁺ T cells in BLV⁺ cattle (54), and the expanded ⁺ cells from AL animals may be CD2 (Table 2), we determined if cells of this phenotype from AL animals were expanded. The phenotypes of cell lines restimulated one to five times (Table 4) were compared for their cytotoxic potential (Fig. 7A). Increasing numbers of ⁺ T cells correlated with the level of cytotoxicity. Conversely, the number of CD8⁺ T cells declined more than 6-fold (Table 4), while env cytotoxicity increased nearly 10-fold (Fig. 7A). Additionally, when we determined the coexpression of CD2 and the -TcR, a correlation between increased cytotoxicity and the number of ⁺ T cells that were CD2 was equally striking (Fig. 7B), suggesting the phenotype of the cytotoxic cell is ⁺ CD2. Similar findings between CD2 ⁺ T cells and increasing cytotoxicity were evident for long-term-cultured cell lines from two other AL animals. The findings from this experiment further support the role of ⁺ T cells from the AL state of infection are responsible for in vitro lysis of cells expressing a BLV antigen.

View larger version (21K): [in this window] [in a new window]   FIG. 7.   Cytotoxic activity against rVVenv-infected D17 cells correlated with CD2 + T cells in cell lines. Short-term cell lines from animal 17 (17-1x, 17-2x, 17-3x, and 17-4x) were restimulated with irradiated PBM cells one, two, three, and four times, respectively. For flow cytometry data on these lines, see Table 4. These are the aggregate data on sequential restimulations of the same culture. (A) Increase in cytolytic activity against rVVenv-infected (filled) but not wild-type vaccinia virus-infected (hatched) D17 cells with each restimulation. Spontaneous release was less than 30%, and determinations were done in triplicate at an E:T ratio of 20:1. (B) Increase in percent CD2 + T cells of total + T cells with each restimulation.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

BLV is among the most persistent pathogens in cattle, whose immune system, like that of all ruminants, is unique in its ⁺ T-cell prevalence and diversity. Despite these two distinct phenomena, the relevance of ⁺ T cells to BLV pathogenesis has not been thoroughly explored. To address this lack of understanding, we determined if ⁺ T cells from BLV-infected animals could recognize cells expressing components of BLV. A large proportion of the expanded effector cell population from adult AL animals were -TcR positive. These ⁺ T cells were cytotoxic to rVVenv-expressing target cells. In contrast to the AL animals, PBM cells from BLV animals typically failed to survive in parallel cultures. Only approximately 1/10 of the number of the cells survived in 3 of 8 attempted BLV cultures, compared to the constant recovery of cells from each of 10 AL and 10 PL cultures (Table 2). Furthermore, cultures from PL animals contained approximately equal numbers of B cells, CD4⁺ T cells, and CD8⁺ T cells, all being threefold more prevalent than ⁺ T cells, and these PL-derived effectors failed to lyse rVVenv-expressing target cells.

The role of ⁺ T cells in ruminants may extend beyond the proposed role of complementing ⁺ T cells suggested for primates (58). The prominence of ⁺ T cells in our in vitro studies and the high proficiency of BLV-specific CTL activity suggests that ⁺ CTL play a significant role in controlling BLV infection in the AL state. The lack of this reactive ⁺ CTL population in PL animals implies that ⁺ T cells are intimately connected to BLV pathogenesis. To our knowledge, this is the first time that ⁺ T cells have been shown to respond specifically to retroviral proteins in ruminants.

Depletion of CD8⁺, CD4⁺, and ⁺ cells indicated that ⁺ cells expanded from AL animals were largely responsible for the target cell lysis. Additionally, the cytotoxicity to Env was not MHC restricted, as evidenced by the lysis of rVVenv-infected D17 cells (Fig. 3). However, expanded PBM cells from AL cattle typically showed no significant cytotoxicity against noninfected and wild-type vaccinia virus-infected autologous target cells, indicating that the cytotoxicity was not the result of NK cells. Cultured cells from AL animals also contained a large proportion of CD4⁺ T lymphocytes, while CD8⁺ T lymphocytes comprised less than a third of the ⁺ T-lymphocyte population. While the 10 to 20% CD8⁺ T lymphocytes may be responsible for the high levels of cytotoxicity observed, depletion of CD8⁺ effector cells did not alter cytotoxicity (Fig. 2), and reduction in CD8⁺ cells occurred while cytotoxicity increased in the short-term cell lines (Table 4 and Fig. 7). Also, the substantially higher levels of CD8⁺ T cells in BLV and PL cattle following culture was not accompanied by increased cytotoxicity (Fig. 3, Fig. 5, and data not shown). The relatively large proportion (>35%) of CD4⁺ T lymphocytes in expanded cultures from AL animals would be additional candidates for cytotoxic effector cells. However, CD4⁺ CTLs are MHC class II restricted (reviewed in reference 21), while autologous fibroblast targets are MHC class II negative and D17 cells are xenogeneic to cattle. Recently, ⁺ T cells were reported to present antigen and stimulate CD4⁺ cells (10). This possiblity would explain the continued presence of CD4⁺ cells in our cultures (Tables 2 to 4). Alternatively, there may be a reciprocal relationship between CD4⁺ and ⁺ cells that is required for ⁺ cell expansion and/or cytotoxicity. Also, CD4⁺ cells may be stimulated nonspecifically in culture through the presence of endogenous IL-2 or other cytokines. Although investigation regarding the continued CD4⁺ T-cell presence in culture was beyond the scope of this study, depletion of CD4⁺ T cells did not affect cytotoxicity in our system (Fig. 2); moreover, despite large proportions (26 to 61%) of CD4⁺ cells in cell lines from BLV and PL animals, these effector populations were not cytotoxic (Table 3, Fig. 3, and data not shown).

Since CD4⁺ and CD8⁺ cells are primarily CD2⁺, the single surface marker staining in Table 2 suggests that cultured cells from AL animals increase in ⁺ cells but not in CD2⁺ cells. Additionally, CD2 ⁺ cells increase in BLV⁺ cattle (54), and we show here that loss of CD2 expression on ⁺ T cells correlated with restimulation of effector cells concomitantly with increased cytotoxicity (Table 4 and Fig. 7). However, decreasing CD2⁺ cells over time may be a consequence of CD2-mediated apoptosis (55). Future experiments should address the relevance of this ⁺ subpopulation in the rVVenv-specific cytotoxic response. In all cytotoxicity assays, the relative numbers of cell subsets, TcR-N3, TcR-N4, TcR-N6, TcR-N7, TcR-N12 (13), and 86D, were determined, but none of these populations demonstrated a correlation with BLV infection status or cytotoxicity in cultured cell populations (data not shown). The exclusive role for ⁺ CTLs is corroborated by the lysis of D17 targets expressing BLV proteins, where a conventional coreceptor model cannot explain the data. While an apparent lack of MHC restriction was observed, nonclassical presentation molecules (such as CD1) cannot be excluded. However, recognition of nonclassical MHC molecules by bovine ⁺-TcR has not been shown to date and may be an unlikely explanation.

Occasionally, AL animals in this study had slightly elevated levels of circulating ⁺ cells relative to noninfected control animals, but the increase was not statistically significant (Table 2). However, the BLV animals used in this study had a slightly higher number of circulating ⁺ cells than previously reported (18), possibly due to the lack of a specific pan--TcR MAb in the earlier study.

Considering that BLV mRNA can be detected ex vivo in sheep (43), the immune system of infected cattle may encounter BLV antigen with relative frequency despite the extended latency of BLV in cattle. Indeed, individual cells of cattle have been shown to express BLV mRNA in vivo (20). In the sheep model, periodic appearance of Rex-specific antibodies and sustained antibodies against other BLV components was detected (43), implying opportunity for repeated contact with BLV antigen and repeated stimulation of BLV-specific ⁺ T cells. Although disease development in cattle is not precisely mimicked by sheep, infected cattle similarly remain seropositive and proviral DNA can be found throughout life. Furthermore, endogenous BLV antigen is produced by B cells from cattle during in vitro culture (references 1, 15, and 29 and data not shown), providing a source of BLV antigen for ⁺ T cells.

In HIV, V9/V2 T-cell responses to HIV-infected targets exist in both uninfected and infected individuals (59), but these cells are diverse in the complementarity-determining region 3 of the TcR and also recognize other virus-infected cells. We have no evidence that the ⁺ T cells identified in this study are similarly limited in chain expression, but they recognize neither wild-type vaccinia virus-infected targets nor any of several common cell lines in our cytotoxicity assay. In HIV-negative humans, V9/V2⁺ T cells recognize HIV- or SIV-infected cells and Daudi cells without a requirement for prior activation (7; reviewed in reference 57), suggesting that antigen-specific stimulation may not be necessary for antiretroviral activity. Additionally, V9/V2⁺ T cells from HIV-positive individuals are functionally defective in the ability to respond to stimulation by Daudi cells and ethyl pyrophosphate (59). Similarly, in SIV, ⁺ CTLs respond to infected target cells and Daudi cells (17, 56). The extent to which the ⁺ T cells in HIV- or SIV-positive primates parallel the PBM cells from BLV⁺ cattle remains to be determined. Additionally, ⁺ CTLs have not been identified in individuals infected with HTLV-1, and the bovine ⁺ CTLs in the present study were unique to AL animals and were not reactive to Daudi cells.

Often, CTL studies use a specific antigen derived from the pathogen of interest, many times in the form of peptide-pulsed antigen-presenting cells (APC). By necessity, peptide-pulsing studies select for a CTL population capable of engaging APC surface molecules carrying the administered peptide antigen. In contrast, the present study relied on endogenous BLV as a source of antigen, followed by expansion of antigen-responsive T lymphocytes in culture. Consequently, the antigen presentation pathway is determined by natural viral expression during effector stimulation. The presence of BLV antigen and reverse transcriptase activity in culture supernatants from BLV-infected animals in this study was confirmed but not quantified (data not shown). Addition of rhIL-2 at the start of the in vitro culture or omission of rhIL-2 during the 7- to 9-day expansion phase resulted in high nonspecific or no cytotoxicity, respectively (data not shown). The use of endogenous BLV as the antigen may more accurately represent the role that BLV plays in vivo. The minimal manipulation of the cultured PBM cells more likely representative than peptide-pulsed APC stimulation in modeling what occurs as the integrated BLV provirus breaks latency.

Aside from antigen availability during culture, correlation of the AL and PL states of infection with BoLA haplotypes (12, 32, 62, 64) and cytokine profiles (36, 44-46, 54) suggests that immune responses from BLV⁺ animals are linked to cytokine production. All PBM cell cultures from BLV⁺ animals produce IL-10 over time (D. Pyeon, personal communication), and macrophages from PL cattle also secrete significant amounts of IL-10 ex vivo (45) whereas macrophages from AL animals secrete IL-12 (44). The combination of IL-2 and IL-12 has been found to elicit highly reactive human ⁺ CTLs (49). Additionally, IL-12 and IL-1 are necessary for the development and activation of ⁺ responses (53). We know from our previous work (reference 11 and data not shown) that large quantities of IL-1 are present at early stages of in vitro culture. Consequently, the choice between IL-10 and IL-12 production and/or secretion may help determine, or result from, the infection state of EBL. Similarly, reactivity to Mycobacterium tuberculosis (35) and HIV (7) by ⁺ T cells is enhanced by IL-12 and abrogated by IL-10 (35). Interestingly, the PBM cells from the less ⁺ T-cell-reactive AL animal 4 contained higher baseline levels of IL-10 mRNA ex vivo than the more reactive AL animals (Pyeon, personal communication). As shown in Fig. 6, restimulation of PBM cells from this animal and removal of macrophages as the source of IL-10 in vitro (45) overcame an initial lack of a ⁺ T-cell response, indicating that unresponsiveness was not permanent. However, under identical culture conditions, cells from PL animals did not possess rVVenv-specific cytotoxicity (Fig. 5). In conclusion, this study shows that AL cattle, but not PL cattle, are capable of eliciting Env-specific ⁺ CTLs. These CTLs are not MHC restricted and may recognize the BLV protein directly. Defining the role of this unique cell population from AL animals could be crucial to understanding the pathology of EBL.